253276-02-7Relevant academic research and scientific papers
PROCESS FOR PRODUCING FLUORINE COMPOUND
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Page/Page column 7, (2008/06/13)
It is to provide a process for synthesizing an intended fluorine-containing compound having a geminal difluoro structure with a high yield, by subjecting a carbonyl compound which is readily available to a two-stage reaction. A compound (1) such as ethyl
A practical new chiral controller for asymmetric Diels-Alder and alkylation reactions
Sarakinos, Georgios,Corey
, p. 1741 - 1744 (2008/02/11)
(formula presented) The enantiomerically pure hydroxy sulfones (+)- and (-)-2 have been prepared from 1,2-epoxycyclohexane by a simple and practical procedure. The acrylate esters of these alcohols undergo BCl3-catalyzed Diels-Alder reactions with a variety of dienes at -78 to -55°C in CH2Cl2 or C7H8 with high dienophile face selectivity (Table 1). The chiral esters so formed are readily cleaved with recovery of the controllers (+)- or (-)-2. Esters of (+)- and (-)-2 can be converted to Z-polassium enolates and alkylated with high face selectivity.
