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  • α-Aryl-substituted allenamides in an imino-Nazarov cyclization cascade catalyzed by Au(I).

α-Aryl-substituted allenamides in an imino-Nazarov cyclization cascade catalyzed by Au(I).

Organic letters (2012-11-06)
Zhi-Xiong Ma, Shuzhong He, Wangze Song, Richard P Hsung
ABSTRACT

An imino-Nazarov cyclization using α-aryl-substituted allenamides is described. This gold(I)-catalyzed cascade is efficient and regioselective in constructing a diverse array of synthetically useful aromatic-ring fused cyclopentenamides. The success in this transformation represents a solution to the challenge in establishing an imino-Nazarov cyclization process.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Gold(I) chloride, 99.9% trace metals basis
Sigma-Aldrich
Gold(III) chloride, ≥99.99% trace metals basis
Sigma-Aldrich
Gold(III) chloride, 99%