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Stereoselective formation of a 3,5-trans-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide

Antonina Vasil'evna Lozanova 1
Antonina Vasil'evna Lozanova
, 
Tanzila Mukharbekovna Ugurchieva 1
Tanzila Mukharbekovna Ugurchieva
, 
Mikhail Vladimirovich Zlokazov 1
Mikhail Vladimirovich Zlokazov
, 
Andrei Valentinovich Stepanov 1
Andrei Valentinovich Stepanov
, 
Vladimir Vsevolodovich Veselovsky 1
Vladimir Vsevolodovich Veselovsky
10.1070/MC2006v016n01ABEH002235
Published 2006-01-31
Communication , Volume 16, Issue 1, 15-16
8
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Lozanova A. V. et al. Stereoselective formation of a 3,5-trans-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide // Mendeleev Communications. 2006. Vol. 16. No. 1. pp. 15-16.
GOST all authors (up to 50) Copy
Lozanova A. V., Ugurchieva T. M., Zlokazov M. V., Stepanov A. V., Veselovsky V. V. Stereoselective formation of a 3,5-trans-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide // Mendeleev Communications. 2006. Vol. 16. No. 1. pp. 15-16.
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TY - JOUR
DO - 10.1070/MC2006v016n01ABEH002235
UR - https://mendcomm.colab.ws/publications/10.1070/MC2006v016n01ABEH002235
TI - Stereoselective formation of a 3,5-trans-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide
T2 - Mendeleev Communications
AU - Lozanova, Antonina Vasil'evna
AU - Ugurchieva, Tanzila Mukharbekovna
AU - Zlokazov, Mikhail Vladimirovich
AU - Stepanov, Andrei Valentinovich
AU - Veselovsky, Vladimir Vsevolodovich
PY - 2006
DA - 2006/01/31
PB - Mendeleev Communications
SP - 15-16
IS - 1
VL - 16
ER -
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@article{2006_Lozanova,
author = {Antonina Vasil'evna Lozanova and Tanzila Mukharbekovna Ugurchieva and Mikhail Vladimirovich Zlokazov and Andrei Valentinovich Stepanov and Vladimir Vsevolodovich Veselovsky},
title = {Stereoselective formation of a 3,5-trans-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide},
journal = {Mendeleev Communications},
year = {2006},
volume = {16},
publisher = {Mendeleev Communications},
month = {Jan},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2006v016n01ABEH002235},
number = {1},
pages = {15--16},
doi = {10.1070/MC2006v016n01ABEH002235}
}
MLA
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Lozanova, Antonina Vasil'evna, et al. “Stereoselective formation of a 3,5-trans-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide.” Mendeleev Communications, vol. 16, no. 1, Jan. 2006, pp. 15-16. https://mendcomm.colab.ws/publications/10.1070/MC2006v016n01ABEH002235.

Abstract

The reaction of N-(2-phenylthiopent-4-enoyl)pyrrolidine with bromine results in the stereoselective formation of 1,4-tetramethylene(5S*-bromomethyl-3R*-phenylthiotetrahydro-2,2-furylidene)ammonium bromide.

References

1.
Zlokazov M.V., Lozanova A.V., Veselovsky V.V.
Mendeleev Communications, 2003
2.
10.1070/MC2006v016n01ABEH002235_bib2
Zlokazov
Izv. Akad. Nauk, Ser. Khim, 2004