Alkylation and Oxidation of 6,7-Dihydro-6-methyl-5H-dibenzo[b,g][1,5]thiazocine. Selective Oxidation of the Sulfide Moiety by Transannular Participation of the Amino Group-Reference-Cited by-同舟云学术

Alkylation and Oxidation of 6,7-Dihydro-6-methyl-5H-dibenzo[b,g][1,5]thiazocine. Selective Oxidation of the Sulfide Moiety by Transannular Participation of the Amino Group

Published:1985-07 Issue:7 Volume:58 Page:1946-1952
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Ohkata Katsuo,Takee Kohichi,Akiba Kin-ya

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/58/7/58_7_1946/_pdf

Reference17 articles.

1. Alkylation of the Sulfur- and Nitrogen-containing Compounds Analogous to Thiazoline Systems

2. Alkylation of Benzothiazolines and the Stevens Rearrangement of the Resulting 2,3,3-Trisubstituted Benzothiazolinium Salts

3. The Structure of Alkylation Products of 2-Substituted 3-Methylbenzolines with Meerwein Reagents

4. General base catalysis and evidence for a sulfurane intermediate in the iodine oxidation of methionine

5. Intramolecular catalysis of organic oxidation and reduction reactions: rapid and microscopically reversible thioether-sulfoxide interconversions in dilute acid

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