Synthesis of β-Hydroxy-α,α-disubstituted Amino Acids through the Orthoamide-Type Overman Rearrangement of an α,β-Unsaturated Ester and Stereodivergent Intramolecular SN2′ Reaction: Development and Application to the Total Synthesis of Sphingofungin F-Reference-Cited by-同舟云学术

Synthesis of β-Hydroxy-α,α-disubstituted Amino Acids through the Orthoamide-Type Overman Rearrangement of an α,β-Unsaturated Ester and Stereodivergent Intramolecular SN2′ Reaction: Development and Application to the Total Synthesis of Sphingofungin F

Published:2018-04-15 Issue:4 Volume:91 Page:594-607
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Sugai Tomoya¹,Usui Shunme¹,Tsuzaki Shun¹,Oishi Hiroki¹,Yasushima Daichi¹,Hisada Shoko¹,Fukuyasu Takahiro¹,Oishi Takeshi²,Sato Takaaki¹,Chida Noritaka¹

Affiliation:

1. Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan

2. School of Medicine, Keio University, 4-1-1 Hiyoshi, Kohoku-ku, Yokohama 223-8521, Japan

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

http://www.journal.csj.jp/doi/pdf/10.1246/bcsj.20170408

Reference69 articles.

1. Total Synthesis of Natural tert-Alkylamino Hydroxy Carboxylic Acids

2. Enantio‐ and Diastereoselective Construction of α,α‐Disubstituted α‐Amino Acids for the Synthesis of Biologically Active Compounds