Enantiospecific approach to a quinane skeleton related to pentalenolactones

DOI: 10.1016/S0040-4039(97)10370-7

Source and publish data:

Tetrahedron Letters p. 8623 - 8626 (1997)

Update date:2022-08-03

Topics:

Authors:

Pellegrinet, Silvina C.

Spanevello, Rolando A.

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Article abstract of DOI:10.1016/S0040-4039(97)10370-7

A novel and general approach has been delineated for the enantiomerically pure synthesis of the angularly fused tricyclic system of the pentalenolactone family of compounds. D-Glucose is used as starting material and a diasteroselective Diels-Alder reaction sets the elements for the ring junctions.

Full text of DOI:10.1016/S0040-4039(97)10370-7

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