4.8 Article

Catalytic Enantioselective 1,4-lodofunctionalizations of Conjugated Dienes

Journal

ORGANIC LETTERS
Volume 17, Issue 18, Pages 4424-4427

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b02026

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Funding

  1. SERB, New Delhi [SB/S1/OC-63/2013]
  2. CSIR, New Delhi

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The first catalytic enantioselective 1,4-iodofunctionalizations of conjugated dienes have been developed. Starting from beta,gamma,delta,epsilon-unsaturated oximes and 4-Ns hydrazones, these N-iodosuccinimide-mediated reactions are catalyzed by newly modified tertiary aminothiourea derivatives and furnish Delta(2)-isoxazoline and Delta(2)-pyrazoline derivatives, respectively, containing an (E)-allyl iodide group at the quaternary stereogenic center generally in high yield and with excellent enantioselectivity (up to 98.5:1.5 er).

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