o-toluenesulfonylchloride

CN1CCC(Oc2ccccc2C(N)=O)C1
Reaction #4875
2-(1-Methyl-3-pyrrolidinyloxy)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
ClCCCSc1ccc2c(-c3c(-c4ccccn4)nn4c3CCC4)ccnc2c1
Reaction #8357
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccccc1S(=O)(=O)n1ccc2c(Br)cccc21
Reaction #8427
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(S(=O)(=O)OCC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #44336
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccccc1S(=O)(=O)Oc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49418
4-(2-methylbenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(S(=O)(=O)OCC2COc3c(F)cc(S(C)(=O)=O)cc3O2)cc1
Reaction #67281
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(S(=O)(=O)OC[C@H]2COc3ccc(S(=O)(=O)C(F)(F)F)cc3O2)cc1
Reaction #67292
[(2R)-7-(TRIFLUOROMETHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL 4-METHYLBENZENESULFONATE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(S(=O)(=O)OC[C@H]2COc3cccc(F)c3O2)cc1
Reaction #67297
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CC1(C=C)CC[C@H](COC(c2ccccc2)(c2ccccc2)c2ccccc2)O1
Reaction #75599
(5R)-5-[(trityloxy)methyl]-2,2-divinyltetrahydrofuran
Yield 47.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccccc1S(=O)(=O)ON=C1c2ccc(-c3ccco3)cc2OCC1C
Reaction #77716
7-furyl-3-methyl-4-chromanone O-(toluenesulfonyl)-oxime
Yield 57.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccc(S(=O)(=O)n2ccc3c(O)c(F)cnc32)cc1
Reaction #162215
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccccc1S(=O)(=O)Nc1cnc(Oc2cc3ccccc3cn2)c(Cl)c1
Reaction #179711
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCC2(S(=O)(=O)c3ccc(Cl)cc3)c3c(F)ccc(F)c3OCC2C1
Reaction #207974
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)COS(=O)(=O)c1ccccc1C
Reaction #209929
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(NS(=O)(=O)c2ccccc2C)cc1
Reaction #212494
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1S(=O)(=O)n1ccc2c(Br)cccc21
Reaction #230386
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccccc1S(=O)(=O)N1N(C2C3CC4CC(C3)CC2C4)C(=O)C1(C)C
Reaction #234890
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccccc1S(=O)(=O)OCCCCc1ccc(CSc2cnn(C(C)(C)C)c(=O)c2Cl)cc1
Reaction #249054
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccccc1S(=O)(=O)NC1CCc2sccc2C1
Reaction #256602
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CCC(c2nnc(-c3ccccc3)o2)CC1
Reaction #309430
tert-butyl 4-(5-phenyl-1,3,4-oxadiazol-2-yl)piperidine-1-carboxylate
Yield 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Page 1Next