IMINE-EPOXIDE REARRANGEMENTS IN THE FORMATION OF SUBSTITUTED PIPERIDINES. A STEREOSELECTIVE SYNTHESIS OF (+-)SOLENOPSIN-A.

DOI: 10.1016/S0040-4039(00)80657-7

Source and publish data:

Tetrahedron Letters p. 4977 - 4980 (1988)

Update date:2022-07-29

Topics:

Authors:

Wasserman, Harry H.

Rusiecki, Victoria

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Article abstract of DOI:10.1016/S0040-4039(00)80657-7

The imine-epoxide rearrangement, followed by hydride reduction has been used to prepare substituted piperidine derivatives with control of stereochemistry.An application to the synthesis of (+-) solenopsin A is reported.

Full text of DOI:10.1016/S0040-4039(00)80657-7

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