para-toluenesulfonic acid

CCCCCCCCCCCCCCCCC(O)COC1CCCCO1
Reaction #1219
1-(2-tetrahydropyranyloxy)-2-octadecanol
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC(=O)c1c(F)cc(F)c(F)c1C
Reaction #1371
ethyl 2-methyl-3,4,6-trifluorobenzoylacetate
Yield 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C1=CCC(C)(C)c2ccc(Br)cc21
Reaction #1457
7-bromo-1-(1,1-dimethylethyl)-3,4-dihydro-4,4-dimethylnaphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C1=CCC(C)(C)c2ccc(Br)cc21
Reaction #1477
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC1=CCC(C)(C)c2cc(C(C)=O)ccc21
Reaction #1483
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCC#CCOC1CCCCO1
Reaction #1659
4-tetrahydropyranoxy-2-butyn-1-ol
Yield 68.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCC#CCOC1CCCCO1
Reaction #2164
4-tetrahydropyranoxy-2-butyn-1-ol
Yield 68.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCC#CCOC1CCCCO1
Reaction #2264
4-tetrahydropyranoxy-2-butyn-1-ol
Yield 68.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #2450
formula VI
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@H]1C=C[C@@H](O)C1
Reaction #2655
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2=CCC(C)(C)c3ccc(Br)cc32)cn1
Reaction #2708
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2=CC(C)(C)Sc3ccc(Br)cc32)cc1
Reaction #2710
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@@H]1[C@H](O)[C@@H](OC(=O)c2ccccc2)[C@H](O[C@@H]2[C@H](O[C@@H]3O[C@@H](C)[C@@H](OCc4ccccc4)[C@@H](OCc4ccccc4)[C@@H]3OCc3ccccc3)[C@@H](OC(=O)c3ccccc3)[C@H](OCC[Si](C)(C)C)O[C@@H]2COC(=O)c2ccccc2)O[C@@H]1COC(=O)c1ccccc1
Reaction #2722
title compound 11a
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCO[C@@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](O[C@@H]2O[C@H](COC(=O)c3ccccc3)[C@H](OC(C)=O)[C@H](O)[C@H]2OC(=O)c2ccccc2)[C@H](O[C@@H]2O[C@@H](C)[C@@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)[C@H]1OC(=O)c1ccccc1
Reaction #2723
23
Yield 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C#N)ccc1N=C(c1ccccc1)c1ccccc1
Reaction #2850
title compound
Yield 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C1=Cc2ccccc2CC1
Reaction #2889
dihydronapthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)CC(=O)OCC(C)C
Reaction #2941
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #3012
salt
Yield 73.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1c(Cc2[nH]c(Cc3[nH]c(C(=O)OCc4ccccc4)c(C)c3CC)c(CC)c2CC)[nH]c(C(=O)OCc2ccccc2)c1C
Reaction #3190
powder
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1c(Cc2[nH]c(C(=O)OCc3ccccc3)c(C)c2CCC(=O)OC)[nH]c(Cc2[nH]c(C(=O)OCc3ccccc3)c(C)c2CCC(=O)OC)c1CC
Reaction #3191
powder
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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