Hydroacylation of 2-vinyl benzaldehyde systems: An efficient method for the synthesis of chiral 3-substituted indanones

…, JV McCullagh, AT Morehead

Index: Kundu, Kousik; McCullagh, James V.; Morehead Jr., Andrew T. Journal of the American Chemical Society, 2005 , vol. 127, # 46 p. 16042 - 16043

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Citation Number: 119

Abstract

Asymmetric rhodium-catalyzed hydroacylation has been utilized in the synthesis of 3- substituted indanones with high conversions and enantioselectivity. The hydroacylation reaction of 2-vinyl benzaldehyde had been previously reported to give a low yield of indanone and an unidentified product. We have identified this compound as a dimer of the starting material. Substitution at the α-position of the 2-vinyl benzaldehyde substrates ...

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