Two pairs of enantiomerically pure cis-fused cyclopenteno-l,2,4-trioxanes (7, en!-7 and 8, ent-8) are prepared (Schemes 1-3). Their identities are established by dye-sensitized photo-oxygenation of ent-7 and 8 to the allylic hydroperoxides, reduction to the corresponding alcohols, and conversion to
The osmium-catalyzed asymmetric dihydroxylation of cis-fused cyclopenteno-1,2,4-trioxanes
✍ Scribed by Charles W. Jefford; Dharmendra Misra; Allan P. Dishington; Géza Timari; Jean-Claude Rossier; Gérald Bernardinelli
- Book ID
- 104214628
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 279 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Absirarr. Submission of racrmir. ris-frrccd ryt-lopeareno-I es 7 4-rrio.w1w.r (I mrd lent) ID caialylic amounls uf K@f_l~ a& (DtiQDJzPHAL and I.2 cquivalenrs af N-melhylnu~r/~hc)/i~,r N-mide icl aqueous arerone a1 2O'c Tetrahedron: Asymmetry 1992.3. 1317.
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