The Enolate Group as Dipolarophile in Intramolecular Cycloaddition of Nitrones

DOI: 10.1016/0040-4020(95)00283-E

Source and publish data:

Tetrahedron p. 6285 - 6292 (1995)

Update date:2022-08-03

Topics:

Authors:

Aurich, Hans Guenter

Koester, Heiner

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Article abstract of DOI:10.1016/0040-4020(95)00283-E

Nitrones 5 were prepared starting from N-benzylalaninol 3.Michael addition of 3 to 3-butenone-2 afforded alcohol 4 which was converted to 5 by Swern oxidation and subsequent treatment of the resulting aldehyde with N-alkylhydroxylamines.The enolate group

Full text of DOI:10.1016/0040-4020(95)00283-E

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