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NCc1ccc(Br)cc1F

O=C(NCc1ccc(Br)cc1F)OCc1ccccc1
Reaction #1300
O-benzyl N-(4-bromo-2-fluorobenzyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Br)cc1F)N1CCCC1
Reaction #44371
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C(=O)c1ccc(Br)cc1F)C(C)C
Reaction #44377
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C(=O)c1ccc(-c2cc(Cl)ccc2O[C@@H](C)C(=O)O)cc1F)C(C)C
Reaction #44378
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(C)C(=O)c1ccc(Br)cc1F
Reaction #44379
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C)C(=O)c1ccc(Br)cc1F
Reaction #44380
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)c1ccc(Br)cc1F
Reaction #44381
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Br)cc1F)N1CCC(F)(F)C1
Reaction #44382
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNC(=O)c1ccc(Br)cc1F
Reaction #44384
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1ccc(Br)cc1F
Reaction #44389
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC1)c1ccc(Br)cc1F
Reaction #44391
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccc(Br)cc1F
Reaction #44395
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(C(=O)OC)ccc2Cl)c(=O)n1Cc1ccc(Br)cc1F
Reaction #64562
title compound
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(Br)cc3F)c2=O)c1
Reaction #64563
4-(4-Bromo-2-fluorobenzyl)-5-n-butyl-2-[5-(N-n-butylcarbamoyl)-2-chloro-phenyl]-2,4-dihydro-3H-1,2,4-triazol-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(Br)cc1F
Reaction #64566
title compound
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #64567
title compound
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(Br)cc1F
Reaction #64571
title compound
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #64572
title compound
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(OCC)c1ccc([C@H](C)N[S@](=O)C(C)(C)C)c(F)c1
Reaction #85697
(R)—N—((S)-1-(4-(1-ethoxyvinyl)-2-fluorophenyl)ethyl)-2-methylpropane-2-sulfinamide
Выход 205.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](N[S@](=O)C(C)(C)C)c1ccc(CC#N)cc1F
Reaction #85699
(R)—N—((S)-1-(4-(cyanomethyl)-2-fluorophenyl)ethyl)-2-methylpropane-2-sulfinamide
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
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