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ClCc1ccccc1

O=C(Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1)c1ccccc1Cl
Reaction #3588
desired product
Выход 72.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(NC(=O)c2ccc(Cl)cc2Cl)cc1Cl
Reaction #3667
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1COc1cccnc1N
Reaction #4387
2-amino-3-(2-methylbenzyloxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn2cccc(OCc3ccccc3Cl)c2n1
Reaction #4391
8-(2-chlorobenzyloxy)-2-methylimidazo[1,2-a]pyridine
Выход 66.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCl)c(Cl)c1
Reaction #7527
title compound
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3Cl)S(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43820
{5-[(2-Chloro-benzyl)-(4-fluoro-benzenesulfonyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Clc1ccc(CSC2=N[C@@H](c3ccccc3)[C@@H](c3ccccc3)N2)c(Cl)c1
Reaction #47029
product 199
Выход 81.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Clc1ccccc1CSC1=N[C@@H](c2ccccc2)[C@@H](c2ccccc2)N1
Reaction #47038
product 208
Выход 32.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1CSC1=N[C@@H](c2ccccc2)[C@@H](c2ccccc2)N1.Cl
Reaction #47056
product 227
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Clc1ccc(Cl)c(CSC2=N[C@@H](c3ccccc3)[C@@H](c3ccccc3)N2)c1
Reaction #47067
product 238
Выход 49.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)cc(Cl)c1C(=O)NC(c1ccccc1)C(C)(C)N1CCCC1
Reaction #49128
title compound
Выход 72.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1)C(=O)O
Reaction #49627
3,5-dinitrobenzoyl-(S)-leucine
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1nn(-c2cccc(S(N)(=O)=O)c2)c2c1ccc1ccc(NC(=O)c3ccccc3Cl)cc12
Reaction #51262
1-[3-(aminosulfonyl)phenyl]-8-[(2-chlorobenzoyl)amino]-1H-benzo[g]indazole-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCc2cc(C(=O)N3CCOCC3)ccc21
Reaction #51458
5-(4-morpholylcarbonyl)phthalid
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc2c(c1)COC2=O
Reaction #51459
5-(N,N-dimethylcarbamyl)phthalid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1ccccc1CN
Reaction #53429
(2-Allyloxy-benzyl)amine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(=C1CNC1)c1cc(F)cc(F)c1
Reaction #53474
3-[(3,5-difluorophenyl)(methylsulfonyl)methylene]azetidine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCCN(Cc2ccc([C@H](c3ccc(Cl)cc3)N3CC(=C(c4cc(F)cc(F)c4)S(C)(=O)=O)C3)cc2)C1
Reaction #53475
1-{(R*)-(4-chlorophenyl)[4-(3,3-dimethylpiperidin-1-ylmethyl)phenyl]methyl}-3-[(3,5-difluorophenyl)(methylsulfonyl)methylene]azetidine
Выход 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(=C1CN([C@@H](c2ccc(Cl)cc2)c2ccc(CN3CCSCC3)cc2)C1)c1cc(F)cc(F)c1
Reaction #53476
1-{(R*)-(4-chlorophenyl)[4-(thiomorpholin-4-ylmethyl)phenyl]methyl}-3-[(3,5-difluorophenyl)(methylsulfonyl)methylene]azetidine
Выход 79.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C[C@@]1(c2ccccc2Cl)C=CC(CN2CC(=C(c3cc(F)cc(F)c3)S(C)(=O)=O)C2)=CC1
Reaction #53477
(R*)-(4-(chlorophenyl)[4-(di-n-propylaminomethyl)phenyl]methyl}-3-[(3,5-difluorophenyl)(methylsulfonyl)methylene]azetidine
DOI: 10.6084/m9.figshare.5104873.v1
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