p-toluenesulfonyl chloride

CCC1(COS(=O)(=O)c2ccc(C)cc2)COC(=O)N1
Reaction #949
beige solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccccc1S(=O)(=O)OCC1(C(F)(F)F)CCN(Cc2ccccc2)C1
Reaction #1986
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCCCOC1CCCCO1
Reaction #2031
1-(Tetrahydopyran-2-yloxy)-4-pentyne
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCOS(=O)(=O)c1ccc(C)cc1
Reaction #2032
2-pentyn-1-yl p-toluenesulphonate
Rendimiento 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOCn1cnc2c1c(=O)[nH]c(=O)n2C
Reaction #2083
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(CCCCCOS(=O)(=O)c1ccc(C)cc1)OCC
Reaction #2106
Diethyl 5-p-toluenesulfonyloxypentylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(S(=O)(=O)n2cnc(CO)c2)cc1
Reaction #2159
title compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)CC(NS(=O)(=O)c1ccc(C)cc1)c1ccc(OCC2CCN(c3ccncc3)CC2)cc1
Reaction #2307
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(S(=O)(=O)OC[C@H](C)CC(=O)OC(C)(C)C)cc1
Reaction #2351
tert-butyl (3R)-3-methyl-4-(p-toluenesulphonyloxy)-butyrate
Rendimiento 96.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(S(=O)(=O)OCC(O)COS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #2438
Compound 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #2487
4-methyl-4'-chlorodiphenylsulfone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NS(=O)(=O)c1ccc(C)cc1
Reaction #2503
title compound
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CO[C@H](C)COS(=O)(=O)c1ccc(C)cc1
Reaction #2837
(+)-(R)-2-methoxypropyl-p-toluenesulphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNC(=O)c1ccc(C)c(I)c1
Reaction #3063
N-methyl-(3-iodo-4-methylphenyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCC(OS(=O)(=O)c1ccc(C)cc1)C(C)=O
Reaction #4384
3-tosyloxy-5-hexyn-2-one
Rendimiento 55.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
[N-]=[N+]=NCCCCCCCCO
Reaction #5222
8-azido-1-octanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)OC1CCCC2(C)C(C(C)CC(Cl)CBr)=CCC12
Reaction #6379
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1ccc(S(=O)(=O)NC(CCCCNC(=O)OCc2ccccc2)C(=O)O)cc1
Reaction #6465
title compound
Rendimiento 81024.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
—
Reaction #6881
material
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(S(=O)(=O)CC2(C)COC2)cc1
Reaction #8381
3-METHYL-3-TOSYLMETHYLOXETANE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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