Serbian Academy of Sciences and Arts [F193]

Link to this page

Serbian Academy of Sciences and Arts [F193]

Authors

Publications

Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications

Bihelović, Filip; Vulović, Bojan; Saičić, Radomir

(Wiley-V C H Verlag Gmbh, Weinheim, 2018)

TY  - JOUR
AU  - Bihelović, Filip
AU  - Vulović, Bojan
AU  - Saičić, Radomir
PY  - 2018
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/2156
AB  - The advent of gold catalysis has transformed hydroxyalkoxylation of alkynes - once a rudimentary, mercury(II)-, or silver(I)-catalyzed process limited to structurally simple substrates - into a sophisticated method that has found application in syntheses of highly complex organic molecules. This transformation can further be combined with carbon-carbon bond-forming reactions into domino sequences that allow for a considerable increase of molecular complexity within a single synthetic step. Some recent examples of the development and synthetic applications of these reactions are provided.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - Israel Journal of Chemistry
T1  - Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications
VL  - 58
IS  - 5
SP  - 521
EP  - 530
DO  - 10.1002/ijch.201700033
ER  - 
@article{
author = "Bihelović, Filip and Vulović, Bojan and Saičić, Radomir",
year = "2018",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2156",
abstract = "The advent of gold catalysis has transformed hydroxyalkoxylation of alkynes - once a rudimentary, mercury(II)-, or silver(I)-catalyzed process limited to structurally simple substrates - into a sophisticated method that has found application in syntheses of highly complex organic molecules. This transformation can further be combined with carbon-carbon bond-forming reactions into domino sequences that allow for a considerable increase of molecular complexity within a single synthetic step. Some recent examples of the development and synthetic applications of these reactions are provided.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "Israel Journal of Chemistry",
title = "Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications",
volume = "58",
number = "5",
pages = "521-530",
doi = "10.1002/ijch.201700033"
}
Bihelović, F., Vulović, B.,& Saičić, R. (2018). Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications.
Israel Journal of Chemistry
Wiley-V C H Verlag Gmbh, Weinheim., 58(5), 521-530.
https://doi.org/10.1002/ijch.201700033
Bihelović F, Vulović B, Saičić R. Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications. Israel Journal of Chemistry. 2018;58(5):521-530
Bihelović Filip, Vulović Bojan, Saičić Radomir, "Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications" Israel Journal of Chemistry, 58, no. 5 (2018):521-530,
https://doi.org/10.1002/ijch.201700033 .
3
2
4

On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-dioxane-5-one to Acyclic Chiral alpha-Branched Aldehydes

Marjanović-Trajković, Jasna; Milanović, Vesna D.; Ferjančić, Zorana; Saičić, Radomir

(Wiley-V C H Verlag Gmbh, Weinheim, 2017)

TY  - JOUR
AU  - Marjanović-Trajković, Jasna
AU  - Milanović, Vesna D.
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2017
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/2410
AB  - Reagent stereocontrol in the proline-catalyzed aldol reaction of 2,2-dimethyl-1,3-dioxane-5-one 1 with chiral aldehydes has been investigated. Synthetically useful levels of diastereoselectivity could be achieved in reactions with acyclic chiral alpha-oxy and alpha-amino aldehydes in both matched and mismatched cases. By using this reaction as a key step, two medicinally relevant azasugars, 1-deoxy-galactonojirimycin (9) and 2,5-dideoxy-2,5-imino-d-altritol (10), were efficiently synthesized.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - European Journal of Organic Chemistry
T1  - On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-dioxane-5-one to Acyclic Chiral alpha-Branched Aldehydes
IS  - 41
SP  - 6146
EP  - 6153
DO  - 10.1002/ejoc.201701073
ER  - 
@article{
author = "Marjanović-Trajković, Jasna and Milanović, Vesna D. and Ferjančić, Zorana and Saičić, Radomir",
year = "2017",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2410",
abstract = "Reagent stereocontrol in the proline-catalyzed aldol reaction of 2,2-dimethyl-1,3-dioxane-5-one 1 with chiral aldehydes has been investigated. Synthetically useful levels of diastereoselectivity could be achieved in reactions with acyclic chiral alpha-oxy and alpha-amino aldehydes in both matched and mismatched cases. By using this reaction as a key step, two medicinally relevant azasugars, 1-deoxy-galactonojirimycin (9) and 2,5-dideoxy-2,5-imino-d-altritol (10), were efficiently synthesized.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "European Journal of Organic Chemistry",
title = "On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-dioxane-5-one to Acyclic Chiral alpha-Branched Aldehydes",
number = "41",
pages = "6146-6153",
doi = "10.1002/ejoc.201701073"
}
Marjanović-Trajković, J., Milanović, V. D., Ferjančić, Z.,& Saičić, R. (2017). On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-dioxane-5-one to Acyclic Chiral alpha-Branched Aldehydes.
European Journal of Organic Chemistry
Wiley-V C H Verlag Gmbh, Weinheim.(41), 6146-6153.
https://doi.org/10.1002/ejoc.201701073
Marjanović-Trajković J, Milanović VD, Ferjančić Z, Saičić R. On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-dioxane-5-one to Acyclic Chiral alpha-Branched Aldehydes. European Journal of Organic Chemistry. 2017;(41):6146-6153
Marjanović-Trajković Jasna, Milanović Vesna D., Ferjančić Zorana, Saičić Radomir, "On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-dioxane-5-one to Acyclic Chiral alpha-Branched Aldehydes" European Journal of Organic Chemistry, no. 41 (2017):6146-6153,
https://doi.org/10.1002/ejoc.201701073 .
1
5
4
7

