Issue 2, 2016

Construction of pyrazolo[5,1-a]isoindol-8(3aH)-one derivatives via phosphine-catalyzed cyclization of electron-deficient alkynes and N-amino substituted phthalimide

Abstract

A novel method for the synthesis of diversely functionalized pyrazolo[5,1-a]isoindol-8(3aH)-ones is developed via phosphine-catalyzed tandem Michael addition/intramolecular Morita–Baylis–Hillman reaction of electron-deficient alkynes and N-amino substituted phthalimide. This cyclization is operationally simple under metal-free reaction conditions.

Graphical abstract: Construction of pyrazolo[5,1-a]isoindol-8(3aH)-one derivatives via phosphine-catalyzed cyclization of electron-deficient alkynes and N-amino substituted phthalimide

Supplementary files

Article information

Article type
Paper
Submitted
26 Aug 2015
Accepted
11 Dec 2015
First published
24 Dec 2015

RSC Adv., 2016,6, 1395-1402

Construction of pyrazolo[5,1-a]isoindol-8(3aH)-one derivatives via phosphine-catalyzed cyclization of electron-deficient alkynes and N-amino substituted phthalimide

Q. Zhou, F. Ge, Q. Chen and T. Lu, RSC Adv., 2016, 6, 1395 DOI: 10.1039/C5RA17267E

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