Teilstruktursuche

1213892

COC(=O)[C@H](Cc1ccc(-c2ccccc2OC)cc1)NC(=O)[C@@H](C)c1ccccc1
Reaction #52904
N-[(S)-2-phenylpropionyl]-4-(2-methoxyphenyl)-L-phenylalanine methyl ester
Ausbeute 79.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2OC)cc1)NC(=O)c1ccc(C(=O)OC(C)(C)C)cc1Cl
Reaction #52946
N-[2-chloro-4-(tert-butoxycarbonyl)benzoyl]-4-(2-methoxyphenyl)-L-phenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1C[C@H]1c1ccc(-c2ccccc2)cc1
Reaction #66394
tert-butyl(trans)-2-(1,1′-biphenyl-4-yl)cyclopropylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)CN(C(=O)OC(C)(C)C)[C@@H]2C[C@H]2c2ccc(-c3ccccc3)cc2)CC1
Reaction #66395
tert-butyl (trans)-2-(1,1′-biphenyl-4-yl)cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)C(Cc1ccc(Cl)cc1)c1ccc(-c2ccsc2)cc1
Reaction #81133
(1RS, 2RS)-3-(4-chlorophenyl)-1-methyl-2-[4-(3-thienyl)phenyl]propylamine
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H](C)[C@@H](Cc1ccc(Cl)c(Cl)c1)c1ccc(-c2ccccc2)c(F)c1
Reaction #81136
(1S, 2S)-N-{3-(3,4-dichlorophenyl)-2-(2-fluoro-4-biphenylyl)-1-methylpropyl}methylamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cccc(N)c2)cc1)NC(=O)CCC(=O)OC
Reaction #158011
(R)-ethyl 4-(3′-aminobiphenyl-4-yl)-3-(4-methoxy-4-oxobutanamido)butanoate
Ausbeute 91.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cccc(NC(C)=O)c2)cc1)NC(=O)CCC(=O)OC
Reaction #158012
(R)-ethyl 4-(3′-acetamidobiphenyl-4-yl)-3-(4-methoxy-4-oxobutanamido)butanoate
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cc(F)ccc2OC)cc1)NC(=O)c1cnco1
Reaction #158022
(R)-ethyl 4-(5′-fluoro-2′-methoxybiphenyl-4-yl)-3-(oxazole-5-carboxamido)butanoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)cc1-c1ccc(C[C@H](CC(=O)O)NC(=O)CCC(=O)O)cc1
Reaction #158028
(R)-4-(1-carboxy-3-(5′-fluoro-2′-methoxybiphenyl-4-yl)propan-2-ylamino)-4-oxobutanoic acid
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)CCc1nnn[nH]1
Reaction #158034
(R)-4-bipheyl-4-yl-3-(3-1H-tetrazol-5-yl-propionylamino)-butyric acid
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NC(=O)C[C@@H](Cc1ccc(-c2cccc(Cl)c2)cc1)NC(=O)CCC(=O)O
Reaction #158038
N—[(R)-1-(3′-chloro-biphenyl-4-ylmethyl)-3-methanesulfonylamino-3-oxo-propyl]-succinamic acid
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)CCC(=O)N[C@@H](CC(=O)NS(C)(=O)=O)Cc1ccc(-c2cccc(Cl)c2)cc1
Reaction #158039
N-[(R)-1-(3′-chloro-biphenyl-4-ylmethyl)-3-methanesulfonylamino-3-oxo-propyl]-succinamic acid butyl ester
Ausbeute 114.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)CCC(=O)O
Reaction #158042
(R)-4-(1-(biphenyl-4-yl)-4-tert-butoxy-4-oxobutan-2-ylamino)-4-oxobutanoic acid
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@H](N)Cc1ccc(-c2cccc(Cl)c2)cc1.Cl
Reaction #158060
(R)-ethyl 3-amino-4-(3′-chlorobiphenyl-4-yl)butanoate hydrochloride
Ausbeute 205.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cccc(Cl)c2)cc1)NC(=O)OC(C)(C)C
Reaction #158062
(R)-ethyl 3-(tert-butoxycarbonylamino)-4-(3′-chlorobiphenyl-4-yl)butanoate
Ausbeute 62.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](O)C(N)Cc1ccc(-c2cccc(Cl)c2)cc1.Cl
Reaction #158093
(R)-3-amino-4-(3′-chloro-biphenyl-4-yl)-2-hydroxy-butyric acid methyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](OC)C(Cc1ccc(-c2cccc(Cl)c2)cc1)NC(=O)OC(C)(C)C
Reaction #158094
(R)-3-tert-butoxycarbonylamino-4-(3′-chloro-biphenyl-4-yl)-2-methoxy-butyric acid methyl ester
Ausbeute 79.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](OC)C(N)Cc1ccc(-c2cccc(Cl)c2)cc1.Cl
Reaction #158095
(R)-3-amino-4-(3′-chloro-biphenyl-4-yl)-2-methoxy-butyric acid methyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](F)C(Cc1ccc(-c2cccc(Cl)c2)cc1)NC(=O)OC(C)(C)C
Reaction #158097
(R)-3-tert-butoxycarbonylamino-4-(3′-chloro-biphenyl-4-yl)-2-fluoro-butyric acid methyl ester
Ausbeute 28.5%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter