Title of article :
Synthesis and photoreactions of 3-oxa-tricyclo[5.2.2.01,5]undecenones: a novel, stereoselective route to oxa-triquinanes and oxa-sterpuranes
Author/Authors :
Vishwakarma Singh، نويسنده , , S.Q Alam، نويسنده , , G.D Praveena، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
8
From page :
9729
To page :
9736
Abstract :
The synthesis of 11-methyl-3-oxa-tricyclo[5.2.2.01,5]undecenones and their photochemical reactions upon triplet (3T) and singlet (1S) excitation is described. Oxidation of hydroxymethylphenol gave a ketoepoxide by intramolecular cycloaddition. Manipulation of the oxirane ring furnished the chromophoric systems. Triplet excitation of these gave tetracyclic compounds containing an oxatriquinane framework. Singlet excitation furnished the tricyclic compound having an oxasterpurane ring system in a stereoselective fashion.
Keywords :
Diels–Alder reaction , Cycloaddition , photo-chemistry , oxa-polyquinanes
Journal title :
Tetrahedron
Serial Year :
2002
Journal title :
Tetrahedron
Record number :
1083684
Link To Document :
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