Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins

Jian Wang; Hao Li; Liansuo Zu; Wei Wang

doi:10.1021/ol0601794

Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins

Jian Wang, Hao Li, Liansuo Zu, Wei Wang

Research output: Contribution to journal › Article › peer-review

127 Scopus citations

Abstract

A method for Michael addition of N-heterocycles to nitroolefins has been developed. The process is promoted by a cinchona alkaloid derivative to give Michael adducts in moderate to high enantioselectivities.

Original language	English (US)
Pages (from-to)	1391-1394
Number of pages	4
Journal	Organic Letters
Volume	8
Issue number	7
DOIs	https://doi.org/10.1021/ol0601794
State	Published - Mar 30 2006
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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title = "Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins",

abstract = "A method for Michael addition of N-heterocycles to nitroolefins has been developed. The process is promoted by a cinchona alkaloid derivative to give Michael adducts in moderate to high enantioselectivities.",

author = "Jian Wang and Hao Li and Liansuo Zu and Wei Wang",

year = "2006",

month = mar,

day = "30",

doi = "10.1021/ol0601794",

language = "English (US)",

volume = "8",

pages = "1391--1394",

journal = "Organic Letters",

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T1 - Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins

AU - Wang, Jian

AU - Li, Hao

AU - Zu, Liansuo

AU - Wang, Wei

PY - 2006/3/30

Y1 - 2006/3/30

N2 - A method for Michael addition of N-heterocycles to nitroolefins has been developed. The process is promoted by a cinchona alkaloid derivative to give Michael adducts in moderate to high enantioselectivities.

AB - A method for Michael addition of N-heterocycles to nitroolefins has been developed. The process is promoted by a cinchona alkaloid derivative to give Michael adducts in moderate to high enantioselectivities.

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JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 7

ER -

Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins

Abstract

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