Teilstruktursuche

COC(=O)CN.Cl

CCOC(=O)C(NCc1cccc(C(F)(F)F)c1)c1cn(Cc2ccccc2)c2ccccc12
Reaction #5704
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(NCc1cccc(C(F)(F)F)c1)c1cn(Cc2ccccc2)c2ccccc12.Cl
Reaction #5705
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](N)C[Si](C)(C)C.Cl
Reaction #40295
(2R)-3-Trimethylsilylalanine methyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(C)(C)NC(=O)c1ccc(Br)s1
Reaction #43379
tert.-butyl 2-[(5-bromo-thiophen-2-yl)-carbonylamino]-isobutyrate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC1C2CCC1CC2)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47642
3-bicyclo[2.2.1]hept-7-yl-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
Ausbeute 47.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2c(OC)ccc(C(N)=O)c2OC)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52970
N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxy-3-carbamoylphenyl)-L-phenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CN)NS(C)(=O)=O.Cl
Reaction #64925
Methyl 2(S)-Methylsulfonylamino-3-aminopropionate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OC[C@H](CCOC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)Cn1cnc2c(Cl)nc(N)nc21
Reaction #76834
(R)-2-Amino-9-(2-stearoyloxymethyl-4-(N-tert-butoxycarbonyl-L-valyloxy)butyl)-6-chloropurine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC(C)(C)C)n1ccc(-c2cc(Cl)ccc2C#C[Si](C)(C)C)cc1=O
Reaction #84917
tert-Butyl 2-[4-{5-chloro-2-[(trimethylsilyl)ethynyl]phenyl}-2-oxopyridin-1(2H)-yl]propanoate
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(Cl)cc1-c1ccn(C(C)C(=O)O)c(=O)c1
Reaction #84918
2-[4-(5-Chloro-2-ethynylphenyl)-2-oxopyridin-1(2H)-yl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC1CC1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84941
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(CC1CC1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84942
2-{4-[5-Chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-cyclopropylpropanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1ccccn1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84952
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Cc1ccccn1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84953
2-{4-[5-Chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-(pyridin-2-yl)propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1cccnc1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84955
Ethyl 2-{4-[5-chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-(pyridin-3-yl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Cc1cccnc1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84956
2-{4-[5-Chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-(pyridin-3-yl)propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1ccncc1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84963
Ethyl 2-{4-[5-chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-(pyridin-4-yl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Cc1ccncc1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84964
2-{4-[5-Chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-(pyridin-4-yl)propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(Cl)CS[C@@H]2C(NC(=O)COc3ccccc3)C(=O)N2C1C(=O)O
Reaction #94054
7-phenoxyacetoamido-3-chloro-3-methyl-cepham-4-carboxylic acid
Ausbeute 51.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)n1cc(I)c2cnc(Cl)nc21
Reaction #169339
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter