Поиск подструктуры

CC1=CSC=C1

O=C(CCCOc1ccccc1Cl)Nc1cscc1C(=O)O
Reaction #42879
title compound
Выход 84.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(Oc1ccc(Cl)c(Cl)c1)C(=O)Nc1cscc1C(=O)O
Reaction #42890
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cscc1NC(=O)C(F)Oc1ccc(Cl)c(Cl)c1
Reaction #42896
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1cc(-c2cncc(N3C[C@@H]4C[C@H]3CN4)c2)cs1
Reaction #51702
oil
Выход 34.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(F)cc2)OC(CC(SC[C@@H](O)[C@H](O)CS)c2ccsc2)=CC1=O
Reaction #78296
5-(2-{[(2S*,3S*)-2,3-dihydroxy-4-mercaptobutyl]thio}-2-thien-3-ylethyl)-2-(4-fluorophenyl)-2methylfuran-3(2H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(F)cc2)OC(CC(SCCO)c2ccsc2)=CC1=O
Reaction #78307
2-(4-fluorophenyl)-5-[2-[(2-hydroxyethyl)thio]-2-(3-thienyl)ethyl]-2-methylfuran-3(2H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3scc(C)c3c2C(=O)O)n1
Reaction #80272
desired compound
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NCc2ccc(F)c(F)c2)sc2ccccc12
Reaction #85428
(3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2ncnc(OCc3cc(-c4ccccc4)no3)c12
Reaction #86057
5-methyl-4-((3-phenyl-isoxazol-5-yl)-methoxy-)-thieno[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2ncnc(OCc3cc(-c4ccccc4)no3)c12.Cl
Reaction #86058
5-methyl-4-((3-phenyl-isoxazol-5-yl)-methoxy-)-thieno[2,3-d]pyrimidine hydrochloride
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O.Cc1csc2ncnc(OCc3cc(-c4ccccc4)no3)c12
Reaction #86059
5-methyl-4-((3-phenyl-isoxazol-5-yl)-methoxy-)-thieno[2,3-d]pyrimidine acetate
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(-c2cncc(N3CC4CC5CC3CN(C5)C4)c2)cs1
Reaction #167617
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCc1csc(B2OCC(C)(C)CO2)c1
Reaction #172530
oil
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCc1csc(-c2sccc2CCCCBr)c1
Reaction #172531
product
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172624
solid
Выход 38.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(SCC(=O)N2CCCc3ccccc32)sc2ccccc12
Reaction #187576
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1c(sc3ccccc13)N2
Reaction #188965
DOI: 10.1039/C8SC04228D
O=C(c1csc(-n2cccn2)c1)N1CCCC2CCCCC21
Reaction #189025
DOI: 10.1039/C8SC04228D
COc1cc(OC)nc(Oc2ccc3scc(C)c3c2C(=O)O)n1
Reaction #195114
DOI: 10.1039/C8SC04228D
CC(C)CC(NC(=O)OC(C)(C)C)C(=O)NC1Cc2cccc(N3CCCC3=O)c2N(Cc2ccsc2)C1=O
Reaction #197698
DOI: 10.1039/C8SC04228D
Страница 1Далее