130562-75-3Relevant academic research and scientific papers
Enantioselective Construction of Quarternary Stereogenic Centres Possessing a Fluorine Atom
Ihara, Masataka,Taniguchi, Nobuaki,Kai, Tomoko,Satoh, Ken,Fukumoto, Keiichiro
, p. 221 - 228 (2007/10/02)
Fluorination of methyl (1R,3R,4S)-8-phenylmenthyl methylmalonates 2 using lithium hexamethyldisilazide and 1-fluoro-2,4,6-trimethylpyridinium triflate (trifluoromethanesulfonate) gave the (R)-3 and (S)-4 isomers in a 3.8:1 ratio, while fluorination of ethyl-, propyl- and benzyl-malonates 10, 11 and 12 provided the (R)-13, 15 and 17 and (S)-14, 16 and 18 isomers in a 1:1.6-2.0 ratio.On the other hand, alkylation of (1R,3R,4S)-8-phenylmenthyl hydrogen fluoromalonates 26 in the presence of lithium hexamethyldisilazide, followed by esterification with diazomethane, produced the (R)-3, 13, 15, 17 and 27 and (S)-4, 14, 16, 18 and 28 isomers in a 1:5.7-35 ratio.
