A Switch of Enantiofacial Selectivities Using Designed Similar Chiral Ligands in Zirconium-Catalyzed Asymmetric Aza Diels−Alder Reactions-Reference-Cited by-同舟云学术

A Switch of Enantiofacial Selectivities Using Designed Similar Chiral Ligands in Zirconium-Catalyzed Asymmetric Aza Diels−Alder Reactions

Published:1999-05-27 Issue:12 Volume:64 Page:4220-4221
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kobayashi Shū¹,Kusakabe Ken-ichi¹,Komiyama Susumu¹,Ishitani Haruro¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, The University of Tokyo, CREST, Japan Science and Technology Corporation (JST), Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan, and Department of Applied Chemistry, Faculty of Science, Science University of Tokyo (SUT), Kagurazaka, Shinjuku-ku, Tokyo 162-0825, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9902300

Reference17 articles.

1. Lanthanide(III)-Catalyzed Enantioselective Diels-Alder Reactions. Stereoselective Synthesis of Both Enantiomers by Using a Single Chiral Source and a Choice of Achiral Ligands

2. Highly Enantioselective Synthesis of Enantiomeric 2,3-Dihydroxy Thioesters by Using Similar Types of Chiral Sources Derived from L-Proline

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