بحث البنية الفرعية

1251296

CCNC(=O)Nc1nc2ccc(-c3cccc(N)c3)cc2s1
Reaction #9241
desired compound
المردود 23.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2cccc(-c3ccc(Cl)cc3Cl)n2n1
Reaction #9278
title compound
المردود 97.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn2c(-c3c(C)cc(C)cc3OC)ccc(OC)c2c1[N+](=O)[O-]
Reaction #9287
title compound
المردود 98.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn2c(-c3c(C)cc(OC)cc3OC)cccc2c1N(CC1CC1)CC1CCOC1
Reaction #9298
title compound
المردود 49.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(C)c1-c1cccc2c(NC(=O)OC(C)(C)C)c(SC)nn12
Reaction #9303
title compound
المردود 102.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)c(-c2cccc3c(NC(=O)OC(C)(C)C)c(OC)nn23)c(OC)c1
Reaction #9322
title compound
المردود 63.4%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(-c2cccc(C(=O)NCCN3CCCC3)c2)c1
Reaction #9869
3′-Formyl-N-[2-(1-pyrrolidinyl)ethyl][1,1′-biphenyl]-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCc1ccc(-c2ccc3c(Cl)c(O)ccc3c2)cc1
Reaction #40267
6-(4-pentylphenyl)-1-chloro-2-naphthol
المردود 78.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2=CCC3(CC2)OCCO3)cc1
Reaction #40328
8-(4-fluorophenyl)-1,4-dioxaspiro[4.5]dec-7-ene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(-n2ccc(OCc3ccccc3)cc2=O)cc1
Reaction #43309
title compound
المردود 58.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2ccc3cc(C)ccc3n2)c1
Reaction #46037
2-(3-methylphenyl)-6-methyl-quinoline
DOI: 10.6084/m9.figshare.5104873.v1
O=C1COCc2cc(-c3ccccc3)ccc21
Reaction #50549
7-phenylisochroman-4-one
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CC=C(C(N)=O)CC2)c2cccc(-c3ccc(Cl)cc3Cl)c2n1
Reaction #51830
title compound
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CC=C(C(=O)OC(C)C)CC2)c2cccc(-c3ccc(Cl)cc3Cl)c2n1
Reaction #51831
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(NS(=O)(=O)C(C)(C)C)c(OB(O)O)c1
Reaction #64387
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(-c3cccc(C)c3)ccc2c1
Reaction #68709
2-(3-methylphenyl)-6-methoxyquinoline
DOI: 10.6084/m9.figshare.5104873.v1
COCc1cc(OC)c(-c2c(SC)sc3c(NC(=O)OC(C)(C)C)c(C)nn23)c(OC)c1
Reaction #69549
title compound
المردود 91.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nnc(NCc3ccc(OC)c(Cl)c3)c3cc(C#N)ccc23)cc1.Cl
Reaction #75570
title compound
المردود 39.1%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccno1
Reaction #80998
desired product
DOI: 10.6084/m9.figshare.5104873.v1
OB(O)Oc1cccc2ccccc12
Reaction #82304
naphthylboric acid
المردود 46.5%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي