子结构搜索

Ic1cccs1

N#Cc1cc(CO)cs1
Reaction #2844
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cccs2)CC1
Reaction #48155
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(C)c1ccccc1NC(=O)c1ccsc1I
Reaction #48241
N-[2-(1,3-dimethylbutyl)phenyl]-2-iodothiophene-3-carboxamide
收率 21.3%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ncnc2sc(I)cc12
Reaction #60882
title compound
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ncnc2sc(-c3c(I)ncn3C)cc12
Reaction #60884
title compound
收率 67.3%DOI: 10.6084/m9.figshare.5104873.v1
Ic1cc2c(-c3ccc4ccccc4c3)n[nH]c2s1
Reaction #62355
title compound
收率 71.3%DOI: 10.6084/m9.figshare.5104873.v1
Ic1cc2c(-c3ccc4ccccc4c3)nn(C(c3ccccc3)(c3ccccc3)c3ccccc3)c2s1
Reaction #62356
title compound
收率 75.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(I)sc2c(N3CCOCC3)nc(Cl)nc12
Reaction #70168
2-chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-c]pyrimidine
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(Cc2ccc(I)s2)cc1
Reaction #80453
2-iodo-5-(4-fluorophenylmethyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](C#Cc1ccc(Cc2ccc(F)cc2)s1)N(O)C(N)=O
Reaction #80455
(R)-N-{3-[5-(4-fluorophenylmethyl)thien-2-yl]-1-methyl-2-propynyl)-N-hydroxyurea
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(Cc2csc(I)c2)cc1
Reaction #80464
2-iodo-4-(4-fluorophenylmethyl)thiophene
收率 87.6%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(Cc2ccsc2I)cc1
Reaction #80466
2-iodo-3-(4fluorophenylmethyl)thiophene
收率 95.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1sccc1Cc1ccc(F)cc1
Reaction #80467
2-methyl-3-(4-fluorophenylmethyl)thiophene
收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1c1nc2cc(-c3cc4cc5sc(-c6ccc7[nH]c(C8CCCN8C(=O)OC(C)(C)C)nc7c6)cc5cc4s3)ccc2[nH]1
Reaction #159064
2-(5-{6-[2-(1-Boc-pyrrolidin-2-yl)-1H-benzoimidazol-5-yl]-1,5-dithia-s-indacen-2-yl}-1H-benzoimidazol-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester
收率 36.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(I)cc1N(C(=O)[C@H]1CC[C@H](C)CC1)C1CCN(C)CC1
Reaction #160393
5-iodo-3-[(trans-4-methyl-cyclohexanecarbonyl)-(1-methyl-piperidin-4-yl)-amino]-thiophene-2-carboxylic acid methyl ester
收率 99.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(-c2ccc(Cl)cc2)cc1N(C(=O)[C@H]1CC[C@H](C)CC1)C1CCN(C)CC1
Reaction #160394
5-(4-chloro-phenyl)-3-[(trans-4-methyl-cyclohexanecarbonyl)-(1-methyl-piperidin-4-yl)-amino]-thiophene-2-carboxylic acid methyl ester
收率 72.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1c1nc2cc(-c3cc4cc5sc(-c6ccc7[nH]c(C8CCCN8C(=O)OC(C)(C)C)nc7c6)cc5cc4s3)ccc2[nH]1
Reaction #167013
2-(5-{6-[2-(1-Boc-pyrrolidin-2-yl)-1H-benzoimidazol-5-yl]-1,5-dithia-s-indacen-2-yl}-1H-benzoimidazol-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester
收率 36.3%DOI: 10.6084/m9.figshare.5104873.v1
COCCN(CCn1cc(-c2cc3nccc(Oc4ccc([N+](=O)[O-])cc4F)c3s2)cn1)C(=O)OC(C)(C)C
Reaction #171552
tert-Butyl 2-(4-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1H-pyrazol-1-yl)ethyl(2-methoxyethyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2cc3nccc(Oc4ccc([N+](=O)[O-])cc4F)c3s2)o1
Reaction #171555
aldehyde
收率 84.2%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2cc3nccc(Oc4ccc([N+](=O)[O-])cc4F)c3s2)nc1
Reaction #171557
title compound 123
收率 50.2%DOI: 10.6084/m9.figshare.5104873.v1
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