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811742

CCc1cc(OCc2ccc(-c3ccccc3-c3nnnn3-c3ccc([N+](=O)[O-])cc3)cc2)c2ccccc2n1
Reaction #5774
2-ethyl-4-[(2'-(1-(4-nitrophenyl)-1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinoline
Выход 58.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c1c(-c1ccc(CO)cc1)cc1[nH]c3ccc(O)cc3c21
Reaction #11120
9-hydroxy-4-(4-hydroxymethylphenyl)pyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Выход 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-c2ccc(CO)cc2)c(-c2ccc(Cl)cc2)n(-c2ccc(S(N)(=O)=O)cc2)c1C
Reaction #46932
5-(4-chloro-phenyl)-4-(4-hydroxymethyl-phenyl)-2-methyl-1-(4-sulfamoyl-phenyl)-1H-pyrrole-3-carboxylic Acid Ethyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(Oc2cc(O[C@@H](C)CO[Si](C)(C)C(C)(C)C)cc(C(=O)Nc3ccn(C)n3)c2)cc1
Reaction #48846
desired compound
Выход 62.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(-c2ccccc2CO)cc(Br)c2c1C(=O)NC2=O
Reaction #49277
3-amino-4-(hydroxymethylphenyl)-6-bromophthalimide
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Oc2ccc(NC(C)=O)cc2)cc1
Reaction #51652
methyl 4-(4-acetamidophenoxy)benzoate
Выход 75.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2c(OC)cc(C3OCCO3)cc2OC)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52943
N-(2,6-dichlorobenzoyl)-4-[4-(1,3-dioxolan-2-yl)-2,6-dimethoxyphenyl]-L-phenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)OB(O)c1ccc(CCCCCCCCCCCO)cc1
Reaction #53274
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(B(O)O)cc1)N1CCN(S(=O)(=O)c2cc3cc(Cl)ccc3[nH]2)CC1
Reaction #56675
4-({4-[(5-chloro-1H-indol-2-yl)sulphonyl]piperazin-1-yl}carbonyl)phenyl boronic acid
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(C(=O)O)c(O)c2)OC1(C)C
Reaction #59012
title compound
Выход 102.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(B(O)O)c(OC)c1
Reaction #59023
4-ethoxycarbonyl-2-methoxyphenylboronic acid
Выход 89.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)ccc1B(O)O
Reaction #59024
title compound
Выход 81.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc(C(=O)O)cc2)cc(C)c1OCCO
Reaction #59033
title compound
Выход 38.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2cc(C)c(OCC(C)=O)c(C)c2)cc1C(C)C
Reaction #59037
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(-c2[nH]c3cccc4c3c2CCNC4=O)cc1
Reaction #61608
4-(6-oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-2-yl)-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(C2=C(c3ccc(CO)cc3)CCC2)cc1
Reaction #65807
1-[2-(4-hydroxymethylphenyl)cyclopenten-1-yl]-4-(methylthio)benzene
Выход 92.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(OCc2ccc(-c3ccccc3-c3nnnn3-c3ccc([N+](=O)[O-])cc3)cc2)c2ccccc2n1
Reaction #65899
2-ethyl-4-[(2'-(1-(4-nitrophenyl)-1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinoline
Выход 58.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(C(=O)N3CC[C@@H](O[Si](C)(C)C(C)(C)C)C3)cc2)OC1(C)C
Reaction #66281
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(C(=O)N3C[C@H](O)[C@@H](O)C3)cc2)OC1(C)C
Reaction #66284
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)OCC)cc3)cc2N=C(N)C1
Reaction #66288
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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