Issue 6, 2008
From the journal:

Organic & Biomolecular Chemistry

Palladium-catalyzed synthesis of indene derivatives via propargylic carbonates with in situ generated organozinc compounds†‡

Zheng-Hui Guan,a   Zhi-Hui Ren,a   Lian-Biao Zhaoa  and  Yong-Min Liang*a  

* Corresponding authors

a State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. China
E-mail: liangym@lzu.edu.cn
Fax: +86-931-8912582
Tel: +86-931-8912593

Abstract

The palladium-catalyzed carboannulation and arylation reaction of propargylic carbonates with in situ generated organozinc compounds produced an important new class of indene derivatives. The reaction proceeded under mild conditions, and indene products were isolated in good to excellent yields.

Graphical abstract: Palladium-catalyzed synthesis of indene derivatives via propargylic carbonates with in situ generated organozinc compounds

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Article information

DOI
https://doi.org/10.1039/B719957K
Article type
Paper
Submitted
02 Jan 2008
Accepted
18 Jan 2008
First published
12 Feb 2008

Org. Biomol. Chem., 2008,6, 1040-1045

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Palladium-catalyzed synthesis of indene derivatives via propargylic carbonates with in situ generated organozinc compounds

Z. Guan, Z. Ren, L. Zhao and Y. Liang, Org. Biomol. Chem., 2008, 6, 1040 DOI: 10.1039/B719957K

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