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Mutual kinetic separation of isotopomers of pentafluorophenyl 2-phenyl propionate using quasi-enantiomeric oxazolidinones.
Chirality. 2007 May 5;19(4):313-20. doi: 10.1002/chir.20364.
Chirality. 2007.
PMID: 17357121
Synthesis of enantiomerically pure isotopomers of 2-phenylpropionic acids.
Chavda S, Coumbarides GS, Dingjan M, Eames J, Flinn A, Ghilagaber S, Northen J, Yohannes Y.
Chavda S, et al. Among authors: dingjan m.
Chirality. 2007 May 15;19(5):366-73. doi: 10.1002/chir.20384.
Chirality. 2007.
PMID: 17357119
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Parallel kinetic resolution of D-labelled 2-aryl-propionic and butanoic acids using quasi-enantiomeric combinations of oxazolidin-2-ones.
Coulbeck E, Dingjan M, Eames J.
Coulbeck E, et al. Among authors: dingjan m.
Chirality. 2010 Feb;22(2):193-205. doi: 10.1002/chir.20727.
Chirality. 2010.
PMID: 19408328
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Parallel kinetic resolution of an oxazolidinone using a quasi-enantiomeric combination of [D,13C]-isotopomers of pentafluorophenyl 2-phenyl propionate.
Coumbarides GS, Dingjan M, Eames J, Flinn A, Northen J.
Coumbarides GS, et al. Among authors: dingjan m.
Chirality. 2007 May 5;19(4):321-8. doi: 10.1002/chir.20367.
Chirality. 2007.
PMID: 17357120
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