Issue 36, 2019

Preparation of isoquinazolines via metal-free [4 + 2] cycloaddition of ynamides with nitriles

Abstract

TfOH-mediated [4 + 2] cycloaddition of ynamides with nitriles to construct 1,2-dihydroquinazolines is realized by a direct reaction in moderate to excellent yields (up to 93%) in a stereospecific manner. A rapid and efficient strategy has been employed for the syntheses of alkyl-substituted 1,2-dihydroquinazoline derivatives, and it exhibits good functional group tolerance, has a short reaction time, shows excellent diastereoselectivity, and is a simple and high-yielding reaction.

Graphical abstract: Preparation of isoquinazolines via metal-free [4 + 2] cycloaddition of ynamides with nitriles

Supplementary files

Article information

Article type
Paper
Submitted
20 Jun 2019
Accepted
15 Aug 2019
First published
03 Sep 2019

Org. Biomol. Chem., 2019,17, 8408-8416

Preparation of isoquinazolines via metal-free [4 + 2] cycloaddition of ynamides with nitriles

H. Wu, Y. Liu, M. He, H. Wen, W. Cao, P. Chen and Y. Tang, Org. Biomol. Chem., 2019, 17, 8408 DOI: 10.1039/C9OB01395D

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