First and mild synthesis of fluorene-9-malonic acid and some substituted derivatives via the intramolecular hydroarylation of 2-phenylbenzylidenemalonic acids-Reference-Cited by-同舟云学术

First and mild synthesis of fluorene-9-malonic acid and some substituted derivatives via the intramolecular hydroarylation of 2-phenylbenzylidenemalonic acids

Published:2011-04 Issue:14 Volume:67 Page:2548-2554
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Chosson Elizabeth,Rochais Christophe,Legay Remi,Sopkova de Oliveira Santos Jana,Rault Sylvain,Dallemagne Patrick

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. BTISA-catalyzed Friedel–Crafts bimolecular cyclization of cinnamic acid under superelectrophilic solvation conditions

2. Structure–Activity Studies on Splitomicin Derivatives as Sirtuin Inhibitors and Computational Prediction of Binding Mode

3. Chemical Libraries via Sequential C−H Functionalization of Phenols

4. An Improved, Scalable, and Impurity-Free Process for Tolterodine Tartrate

5. Facile and Regioselective Synthesis of Phenylpropanoid-Substituted Flavan-3-ols

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