Stereocontrol in the Addition of Allyl Metal Reagents to an Optically Active Imine Derived from Malic Acid, Leading to a Formal Synthesis of (+)-Negamycin-Reference-Cited by-同舟云学术

Stereocontrol in the Addition of Allyl Metal Reagents to an Optically Active Imine Derived from Malic Acid, Leading to a Formal Synthesis of (+)-Negamycin

Published:1998-05 Issue:5 Volume:27 Page:467-468
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Shimizu Makoto,Morita Asato,Fujisawa Tamotsu

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/27/5/27_5_467/_pdf

Reference19 articles.

1. Very high 1,2- and 1,3-asymmetric induction in the reactions of allylic boron compounds with chiral imines

2. Stereocontrolled reductive amination of 3-hydroxy ketones

3. Diastereoface Discrimination in the Addition of Acetylide to a Chiral Aldehyde, Leading to a Synthesis of (+)-Deoxybiotin in Enantiomerically Pure Form Starting from L-Cysteine

4. Stereocontrol in the addition of nucleophiles to an optically active aldehyde derived from L-serine, leading to a short-step synthesis of (2S,3S,4R)-phytosphingosine

5. A NEW ANTIBIOTIC, NEGAMYCIN

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