Участвует в 75 реакциях

1140

CC(O)(c1ccsc1)c1cncs1
Reaction #2915
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(Br)ccc1C(=O)c1nccs1
Reaction #225403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC(c1nccs1)C1CN2CCC1CC2
Reaction #254652
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cncs1
Reaction #279588
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C[Si](C)(C)c1ncc(C(=O)c2ccccc2[N+](=O)[O-])s1
Reaction #280197
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)Nc1ccc(NC(=O)c2nccs2)cc1
Reaction #306738
product
Выход 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)Nc1ccc(OC(=O)c2nccs2)cc1
Reaction #306739
product
Выход 12.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
OC(c1ccc2c(cnn2-c2ccc(F)cc2)c1)(c1cncs1)C(F)(F)F
Reaction #331670
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C[Si](C)(C)c1nccs1
Reaction #406130
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C[Si](C)(C)c1ncc(C23CN(C(=O)OCc4ccccc4)CC2CON3)s1
Reaction #425271
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
C[Si](C)(C)c1ncc(C23CN(C(=O)OCc4ccccc4)CC2CON3)s1
Reaction #557398
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCOC(=O)c1nccs1
Reaction #588407
ethyl 2-thiazolecarboxylate
Выход 51.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
C[Si](C)(C)c1nccs1
Reaction #590964
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C(c1ccc(F)cc1)c1nccs1
Reaction #594799
title compound
Выход 77.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
OC(c1ccc(F)cc1)c1cncs1
Reaction #594819
product
Выход 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC(C)(C)OC(=O)N1CCC2=Cc3c(cnn3-c3ccc(F)cc3)C[C@]2(C(=O)c2cnc([Si](C)(C)C)s2)C1
Reaction #624433
(R)-tert-butyl 1-(4-fluorophenyl)-4a-(2-(trimethylsilyl)thiazole-5-carbonyl)-4a,5,7,8-tetrahydro-1H-pyrazolo[3,4-g]isoquinoline-6(4H)-carboxylate
Выход 27.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cnc([Si](C)(C)C)s1
Reaction #747906
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
C[Si](C)(C)CCN1C(=O)CN(c2ccc(-c3nccs3)cc2OCc2ccccc2)S1(=O)=O
Reaction #747910
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CC(C)CC(NC(=O)OC(C)(C)C)C(O)c1nccs1
Reaction #762634
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
C[Si](C)(C)CCN1C(=O)CN(c2ccc(-c3nccs3)cc2OCc2ccccc2)S1(=O)=O
Reaction #788434
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
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