Participa en 179 reacciones

4635

FC(F)=CCCSc1nc2ccccc2s1
Reaction #2424
2-(4,4-difluorobut-3-enyl)thiobenzthiazole
Rendimiento 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1CCCN(Sc2nc3ccccc3s2)C1
Reaction #54172
1-(2-benzothiazolylthio)-3-methyl-piperidine
Rendimiento 95.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC(=O)c1ccc(-n2c3ccc(C(C)=O)cc3c3cc(C(=O)c4ccc(Sc5nc6ccccc6s5)cc4)ccc32)cc1
Reaction #66037
1-{9-(4-Acetyl-phenyl)-6-[4-(benzothiazol-2-ylsulfanyl)-benzoyl]-9H-carbazol-3-yl}-ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(Nc1ccc2cn[nH]c2c1)c1cccc(N(Cc2ccccc2)S(=O)(=O)c2ccccc2)c1
Reaction #91097
title compound
Rendimiento 45.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)CC(C(O)=S)c1nc2ccccc2s1
Reaction #93400
benzothiazol-2-ylthiosuccinic acid
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(O)CC(CSc1nc2ccccc2s1)C(=O)O
Reaction #93401
3-(benzothiazol-2-ylthio)-propane-1,2-dicarboxylic acid
Rendimiento 50.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(O)CC(CC(=O)O)Sc1nc2ccccc2s1
Reaction #93402
3-(benzothiazol-2-ylthio)-glutaric acid
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(O)CC(C(=O)O)C(CSc1nc2ccccc2s1)C(=O)O
Reaction #93404
4-(benzothiazol-2-ylthio)-butane-1,2,3-tricarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
Sc1nc2ccccc2s1
Reaction #95224
2-mercaptobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
C=C(C)c1cccc(C(C)(C)NSc2nc3ccccc3s2)c1
Reaction #175374
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(NSc1nc2ccccc2s1)c1ccccc1
Reaction #189572
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc2scnc2c1
Reaction #197879
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CC(CC(=O)O)Sc1nc2ccccc2s1
Reaction #209603
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ncc(-c2ccccc2)nc1Sc1nc2ccccc2s1
Reaction #233738
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)c1nc(N(C)S(C)(=O)=O)nc(-c2ccc(F)cc2)c1CS(=O)(=O)c1nc2ccccc2s1
Reaction #243109
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(N2CCCC2)c(NC(=O)CN2CCN(CCSc3nc4ccccc4s3)CC2)c(N2CCCC2)n1
Reaction #246475
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(Sc1nc2ccccc2s1)C(N)=O
Reaction #257204
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=C(C)C(C(=O)OCc1ccc(OC)cc1)N1C(=O)C(NC(=O)Cc2ccccc2)C1SS(=O)(=O)c1ccccc1
Reaction #290499
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCC(O)CSc1nc2ccccc2s1
Reaction #291238
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1CCCC(C)C1NSc1nc2ccccc2s1
Reaction #292575
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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