This paper describes the synthesis of dithioindoles from the free-radical cyclizations of arylisonitriles having pendant alkynes. Also described is the synthesis of substituted indoles and spiro-fused indoles from the coupling of dithioindoles with active hydrogen-containing compounds.
The Use of Sulfur Ylides in the Synthesis of Substituted Indoles
作者:Abigail R. Kennedy、Michael H. Taday、Jon D. Rainier
DOI:10.1021/ol0162320
日期:2001.7.1
[GRAPHICS]This letter describes the insertion of rhodium carbenoids into thioindoles, C-10 thioindoles undergo fragmentation-coupling reactions when exposed to rhodium carbenoids. In an analogous fashion, ketoester- and malonate-substituted carbenoids have been found to insert into C-2 thioindoles, In contrast, vinylogous carbenoids were found to alkylate C-2 thioindoles at C-3.
Sulfur Ylide-Initiated Thio-Claisen Rearrangements. The Synthesis of Highly Substituted Indolines
作者:Alexei V. Novikov、Abigail R. Kennedy、Jon D. Rainier
DOI:10.1021/jo026582f
日期:2003.2.1
The coupling of rhodium carbenoids from vinyl diazoacetates with 2-thio-3-alkyl indoles was found to generate C(3) quaternarysubstitutedindolines via a thionium ylide-initiated [3,3]-sigmatropic rearrangement.
This paper describes the synthesis of dithioindoles from the free-radical cyclizations of arylisonitriles having pendant alkynes. Also described is the synthesis of substituted indoles and spiro-fused indoles from the coupling of dithioindoles with active hydrogen-containing compounds.