A Formal Synthesis of Brassinolide. -Enantiodifferentiation of the C2-symmetrical tetraol-sulfide (I) by an enzyme-catalyzed acylation and an E-stereoconvergent Ramberg-Baecklund process are key steps in the construction of the side-chain synthon ( IV). Its introduction to the steroid skeleton affo
โฆ LIBER โฆ
A formal synthesis of brassinolide
โ Scribed by T. Schmittberger; D. Uguen
- Book ID
- 104256839
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 256 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Enzyme-catalysed differentiation of hydroxy groups in a C2v-shaped tetraol-sulfide, combined with a E-stereoconvergent Ramberg-Backlund process, allowed to prepare pure (2S)-2,3-dimethyl-1iodobatane, which could be coupled with a 3,5-cyclopregnane-20-thioracthanol derivative so as to give an e Ofcient precursor of the title vegetal hormone.
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