Indole chemistry continues to gain credit within organic synthesis owing to the ubiquitous presence of this heteroaromatic ring in pharmaceuticals, agrochemicals, and organic functional material science.[1] Over the past few years, metal and metal-free catalysis has played a major role in the area, contributing to the development of a number of sustainable procedures for both synthesis and asymmetric decoration of the indolyl core.

Merging Synthesis and Enantioselective Functionalization of Indoles by a Gold-Catalyzed Asymmetric Cascade Reaction / M. Chiarucci; R. Mocci; LD Syntrivanis; G. Cera; A. Mazzanti; M. Bandini. - In: ANGEWANDTE CHEMIE. INTERNATIONAL EDITION. - ISSN 1433-7851. - ELETTRONICO. - 52:(2013), pp. 10850-10853. [10.1002/anie.201304619]

Merging Synthesis and Enantioselective Functionalization of Indoles by a Gold-Catalyzed Asymmetric Cascade Reaction.

CHIARUCCI, MICHEL;CERA, GIANPIERO;MAZZANTI, ANDREA;BANDINI, MARCO
2013

Abstract

Indole chemistry continues to gain credit within organic synthesis owing to the ubiquitous presence of this heteroaromatic ring in pharmaceuticals, agrochemicals, and organic functional material science.[1] Over the past few years, metal and metal-free catalysis has played a major role in the area, contributing to the development of a number of sustainable procedures for both synthesis and asymmetric decoration of the indolyl core.
2013
Merging Synthesis and Enantioselective Functionalization of Indoles by a Gold-Catalyzed Asymmetric Cascade Reaction / M. Chiarucci; R. Mocci; LD Syntrivanis; G. Cera; A. Mazzanti; M. Bandini. - In: ANGEWANDTE CHEMIE. INTERNATIONAL EDITION. - ISSN 1433-7851. - ELETTRONICO. - 52:(2013), pp. 10850-10853. [10.1002/anie.201304619]
M. Chiarucci; R. Mocci; LD Syntrivanis; G. Cera; A. Mazzanti; M. Bandini
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/184135
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