New Methods of Resolution and Enrichment of Enantiomeric Excesses of 1,1‘-Bi-2-naphthol-Reference-Cited by-同舟云学术

New Methods of Resolution and Enrichment of Enantiomeric Excesses of 1,1‘-Bi-2-naphthol

Published:1997-06-01 Issue:13 Volume:62 Page:4302-4306
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Periasamy Mariappan¹,Venkatraman Lakshmanan¹,Thomas K. R. Justin¹

Affiliation:

1. School of Chemistry, University of Hyderabad, Central University P.O., Hyderabad 500 046, India, and RSIC, Indian Institute of Technology, Madras 600 036, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo961937e

Reference31 articles.

1. Synthesis and Applications of Binaphthylic C2-Symmetry Derivatives as Chiral Auxiliaries in Enantioselective Reactions

2. Asymmetric synthesis via axially dissymmetric molecules. 6. Rational designing of efficient chiral reducing agents. Highly enantioselective reduction of aromatic ketones by binaphthol-modified lithium aluminum hydride reagents

3. Catalytic asymmetric Diels Alder reactions

4. Vaulted biaryls as chiral ligands for asymmetric catalytic Diels-Alder reactions

5. A Chiral Scandium Catalyst for Enantioselective Diels-Alder Reactions

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