A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF)

Marjanović-Trajković, Jasna; Ferjančić, Zorana; Saičić, Radomir

(Pergamon-Elsevier Science Ltd, Oxford, 2017)

TY  - JOUR
AU  - Marjanović-Trajković, Jasna
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2017
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/2452
AB  - A catalytic asymmetric synthesis of (+)-aza-galacto-fagomine (AGF) - the most promising compound for the pharmacological chaperone therapy of Krabbe disease was accomplished in six steps, in 14% overall yield. The synthesis hinges on the combination of organocatalyzed aldolization and reductive hydrazination.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron
T1  - A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF)
VL  - 73
IS  - 18
SP  - 2630
DO  - 10.1016/j.tet.2017.03.052
ER  - 
@article{
author = "Marjanović-Trajković, Jasna and Ferjančić, Zorana and Saičić, Radomir",
year = "2017",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2452",
abstract = "A catalytic asymmetric synthesis of (+)-aza-galacto-fagomine (AGF) - the most promising compound for the pharmacological chaperone therapy of Krabbe disease was accomplished in six steps, in 14% overall yield. The synthesis hinges on the combination of organocatalyzed aldolization and reductive hydrazination.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron",
title = "A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF)",
volume = "73",
number = "18",
pages = "2630",
doi = "10.1016/j.tet.2017.03.052"
}
Marjanović-Trajković, J., Ferjančić, Z.,& Saičić, R. (2017). A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF).
Tetrahedron
Pergamon-Elsevier Science Ltd, Oxford., 73(18), 2630.
https://doi.org/10.1016/j.tet.2017.03.052
Marjanović-Trajković J, Ferjančić Z, Saičić R. A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF). Tetrahedron. 2017;73(18):2630
Marjanović-Trajković Jasna, Ferjančić Zorana, Saičić Radomir, "A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF)" Tetrahedron, 73, no. 18 (2017):2630,
https://doi.org/10.1016/j.tet.2017.03.052 .
1
1
3

A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF)

Marjanović-Trajković, Jasna; Ferjančić, Zorana; Saičić, Radomir

(Pergamon-Elsevier Science Ltd, Oxford, 2017)

TY  - JOUR
AU  - Marjanović-Trajković, Jasna
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2017
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/3025
AB  - A catalytic asymmetric synthesis of (+)-aza-galacto-fagomine (AGF) - the most promising compound for the pharmacological chaperone therapy of Krabbe disease was accomplished in six steps, in 14% overall yield. The synthesis hinges on the combination of organocatalyzed aldolization and reductive hydrazination.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron
T1  - A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF)
VL  - 73
IS  - 18
SP  - 2630
DO  - 10.1016/j.tet.2017.03.052
ER  - 
@article{
author = "Marjanović-Trajković, Jasna and Ferjančić, Zorana and Saičić, Radomir",
year = "2017",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3025",
abstract = "A catalytic asymmetric synthesis of (+)-aza-galacto-fagomine (AGF) - the most promising compound for the pharmacological chaperone therapy of Krabbe disease was accomplished in six steps, in 14% overall yield. The synthesis hinges on the combination of organocatalyzed aldolization and reductive hydrazination.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron",
title = "A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF)",
volume = "73",
number = "18",
pages = "2630",
doi = "10.1016/j.tet.2017.03.052"
}
Marjanović-Trajković, J., Ferjančić, Z.,& Saičić, R. (2017). A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF).
Tetrahedron
Pergamon-Elsevier Science Ltd, Oxford., 73(18), 2630.
https://doi.org/10.1016/j.tet.2017.03.052
Marjanović-Trajković J, Ferjančić Z, Saičić R. A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF). Tetrahedron. 2017;73(18):2630
Marjanović-Trajković Jasna, Ferjančić Zorana, Saičić Radomir, "A short stereoselective synthesis of (+)-aza-galacto-fagomine (AGF)" Tetrahedron, 73, no. 18 (2017):2630,
https://doi.org/10.1016/j.tet.2017.03.052 .
1
1
3

