Recherche de Sous-structure

10834

C=Cc1ccc(CCOC(=O)C(=O)OCC)cc1
Reaction #6503
aimed compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(CC)NC(C)=O
Reaction #7632
Ethyl 3-(acetylamino)-2-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(CC)NC(=O)C1CCCC1
Reaction #7645
Ethyl 3-[(cyclopentylcarbonyl)amino]-2-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)C(=O)OC(C)(C)C)c1
Reaction #41363
tert-Butyl[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]carbamoylformate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)C(=O)OC(C)C)c1
Reaction #41365
Propan-2-yl[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]carbamoylformate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N[C@@H](C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1cccc(OC)c1
Reaction #41366
Ethyl[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]carbamoylformate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(NC(=O)C1CCC1)c1cccc(OCc2ccccc2)c1
Reaction #46253
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N1CCc2ccccc21
Reaction #80737
N-ethoxalylindoline
Rendement 108.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N1C2=CC=CCC2CCC1CO[Si](C)(C)C
Reaction #80765
N-ethoxalyl-2-trimethylsilyloxymethyltetrahydroquinoline
Rendement 106.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)NCC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80773
title compound
Rendement 21.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(-c2ccc([N+](=O)[O-])cc2)no1
Reaction #82821
5-ethoxycarbonyl-3-(4-nitrophenyl)-1,2,4-oxadiazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(=O)Cl
Reaction #84024
t-butyl 2-chloro-2-oxoacetate
Rendement 40.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(=O)Cl
Reaction #84025
Compound 34
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ncc(-c2ccccc2)o1
Reaction #86833
ethyl 5-phenyloxazole-2-carboxylate
Rendement 22.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)NCCc1c[nH]c2ccc(Cl)cc12
Reaction #86843
2-(2-(5-chloro-1H-indol-3-yl)ethylamino)-2-oxoacetic acid
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)N[C@H](CO)Cc1ccccc1
Reaction #86845
(S)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acid
Rendement 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)N[C@@H](CO)Cc1ccccc1
Reaction #86847
(R)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acid
Rendement 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1cccn1CCOC(C)=O
Reaction #95388
ethyl 1-(2-acetoxyethyl)pyrrole-2-glyoxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)NCC(C)O
Reaction #156269
title compound
Rendement 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cccc(Cl)c2)cc1)NC(=O)C(=O)OCC
Reaction #158072
(R)-ethyl 4-(3′-chlorobiphenyl-4-yl)-3-(2-ethoxy-2-oxoacetamido)butanoate
Rendement 83.8%DOI: 10.6084/m9.figshare.5104873.v1
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