Stereocontrolled derivatization of 3-methoxyestra-1,3,5(10), n-tetraenes via lewis acid promoted prins reactions, (n=7; 8(9))

DOI: 10.1016/S0040-4039(00)74873-8

Source and publish data:

Tetrahedron Letters p. 743 - 746 (1991)

Update date:2022-08-04

Topics:

Authors:

Kuenzer, Hermann

Sauer, Gerhard

Wiechert, Rudolf

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Article abstract of DOI:10.1016/S0040-4039(00)74873-8

Steroidal olefins 1 and 3 undergo dimethylaluminum chloride-mediated Prins reactions with paraformaldehyde to furnish homoallylic alcohols 4 and 16 as major products. These ene reaction-type intermediates are converted into 6 and 17 by hydroxyl group-assi

Full text of DOI:10.1016/S0040-4039(00)74873-8

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