Enantioselective Morita-Baylis-Hillman Reaction Organocatalyzed by Glucose-based Phosphinothiourea

Тип публикации: Journal Article
Дата публикации: 2012-09-27
Wiley
SCImago Q1
WOS Q2
БС1
SJR: 1.12
CiteScore: 9
Impact factor: 5.7
ISSN: 1001604X, 16147065
General Chemistry
Краткое описание
A class of bifunctional phosphinothioureas derived from saccharide was developed as new organocatalysts for the enantioselective Morita-Baylis-Hillman reaction between acrylates and aldehydes. With 10 mol% of glucose-based phosphinothiourea 1d, the allylic alcohols were obtained in up to 96% yield and 83% ee under mild reaction conditions.
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Yang W. et al. Enantioselective Morita-Baylis-Hillman Reaction Organocatalyzed by Glucose-based Phosphinothiourea // Chinese Journal of Chemistry. 2012.
ГОСТ со всеми авторами (до 50) Скопировать
Yang W., Sha F., Zhang X., Yuan K., Wu X. Enantioselective Morita-Baylis-Hillman Reaction Organocatalyzed by Glucose-based Phosphinothiourea // Chinese Journal of Chemistry. 2012.
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TY - JOUR
DO - 10.1002/cjoc.201200740
UR - https://doi.org/10.1002/cjoc.201200740
TI - Enantioselective Morita-Baylis-Hillman Reaction Organocatalyzed by Glucose-based Phosphinothiourea
T2 - Chinese Journal of Chemistry
AU - Yang, Weihong
AU - Sha, Feng
AU - Zhang, Xin
AU - Yuan, Kui
AU - Wu, Xinyan
PY - 2012
DA - 2012/09/27
PB - Wiley
SN - 1001-604X
SN - 1614-7065
ER -
BibTex
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@article{2012_Yang,
author = {Weihong Yang and Feng Sha and Xin Zhang and Kui Yuan and Xinyan Wu},
title = {Enantioselective Morita-Baylis-Hillman Reaction Organocatalyzed by Glucose-based Phosphinothiourea},
journal = {Chinese Journal of Chemistry},
year = {2012},
publisher = {Wiley},
month = {sep},
url = {https://doi.org/10.1002/cjoc.201200740},
doi = {10.1002/cjoc.201200740}
}
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