INTRAMOLECULAR PHOTOCHEMICAL [2-CYCLOADDITIONS OF ENANTIOMERICALLY PURE 4,4-DISUBSTITUTED CYCLOHEXENONES - AN APPROACH TO THE TOTAL ASYMMETRIC-SYNTHESIS OF LINTENONE(2])

Authors
RESEK JE MEYERS AI
Citation
Je. Resek et Ai. Meyers, INTRAMOLECULAR PHOTOCHEMICAL [2-CYCLOADDITIONS OF ENANTIOMERICALLY PURE 4,4-DISUBSTITUTED CYCLOHEXENONES - AN APPROACH TO THE TOTAL ASYMMETRIC-SYNTHESIS OF LINTENONE(2]), Synlett, (2), 1995, pp. 145-146
Citations number
10
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
2
Year of publication
1995
Pages
145 - 146
Database
ISI
SICI code
0936-5214(1995):2<145:IP[OEP>2.0.ZU;2-0
Abstract
Enantiomerically pure 4,4-dialkylcyclohexenones 12-14 have been prepar ed which undergo photochemical [2 + 2] cycloadditions to give the ring system of lintenone 1.