INTRAMOLECULAR OXIME OLEFIN CYCLOADDITIONS. STEREOSPECIFIC FORMATION OF FUNCTIONALIZED PYRROLIDINES.

DOI: 10.1016/S0040-4039(00)80746-7

Source and publish data:

Tetrahedron Letters p. 5313 - 5316 (1988)

Update date:2022-08-05

Topics:

Authors:

Hassner, Alfred

Maurya, Rakesh

Mesko, Eszter

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Article abstract of DOI:10.1016/S0040-4039(00)80746-7

Allylamines possessing a properly positioned aldoxime or ketoxime chain undergo thermally induced dipolar cycloaddition to bicylic isoxazolidines, with stereospecific introduction of three stereo centers.This provides an entry into stereospecifically func

Full text of DOI:10.1016/S0040-4039(00)80746-7

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