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Vibralactone

Stereocontrol led Carbocyclic Construction (-)-Mintlactone (Bates), (-)-Gleenol (Kobayashi), (-)-Vibralactone C (Snider)... [Pg.158]

Roderick W. Bates of Nanyang Technological University found (J. Org. Chem. 2008, 73, 8104), in a synthesis of (-)-Mintlactone 29, that the diastereocontroUed reductive cyclization of 27 to 28 worked best in wet DMF. Susianu Kobayashi of the Tokyo University of Science showed (Chemistry Lett. 2008, 37, 770), en route to (-)-Gleenol 32, that the Claisen rearrangement of 30 deUvered the cyclohexene 31 with high diastereocontrol. Barry B. Snider of Brandeis University prepared (J. Org. Chem. 2008, 73, 8049) (-)-Vibralactone C 36 from 33, available from o-anisic acid by the Schultz protocol. [Pg.159]

See other pages where Vibralactone is mentioned: [Pg.102]    [Pg.102]    [Pg.366]    [Pg.99]    [Pg.99]    [Pg.102]    [Pg.102]    [Pg.366]    [Pg.99]    [Pg.99]   
See also in sourсe #XX -- [ Pg.366 ]



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Stereocontrolled Carbocyclic Construction (-)-Mintlactone (Bates), -Gleenol (Kobayashi), (-)-Vibralactone C (Snider)

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