Controlling chemoselectivity in copper-catalyzed decarboxylative A3/A3 cross-couplings: direct formation of unsymmetrical 1,4-diamino-2-butynes-Reference-Cited by-同舟云学术

Controlling chemoselectivity in copper-catalyzed decarboxylative A3/A3 cross-couplings: direct formation of unsymmetrical 1,4-diamino-2-butynes

Published:2017 Issue:1 Volume:4 Page:37-41
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zhao Panfeng¹²³⁴,Feng Huangdi¹²³⁴,Pan Haoran¹²³⁴,Sun Zhihua¹²³⁴,Tong Minchao⁵⁶⁷³⁴

Affiliation:

1. College of Chemistry and Chemical Engineering

2. Shanghai University of Engineering Science

3. Shanghai

4. China

5. State Key Laboratory of Organometallic Chemistry

6. Shanghai Institute of Organic Chemistry

7. Chinese Academy of Sciences

Abstract

A direct cross-coupling of propiolic acid with two kinds of in situ formed iminiums has been achieved via a CuI/CuCl₂-catalyzed decarboxylative A³/A³ domino process.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QO/C6QO00499G

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