Issue 2, 2004
From the journal:

Chemical Communications

The intramolecular Baylis–Hillman reaction: easy preparation of versatile substrates, facile reactions, and synthetic applications†

Jung Eun Yeo,a   Xiuling Yang,a   Hee Jin Kima  and  Sangho Koo*a  

* Corresponding authors

a Department of Chemistry, Myong Ji University, Yongin, Kyunggi-Do, 449-728, Korea
E-mail: sangkoo@mju.ac.kr
Fax: +82 31 335 7248
Tel: +82 31 330 6185

Abstract

We have developed a general and highly efficient method for the preparation of diverse ω-formyl-α,β-unsaturated carbonyl compounds and optimized the conditions for the intramolecular Baylis–Hillman reactions of these compounds to provide various biologically important polycyclic compounds.

Graphical abstract: The intramolecular Baylis–Hillman reaction: easy preparation of versatile substrates, facile reactions, and synthetic applications

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Article information

DOI
https://doi.org/10.1039/B311951C
Article type
Communication
Submitted
26 Sep 2003
Accepted
20 Oct 2003
First published
10 Nov 2003

Chem. Commun., 2004, 236-237

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The intramolecular Baylis–Hillman reaction: easy preparation of versatile substrates, facile reactions, and synthetic applications

J. E. Yeo, X. Yang, H. J. Kim and S. Koo, Chem. Commun., 2004, 236 DOI: 10.1039/B311951C

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