Enantioselective synthesis of dihydro-1H-benzindoles.

The Journal of organic chemistry (2013-03-14)
Gustavo P Silveira, Joseph P Marino

The first examples of dihydro-1H-benzindoles by enantioselective γ-lactamization reaction of naphthyl sulfilimines with trichloroacetyl chloride in the presence of ZnCu as catalyst (≥98:2 er and 65-80% yields) are described. Products are obtained by [3,3]-sigmatropic rearrangement of the azasulfonium enolate or followed by a second allylic rearrangement that transfers chirality. The absolute stereochemistry was confirmed by X-ray crystallography, which provides support for the mechanisms proposed.

Product Number
Product Description

Trichloroacetyl chloride, 99%

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