Sulfur Ylide-Initiated Thio-Claisen Rearrangements. The
Synthesis of Highly Substituted Indolines

Novikov, Alexei V.; Kennedy, Abigail R.; Rainier, Jon D.

doi:10.1021/jo026582f.s002

jo026582f_si_002.pdf (62.84 kB)

Sulfur Ylide-Initiated Thio-Claisen Rearrangements. The Synthesis of Highly Substituted Indolines

journal contribution

posted on 2002-12-24, 00:00 authored by Alexei V. Novikov, Abigail R. Kennedy, Jon D. Rainier

The coupling of rhodium carbenoids from vinyl diazoacetates with 2-thio-3-alkyl indoles was found to generate C(3) quaternary substituted indolines via a thionium ylide-initiated [3,3]-sigmatropic rearrangement.

Sulfur Ylide-Initiated Thio-Claisen Rearrangements. The Synthesis of Highly Substituted Indolines

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