Supplementary data for article: Marjanović-Trajković, J.; Ferjančić, Z.; Saičić, R. A Short Stereoselective Synthesis of (+)-Aza-Galacto-Fagomine (AGF). Tetrahedron 2017, 73 (18), 2630. https://doi.org/10.1016/j.tet.2017.03.052

Marjanović-Trajković, Jasna; Ferjančić, Zorana; Saičić, Radomir

(Pergamon-Elsevier Science Ltd, Oxford, 2017)

TY  - BOOK
AU  - Marjanović-Trajković, Jasna
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2017
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/3026
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron
T1  - Supplementary data for article: Marjanović-Trajković, J.; Ferjančić, Z.; Saičić, R. A Short Stereoselective Synthesis of (+)-Aza-Galacto-Fagomine (AGF). Tetrahedron 2017, 73 (18), 2630. https://doi.org/10.1016/j.tet.2017.03.052
ER  - 
@book{
author = "Marjanović-Trajković, Jasna and Ferjančić, Zorana and Saičić, Radomir",
year = "2017",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3026",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron",
title = "Supplementary data for article: Marjanović-Trajković, J.; Ferjančić, Z.; Saičić, R. A Short Stereoselective Synthesis of (+)-Aza-Galacto-Fagomine (AGF). Tetrahedron 2017, 73 (18), 2630. https://doi.org/10.1016/j.tet.2017.03.052"
}
Marjanović-Trajković, J., Ferjančić, Z.,& Saičić, R. (2017). Supplementary data for article: Marjanović-Trajković, J.; Ferjančić, Z.; Saičić, R. A Short Stereoselective Synthesis of (+)-Aza-Galacto-Fagomine (AGF). Tetrahedron 2017, 73 (18), 2630. https://doi.org/10.1016/j.tet.2017.03.052.
Tetrahedron
Pergamon-Elsevier Science Ltd, Oxford..
Marjanović-Trajković J, Ferjančić Z, Saičić R. Supplementary data for article: Marjanović-Trajković, J.; Ferjančić, Z.; Saičić, R. A Short Stereoselective Synthesis of (+)-Aza-Galacto-Fagomine (AGF). Tetrahedron 2017, 73 (18), 2630. https://doi.org/10.1016/j.tet.2017.03.052. Tetrahedron. 2017;
Marjanović-Trajković Jasna, Ferjančić Zorana, Saičić Radomir, "Supplementary data for article: Marjanović-Trajković, J.; Ferjančić, Z.; Saičić, R. A Short Stereoselective Synthesis of (+)-Aza-Galacto-Fagomine (AGF). Tetrahedron 2017, 73 (18), 2630. https://doi.org/10.1016/j.tet.2017.03.052" Tetrahedron (2017)

Supplementary data for the article: Marjanovic Trajkovic, J.; Milanovic, V.; Ferjancic, Z.; Saicic, R. N. On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-Dioxane-5-One to Acyclic Chiral α-Branched Aldehydes. European Journal of Organic Chemistry 2017, 2017 (41), 6146–6153. https://doi.org/10.1002/ejoc.201701073

Marjanović-Trajković, Jasna; Milanović, Vesna D.; Ferjančić, Zorana; Saičić, Radomir

(Wiley-V C H Verlag Gmbh, Weinheim, 2017)

TY  - BOOK
AU  - Marjanović-Trajković, Jasna
AU  - Milanović, Vesna D.
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2017
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/3229
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - European Journal of Organic Chemistry
T1  - Supplementary data for the article: Marjanovic Trajkovic, J.; Milanovic, V.; Ferjancic, Z.; Saicic, R. N. On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-Dioxane-5-One to Acyclic Chiral α-Branched Aldehydes. European Journal of Organic Chemistry 2017, 2017 (41), 6146–6153. https://doi.org/10.1002/ejoc.201701073
ER  - 
@book{
author = "Marjanović-Trajković, Jasna and Milanović, Vesna D. and Ferjančić, Zorana and Saičić, Radomir",
year = "2017",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3229",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "European Journal of Organic Chemistry",
title = "Supplementary data for the article: Marjanovic Trajkovic, J.; Milanovic, V.; Ferjancic, Z.; Saicic, R. N. On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-Dioxane-5-One to Acyclic Chiral α-Branched Aldehydes. European Journal of Organic Chemistry 2017, 2017 (41), 6146–6153. https://doi.org/10.1002/ejoc.201701073"
}
Marjanović-Trajković, J., Milanović, V. D., Ferjančić, Z.,& Saičić, R. (2017). Supplementary data for the article: Marjanovic Trajkovic, J.; Milanovic, V.; Ferjancic, Z.; Saicic, R. N. On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-Dioxane-5-One to Acyclic Chiral α-Branched Aldehydes. European Journal of Organic Chemistry 2017, 2017 (41), 6146–6153. https://doi.org/10.1002/ejoc.201701073.
European Journal of Organic Chemistry
Wiley-V C H Verlag Gmbh, Weinheim..
Marjanović-Trajković J, Milanović VD, Ferjančić Z, Saičić R. Supplementary data for the article: Marjanovic Trajkovic, J.; Milanovic, V.; Ferjancic, Z.; Saicic, R. N. On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-Dioxane-5-One to Acyclic Chiral α-Branched Aldehydes. European Journal of Organic Chemistry 2017, 2017 (41), 6146–6153. https://doi.org/10.1002/ejoc.201701073. European Journal of Organic Chemistry. 2017;
Marjanović-Trajković Jasna, Milanović Vesna D., Ferjančić Zorana, Saičić Radomir, "Supplementary data for the article: Marjanovic Trajkovic, J.; Milanovic, V.; Ferjancic, Z.; Saicic, R. N. On the Asymmetric Induction in Proline-Catalyzed Aldol Reactions: Reagent-Controlled Addition Reactions of 2,2-Dimethyl-1,3-Dioxane-5-One to Acyclic Chiral α-Branched Aldehydes. European Journal of Organic Chemistry 2017, 2017 (41), 6146–6153. https://doi.org/10.1002/ejoc.201701073" European Journal of Organic Chemistry (2017)

Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898

Vulović, Bojan; Kolarski, Dušan; Bihelović, Filip; Matović, Radomir; Gruden-Pavlović, Maja; Saičić, Radomir

(Amer Chemical Soc, Washington, 2016)

TY  - BOOK
AU  - Vulović, Bojan
AU  - Kolarski, Dušan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Gruden-Pavlović, Maja
AU  - Saičić, Radomir
PY  - 2016
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/3520
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898
ER  - 
@book{
author = "Vulović, Bojan and Kolarski, Dušan and Bihelović, Filip and Matović, Radomir and Gruden-Pavlović, Maja and Saičić, Radomir",
year = "2016",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3520",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898"
}
Vulović, B., Kolarski, D., Bihelović, F., Matović, R., Gruden-Pavlović, M.,& Saičić, R. (2016). Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898.
Organic Letters
Amer Chemical Soc, Washington..
Vulović B, Kolarski D, Bihelović F, Matović R, Gruden-Pavlović M, Saičić R. Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898. Organic Letters. 2016;
Vulović Bojan, Kolarski Dušan, Bihelović Filip, Matović Radomir, Gruden-Pavlović Maja, Saičić Radomir, "Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898" Organic Letters (2016)

Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H

Vulović, Bojan; Kolarski, Dušan; Bihelović, Filip; Matović, Radomir; Gruden-Pavlović, Maja; Saičić, Radomir

(Amer Chemical Soc, Washington, 2016)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Kolarski, Dušan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Gruden-Pavlović, Maja
AU  - Saičić, Radomir
PY  - 2016
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/2290
AB  - 1,6-Diynes with a t-butylcarbonate group in the propargylic position undergo gold(I)-catalyzed dominocyclization which affords alpha-hydroxycyclohexenones. The described sequence can be applied on functionalized, highly oxygenated substrates, as examplified in the synthesis of (-)-gabosine H and its epimer.
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H
VL  - 18
IS  - 15
SP  - 3886
EP  - 3889
DO  - 10.1021/acs.orglett.6b01898
ER  - 
@article{
author = "Vulović, Bojan and Kolarski, Dušan and Bihelović, Filip and Matović, Radomir and Gruden-Pavlović, Maja and Saičić, Radomir",
year = "2016",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2290",
abstract = "1,6-Diynes with a t-butylcarbonate group in the propargylic position undergo gold(I)-catalyzed dominocyclization which affords alpha-hydroxycyclohexenones. The described sequence can be applied on functionalized, highly oxygenated substrates, as examplified in the synthesis of (-)-gabosine H and its epimer.",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H",
volume = "18",
number = "15",
pages = "3886-3889",
doi = "10.1021/acs.orglett.6b01898"
}
Vulović, B., Kolarski, D., Bihelović, F., Matović, R., Gruden-Pavlović, M.,& Saičić, R. (2016). Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H.
Organic Letters
Amer Chemical Soc, Washington., 18(15), 3886-3889.
https://doi.org/10.1021/acs.orglett.6b01898
Vulović B, Kolarski D, Bihelović F, Matović R, Gruden-Pavlović M, Saičić R. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H. Organic Letters. 2016;18(15):3886-3889
Vulović Bojan, Kolarski Dušan, Bihelović Filip, Matović Radomir, Gruden-Pavlović Maja, Saičić Radomir, "Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H" Organic Letters, 18, no. 15 (2016):3886-3889,
https://doi.org/10.1021/acs.orglett.6b01898 .
11
12
11
13

Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids

Marjanović-Trajković, Jasna; Ferjančić, Zorana; Saičić, Radomir

(Pergamon-Elsevier Science Ltd, Oxford, 2015)

TY  - JOUR
AU  - Marjanović-Trajković, Jasna
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2015
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/3389
AB  - The enantioselective synthesis of 4-epi-fagomine was accomplished starting from dioxanone and Cbz-protected benyzlamine, in 4 steps, with 18% overall yield. The key feature of this synthetic approach is the tactical combination of reactions: organocatalyzed aldolization/reductive amination, which allows for a quick formation of heterocyclic rings with defined absolute configuration of all stereogenic centers. Two hydroxypipecolic acids and a reduced fagomine analogue were also synthesized.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron
T1  - Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids
VL  - 71
IS  - 38
SP  - 6784
EP  - 6789
DO  - 10.1016/j.tet.2015.07.036
ER  - 
@article{
author = "Marjanović-Trajković, Jasna and Ferjančić, Zorana and Saičić, Radomir",
year = "2015",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3389",
abstract = "The enantioselective synthesis of 4-epi-fagomine was accomplished starting from dioxanone and Cbz-protected benyzlamine, in 4 steps, with 18% overall yield. The key feature of this synthetic approach is the tactical combination of reactions: organocatalyzed aldolization/reductive amination, which allows for a quick formation of heterocyclic rings with defined absolute configuration of all stereogenic centers. Two hydroxypipecolic acids and a reduced fagomine analogue were also synthesized.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron",
title = "Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids",
volume = "71",
number = "38",
pages = "6784-6789",
doi = "10.1016/j.tet.2015.07.036"
}
Marjanović-Trajković, J., Ferjančić, Z.,& Saičić, R. (2015). Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids.
Tetrahedron
Pergamon-Elsevier Science Ltd, Oxford., 71(38), 6784-6789.
https://doi.org/10.1016/j.tet.2015.07.036
Marjanović-Trajković J, Ferjančić Z, Saičić R. Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids. Tetrahedron. 2015;71(38):6784-6789
Marjanović-Trajković Jasna, Ferjančić Zorana, Saičić Radomir, "Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids" Tetrahedron, 71, no. 38 (2015):6784-6789,
https://doi.org/10.1016/j.tet.2015.07.036 .
1
5
6
7

Supplementary data for article: Marjanovic, J.; Ferjancic, Z.; Saicic, R. N. Organocatalyzed Synthesis of (-)-4-Epi-Fagomine and the Corresponding Pipecolic Acids. Tetrahedron 2015, 71 (38), 6784–6789. https://doi.org/10.1016/j.tet.2015.07.036

Marjanović-Trajković, Jasna; Ferjančić, Zorana; Saičić, Radomir

(Pergamon-Elsevier Science Ltd, Oxford, 2015)

TY  - BOOK
AU  - Marjanović-Trajković, Jasna
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2015
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/3390
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron
T1  - Supplementary data for article: Marjanovic, J.; Ferjancic, Z.; Saicic, R. N. Organocatalyzed Synthesis of (-)-4-Epi-Fagomine and the Corresponding Pipecolic Acids. Tetrahedron 2015, 71 (38), 6784–6789. https://doi.org/10.1016/j.tet.2015.07.036
ER  - 
@book{
author = "Marjanović-Trajković, Jasna and Ferjančić, Zorana and Saičić, Radomir",
year = "2015",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3390",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron",
title = "Supplementary data for article: Marjanovic, J.; Ferjancic, Z.; Saicic, R. N. Organocatalyzed Synthesis of (-)-4-Epi-Fagomine and the Corresponding Pipecolic Acids. Tetrahedron 2015, 71 (38), 6784–6789. https://doi.org/10.1016/j.tet.2015.07.036"
}
Marjanović-Trajković, J., Ferjančić, Z.,& Saičić, R. (2015). Supplementary data for article: Marjanovic, J.; Ferjancic, Z.; Saicic, R. N. Organocatalyzed Synthesis of (-)-4-Epi-Fagomine and the Corresponding Pipecolic Acids. Tetrahedron 2015, 71 (38), 6784–6789. https://doi.org/10.1016/j.tet.2015.07.036.
Tetrahedron
Pergamon-Elsevier Science Ltd, Oxford..
Marjanović-Trajković J, Ferjančić Z, Saičić R. Supplementary data for article: Marjanovic, J.; Ferjancic, Z.; Saicic, R. N. Organocatalyzed Synthesis of (-)-4-Epi-Fagomine and the Corresponding Pipecolic Acids. Tetrahedron 2015, 71 (38), 6784–6789. https://doi.org/10.1016/j.tet.2015.07.036. Tetrahedron. 2015;
Marjanović-Trajković Jasna, Ferjančić Zorana, Saičić Radomir, "Supplementary data for article: Marjanovic, J.; Ferjancic, Z.; Saicic, R. N. Organocatalyzed Synthesis of (-)-4-Epi-Fagomine and the Corresponding Pipecolic Acids. Tetrahedron 2015, 71 (38), 6784–6789. https://doi.org/10.1016/j.tet.2015.07.036" Tetrahedron (2015)

