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: Stereoselective Preparation of Vitamin D Precursors Using the Intramolecular Coupling of Alkynes and Cyclopropylcarbene—Chromium Complexes: A Formal Total Synthesis of (.+-.)-Vitamin D3.
✍ Scribed by J. YAN; J. W. HERNDON
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 37 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Stereoselective Preparation of Vitamin D Precursors Using the Intramolecular Coupling of Alkynes and Cyclopropylcarbene-Chromium Complexes: A Formal Total Synthesis of (±)-Vitamin D 3 . -The intramolecular coupling of the complexes (III) proceeds with high diastereoselectivity. Catalytic hydrogenation of the resulting pyrans leads to ring opening products like (V). (V) can easily be transformed into the precursor (VI) of vitamin D 3 . -(YAN,
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