A concise route to functionalized benzofurans directly from gem-dibromoalkenes and phenols-Reference-Cited by-同舟云学术

A concise route to functionalized benzofurans directly from gem-dibromoalkenes and phenols

Published:2015 Issue:80 Volume:5 Page:65462-65470
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Rao Maddali L. N.¹²³⁴,Dasgupta Priyabrata¹²³⁴

Affiliation:

1. Department of Chemistry

2. Indian Institute of Technology Kanpur

3. Kanpur

4. India

Abstract

A tandem strategy for the construction of benzofuran motifs has been developed directly from gem-dibromoalkenes and phenols under palladium-catalyzed conditions.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA13213D

Reference39 articles.

1. Synthesis and Metal-Catalyzed Reactions of gem-Dihalovinyl Systems

2. Pd-Catalyzed Domino Synthesis of Internal Alkynes Using Triarylbismuths as Multicoupling Organometallic Nucleophiles

3. Pd-Catalyzed Tandem Chemoselective Synthesis of 2-Arylbenzofurans using Threefold Arylating Triarylbismuth Reagents

4. New synthesis of benzo[b]furan and indole derivatives from 1,1-dibromo-1-alkenes using a tandem Pd-assisted cyclization–coupling reaction

5. A Highly Efficient Tandem Reaction of 2-(gem-Dibromovinyl)phenols(thiophenols) with Organosilanes to 2-Arylbenzofurans (thiophenes)

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