Amide-based bifunctional organocatalysts in asymmetric reactions
Тип публикации: Journal Article
Дата публикации: 2009-08-27
scimago Q1
wos Q2
БС1
SJR: 1.037
CiteScore: 7.4
Impact factor: 4.2
ISSN: 13597345, 1364548X
PubMed ID:
19826653
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
A series of amide-based bifunctional organocatalysts have been utilized in asymmetric reactions. Prolinamide analogues have been designed to catalyze asymmetric reactions via enamine intermediates with the assistance of tunable hydrogen bonding. In addition, the combination of various Lewis base functional groups, such as guanidine, N-oxide and phosphane, with an amide moiety have also constituted efficient bifunctional organocatalysts with unique reactivity and selectivity.
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ГОСТ
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Liu X., Lin L., Feng X. Amide-based bifunctional organocatalysts in asymmetric reactions // Chemical Communications. 2009. Vol. 41. p. 6145.
ГОСТ со всеми авторами (до 50)
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Liu X., Lin L., Feng X. Amide-based bifunctional organocatalysts in asymmetric reactions // Chemical Communications. 2009. Vol. 41. p. 6145.
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TY - JOUR
DO - 10.1039/b913411e
UR - https://doi.org/10.1039/b913411e
TI - Amide-based bifunctional organocatalysts in asymmetric reactions
T2 - Chemical Communications
AU - Liu, Xiaohua
AU - Lin, Li-Li
AU - Feng, Xiaoming
PY - 2009
DA - 2009/08/27
PB - Royal Society of Chemistry (RSC)
SP - 6145
IS - 41
PMID - 19826653
SN - 1359-7345
SN - 1364-548X
ER -
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BibTex (до 50 авторов)
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@article{2009_Liu,
author = {Xiaohua Liu and Li-Li Lin and Xiaoming Feng},
title = {Amide-based bifunctional organocatalysts in asymmetric reactions},
journal = {Chemical Communications},
year = {2009},
publisher = {Royal Society of Chemistry (RSC)},
month = {aug},
url = {https://doi.org/10.1039/b913411e},
number = {41},
pages = {6145},
doi = {10.1039/b913411e}
}