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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.


📜 SIMILAR VOLUMES


ChemInform Abstract: Efficient and Versa
✍ A. MOURINO; M. TORNEIRO; C. VITALE; S. FERNANDEZ; J. PEREZ-SESTELO; S. ANNE; C. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

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

ChemInform Abstract: Efficient Synthesis
✍ Andrzej R. Daniewski; Lisa M. Garofalo; Stanley D. Hutchings; Marek M. Kabat; We 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 40 KB 👁 2 views

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