Eaton's reagent

O=C1CCNC(=O)c2[nH]ccc21
Reaction #42649
aldisine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CS(=O)(=O)Oc1ccc(-c2ncco2)cc1
Reaction #44777
4-(oxazol-2-yl)phenyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Ic1ccc(-c2ncco2)cc1
Reaction #44783
2-(4-iodophenyl)oxazole
Yield 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CS(=O)(=O)[O-].Cc1cc(C)c([S+](c2ccccc2)c2ccccc2)c(C)c1
Reaction #52135
2,4,6-trimethylphenyldiphenylsulfonium mesylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cc2c(cc1Br)C(C)(C)c1[nH]c3cc(C#N)ccc3c1C2=O
Reaction #90091
title compound
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCc1cc2c(cc1I)C(C)(C)c1[nH]c3cc(C#N)ccc3c1C2=O
Reaction #90155
title compound
Yield 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
—
Reaction #161643
material
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(O)nc2c1CN(Cc1ccccc1)CC2
Reaction #168003
6-benzyl-4-methyl-5,6,7,8-tetrahydro-1,6-naphthyridin-2-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1CCNC(=O)c2[nH]ccc21
Reaction #219169
aldisine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Cc1nccn2c(C3CC(=O)N(C)C3)ncc12
Reaction #332953
1-methyl-4-(8-methylimidazo[1,5-a]pyrazin-3-yl)pyrrolidin-2-one
Yield 108.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(O)c1ccccc1C1(c2ccccc2C(=O)O)c2cc(C34CC5CC(CC(C5)C3)C4)ccc2-c2ccc(C34CC5CC(CC(C5)C3)C4)cc21
Reaction #338898
2,7-di(1-adamantyl)-fluorene-9,9-bisbenzoic acid
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1ccc([S+](c2ccc(C)cc2)c2ccc(C3CCCCC3)cc2)cc1.O=S(=O)([O-])C(F)(F)C(F)C(F)(F)F
Reaction #364867
contemplated material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1ccc([S+](C)C)cc1.O=S(=O)([O-])C(F)(F)C(F)C(F)(F)F
Reaction #364869
contemplated material
Yield 169.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
O=C1CCCc2cc(F)cc(F)c21
Reaction #426374
6,8-Difluoro-3,4-dihydro-2H-naphthalen-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCOC(=O)C1CC=C(c2ncc(-c3cc(C)cc(Nc4nccc(C(F)(F)F)n4)c3)s2)CC1
Reaction #497728
ethyl 4-[5-(3-methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)-1,3-thiazol-2-yl]-cyclohex-3-ene-1-carboxylate
Yield 83.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Cc1cc(Nc2nccc(C(F)(F)F)n2)cc(-c2cnc(C3=CCSCC3)s2)c1
Reaction #497855
title compound
Yield 41.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Cc1cc(Nc2nccc(C(F)(F)F)n2)cc(-c2cnc(C3=CCS(=O)(=O)CC3)s2)c1
Reaction #497858
N-{3-[2-(1,1-dioxido-3,6-dihydro-2H-thiopyran-4-yl)-1,3-thiazol-5-yl]-5-methylphenyl}-4-(trifluoromethyl)pyrimidin-2-amine
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCOC(=O)c1cn(C)c2sc(CN3CCOCC3)nc2c1=O
Reaction #498394
title compound
Yield 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
O=C1CCCc2cc(F)cc(F)c21
Reaction #507383
6,8-Difluoro-3,4-dihydro-2H-naphthalen-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COc1ccc(Oc2c(Cl)cc([N+](=O)[O-])cc2Cl)cc1S(=O)(=O)c1ccc(F)cc1
Reaction #520099
title compound
Yield 29.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
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