Supplementary data for article: Novkovic, L.; Trmcic, M.; Rodic, M.; Bihelovic, F.; Zlatar, M.; Matovic, R.; Saicic, R. N. Synthesis of Endoperoxides by Domino Reactions of Ketones and Molecular Oxygen. RSC Advances 2015, 5 (120), 99577–99584. https://doi.org/10.1039/c5ra13476e

Novković, Luka P.; Trmčić, Milena; Rodić, M.; Bihelović, Filip; Zlatar, Matija; Matović, Radomir; Saičić, Radomir

(Royal Soc Chemistry, Cambridge, 2015)

TY  - BOOK
AU  - Novković, Luka P.
AU  - Trmčić, Milena
AU  - Rodić, M.
AU  - Bihelović, Filip
AU  - Zlatar, Matija
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2015
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/3442
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Supplementary data for article: Novkovic, L.; Trmcic, M.; Rodic, M.; Bihelovic, F.; Zlatar, M.; Matovic, R.; Saicic, R. N. Synthesis of Endoperoxides by Domino Reactions of Ketones and Molecular Oxygen. RSC Advances 2015, 5 (120), 99577–99584. https://doi.org/10.1039/c5ra13476e
ER  - 
@book{
author = "Novković, Luka P. and Trmčić, Milena and Rodić, M. and Bihelović, Filip and Zlatar, Matija and Matović, Radomir and Saičić, Radomir",
year = "2015",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3442",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Supplementary data for article: Novkovic, L.; Trmcic, M.; Rodic, M.; Bihelovic, F.; Zlatar, M.; Matovic, R.; Saicic, R. N. Synthesis of Endoperoxides by Domino Reactions of Ketones and Molecular Oxygen. RSC Advances 2015, 5 (120), 99577–99584. https://doi.org/10.1039/c5ra13476e"
}
Novković, L. P., Trmčić, M., Rodić, M., Bihelović, F., Zlatar, M., Matović, R.,& Saičić, R. (2015). Supplementary data for article: Novkovic, L.; Trmcic, M.; Rodic, M.; Bihelovic, F.; Zlatar, M.; Matovic, R.; Saicic, R. N. Synthesis of Endoperoxides by Domino Reactions of Ketones and Molecular Oxygen. RSC Advances 2015, 5 (120), 99577–99584. https://doi.org/10.1039/c5ra13476e.
RSC Advances
Royal Soc Chemistry, Cambridge..
Novković LP, Trmčić M, Rodić M, Bihelović F, Zlatar M, Matović R, Saičić R. Supplementary data for article: Novkovic, L.; Trmcic, M.; Rodic, M.; Bihelovic, F.; Zlatar, M.; Matovic, R.; Saicic, R. N. Synthesis of Endoperoxides by Domino Reactions of Ketones and Molecular Oxygen. RSC Advances 2015, 5 (120), 99577–99584. https://doi.org/10.1039/c5ra13476e. RSC Advances. 2015;
Novković Luka P., Trmčić Milena, Rodić M., Bihelović Filip, Zlatar Matija, Matović Radomir, Saičić Radomir, "Supplementary data for article: Novkovic, L.; Trmcic, M.; Rodic, M.; Bihelovic, F.; Zlatar, M.; Matovic, R.; Saicic, R. N. Synthesis of Endoperoxides by Domino Reactions of Ketones and Molecular Oxygen. RSC Advances 2015, 5 (120), 99577–99584. https://doi.org/10.1039/c5ra13476e" RSC Advances (2015)

Synthesis of endoperoxides by domino reactions of ketones and molecular oxygen

Novković, Luka P.; Trmčić, Milena; Rodić, M.; Bihelović, Filip; Zlatar, Matija; Matović, Radomir; Saičić, Radomir

(Royal Soc Chemistry, Cambridge, 2015)

