Поиск подструктуры

1433998

C=Cc1cc(C)c(C(=O)N=C(N)N)cc1S(C)(=O)=O
Reaction #2991
N-diaminomethylene-2-methyl-4-ethenyl-5-methylsulfonyl-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1ccc(CO)cc1Br
Reaction #11986
OBS02002
Выход 96.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1ccc(CCl)cc1Br
Reaction #11987
OBS02003
Выход 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1c(Br)cc(CO)cc1Br
Reaction #11988
OBS02015
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1c(Br)cc(CCl)cc1Br
Reaction #11989
OBS02018
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccccc1SCC1OCCO1
Reaction #43680
(2-bromophenylthiomethyl)-1,3-dioxolane
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cccc2ccsc12
Reaction #43681
title compound
Выход 40.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1ccc(CO)cc1Br
Reaction #48228
OBS02002
Выход 96.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1ccc(CCl)cc1Br
Reaction #48229
OBS02003
Выход 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1c(Br)cc(CO)cc1Br
Reaction #48230
OBS02015
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1c(Br)cc(CCl)cc1Br
Reaction #48231
OBS02018
DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(C(F)(F)F)ccc1C(=O)O
Reaction #49739
2-(methylsulphenyl)-4-trifluoromethylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(C(F)(F)F)ccc1Br
Reaction #49740
4-bromo-3-(methylsulphenyl)benzotrifluoride
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2ccccc2)c(S(=O)(=O)Nc2ccc(Cl)c(OCCN(C)C)c2)cc1OC
Reaction #51042
title compound
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1CCC[C@@H](OC)[C@@H]1CC(=O)Cn1cnc2cc(Br)c(SC)cc2c1=O
Reaction #62894
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1CCC[C@@H](OC)[C@@H]1CC(=O)Cn1cnc2cc(Br)c(SCC)cc2c1=O
Reaction #62895
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(SC#N)c(Br)cc1N
Reaction #62903
ethyl 2-amino-4-bromo-5-thiocyanatobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1Br
Reaction #64461
title compound
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1
Reaction #64463
title compound
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(S(=O)(=O)c2ccc(C(F)(F)F)cc2Br)CCN1C(=O)OC(C)(C)C
Reaction #71657
title compound
Выход 80.8%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее