Issue 25, 2017

Synthesis of seven-membered heterocycles via copper-catalyzed cross-coupling of terminal alkynes with diazo compounds and sequential Michael addition

Abstract

A novel approach to synthesize seven-membered heterocycles is established by reacting amide tethered terminal alkynes with aryl diazoacetates in a one-pot reaction. This reaction involves copper-catalyzed cross coupling followed by base-promoted intramolecular Michael addition and yields products with a medium-sized ring.

Graphical abstract: Synthesis of seven-membered heterocycles via copper-catalyzed cross-coupling of terminal alkynes with diazo compounds and sequential Michael addition

Supplementary files

Article information

Article type
Communication
Submitted
04 May 2017
Accepted
07 Jun 2017
First published
07 Jun 2017

Org. Biomol. Chem., 2017,15, 5272-5274

Synthesis of seven-membered heterocycles via copper-catalyzed cross-coupling of terminal alkynes with diazo compounds and sequential Michael addition

S. Yan, S. Cao and J. Sun, Org. Biomol. Chem., 2017, 15, 5272 DOI: 10.1039/C7OB01091E

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