An Efficient and Selective conversion of Hydrazides into Esters and Acids-Reference-Cited by-同舟云学术

An Efficient and Selective conversion of Hydrazides into Esters and Acids

Published:2000-08 Issue:8 Volume:2000 Page:376-377
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Srinivas R.¹,Reddy B.V. Subba¹,Yadav J.S.¹,Ramalingam T.¹

Affiliation:

1. Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad-500 007, India

Abstract

Hydrazides are selectively oxidised to esters/acids in high yields using Oxone® in the presence of an appropriate alcohol/water as a nucleophile at ambient temperature. A variety of functional groups including alkenes, alcohols, ethers, cyclopropyl groups and nitriles are unaffected.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823400103167958

Reference18 articles.

1. N-Acylethoxymethylene Hydrazones as the Source of a C1Fragment

2. A General and Simple Approach to N1-Acylformamidrazones

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4. Migration of an acyl group in the pyrazole system: synthesis of 1-acyl-3-hydroxy-1H-pyrazoles and related derivatives. A new preparation of N,N ′-diacylhydrazines

5. Studies on pyrrolidinones. A convenient synthesis of 2-methyl-5-(5-oxo-1-benzyl-2-pyrrolidinyl)-1,3,4-oxadiazole

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