TY  - JOUR
AU  - Novković, Luka P.
AU  - Trmčić, Milena
AU  - Rodić, M.
AU  - Bihelović, Filip
AU  - Zlatar, Matija
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2015
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/2000
AB  - Domino reactions of ketones with molecular oxygen in the presence of potassium hydroxide and potassium t-butoxide afford cyclic hydroperoxy acetals (3,5-dihydroxy-1,2-dioxanes). Mixed endoperoxides can also be obtained in a three-component reaction of two ketones and oxygen.
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Synthesis of endoperoxides by domino reactions of ketones and molecular oxygen
VL  - 5
IS  - 120
SP  - 99577
EP  - 99584
DO  - 10.1039/c5ra13476e
ER  - 
@article{
author = "Novković, Luka P. and Trmčić, Milena and Rodić, M. and Bihelović, Filip and Zlatar, Matija and Matović, Radomir and Saičić, Radomir",
year = "2015",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2000",
abstract = "Domino reactions of ketones with molecular oxygen in the presence of potassium hydroxide and potassium t-butoxide afford cyclic hydroperoxy acetals (3,5-dihydroxy-1,2-dioxanes). Mixed endoperoxides can also be obtained in a three-component reaction of two ketones and oxygen.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Synthesis of endoperoxides by domino reactions of ketones and molecular oxygen",
volume = "5",
number = "120",
pages = "99577-99584",
doi = "10.1039/c5ra13476e"
}
Novković, L. P., Trmčić, M., Rodić, M., Bihelović, F., Zlatar, M., Matović, R.,& Saičić, R. (2015). Synthesis of endoperoxides by domino reactions of ketones and molecular oxygen.
RSC Advances
Royal Soc Chemistry, Cambridge., 5(120), 99577-99584.
https://doi.org/10.1039/c5ra13476e
Novković LP, Trmčić M, Rodić M, Bihelović F, Zlatar M, Matović R, Saičić R. Synthesis of endoperoxides by domino reactions of ketones and molecular oxygen. RSC Advances. 2015;5(120):99577-99584
Novković Luka P., Trmčić Milena, Rodić M., Bihelović Filip, Zlatar Matija, Matović Radomir, Saičić Radomir, "Synthesis of endoperoxides by domino reactions of ketones and molecular oxygen" RSC Advances, 5, no. 120 (2015):99577-99584,
https://doi.org/10.1039/c5ra13476e .
7
4
5

Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids

Marjanović-Trajković, Jasna; Ferjančić, Zorana; Saičić, Radomir

(Pergamon-Elsevier Science Ltd, Oxford, 2015)

TY  - JOUR
AU  - Marjanović-Trajković, Jasna
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2015
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/1951
AB  - The enantioselective synthesis of 4-epi-fagomine was accomplished starting from dioxanone and Cbz-protected benyzlamine, in 4 steps, with 18% overall yield. The key feature of this synthetic approach is the tactical combination of reactions: organocatalyzed aldolization/reductive amination, which allows for a quick formation of heterocyclic rings with defined absolute configuration of all stereogenic centers. Two hydroxypipecolic acids and a reduced fagomine analogue were also synthesized.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron
T1  - Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids
VL  - 71
IS  - 38
SP  - 6784
EP  - 6789
DO  - 10.1016/j.tet.2015.07.036
ER  - 
@article{
author = "Marjanović-Trajković, Jasna and Ferjančić, Zorana and Saičić, Radomir",
year = "2015",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/1951",
abstract = "The enantioselective synthesis of 4-epi-fagomine was accomplished starting from dioxanone and Cbz-protected benyzlamine, in 4 steps, with 18% overall yield. The key feature of this synthetic approach is the tactical combination of reactions: organocatalyzed aldolization/reductive amination, which allows for a quick formation of heterocyclic rings with defined absolute configuration of all stereogenic centers. Two hydroxypipecolic acids and a reduced fagomine analogue were also synthesized.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron",
title = "Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids",
volume = "71",
number = "38",
pages = "6784-6789",
doi = "10.1016/j.tet.2015.07.036"
}
Marjanović-Trajković, J., Ferjančić, Z.,& Saičić, R. (2015). Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids.
Tetrahedron
Pergamon-Elsevier Science Ltd, Oxford., 71(38), 6784-6789.
https://doi.org/10.1016/j.tet.2015.07.036
Marjanović-Trajković J, Ferjančić Z, Saičić R. Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids. Tetrahedron. 2015;71(38):6784-6789
Marjanović-Trajković Jasna, Ferjančić Zorana, Saičić Radomir, "Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids" Tetrahedron, 71, no. 38 (2015):6784-6789,
https://doi.org/10.1016/j.tet.2015.07.036 .
1
5
6
7

Total synthesis and biological evaluation of atrop-O-benzyl-desmethylabyssomicin C

Matović, Radomir; Bihelović, Filip; Gruden-Pavlović, Maja; Saičić, Radomir

(Royal Soc Chemistry, Cambridge, 2014)

