α-ACYLAMINORADICAL ANNELATION IN THE DIASTEREOSELECTIVE SYNTHESIS OF 1- AND 5-SUBSTITUTED TETRAHYDROPYRROLOOXAZOLE AND 1-SUBSTITUTED PYRROLIZIDINE DERIVATIVES

DOI: 10.1246/cl.1986.735

Source and publish data:

Chemistry Letters p. 735 - 736 (1986)

Update date:2022-08-03

Topics:

Authors:

Kano, Shinzo

Yuasa, Yoko

Asami, Kenji

Shibuya, Shiroshi

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Article abstract of DOI:10.1246/cl.1986.735

Diastereoselective synthesis of 1,8-trans-1-substituted and 5,8-trans-5-substituted tetrahydropyrrolo<1,2-c>oxazoles was achieved by an application of α-acylaminoradical cyclization at a silylated triple bond.The method was applied to an enantioselective

Full text of DOI:10.1246/cl.1986.735

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