Silylmethyl-substituted cyclopropyl and other strained ring systems: cycloaddition with dipolarophiles
Тип публикации: Journal Article
Дата публикации: 2008-11-18
scimago Q1
wos Q2
БС1
SJR: 1.037
CiteScore: 7.4
Impact factor: 4.2
ISSN: 13597345, 1364548X
PubMed ID:
19057754
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
Small ring compounds represent a class of versatile building blocks in organic synthesis. Three- and four-membered ring carbo- and heterocycles are regarded as unique functional groups. Lewis acid-assisted cycloaddition of cyclopropanes, aziridines and azetidines substituted by vicinal electron-donor and electron-acceptor groups takes place in a regio- and stereocontrolled fashion. Trialkylsilylmethyl is an interesting donor substituent. In this feature article, we provide an overview of the cycloaddition of different dipolarophiles to silylmethyl-substituted small ring compounds and discuss their possible applications in synthesis.
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Agrawal D., Yadav V. K. Silylmethyl-substituted cyclopropyl and other strained ring systems: cycloaddition with dipolarophiles // Chemical Communications. 2008. Vol. 48. p. 6471.
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Agrawal D., Yadav V. K. Silylmethyl-substituted cyclopropyl and other strained ring systems: cycloaddition with dipolarophiles // Chemical Communications. 2008. Vol. 48. p. 6471.
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TY - JOUR
DO - 10.1039/b812285g
UR - https://doi.org/10.1039/b812285g
TI - Silylmethyl-substituted cyclopropyl and other strained ring systems: cycloaddition with dipolarophiles
T2 - Chemical Communications
AU - Agrawal, Divya
AU - Yadav, Veejendra K.
PY - 2008
DA - 2008/11/18
PB - Royal Society of Chemistry (RSC)
SP - 6471
IS - 48
PMID - 19057754
SN - 1359-7345
SN - 1364-548X
ER -
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BibTex (до 50 авторов)
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@article{2008_Agrawal,
author = {Divya Agrawal and Veejendra K. Yadav},
title = {Silylmethyl-substituted cyclopropyl and other strained ring systems: cycloaddition with dipolarophiles},
journal = {Chemical Communications},
year = {2008},
publisher = {Royal Society of Chemistry (RSC)},
month = {nov},
url = {https://doi.org/10.1039/b812285g},
number = {48},
pages = {6471},
doi = {10.1039/b812285g}
}