Careful control of reaction temperature can improve the stereoselectivity of the aza-Claisen rearrangement. Conducting the reaction at lower temperatures can favor the formation of the desired enantiomer.
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N-((S)-1-phenylethyl)-(2S,3S)-2,3-dimethylpent-4-enamide
3-phenyl-2-(phenylamino)-2-(phenylmethyl)propanenitrile
C30H36N2O9
C26H27NO3S2
(S)-2,2-Dimethyl-3-((R)-2-morpholin-4-yl-2-oxo-1-phenyl-ethylamino)-3-phenyl-propionic acid ethyl ester
2-[3,5-bis(trifluoromethyl)phenyl]-4,4,6-trimethyl-1,3,2-dioxaborinane
(3-methoxyphenyl)methyl methyl carbonate
1-(3-phenoxyphenyl)ethanol
9-(3-nitrophenyl)-2-phenyl-9H-carbazole
1,2-Cyclohexanediol, 1-(4-methoxyphenyl)-, (1R,2R)-rel-
((1S,2R,3S,4R)-1-Benzyl-4-tert-butoxycarbonylamino-2,3-dihydroxy-5-phenyl-pentyl)-carbamic acid tert-butyl ester
4-Cyano-2,3-diphenyl-1-hydroxy-9,10-dihydrophenanthrene
1-Propanone, 2-hydroxy-1-(4-methoxyphenyl)-
2-(4-methoxyphenyl)-4-quinolinecarboxaldehyde
4-Isoquinolinecarboxylic acid, 1,2,3,4-tetrahydro-1-oxo-2,3-diphenyl-, (3R,4S)-rel-
1,1-dichloro-2-methyl-2-(4-nitrophenyl)cyclopropane
1-(3-hydroxy-cyclohexyl)-ethanone
(+/-)-1-[2H1]-Cyclopente-2-en-1-ol
1-(4-hydroxy-3-methoxyphenyl)-2-{4-[(E)-3-hydroxy-1-propenyl]-2-methoxyphenoxy}-1,3-propanediol
1-[(3-methoxyphenyl)ethynyl]cyclohexanol
2,4-dichlorophenyl 2-nitrophenyl sulfide
2',5'-dimethyl-2,3':4',2''-terthiophene
N-BOC-L-ALA-NHOBN
N4-(4-methylphenyl)-3,4-Pyridinediamine
3-(2-Hydroxy-1-propyl)amino-1-phenyl-2-buten-1-on
