Direct olefination of benzaldehydes into 1,3-diarylpropenes via a copper-catalyzed heterodomino Knoevenagel-decarboxylation-Csp3-H activation sequence-Reference-Cited by-同舟云学术

Direct olefination of benzaldehydes into 1,3-diarylpropenes via a copper-catalyzed heterodomino Knoevenagel-decarboxylation-Csp3-H activation sequence

Published:2014 Issue:21 Volume:12 Page:3493-3498
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhao Yaping¹²³⁴,Sun Lu¹²³⁴,Zeng Tieqiang¹²³⁴,Wang Jiayi¹²³⁴,Peng Yanqing¹²³⁴,Song Gonghua¹²³⁴

Affiliation:

1. Shanghai Key Laboratory of Chemical Biology

2. Institute of Pesticides and Pharmaceuticals

3. East China University of Science and Technology

4. Shanghai 200237, P.R. China

Abstract

Copper-catalyzed direct olefination of benzaldehydes into unsymmetrical 1,3-diarylpropenes by a novel domino Knoevenagel-decarboxylation-Csp³-H activation sequence using simpler substrates like benzaldehydes.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB00155A

Reference61 articles.

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5. Palladium(ii)-catalyzed coupling reactions with a chelating vinyl ether and arylboronic acids: a new Heck/Suzuki domino diarylation reaction

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