Formation of a novel thiopyranoindole ring system

Published

Journal Article

The novel thiopyran[2,3,4-c,d]indole ring system (e.g.3) has been prepared from a substituted indole by intramolecular cyclisation of a t-BuS group onto an allyl substituent. The reaction occurs in high yield under the influence of protic acids, Lewis acids or electrophiles (Br2, I2, Hg(OAc)2). © 1992.

Full Text

Published version (via Digital Object Identifier)

Duke Authors

Therien, Michael J.

Cited Authors

Hutchinson, JH; McEachern, EJ; Scheigetz, J; Macdonald, D; Thérien, M

Published Date

August 11, 1992

Published In

Tetrahedron Letters

Volume / Issue

33 / 33

Start / End Page

4713 - 4716

International Standard Serial Number (ISSN)

0040-4039

Digital Object Identifier (DOI)

10.1016/S0040-4039(00)61266-2

Citation Source

Scopus