A quantitative study of substituent effects on oxidative cyclization of some 2-methylsubstituted aldehydes. Thiosemicarbazones induced by ferric chloride-Reference-Cited by-同舟云学术

A quantitative study of substituent effects on oxidative cyclization of some 2-methylsubstituted aldehydes. Thiosemicarbazones induced by ferric chloride

Published:1996-05 Issue:3 Volume:33 Page:863-872
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Noto Renato,Meo Paolo Lo,Gruttadauria Michelangelo,Werber Giuseppe

Publisher

Wiley

Subject

Organic Chemistry

Reference25 articles.

1. Novel [2-(4-Piperidinyl)ethyl](thio)ureas: synthesis and antiacetylcholinesterase activity

2. Discovery of a novel class of potent HIV-1 protease inhibitors containing the (R)-(hydroxyethyl)urea isostere

3. The semicarbazone peptidomimetic group in imino aza peptides

4. Substituent effect on oxidative cyclization of aldehyde thiosemicarbazones with ferric chloride

5. Oxidative cyclization of some aldehyde semicarbazones induced by metallic salts

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