TY  - JOUR
AU  - Mihailović, ML
AU  - Gojkovic, S
AU  - Milosavljevic, S
AU  - Konstantinovic, S
PY  - 1999
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/412
AB  - The reaction of 4-tert-butyl-4-penten-1-ol 3 with some electrophilic reagents (such as mineral acids, mercuric acetate, peracids) has been investigated. It is found that in the acid (H2SO4) catalysed reaction of 3, the products of 1,2-methyl rearrangement are produced. The oxymercuration/demercuration reaction of 3 and its reaction with meta-chloroperbenzoic acid afford in high yields exclusively Markovnikov-type products.
PB  - Natl Inst Science Communication, New Delhi
T2  - Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry
T1  - Ring closure reaction of 4-tert-butyl-4-penten-1-ol with electrophilic reagents
VL  - 38
IS  - 1
SP  - 101
EP  - 105
UR  - https://hdl.handle.net/21.15107/rcub_cherry_412
ER  - 

@article{
author = "Mihailović, ML and Gojkovic, S and Milosavljevic, S and Konstantinovic, S",
year = "1999",
abstract = "The reaction of 4-tert-butyl-4-penten-1-ol 3 with some electrophilic reagents (such as mineral acids, mercuric acetate, peracids) has been investigated. It is found that in the acid (H2SO4) catalysed reaction of 3, the products of 1,2-methyl rearrangement are produced. The oxymercuration/demercuration reaction of 3 and its reaction with meta-chloroperbenzoic acid afford in high yields exclusively Markovnikov-type products.",
publisher = "Natl Inst Science Communication, New Delhi",
journal = "Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry",
title = "Ring closure reaction of 4-tert-butyl-4-penten-1-ol with electrophilic reagents",
volume = "38",
number = "1",
pages = "101-105",
url = "https://hdl.handle.net/21.15107/rcub_cherry_412"
}

Mihailović, M., Gojkovic, S., Milosavljevic, S.,& Konstantinovic, S.. (1999). Ring closure reaction of 4-tert-butyl-4-penten-1-ol with electrophilic reagents. in Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry
Natl Inst Science Communication, New Delhi., 38(1), 101-105.
https://hdl.handle.net/21.15107/rcub_cherry_412

Mihailović M, Gojkovic S, Milosavljevic S, Konstantinovic S. Ring closure reaction of 4-tert-butyl-4-penten-1-ol with electrophilic reagents. in Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry. 1999;38(1):101-105.
https://hdl.handle.net/21.15107/rcub_cherry_412 .

Mihailović, ML, Gojkovic, S, Milosavljevic, S, Konstantinovic, S, "Ring closure reaction of 4-tert-butyl-4-penten-1-ol with electrophilic reagents" in Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry, 38, no. 1 (1999):101-105,
https://hdl.handle.net/21.15107/rcub_cherry_412 .

TY  - JOUR
AU  - Petrović, ZD
AU  - Konstantinovic, S
AU  - Scheffold, R
AU  - Milosavljevic, S
PY  - 1997
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/363
AB  - Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12 have been studied. Geranyl bromide 1 and methyl (2E, 6E) 8-bromo-3,7-dimethylocta-2,6-dienoate 2 have been used as substrates and subjected to chemical and electrochemical reduction. The formation and distribution of the reaction products of these substrates can be explained by free radical mechanisms, namely by reductive reactions of some functional groups, rearrangements and intermolecular coupling of intermediate radicals.
PB  - Natl Inst Science Communication & Information Resources-Niscair, New Delhi
T2  - Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry
T1  - Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12
VL  - 36
IS  - 9
SP  - 765
EP  - 768
UR  - https://hdl.handle.net/21.15107/rcub_cherry_363
ER  - 

@article{
author = "Petrović, ZD and Konstantinovic, S and Scheffold, R and Milosavljevic, S",
year = "1997",
abstract = "Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12 have been studied. Geranyl bromide 1 and methyl (2E, 6E) 8-bromo-3,7-dimethylocta-2,6-dienoate 2 have been used as substrates and subjected to chemical and electrochemical reduction. The formation and distribution of the reaction products of these substrates can be explained by free radical mechanisms, namely by reductive reactions of some functional groups, rearrangements and intermolecular coupling of intermediate radicals.",
publisher = "Natl Inst Science Communication & Information Resources-Niscair, New Delhi",
journal = "Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry",
title = "Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12",
volume = "36",
number = "9",
pages = "765-768",
url = "https://hdl.handle.net/21.15107/rcub_cherry_363"
}

Petrović, Z., Konstantinovic, S., Scheffold, R.,& Milosavljevic, S.. (1997). Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12. in Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry
Natl Inst Science Communication & Information Resources-Niscair, New Delhi., 36(9), 765-768.
https://hdl.handle.net/21.15107/rcub_cherry_363

Petrović Z, Konstantinovic S, Scheffold R, Milosavljevic S. Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12. in Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry. 1997;36(9):765-768.
https://hdl.handle.net/21.15107/rcub_cherry_363 .

Petrović, ZD, Konstantinovic, S, Scheffold, R, Milosavljevic, S, "Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12" in Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry, 36, no. 9 (1997):765-768,
https://hdl.handle.net/21.15107/rcub_cherry_363 .