Поиск подструктуры

Cc1ccc(S)c(C)c1

Cc1cc(C)c(S(=O)(=O)N[C@H](CNc2cccc3c2cnn3-c2ccc(F)cc2)C(C)C)c(C)c1
Reaction #654
Выход 11.4%
Cc1ccc(C2=CC(C)(C)Sc3ccc(C=O)cc32)s1
Reaction #2720
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(/C(=C/c2ccc3c(c2)C(c2ccc(C)cc2)=CCC3(C)C)CC(OC)OC)cc1
Reaction #2721
product E
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(-c2cc(Cl)ccc2O)cc1C(F)(F)F)N1CCOCC1
Reaction #44363
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(S(=O)(=O)NCCc2ccc(C(=CCCCC(=O)O)c3cccnc3)cc2)c(C)c1
Reaction #50409
crude product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64546
desired material
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1
Reaction #64554
title compound
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F
Reaction #64574
title compound
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CS[C@@H]1CCC[C@H]1CCc1cc(C(C)(C)C)cc(C(C)(C)C)c1
Reaction #65913
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #71681
12S
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)N2CCN(S(=O)(=O)c3ccc(C(F)(F)F)cc3C)C[C@@H]2C)cn1.Cl
Reaction #71703
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1S(=O)(=O)N1CCN(C(=O)c2ccc(C3CC3)nc2)[C@@H](C)C1
Reaction #71707
title compound
Выход 2.4%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)CCC2)c(Cl)c1C1=NOC2OCCC12
Reaction #76423
3-Oxocyclohex-1-enyl 2-chloro-4-ethylsulfonyl-3-(3a,4,5,6a-tetrahydrofuro[3,2-d]isoxazol-3-yl)-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc2scc(N)c(=O)c2c1
Reaction #93747
3-amino-6-ethyl-4H-1-benzothiopyran-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)O)ccc1SC(C)C
Reaction #160113
4-(isopropylthio)-3-methylbenzoic acid
Выход 35.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(S(=O)(=O)N(Cc2ccc3c(ccn3C)c2)c2ncc(C(F)(F)F)cc2Cl)c(C)c1
Reaction #160256
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(-c2ccc3c(c2)C=C(C(=O)Nc2ccc(CN(C)C4CCC(=O)CC4)cc2)CCS3(=O)=O)cc1
Reaction #173751
DOI: 10.1039/C8SC04228D
Cn1ncc(C(=O)c2ccc(S(C)(=O)=O)c(C3=NOCC3)c2Cl)c1O
Reaction #179344
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(C)ccc1Sc1ccccc1
Reaction #182889
DOI: 10.1039/C8SC04228D
CCOCCCc1ccc(-c2ccc3c(c2)C=C(C(=O)Nc2ccc(CN(C)C4CCOCC4)cc2)CCS3(=O)=O)cc1
Reaction #184486
DOI: 10.1039/C8SC04228D
Страница 1Далее