110480-82-5Relevant articles and documents
Naphthyl-substituted bisoxazoline and pyridylbisoxazoline-copper(I) catalysts for asymmetric allylic oxidation
Zhou, Ziniu,Andrus, Merritt B.
, p. 4518 - 4521 (2012)
The synthesis of naphthyl substituted malonyl-derived and pyridine-based bisoxazolines and their applications in the asymmetric allylic oxidation of cyclohexene with t-butyl p-nitroperbenzoate have been performed with much improved reactivity (75% yield)
A general asymmetric synthesis of phenylglycinols
Pan, Xingang,Jia, Liangbin,Liu, Xuejian,Ma, Haikuo,Yang, Wenqian,Schwarz, Jacob B.
experimental part, p. 329 - 337 (2011/05/17)
Hydride reduction and deprotection of siloxymethyl sulfinimines 2 reliably furnished chiral phenylglycinols 1 or 10 in high overall yield and enantiomeric purity.
An efficient synthesis of 1-naphthylbis(oxazoline) and exploration of the scope in asymmetric catalysis
Van Lingen, Hester L.,Van de Mortel, Jeroen K. W.,Hekking, Koen F. W.,Van Delft, Floris L.,Sonke, Theo,Rutjes, Floris P. J. T.
, p. 317 - 324 (2007/10/03)
Both enantiomers of 1-naphthylglycine were obtained in 99% ee by enzymatic resolution of the corresponding racemic amino acid amide, giving access to the novel ligands (R)- and (S)-naphthylbis(oxazoline). Initial studies provided insight into the scope an