Title of article
Stereoselective synthesis of 22-oxacalcitriol (OCT) and analogues modified at C25
Author/Authors
Fall، نويسنده , , Yagamare and Gonzلlez، نويسنده , , Victoria and Vidal، نويسنده , , Beatriz and Mouriٌo، نويسنده , , Antonio، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
3
From page
427
To page
429
Abstract
The stereoselective synthesis of 22-oxacalcitriol (OCT) has been achieved. The triene system was introduced using the Lythgoe–Hoffmann La Roche convergent Wittig–Horner approach to couple ketoester 7 with A ring phosphine oxide 8. The value of the resulting ester 6 for synthesis of C25-modified OCT analogues is exemplified by the synthesis of 5.
Journal title
Tetrahedron Letters
Serial Year
2002
Journal title
Tetrahedron Letters
Record number
1649285
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