Issue 40, 2018

Palladium-catalyzed heck-type cascade cyclization of (Z)-1-iodo-1,6-dienes with N-tosyl hydrazones

Abstract

A palladium-catalyzed heck-type cascade cyclization of (Z)-1-iodo-1,6-dienes with N-tosyl hydrazones is reported. The alkylpalladium intermediate coupled with the diazo compound, generating the second alkylpalladium species bearing two β-H, which generated a terminal alkene as the major products in the anti-Zaitsev way via the highly regioselective β-H elimination. It provided a new way to synthesize tetrahydropyridine derivatives bearing a terminal alkene.

Graphical abstract: Palladium-catalyzed heck-type cascade cyclization of (Z)-1-iodo-1,6-dienes with N-tosyl hydrazones

Supplementary files

Article information

Article type
Communication
Submitted
28 Jul 2018
Accepted
24 Sep 2018
First published
25 Sep 2018

Org. Biomol. Chem., 2018,16, 7356-7360

Palladium-catalyzed heck-type cascade cyclization of (Z)-1-iodo-1,6-dienes with N-tosyl hydrazones

J. Li, X. Chi, L. Meng, L. Jiao, W. Shang, P. Wang, D. Zhang, Y. Dong, Q. Liu and H. Liu, Org. Biomol. Chem., 2018, 16, 7356 DOI: 10.1039/C8OB01821A

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