SYRTHESES of S-isotestosterone and the corresponding antbracene analogue using trsns-Q-hydroxy-S-methyl-%+ -(3'-methyl-+'-methorybenzo)-hydradane (I) were earlier 1 reported . The present corununicatlon describes the preparatlon of 178-hydroxp-des-A-androst-9-ene-Gone (IIR=OH) and
The stereospecific olefin formation reaction of 10-P-5 β-hydroxy-α,β-diphenylethylphosphoranes
✍ Scribed by Satoshi Kojima; Kazuhiro Kawaguchi; Kin-ya Akiba
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 238 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
The Westphalen rearrangement' of 38,68-substituted-cholestan-5u-ols (1) to give 5g-methyl-A'-compounds (2) has received considerable study2. No rearrangement products are obtained from 5J3-hydroxy-3, 6a-substituted-4, 6f3-methyl-5 or 6-keto-derivatives 6 . Recently Davies and Summers' reported t
## Per-n Preee.
## Abstract (Z)‐3β‐Acetoxy‐ and (Z)‐3 α‐acetoxy‐5, 10‐__seco__‐1 (10)‐cholesten‐5‐one (**6a**) and (**7a**) were synthesized by fragmentation of 3β‐acetoxy‐5α‐cholestan‐5‐ol (**1**) and 3α‐acetoxy‐5β‐cholestan‐5‐ol (**2**), respectively, using in both cases the hypoiodite reaction (the lead tetraac