역학 분할은 두 개의 대영사 반응 속도의 차이를 이용하여 외소회 혼합물에서 쌍영체를 분리하는 방법입니다.C-H엔화 반응 중 하나는 영사체에 대해 시약에 우선 반응하고 다른 하나는 불반응을 유지합니다.이 프로세스로 인해 시작 원료의 한 쌍이 제품으로 변환되고 다른 하나는 동일하게 유지됩니다.고도의 선택성을 구현하는 것은 고도의 대영체 부집물을 얻는 열쇠이다.
화학 원료를 구입해야하는 경우 요청 정보를 제출하여최신견적을받으십시오.
(S)-2-(4-methoxyphenyl)-2-pivalamidoacetic acid
dimethyl (S)-2-(1-phenylallyl)malonate
(R)-2-nitro-1-(4-nitrophenyl)ethyl acetate
benzyl 2-cyclohexyl-2-hydroxy-2-phenylacetate
Benzenemethanol, 3-iodo-a-methyl-
Butanamide, N-(1-methyl-3-phenylpropyl)-, (S)-
1-Cyclopentene-1-carboxylic acid, 3-(phenylmethyl)-, 1,1-dimethylethyl ester
Butanedioic acid, [(4-methoxyphenyl)methyl]-, 1-methyl ester
C19H19NO4
5-Cyclohexadecen-1-one, 3-methyl-, (3R)-
HCl
1-fluoro-4-(4-tolylsulfonylmethyl)benzene
(5E,3S)-1-phenylpent-3-en-1-ol
C11H13(2)H2N
(R)-N-(1-phenylpentyl)benzamide
C14H18O
benzyl (R)-2-(diphenylacetyloxy)propanoate
(4S)-4-phenyl-3-[(2R)-2-phenylpropionyl]oxazolidin-2-one
(S)-(-)-α-methoxy-α-(trifluoromethyl)pnenylacetyl acid ester of methyl (+)-(1R,2R,3S,5S)-3-hydroxy-7-oxobicyclo<3.3.0>octane-2-carboxylate
(3,5-bis(trifluoromethyl)phenyl)sulfamoyl chloride
2-methoxy-N-[1-(4-fluorophenyl)ethyl]acetamide
N-(((S)-4-phenylbutan-2-ylcarbamoyl)methyl)octanamide
2-methyl-5-phenylpyrrolidine
Phosphine oxide, (2-methoxy-1-naphthalenyl)methylphenyl-, (S)-
3-benzyl-5-bromo-1-methylindolin-2-one
3,4,5- 트리메틸 옥사 졸
Benzenepropanoic acid, b-(1-oxobutoxy)-, ethyl ester
(R)-3-oxocyclohexyl acetate
(Z)-5-benzylidenepyrrolidine-2,4-dione
3-[(2-Methylpropanoyl)amino]-2-[(S)-1-tert-butyldimethylsilyloxy-2-methylpropyl]quinazolin-4(3H)-one
N-[(2S)-2-(4-isobutylphenyl)propionyl]-7,8-difluoro-(3S)-3-methyl-2,3-dihydro-4H-[1,4]benzoxazine
1-(pyridin-2-ylsulfanyl)propan-2-one
C29H28O2Si
L-2-(4-fluoro-phenyl)-2-(2-methoxy-acetylamino)-acetamide
(R)-1-(4-fluorophenyl)butane-1,4-diol
Butyric acid (Z)-(R)-1-methyl-3-phenyl-allyl ester
(S)-methyl 3-methyl-3-phenyl-2-propylaminocarbonyloxybutanoate
(+)-(1S,2S,6R,7R)-tricyclo[5.2.1.02,6]deca-4,8-dien-3-one
Benzeneethanamine, a-3-butenyl-