TY  - DATA
AU  - Tasić, Gordana
AU  - Simić, Milena R.
AU  - Popovic, Stanimir
AU  - Husinec, Suren
AU  - Maslak, Veselin
AU  - Savić, Vladimir
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3501
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - Supplementary data for article: Tasić, G.; Simić, M. R.; Popovic, S.; Husinec, S.; Maslak, V.; Savić, V. Indirect N-Vinylation of Indoles via Isomerisation of N-Allyl Derivatives: Synthesis of (+/-)-Debromoarborescidine B. Tetrahedron Letters 2013, 54 (34), 4536–4539. https://doi.org/10.1016/j.tetlet.2013.06.069
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3501
ER  - 

@misc{
author = "Tasić, Gordana and Simić, Milena R. and Popovic, Stanimir and Husinec, Suren and Maslak, Veselin and Savić, Vladimir",
year = "2013",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "Supplementary data for article: Tasić, G.; Simić, M. R.; Popovic, S.; Husinec, S.; Maslak, V.; Savić, V. Indirect N-Vinylation of Indoles via Isomerisation of N-Allyl Derivatives: Synthesis of (+/-)-Debromoarborescidine B. Tetrahedron Letters 2013, 54 (34), 4536–4539. https://doi.org/10.1016/j.tetlet.2013.06.069",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3501"
}

Tasić, G., Simić, M. R., Popovic, S., Husinec, S., Maslak, V.,& Savić, V.. (2013). Supplementary data for article: Tasić, G.; Simić, M. R.; Popovic, S.; Husinec, S.; Maslak, V.; Savić, V. Indirect N-Vinylation of Indoles via Isomerisation of N-Allyl Derivatives: Synthesis of (+/-)-Debromoarborescidine B. Tetrahedron Letters 2013, 54 (34), 4536–4539. https://doi.org/10.1016/j.tetlet.2013.06.069. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford..
https://hdl.handle.net/21.15107/rcub_cherry_3501

Tasić G, Simić MR, Popovic S, Husinec S, Maslak V, Savić V. Supplementary data for article: Tasić, G.; Simić, M. R.; Popovic, S.; Husinec, S.; Maslak, V.; Savić, V. Indirect N-Vinylation of Indoles via Isomerisation of N-Allyl Derivatives: Synthesis of (+/-)-Debromoarborescidine B. Tetrahedron Letters 2013, 54 (34), 4536–4539. https://doi.org/10.1016/j.tetlet.2013.06.069. in Tetrahedron Letters. 2013;.
https://hdl.handle.net/21.15107/rcub_cherry_3501 .

Tasić, Gordana, Simić, Milena R., Popovic, Stanimir, Husinec, Suren, Maslak, Veselin, Savić, Vladimir, "Supplementary data for article: Tasić, G.; Simić, M. R.; Popovic, S.; Husinec, S.; Maslak, V.; Savić, V. Indirect N-Vinylation of Indoles via Isomerisation of N-Allyl Derivatives: Synthesis of (+/-)-Debromoarborescidine B. Tetrahedron Letters 2013, 54 (34), 4536–4539. https://doi.org/10.1016/j.tetlet.2013.06.069" in Tetrahedron Letters (2013),
https://hdl.handle.net/21.15107/rcub_cherry_3501 .

TY  - JOUR
AU  - Tasić, Gordana
AU  - Simić, Milena R.
AU  - Popovic, Stanimir
AU  - Husinec, Suren
AU  - Maslak, Veselin
AU  - Savić, Vladimir
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1382
AB  - Double bond migration in N-allylindoles has been investigated as a method to access N-vinyl derivatives of this heterocycle. The optimal reaction conditions employed t-BuOK or NaH in DMSO as the solvent at room temperature to afford the products in yields ranging from 51 to 99%. Although in some cases a high degree of stereoselectivity was observed, preferential formation of either the Z- or E-isomer was not predictable. The developed methodology was employed in the synthesis of (+/-)-debromoarborescidine B.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - Indirect N-vinylation of indoles via isomerisation of N-allyl derivatives: synthesis of (+/-)-debromoarborescidine B
VL  - 54
IS  - 34
SP  - 4536
EP  - 4539
DO  - 10.1016/j.tetlet.2013.06.069
ER  - 

@article{
author = "Tasić, Gordana and Simić, Milena R. and Popovic, Stanimir and Husinec, Suren and Maslak, Veselin and Savić, Vladimir",
year = "2013",
abstract = "Double bond migration in N-allylindoles has been investigated as a method to access N-vinyl derivatives of this heterocycle. The optimal reaction conditions employed t-BuOK or NaH in DMSO as the solvent at room temperature to afford the products in yields ranging from 51 to 99%. Although in some cases a high degree of stereoselectivity was observed, preferential formation of either the Z- or E-isomer was not predictable. The developed methodology was employed in the synthesis of (+/-)-debromoarborescidine B.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "Indirect N-vinylation of indoles via isomerisation of N-allyl derivatives: synthesis of (+/-)-debromoarborescidine B",
volume = "54",
number = "34",
pages = "4536-4539",
doi = "10.1016/j.tetlet.2013.06.069"
}

Tasić, G., Simić, M. R., Popovic, S., Husinec, S., Maslak, V.,& Savić, V.. (2013). Indirect N-vinylation of indoles via isomerisation of N-allyl derivatives: synthesis of (+/-)-debromoarborescidine B. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford., 54(34), 4536-4539.
https://doi.org/10.1016/j.tetlet.2013.06.069

Tasić G, Simić MR, Popovic S, Husinec S, Maslak V, Savić V. Indirect N-vinylation of indoles via isomerisation of N-allyl derivatives: synthesis of (+/-)-debromoarborescidine B. in Tetrahedron Letters. 2013;54(34):4536-4539.
doi:10.1016/j.tetlet.2013.06.069 .

Tasić, Gordana, Simić, Milena R., Popovic, Stanimir, Husinec, Suren, Maslak, Veselin, Savić, Vladimir, "Indirect N-vinylation of indoles via isomerisation of N-allyl derivatives: synthesis of (+/-)-debromoarborescidine B" in Tetrahedron Letters, 54, no. 34 (2013):4536-4539,
https://doi.org/10.1016/j.tetlet.2013.06.069 . .