Stereoselectivity of the Benzannulation Reaction: Efficient Central-to-Axial Chirality Transfer-Reference-Cited by-同舟云学术

Stereoselectivity of the Benzannulation Reaction: Efficient Central-to-Axial Chirality Transfer

Published:2002-05-16 Issue:23 Volume:124 Page:6512-6513
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Vorogushin Andrei V.¹,Wulff William D.¹,Hansen Hans-Jürgen¹

Affiliation:

1. Department of Chemistry, Michigan State University, East Lansing, Michigan 48824, and Institute of Organic Chemistry, University of Zürich, Winterthurerstrasse 190, CH-8057, Zürich, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0201505

Reference19 articles.

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3. Asymmetric total synthesis of natural (-)-and unnatural (+)-steganacin

4. 1,1‘-Binaphthyl Dimers, Oligomers, and Polymers: Molecular Recognition, Asymmetric Catalysis, and New Materials

5. For example: (a) Jacques, J.; Fouquey, C.Organic Synthses; Wiley: New York, 1993; Collect. Vol. 8, p 50. (b) Takaya, H.; Akutagawa, S.; Noyori, R.Organic Synthses; Wiley: New York, 1993; Collect. Vol. 8, p 57.

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