Issue 91, 2015

Diversity-oriented heterocyclic synthesis using divergent reactivity of N-substituted iso(thio)cyanates

Abstract

Carbon-substituted isocyanates and isothiocyanates are common building blocks in organic synthesis. In contrast, synthetic uses of N-substituted isocyanates and isothiocyanates are severely underdeveloped: few have been reported and their reactivity had not been compared. Herein, we compare the reactivity of blocked (masked) N-isocyanate and N-isothiocyanate precursors in cascade reactions. Divergent reactivity is observed with secondary propargylic and allylic systems, leading to new syntheses of imidazolones, thiazolidines, and a tool to form complex azomethine imines.

Graphical abstract: Diversity-oriented heterocyclic synthesis using divergent reactivity of N-substituted iso(thio)cyanates

Supplementary files

Article information

Article type
Communication
Submitted
27 Aug 2015
Accepted
18 Sep 2015
First published
21 Sep 2015

Chem. Commun., 2015,51, 16405-16408

Author version available

Diversity-oriented heterocyclic synthesis using divergent reactivity of N-substituted iso(thio)cyanates

J. Vincent-Rocan, J. S. Derasp and A. M. Beauchemin, Chem. Commun., 2015, 51, 16405 DOI: 10.1039/C5CC07212C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements