Title of article :
Vitamin D: a concise synthesis of the C19 hydroxylated enyne A-ring, an interesting precursor for the preparation of C19 substituted vitamin D analogues
Author/Authors :
Rodriguez، نويسنده , , Raphaël and Ollivier، نويسنده , , Cyril and Santelli، نويسنده , , Maurice، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Pages :
4
From page :
2289
To page :
2292
Abstract :
A new C19 hydroxylated enyne 15, as potential A-ring building block of vitamin D analogues, was synthesized in enantiomerically pure form in nine steps from (−)-(S)-limonene. This short synthesis involved ozonolyzis of 1,2-limonene oxide followed by a Criegee rearrangement, epoxide trans diaxial ring opening by lithium acetylide, elimination, epoxidation and syn β-elimination of the resulting homopropargylic oxirane.
Keywords :
limonene , Vitamin D , Epoxide ring opening , Criegee rearrangement
Journal title :
Tetrahedron Letters
Serial Year :
2004
Journal title :
Tetrahedron Letters
Record number :
1657531
Link To Document :
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