tetrabutylammonium hydroxide

COc1cc(CC(=O)Nc2cccc(I)c2)ccc1OCCNC(=O)OC(C)(C)C
Reaction #7153
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(CC(=O)Nc2cccc(C3CCC(C(C)(C)C)CC3)c2)ccc1OCCBr
Reaction #7154
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCC[N+](CCCC)(CCCC)CCCC.O=S([O-])c1cccc2ccccc12
Reaction #43891
Tetrabutylammonium 1-Naphthalene Sulfinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CC(=O)[O-].CCCC[N+](CCCC)(CCCC)CCCC
Reaction #50320
tetrabutylammonium acrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(=O)N1CCc2ccc(S(=O)(=O)n3ccc4ccccc43)cc2C1
Reaction #51094
title compound ( D1 )
수율 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
N#CSCOn1cc(Cl)cn1
Reaction #63230
4-chloro-1-[(thiocyanato)-methoxy]-pyrazole
수율 71.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCC[N+](CCCC)(CCCC)CCCC
Reaction #64603
tetra(n-butyl)ammonium
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCC[N+](CCCC)(CCCC)CCCC
Reaction #64604
tetra(n-butyl)ammonium
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCC[N+](CCCC)(CCCC)CCCC
Reaction #64681
tetra (n-butyl) ammonium
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCC[N+](CCCC)(CCCC)CCCC
Reaction #64682
tetra (n-butyl) ammonium
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
N#Cc1cccc(C(=O)N2CCC(c3cn(Cc4ccc(F)cc4)c4ccccc34)CC2)c1
Reaction #70512
3-{4-[1-(4-Fluoro-benzyl)-1H-indol-3-yl]-piperidine-1-carbonyl}-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1C(c2cccc(-c3ccccc3)c2)=C(c2ccc(Br)cc2)C(c2ccc(Br)cc2)=C1c1cccc(-c2ccccc2)c1
Reaction #85586
tetraarylcyclopentadienone
수율 53.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C1C(c2cccc(-c3ccccc3)c2)=C(c2ccc(Cl)cc2)C(c2ccc(Cl)cc2)=C1c1cccc(-c2ccccc2)c1
Reaction #85588
tetraarylcyclopentadienone
수율 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1ccc(-n2ccc(C(=O)O)cc2=O)cc1
Reaction #158904
1-(4-Ethoxycarbonyl-phenyl)-2-oxo-1,2-dihydro-pyridine-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1ccc(-n2ccc(C(=O)O)cc2=O)cc1
Reaction #166859
1-(4-Ethoxycarbonyl-phenyl)-2-oxo-1,2-dihydro-pyridine-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)NC(=O)N1CCCC1c1ncc(-c2ccc(-c3ccn(-c4cn(COCC[Si](C)(C)C)c(C5CCCN5C(=O)OC(C)(C)C)n4)c(=O)c3)cc2)n1COCC[Si](C)(C)C
Reaction #166864
2-[4-(4-{4-[2-(1-tert-butylcarbamyl-pyrrolidin-2-yl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-phenyl}-2-oxo-2H-pyridin-1-yl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCC[N+](CCCC)(CCCC)CCCC.c1nc[nH]n1
Reaction #215623
tetrabutylammonium 1H-1,2,4-triazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCCC[N+](CCCC)(CCCC)CCCC.O=C([O-])c1ccccc1O
Reaction #217752
Tetrabutylammonium Salicylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)c(O)c1)C(=O)[O-].CCCC[N+](CCCC)(CCCC)CCCC
Reaction #303827
title compound
수율 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)c(O)c1)C(=O)[O-].CCCC[N+](CCCC)(CCCC)CCCC
Reaction #316677
title compound
수율 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
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