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.

M. Chiarucci, R. Mocci, LD Syntrivanis, G. Cera, A. Mazzanti, M. Bandini (2013). Merging Synthesis and Enantioselective Functionalization of Indoles by a Gold-Catalyzed Asymmetric Cascade Reaction. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, 52, 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
M. Chiarucci, R. Mocci, LD Syntrivanis, G. Cera, A. Mazzanti, M. Bandini (2013). Merging Synthesis and Enantioselective Functionalization of Indoles by a Gold-Catalyzed Asymmetric Cascade Reaction. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, 52, 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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