Catalytic Enantioselective Michael Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes Catalyzed by Well-Defined Chiral Ru Amido Complexes-Reference-Cited by-同舟云学术

Catalytic Enantioselective Michael Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes Catalyzed by Well-Defined Chiral Ru Amido Complexes

Published:2004-08-20 Issue:36 Volume:126 Page:11148-11149
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Watanabe Masahito¹,Ikagawa Ayako¹,Wang Hui¹,Murata Kunihiko¹,Ikariya Takao¹

Affiliation:

1. Department of Applied Chemistry, Graduate School of Science and Engineering, Tokyo Institute of Technology and Frontier Collaborative Research Center, O-okayama, Meguro-ku, Tokyo 152-8552, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja046296g

Reference16 articles.

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2. Enantioselective conjugate addition of primary dialkylzinc reagents to 2-aryl- and 2-heteroaryl-nitroolefins mediated by titanium-TADDOLates preparation of enantioenriched 2-aryl-alkylamines

3. Catalytic Enantioselective Conjugate Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes

4. Rhodium-Catalyzed Asymmetric Conjugate Addition of Organoboronic Acids to Nitroalkenes

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