Issue 29, 2019

Gold(i)-catalyzed enantioselective synthesis of polycyclic indoline skeletons and enantiomerically enriched β-substituted tryptamine-allenes by kinetic resolution

Abstract

A gold(I)-catalyzed highly efficient kinetic resolution of indole–allene derivatives has been demonstrated, providing enantiomerically enriched polycyclic indolines possessing four stereogenic centers including an all-carbon quaternary center in a spirocyclic framework and β-substituted tryptamine derivatives in good to excellent ee values and high s selectivities with good functional group tolerance under mild conditions in an atom-economical way.

Graphical abstract: Gold(i)-catalyzed enantioselective synthesis of polycyclic indoline skeletons and enantiomerically enriched β-substituted tryptamine-allenes by kinetic resolution

Supplementary files

Article information

Article type
Communication
Submitted
17 Jan 2019
Accepted
12 Mar 2019
First published
13 Mar 2019

Chem. Commun., 2019,55, 4210-4213

Gold(I)-catalyzed enantioselective synthesis of polycyclic indoline skeletons and enantiomerically enriched β-substituted tryptamine-allenes by kinetic resolution

Y. Zhang, Y. Wei and M. Shi, Chem. Commun., 2019, 55, 4210 DOI: 10.1039/C9CC00412B

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