Highly Stereoselective 1,4-Conjugate Addition of Organocopper Reagents to Methyl α-d-Glucopyranoside Derivatives Tethering an Unsaturated Ester Moiety at C-4 or C-61-Reference-Cited by-同舟云学术

Highly Stereoselective 1,4-Conjugate Addition of Organocopper Reagents to Methyl α-d-Glucopyranoside Derivatives Tethering an Unsaturated Ester Moiety at C-4 or C-61

Published:1999-09-30 Issue:9 Volume:1 Page:1447-1450
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Totani Kiichiro¹,Nagatsuka Takayuki¹,Takao Ken-ichi¹,Ohba Shigeru¹,Tadano Kin-ichi¹

Affiliation:

1. Department of Applied Chemistry, Keio University, Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan, and Department of Chemistry, Keio University, Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol9909942

Reference9 articles.

1. Asymmetric synthesis of α-amino acids from carbohydrates as chiral templates

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