Cyclocondensation reactions of 2-acyl-3-indoleacetic acid derivatives with phenylglycinol. Enantioselective synthesis of 1-substituted tetrahydro-b-carboline alkaloids

Publication date

2020-06-04T07:42:42Z

2020-06-04T07:42:42Z

2012-03

2020-06-04T07:42:42Z

Abstract

Cyclocondensation reactions between a variety of 2‐acyl‐3‐indoleacetic acid derivatives and (R )‐phenylglycinol were studied. Successful results were obtained from N ‐alkyl keto acid derivatives. The resulting tetracyclic lactams provide straightforward access to enantiopure 1‐substituted tetrahydro‐β‐carboline alkaloids.

Document Type

Article


Accepted version

Language

English

Publisher

Wiley-VCH

Related items

Versió postprint del document publicat a: https://doi.org/10.1002/ejoc.201101718

European Journal of Organic Chemistry, 2012, vol. 2012, num. 9, p. 1835-1842

https://doi.org/10.1002/ejoc.201101718

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(c) Wiley-VCH, 2012