Efficient and Versatile Synthesis of A-Ring Precursors of 1α,25-Dihydroxy-Vitamin D3 and Analogues. Application to the Synthesis of Lythgoe-Roche Phosphine Oxide. -Starting from 1-carvone (I) an efficient approach to the Lythgoe-Roche phosphine oxide (XII), an important vitamin D synthon, is report
Efficient and versatile synthesis of a-ring precursors of 1α,25-dihydroxy-vitamin D3 and analogues. Application to the synthesis of Lythgoe-Roche phosphine oxide
✍ Scribed by Antonio Mouriño; Mercedes Torneiro; Cristian Vitale; Sara Fernández; José Pérez-Sestelo; Sofia Anné; Carlos Gregorio
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 202 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
An efficient, versatile synthesis of Lythgoe-Phosphine Oxide has been developed starting from /-carvone. The key steps are rupture of protected epoxide 7 to give dicarbonyl compound 8, preparation of vinylic triflate 2, and palladium-catalysed cyclization-carbonylation of vinylic triflate 2.
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