том 74 издание 9 страницы 1341-1349

Regio- and stereoselectivity of [2+3]cycloaddition of nitroethene to (Z)-N-aryl-C-phenylnitrones

Тип публикацииJournal Article
Дата публикации2009-09-11
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ISSN00100765, 12126950
General Chemistry
Краткое описание

The cycloaddition reactions of nitroethene to (Z)-N-aryl-C-phenylnitrones lead to mixtures of stereoisomeric cis- and trans-2-aryl-4-nitro-3-phenylisoxazolidines. Regioselectivity of these reactions is determined by the character of nucleophile–electrophile interactions, while stereoselectivity is determined by the steric factors and the character of secondary orbital interactions.

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ГОСТ |
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Jasiński R. Regio- and stereoselectivity of [2+3]cycloaddition of nitroethene to (Z)-N-aryl-C-phenylnitrones // Collection of Czechoslovak Chemical Communications. 2009. Vol. 74. No. 9. pp. 1341-1349.
ГОСТ со всеми авторами (до 50) Скопировать
Jasiński R. Regio- and stereoselectivity of [2+3]cycloaddition of nitroethene to (Z)-N-aryl-C-phenylnitrones // Collection of Czechoslovak Chemical Communications. 2009. Vol. 74. No. 9. pp. 1341-1349.
RIS |
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TY - JOUR
DO - 10.1135/cccc2009037
UR - https://doi.org/10.1135/cccc2009037
TI - Regio- and stereoselectivity of [2+3]cycloaddition of nitroethene to (Z)-N-aryl-C-phenylnitrones
T2 - Collection of Czechoslovak Chemical Communications
AU - Jasiński, Ryszard
PY - 2009
DA - 2009/09/11
PB - Institute of Organic Chemistry & Biochemistry
SP - 1341-1349
IS - 9
VL - 74
SN - 0010-0765
SN - 1212-6950
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2009_Jasiński,
author = {Ryszard Jasiński},
title = {Regio- and stereoselectivity of [2+3]cycloaddition of nitroethene to (Z)-N-aryl-C-phenylnitrones},
journal = {Collection of Czechoslovak Chemical Communications},
year = {2009},
volume = {74},
publisher = {Institute of Organic Chemistry & Biochemistry},
month = {sep},
url = {https://doi.org/10.1135/cccc2009037},
number = {9},
pages = {1341--1349},
doi = {10.1135/cccc2009037}
}
MLA
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Jasiński, Ryszard. “Regio- and stereoselectivity of [2+3]cycloaddition of nitroethene to (Z)-N-aryl-C-phenylnitrones.” Collection of Czechoslovak Chemical Communications, vol. 74, no. 9, Sep. 2009, pp. 1341-1349. https://doi.org/10.1135/cccc2009037.