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Cc1cccs1

CCCc1nc(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c(-c2ccc(C)cc2)c(OCCOc2ncc(-c3cccs3)cn2)n1
Reaction #2388
4-tert-butyl-N-[6-{2-(5-(2-thienyl)pyrimidin-2-yloxy)ethoxy}-5-(4-methylphenyl)-2-n-propylpyrimidin-4-yl]-benzenesulfonamide
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)Cc3cccs3)[C@H]2SC1
Reaction #56298
7β-(thienylacetamido)-3-azidomethyl-3-cephem-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc2c(O)c(-c3ccccc3)sc2n1
Reaction #63812
pale yellow needles
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1c(-c2ccccc2)sc2nc(C(C)(C)C)ccc12
Reaction #63813
fine white needles
Ausbeute 91.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(O)=C(C(=O)Nc2ccc(Br)cc2)c2sccc2S1(=O)=O
Reaction #75012
4'-bromo-3-hydroxy-2-methyl-2H-thieno[2,3-e]1,2-thiazine-4-carboxanilide 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(-c2ccc3cc(O)ccc3n2)s1
Reaction #84073
5-(6-hydroxyquinolin-2-yl)thiophene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)N1CCC(N(C(=O)C2CCC(C)CC2)c2cc(-c3ccccc3)sc2C(=O)OC)CC1
Reaction #160342
3-[(1-Methylcarbamoyl-piperidin-4-yl)-(4-methyl-cyclohexanecarbonyl)-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCC(N(c2cc(-c3ccccc3)sc2C(=O)O)C(=O)[C@H]2CC[C@@H](C)CC2)CC1
Reaction #160406
cis-3-[(4-Hydroxy-4-methyl-cyclohexyl)-(4-methyl-cyclohexanecarbonyl)-amino]-5-phenyl-thiophene-2-carboxylic acid
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCCO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)c1ccc(C=Cc2ccc(C=O)s2)c(OCc2ccccc2)c1
Reaction #172514
5-[2-[2-benzyloxy-4-[butyl[4-(tert-butyldiphenylsiloxy) butyl]amino]phenyl]vinyl]thiophene-2-carboaldehyde
Ausbeute 57.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC1OC(c2ccc(Cl)c(Cc3ccc(-c4ccc(C=O)c(F)c4)s3)c2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #173799
DOI: 10.1039/C8SC04228D
CC(C)(C#Cc1cc2nccc(Oc3ccc(N(C(=O)C4(C(N)=O)CC4)c4ccc(F)cc4)cc3F)c2s1)N1CCCCC1
Reaction #173969
DOI: 10.1039/C8SC04228D
CC(C)(Oc1ccc(CCC(OCC2CCCCC2)c2ccc(-c3ccc(C(F)(F)F)cc3)s2)c(Cl)c1Cl)C(=O)O
Reaction #178640
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1cccc(-c2ccc(CN(CC3CC3)S(=O)(=O)c3ccccc3C(F)(F)F)s2)c1
Reaction #182346
DOI: 10.1039/C8SC04228D
CCCN(CCSc1ccc(OCC(=O)O)c(C)c1)S(=O)(=O)c1c(C)sc2ccc(Cl)cc12
Reaction #183858
DOI: 10.1039/C8SC04228D
CCCc1nc(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c(-c2ccc(C)cc2)c(OCCOc2ncc(-c3cccs3)cn2)n1
Reaction #185110
DOI: 10.1039/C8SC04228D
COC(=O)c1sc(-c2ccc(Cl)cc2)cc1N(C(=O)C1CCC(C)CC1)C1CCN(C)CC1
Reaction #188611
DOI: 10.1039/C8SC04228D
NC(=O)c1ccc(-c2cc3ccccc3s2)cn1
Reaction #188657
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(-c2cccc(N(C(=O)C(F)(F)F)C3CCN(S(=O)(=O)Cc4cccc(N)c4)CC3)c2)c(Br)c1OCC(=O)OC
Reaction #190655
DOI: 10.1039/C8SC04228D
O=C(O)COc1c(C(=O)O)sc(-c2cccc(NC3CCN(S(=O)(=O)Cc4cc(Cl)cc(Cl)c4)CC3)c2)c1Br
Reaction #193052
DOI: 10.1039/C8SC04228D
COc1cc(-n2cnc3cc(-c4ccc(Cl)cc4Cl)sc3c2=O)ccc1OCC(C)(C)O
Reaction #194291
DOI: 10.1039/C8SC04228D
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