A New Strategy for the One Pot Synthesis of (Aryloxyimino)Ethylcoumarins Promoted by CuCl2-Reference-Cited by-同舟云学术

A New Strategy for the One Pot Synthesis of (Aryloxyimino)Ethylcoumarins Promoted by CuCl2

Published:2012-01 Issue:1 Volume:36 Page:5-8
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Pal Gargi¹,Bhattacharyya Pranabes¹,Medda Arunima¹,Das Asish R.¹

Affiliation:

1. Department of Chemistry, University of Calcutta, 92, A.P.C. Road, Kolkata – 700009, India

Abstract

Cupric chloride showed efficient catalytic activity for the cross coupling reaction of arylboronic acids and (hydroxyi mino)ethylcoumarins at room temperature in the presence of NEt3 as base. A simple and convenient protocol for the synthesis of O-aryloxime ethers having the highly base sensitive coumarin nucleus is reported. O-Aryloxime ethers are important as they provide access to scaffolds for the generation of various biologically active compounds. They are potential precursors to benzofurans and benzisoxazoles.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/174751912X13247245983221

Reference20 articles.

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3. Antileishmanial activity of benzocycloalkyl azole oximino ethers: The conformationally constraint analogues of oxiconazole

4. Oximino Ethers: Dialkylaminoalkyl Derivatives

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