ENANTIOSELECTIVE PREPARATION OF KEY INTERMEDIATES FOR STEROID SYNTHESIS THROUGH THE ASYMMETRIC MICHAEL ADDITION PROCESS INVOLVING CHIRAL IMINES.

DOI: 10.1016/S0040-4039(00)80513-4

Source and publish data:

Tetrahedron Letters p. 4427 - 4430 (1988)

Update date:2022-09-26

Topics:

Authors:

d'Angelo, Jean

Revial, Gilbert

Volpe, Tony

Pfau, Michel

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Article abstract of DOI:10.1016/S0040-4039(00)80513-4

(S)-Phenanthrone 7, prepared from ketone 4 (80 percent yield, 93 percent ee), was transformed into compounds 8, 9, 13, 15 and 16, useful intermediates in steroid synthesis.

Full text of DOI:10.1016/S0040-4039(00)80513-4

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