Issue 24, 2011
From the journal:

Chemical Communications

A domino pericyclic route to polysubstituted salicylic acid derivatives: four sequential processes from enynones and ketenesilyl acetals†

Toshiyuki Hamura,‡a   Shin Iwataa  and  Keisuke Suzuki*a  

* Corresponding authors

a Department of Chemistry, Tokyo Institute of Technology, and SORST, JST Agency, 2-12-1 O-okayama, Meguro-ku, Tokyo 152-8551, Japan
E-mail: ksuzuki@chem.titech.ac.jp
Fax: +81 3-5734-2788

Abstract

Alkenyl alkynyl ketones and ketene silyl acetals (KSAs) undergo regioselective [2+2]-cycloaddition under thermal conditions, triggering domino pericyclic reactions en route to various poly-substituted salicylic acid derivatives.

Graphical abstract: A domino pericyclic route to polysubstituted salicylic acid derivatives: four sequential processes from enynones and ketene silyl acetals

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Article information

DOI
https://doi.org/10.1039/C1CC11758K
Article type
Communication
Submitted
28 Mar 2011
Accepted
04 May 2011
First published
19 May 2011

Chem. Commun., 2011,47, 6891-6893

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A domino pericyclic route to polysubstituted salicylic acid derivatives: four sequential processes from enynones and ketene silyl acetals

T. Hamura, S. Iwata and K. Suzuki, Chem. Commun., 2011, 47, 6891 DOI: 10.1039/C1CC11758K

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