Issue 75, 2015

[3 + 2] Annulations between indoles and α,β-unsaturated ketones: access to pyrrolo[1,2-a]indoles and model reactions toward the originally assigned structure of yuremamine

Abstract

A direct [3 + 2] annulation reaction between indoles and α,β-unsaturated ketones is reported, which allows for the efficient assembly of densely substituted, highly functionalized pyrrolo[1,2-a]indoles. Model reactions toward the originally assigned structure of yuremamine are also described, leading to the successful construction of the core with required functionality.

Graphical abstract: [3 + 2] Annulations between indoles and α,β-unsaturated ketones: access to pyrrolo[1,2-a]indoles and model reactions toward the originally assigned structure of yuremamine

Supplementary files

Article information

Article type
Communication
Submitted
20 Jun 2015
Accepted
09 Jul 2015
First published
09 Jul 2015

RSC Adv., 2015,5, 60962-60965

Author version available

[3 + 2] Annulations between indoles and α,β-unsaturated ketones: access to pyrrolo[1,2-a]indoles and model reactions toward the originally assigned structure of yuremamine

H. Li, Z. Wang and L. Zu, RSC Adv., 2015, 5, 60962 DOI: 10.1039/C5RA11904A

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