Specification
Synonyms
(R)-DPMPM; [(2R)-1-methylpyrrolidin-2-yl]-diphenyl-methanol; (r)-n-methyl-alpha,alpha-diphenyl-2-pyrrolidinemethanol; AJ-20718; alpha,alpha-Diphenyl-N-methyl-D-prolinol; OR10013; AKOS007930843; (R)-alpha,alpha-Diphenyl-N-methyl-2-pyrrolidinemethanol; ((r)-1-methylpyrrolidin-2-yl)diphenylmethanol; KS-00000IVK;
IUPAC Name
[(2R)-1-methylpyrrolidin-2-yl]-diphenylmethanol;
Canonical SMILES
CN1CCCC1C(C2=CC=CC=C2)(C3=CC=CC=C3)O;
InChI
InChI=1S/C18H21NO/c1-19-14-8-13-17(19)18(20,15-9-4-2-5-10-15)16-11-6-3-7-12-16/h2-7,9-12,17,20H,8,13-14H2,1H3/t17-/m1/s1;
InChI Key
XIJAGFLYYNXCAB-QGZVFWFLSA-N;
Application
Chiral amino alcohol assisted asymmetric, enantioselective, aryl transfer of triphenylboroxin to a set of aryl aldehydes in the presence of chiral amino alcohols derived from (S)-proline.
Pyrrolidinylmethanol compound used for the zinc-catalyzed addition of arylboronic acids to aromatic aldehydes, proceeding in high yields and high enantioselectivities (up to 98% ee).
Covalently-Bonded Unit Count
1
Defined Atom Stereocenter Count
1
Monoisotopic Mass
267.162g/mol
Topological Polar Surface Area
23.5A^2