Parallel kinetic resolution of an oxazolidinone using a  quasi ‐enantiomeric combination of [D, 13 C]‐isotopomers of pentafluorophenyl 2‐phenyl propionate | Zendy

Coumbarides Gregory S. | Zendy; Dingjan Marco | Zendy; Eames Jason | Zendy; Flinn Anthony | Zendy; Northen Julian | Zendy

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Parallel kinetic resolution of an oxazolidinone using a quasi ‐enantiomeric combination of [D, 13 C]‐isotopomers of pentafluorophenyl 2‐phenyl propionate

Author(s) -

Coumbarides Gregory S.,

Dingjan Marco,

Eames Jason,

Flinn Anthony,

Northen Julian

Publication year - 2007

Publication title -

chirality

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.43

H-Index - 77

eISSN - 1520-636X

pISSN - 0899-0042

DOI - 10.1002/chir.20367

Subject(s) - chemistry , isotopomers , enantiomer , kinetic resolution , chirality (physics) , propionate , stereochemistry , resolution (logic) , kinetic energy , enantiomeric excess , propionates , enantioselective synthesis , organic chemistry , catalysis , molecule , nambu–jona lasinio model , chiral symmetry breaking , physics , quantum mechanics , artificial intelligence , quark , computer science

Parallel kinetic resolution of Evans' phenylglycine derived oxazolidinone using an equimolar combination of quasi ‐enantiomeric active esters (derived from [D, 13 C]‐labeled 2‐phenylpropionic acid) was achieved. The levels of stereocontrol were high, leading to products with predictable configurations. Chirality, 2007. © 2007 Wiley‐Liss, Inc.

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