Versatile One-Pot Synthesis of 3-Alkenylcoumarins

Autor: Olga N. Kataeva, Siegfried R. Waldvogel, Olivia Neumann, Kristina Hackelöer, Pia Königs
Rok vydání: 2008
Předmět:
Zdroj: European Journal of Organic Chemistry. 2008:343-349
ISSN: 1099-0690
1434-193X
DOI: 10.1002/ejoc.200700819
Popis: A variety of 2-acyl-, 2-aroyl- and 2-formyl-substituted phenols are converted in a one-pot reaction with α,β-unsaturated carboxylic acid chlorides into the corresponding 3-alkenylcoumarins. Especially the labile 3-vinylcoumarins are readily available by the simple to perform protocol. If longer alkenyl chains are involved in position 3, small molecules with excellent organo gelating properties are established. The mode of action for such aggregates is confirmed by X-ray analysis of an analogue.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
Databáze: OpenAIRE