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Highly Efficient Construction of Pentacyclic Carboline‐Containing Salts via a [Cp*RhCl2]2‐Catalyzed Tandem Reaction

Highly Efficient Construction of Pentacyclic Carboline‐Containing Salts via a... A [Cp*RhCl2]2‐catalyzed tandem reaction of indolyl aldehydes, amines, and alkynes featuring the formation of two C−C bonds, two C−N bonds, and one C=N bond is described. This strategy involves double C−H activation and double insertion of alkynes, furnishing a series of pentacyclic carboline‐containing salts in good yields under mild conditions. It provides a good choice for rapidly constructing libraries of such pentacyclic carboline‐containing salts. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Asian Journal of Organic Chemistry Wiley

Highly Efficient Construction of Pentacyclic Carboline‐Containing Salts via a [Cp*RhCl2]2‐Catalyzed Tandem Reaction

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References (70)

Publisher
Wiley
Copyright
© 2019 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
ISSN
2193-5807
eISSN
2193-5815
DOI
10.1002/ajoc.201800642
Publisher site
See Article on Publisher Site

Abstract

A [Cp*RhCl2]2‐catalyzed tandem reaction of indolyl aldehydes, amines, and alkynes featuring the formation of two C−C bonds, two C−N bonds, and one C=N bond is described. This strategy involves double C−H activation and double insertion of alkynes, furnishing a series of pentacyclic carboline‐containing salts in good yields under mild conditions. It provides a good choice for rapidly constructing libraries of such pentacyclic carboline‐containing salts.

Journal

Asian Journal of Organic ChemistryWiley

Published: Jan 1, 2019

Keywords: ; ; ; ;

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