Chiral bifunctional bisphosphine enabled enantioselective tandem Michael addition of tryptamine-derived oxindoles to ynones
Тип публикации: Journal Article
Дата публикации: 2019-07-04
SCImago Q1
WOS Q2
БС1
SJR: 0.907
CiteScore: 7.2
Impact factor: 4.3
ISSN: 13597345, 1364548X
PubMed ID:
31305812
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
A chiral phosphine-catalyzed tandem Michael addition of tryptamine-derived oxindoles to ynones has been developed, which provides facile access to a series of optically enriched spiro[pyrrolidine-3,3′-oxindole] compounds in good yields with good to excellent enantio- (up to 97% ee) and diastereoselectivities (up to 20 : 1 dr). Mechanistic studies indicate that this tandem reaction proceeds via an intermolecular aza-Michael/intramolecular Michael addition process.
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ГОСТ
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Cong T. et al. Chiral bifunctional bisphosphine enabled enantioselective tandem Michael addition of tryptamine-derived oxindoles to ynones // Chemical Communications. 2019. Vol. 55. No. 62. pp. 9176-9179.
ГОСТ со всеми авторами (до 50)
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Cong T., Wang H., Li X., Wu H. H., Zhang J. Chiral bifunctional bisphosphine enabled enantioselective tandem Michael addition of tryptamine-derived oxindoles to ynones // Chemical Communications. 2019. Vol. 55. No. 62. pp. 9176-9179.
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RIS
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TY - JOUR
DO - 10.1039/c9cc04357h
UR - https://xlink.rsc.org/?DOI=C9CC04357H
TI - Chiral bifunctional bisphosphine enabled enantioselective tandem Michael addition of tryptamine-derived oxindoles to ynones
T2 - Chemical Communications
AU - Cong, Tiantian
AU - Wang, Huamin
AU - Li, Xiuzheng
AU - Wu, Hai Hong
AU - Zhang, Junliang
PY - 2019
DA - 2019/07/04
PB - Royal Society of Chemistry (RSC)
SP - 9176-9179
IS - 62
VL - 55
PMID - 31305812
SN - 1359-7345
SN - 1364-548X
ER -
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BibTex (до 50 авторов)
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@article{2019_Cong,
author = {Tiantian Cong and Huamin Wang and Xiuzheng Li and Hai Hong Wu and Junliang Zhang},
title = {Chiral bifunctional bisphosphine enabled enantioselective tandem Michael addition of tryptamine-derived oxindoles to ynones},
journal = {Chemical Communications},
year = {2019},
volume = {55},
publisher = {Royal Society of Chemistry (RSC)},
month = {jul},
url = {https://xlink.rsc.org/?DOI=C9CC04357H},
number = {62},
pages = {9176--9179},
doi = {10.1039/c9cc04357h}
}
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MLA
Скопировать
Cong, Tiantian, et al. “Chiral bifunctional bisphosphine enabled enantioselective tandem Michael addition of tryptamine-derived oxindoles to ynones.” Chemical Communications, vol. 55, no. 62, Jul. 2019, pp. 9176-9179. https://xlink.rsc.org/?DOI=C9CC04357H.
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