4.8 Article

Highly Enantioselective Friedel-Crafts Reaction of Thiophenes with Glyoxylates: Formal Synthesis of Duloxetine

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ORGANIC LETTERS
卷 11, 期 20, 页码 4636-4639

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AMER CHEMICAL SOC
DOI: 10.1021/ol901906r

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  1. Polish Ministry of Science and Higher Education [PBZ-KBN-126/T09/06]
  2. Foundation for Polish Science

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An efficient Friedel-Crafts reaction of a series of 2-substituted thiophenes with alkyl glyoxylates has been developed using a catalytic amount of an easy accessible 6,6'-dibromo-BINOL/Ti(IV) complex. A variety of hydroxy(thiophene-2-yl)acetates can be synthesized in high enantioselectivites (92-98% ee) and good yields. This is the first report on the efficient asymmetric F-C reaction of thiophenes with alkyl glyoxylates. Starting from simple thiophene and n-butyl glyoxylate, we demonstrated the formal synthesis of duloxetine.

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