DIASTEREOSELEKTIVE SYNTHESE DES SESQUITERPENS (+/-)-OPLOPANON DURCH KATIONISCHE ?-CYCLISIERUNG

DOI: 10.1016/S0040-4039(01)82031-1

Source and publish data:

Tetrahedron Letters p. 3937 - 3940 (1981)

Update date:2022-08-04

Topics:

Authors:

Koester, Frank-Hinrich

Wolf, Herbert

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Article abstract of DOI:10.1016/S0040-4039(01)82031-1

Enone 3, obtained by regioselective alkylation of 4 with 5, was cyclized stereoselectively to the enol acetate 9, subsequently transformed to (+/-)-oplopanone (1) by a short reaction sequence.

Full text of DOI:10.1016/S0040-4039(01)82031-1

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