Enantioselective Michael Additions of Nitromethane by a Catalytic Double Activation Method Using Chiral Lewis Acid and Achiral Amine Catalysts-Reference-Cited by-同舟云学术

Enantioselective Michael Additions of Nitromethane by a Catalytic Double Activation Method Using Chiral Lewis Acid and Achiral Amine Catalysts

Published:2002-10-17 Issue:45 Volume:124 Page:13394-13395
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Itoh Kennosuke¹,Kanemasa Shuji¹

Affiliation:

1. Institute of Advanced Material Study, CREST of JST (Japan Science and Technology), Kyushu University, 6-1 Kasugakoen, Kasuga 816-8580, Japan, and Department of Molecular and Material Sciences, Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasugakoen, Kasuga 816-8580, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja027313%2B

Reference17 articles.

1. Cationic Aqua Complexes of the C2-Symmetric trans-Chelating Ligand (R,R)-4,6-Dibenzofurandiyl-2,2‘-bis(4- phenyloxazoline). Absolute Chiral Induction in Diels−Alder Reactions Catalyzed by Water-Tolerant Enantiopure Lewis Acids

2. Lewis Acid-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Diazoalkane: Chiral Ligand/Achiral Auxiliary Cooperative Chirality Control

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