The synthesis of functionalised hydroazulenes: a new acess to the lactarane skeleton

DOI: 10.1016/S0040-4020(01)85534-4

Source and publish data:

Tetrahedron p. 9657 - 9670 (1994)

Update date:2022-07-29

Topics:

Authors:

Tochtermann

Bruhn Bruhn

Meints Meints

Wolff Wolff

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Article abstract of DOI:10.1016/S0040-4020(01)85534-4

An efficient regioselective and stereoselective approach to the hydroazulenic skeleton of the lactarane sesquiterpenes is described. The furan 1 is transformed to the key intermediate 4. Regioselective intramolecular aldol reaction of 4 leads to the hydro

Full text of DOI:10.1016/S0040-4020(01)85534-4

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