000 01633 a2200385 4500
005 20250515004044.0
264 0 _c20060216
008 200602s 0 0 eng d
022 _a0002-7863
024 7 _a10.1021/ja0535561
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSoloshonok, Vadim A
245 0 0 _aMichael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity.
_h[electronic resource]
260 _bJournal of the American Chemical Society
_cNov 2005
300 _a15296-303 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aCatalysis
650 0 4 _aGlycine
_xchemistry
650 0 4 _aKinetics
650 0 4 _aModels, Chemical
650 0 4 _aMolecular Structure
650 0 4 _aNickel
_xchemistry
650 0 4 _aOxazolidinones
_xchemistry
650 0 4 _aPyrrolidonecarboxylic Acid
_xchemistry
650 0 4 _aSchiff Bases
_xchemistry
650 0 4 _aSpectrometry, Mass, Fast Atom Bombardment
650 0 4 _aStereoisomerism
700 1 _aCai, Chaozhong
700 1 _aYamada, Takeshi
700 1 _aUeki, Hisanori
700 1 _aOhfune, Yasufumi
700 1 _aHruby, Victor J
773 0 _tJournal of the American Chemical Society
_gvol. 127
_gno. 43
_gp. 15296-303
856 4 0 _uhttps://doi.org/10.1021/ja0535561
_zAvailable from publisher's website
999 _c15876167
_d15876167