Syntheses of .alpha.-phenylneopentyl chloride enantiomers: (S)-(-)-1-chloro-1-phenyl-2,2-dimethylpropane from (R)-(+)-1-phenyl-2,2-dimethyl-1-propanol via the reaction of tri-n-butylphosphine in carbon tetrachloride and (R)-(+)-1-chloro-1-phenyl-2,2-dimethylpropane from anthranilic acid
ZIEGER, H. E.;BRIGHT, D. A.;HAUBENSTOCK, H., J. ORG. CHEM., 1986, 51, N 8, 1180-1184
作者:ZIEGER, H. E.、BRIGHT, D. A.、HAUBENSTOCK, H.
DOI:——
日期:——
Metal-free intramolecular oxidative decarboxylative amination of primary α-amino acids with product selectivity
作者:Yizhe Yan、Zhiyong Wang
DOI:10.1039/c1cc12885j
日期:——
A novel metal-free intramolecular oxidative decarboxylative coupling of primary α-amino acids with 2-aminobenzoketones under mild and neutral conditions was developed. Different quinazolines can be selectively obtained by various oxidants.
Syntheses of .alpha.-phenylneopentyl chloride enantiomers: (S)-(-)-1-chloro-1-phenyl-2,2-dimethylpropane from (R)-(+)-1-phenyl-2,2-dimethyl-1-propanol via the reaction of tri-n-butylphosphine in carbon tetrachloride and (R)-(+)-1-chloro-1-phenyl-2,2-dimethylpropane from anthranilic acid
作者:Herman E. Zieger、Danielle Angrand Bright、H. Haubenstock