Singlet oxygen addition to chiral allylic alcohols and subsequent peroxyacetalization with β-naphthaldehyde: synthesis of diastereomerically pure 3-β-naphthyl-substituted 1,2,4-trioxanes
作者:Axel G. Griesbeck、Tamer T. El-Idreesy、Johann Lex
DOI:10.1016/j.tet.2006.05.093
日期:2006.11
The synthesis of a series of eight β-naphthyl-substituted 1,2,4-trioxanes 3a–h by a sequence of singlet oxygen ene reaction of allylic alcohols 1a–h and Lewis acid catalyzed peroxyacetalization of the allylic hydroperoxides 2a–h with β-naphthaldehyde is reported. The ene reactions were performed by solid-state photooxygenation in dye-crosslinked polystyrene beads and resulted in mixtures of diastereoisomeric
Processes for Highly Enantio- and Diastereoselective Synthesis of Acyclic Epoxy Alcohols and Allylic Epoxy Alcohols
申请人:Walsh Patrick
公开号:US20090163728A1
公开(公告)日:2009-06-25
The inventive subject matter relates to novel processes for making an epoxy alcohol from an aldehyde, comprising the steps of: (a) adding (i) an organozinc compound or (ii) divinylzinc compound and an diorganozinc compound to said aldehyde in the presence of a first catalyst to form an allylic alkoxide compound; and (b) epoxidizing said allylic alkoxide compound in the presence of an oxidant and a second catalyst.