204119-07-3Relevant academic research and scientific papers
New approaches to enantioselective fluorination: Cinchona alkaloids combinations and chiral ligands/metal complexes
Shibata, Norio,Ishimaru, Takehisa,Nakamura, Shuichi,Toru, Takeshi
, p. 469 - 483 (2007)
The selective construction of carbon-fluorine bonds is of great interest to medicinal chemists because the replacement of a hydrogen or an oxygen atom with a fluorine atom in biologically active molecules can confer the molecules with improved physicochem
Enantioselective fluorination mediated by cinchona alkaloid derivatives/Selectfluor combinations: Reaction scope and structural information for N-fluorocinchona alkaloids
Shibata,Suzuki,Asahi,Shiro
, p. 7001 - 7009 (2001)
Cinchona-alkaloid/Selectfluor combinations efficiently fluorinate a variety of carbonyl compounds in a highly enantioselective manner to furnish chiral α-fluorocarbonyl compounds. The DHQB/Selectfluor combination is effective for the enantioselective fluo
SPANphos ligands in palladium-catalyzed asymmetric fluorination
Jacquet, Olivier,Clement, Nicolas D.,Blanco, Carolina,Belmonte, Marta Martinez,Benet-Buchholz, Jordi,Van Leeuwen, Piet W. N. M.
experimental part, p. 4844 - 4852 (2012/10/18)
The synthesis of new enantiopure wide-bite-angle diphosphanes is described as well as their use in the palladium-catalyzed asymmetric fluorination of α-cyanoacetates. Enantiomeric excesses up to 93 % were obtained when Pd(OAc)2-SPANphos was use
Efficient synthesis of a new, highly versatile chiral derivatizing agent, α-cyano-α-fluoro-p-tolylacetic acid (CFTA)
Takeuchi, Yoshio
, p. 365 - 366 (2007/10/03)
The new and versatile chiral derivatizing agent, α-cyano-α-fluoro-p-tolylacetic acid (CFTA), has been efficiently synthesized in optically pure form by Candida rugosa lipase-mediated kinetic resolution of racemic CFTA ethyl ester, the latter being readily