TY  - JOUR
AU  - Matović, Radomir
AU  - Bihelović, Filip
AU  - Gruden-Pavlović, Maja
AU  - Saičić, Radomir
PY  - 2014
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/1860
AB  - The total synthesis of desmethylabyssomicin C analogue 1 was accomplished using diastereotopos-selective ring closing metathesis and Nozaki-Hiyama-Kishi cyclization as the key steps. The synthetic analogue retained its antibacterial activity against methicillin-resistant S. aureus strains, whereas its cytotoxicity decreased for three orders of magnitude, as compared to atrop-abyssomicin C.
PB  - Royal Soc Chemistry, Cambridge
T2  - Organic and Biomolecular Chemistry
T1  - Total synthesis and biological evaluation of atrop-O-benzyl-desmethylabyssomicin C
VL  - 12
IS  - 39
SP  - 7682
EP  - 7685
DO  - 10.1039/c4ob01436g
ER  - 
@article{
author = "Matović, Radomir and Bihelović, Filip and Gruden-Pavlović, Maja and Saičić, Radomir",
year = "2014",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/1860",
abstract = "The total synthesis of desmethylabyssomicin C analogue 1 was accomplished using diastereotopos-selective ring closing metathesis and Nozaki-Hiyama-Kishi cyclization as the key steps. The synthetic analogue retained its antibacterial activity against methicillin-resistant S. aureus strains, whereas its cytotoxicity decreased for three orders of magnitude, as compared to atrop-abyssomicin C.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Organic and Biomolecular Chemistry",
title = "Total synthesis and biological evaluation of atrop-O-benzyl-desmethylabyssomicin C",
volume = "12",
number = "39",
pages = "7682-7685",
doi = "10.1039/c4ob01436g"
}
Matović, R., Bihelović, F., Gruden-Pavlović, M.,& Saičić, R. (2014). Total synthesis and biological evaluation of atrop-O-benzyl-desmethylabyssomicin C.
Organic and Biomolecular Chemistry
Royal Soc Chemistry, Cambridge., 12(39), 7682-7685.
https://doi.org/10.1039/c4ob01436g
Matović R, Bihelović F, Gruden-Pavlović M, Saičić R. Total synthesis and biological evaluation of atrop-O-benzyl-desmethylabyssomicin C. Organic and Biomolecular Chemistry. 2014;12(39):7682-7685
Matović Radomir, Bihelović Filip, Gruden-Pavlović Maja, Saičić Radomir, "Total synthesis and biological evaluation of atrop-O-benzyl-desmethylabyssomicin C" Organic and Biomolecular Chemistry, 12, no. 39 (2014):7682-7685,
https://doi.org/10.1039/c4ob01436g .
12
11
10

Total synthesis of (+)-swainsonine and (+)-8-epi-swainsonine

Trajković, Milos; Balanac, Vesna; Ferjančić, Zorana; Saičić, Radomir

(Royal Soc Chemistry, Cambridge, 2014)

TY  - JOUR
AU  - Trajković, Milos
AU  - Balanac, Vesna
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2014
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/1876
AB  - Enantioselective synthesis of (+)-swainsonine was achieved in 9 steps, with 24% overall yield. The key feature of the synthesis is the tactical combination of reactions: organocatalyzed aldolization/reductive amination, which allows for a rapid construction of highly functionalized heterocyclic systems. In a similar way (+)-8-epi-swainsonine was synthesized (7 steps, 28%).
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Total synthesis of (+)-swainsonine and (+)-8-epi-swainsonine
VL  - 4
IS  - 96
SP  - 53722
EP  - 53724
DO  - 10.1039/c4ra11978a
ER  - 
@article{
author = "Trajković, Milos and Balanac, Vesna and Ferjančić, Zorana and Saičić, Radomir",
year = "2014",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/1876",
abstract = "Enantioselective synthesis of (+)-swainsonine was achieved in 9 steps, with 24% overall yield. The key feature of the synthesis is the tactical combination of reactions: organocatalyzed aldolization/reductive amination, which allows for a rapid construction of highly functionalized heterocyclic systems. In a similar way (+)-8-epi-swainsonine was synthesized (7 steps, 28%).",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Total synthesis of (+)-swainsonine and (+)-8-epi-swainsonine",
volume = "4",
number = "96",
pages = "53722-53724",
doi = "10.1039/c4ra11978a"
}
Trajković, M., Balanac, V., Ferjančić, Z.,& Saičić, R. (2014). Total synthesis of (+)-swainsonine and (+)-8-epi-swainsonine.
RSC Advances
Royal Soc Chemistry, Cambridge., 4(96), 53722-53724.
https://doi.org/10.1039/c4ra11978a
Trajković M, Balanac V, Ferjančić Z, Saičić R. Total synthesis of (+)-swainsonine and (+)-8-epi-swainsonine. RSC Advances. 2014;4(96):53722-53724
Trajković Milos, Balanac Vesna, Ferjančić Zorana, Saičić Radomir, "Total synthesis of (+)-swainsonine and (+)-8-epi-swainsonine" RSC Advances, 4, no. 96 (2014):53722-53724,
https://doi.org/10.1039/c4ra11978a .
10
8
10