MgBr2-PROMOTED ELECTROSYNTHESIS OF SULFENIMINES (THIOOXIMES) FROM α-AMINOALKANOATES AND DIARYL/DIALKYL DISULFIDES IN A CH2Cl2–H2O TWO-PHASE SYSTEM. A STRAIGHTFORWARD PREPARATION OF C(6)/C(7)-SULFENIMINE DERIVATIVES OF PENICILLIN AND CEPHALOSPORIN-Reference-Cited by-同舟云学术

MgBr2-PROMOTED ELECTROSYNTHESIS OF SULFENIMINES (THIOOXIMES) FROM α-AMINOALKANOATES AND DIARYL/DIALKYL DISULFIDES IN A CH2Cl2–H2O TWO-PHASE SYSTEM. A STRAIGHTFORWARD PREPARATION OF C(6)/C(7)-SULFENIMINE DERIVATIVES OF PENICILLIN AND CEPHALOSPORIN

Published:1984-10-05 Issue:10 Volume:13 Page:1823-1826
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Torii Sigeru,Tanaka Hideo,Hamano Sin-ichi,Tada Nobuhito,Nokami Junzo,Sasaoka Michio

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference10 articles.

1. Studies on the preparation and reactions of tritylsulfenimines

2. Studies on the development of the tritylsulfenyl group as a nitrogen protecting group and application in a synthesis of .delta.-coniceine

3. Sulfenyl transfer rearrangement of sulfenimines (thiooximes). A novel synthesis of 7.alpha.-methoxycephalosporins and 6.alpha.-methoxypenicillins

4. A novel synthetic route to 7.ALPHA.-methoxycephalosporins.

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