Substructure Search

260579

CC(C)(C)c1ccc(NC(=O)c2cccc(-c3nn4c(c3-c3ccncc3)SCC4)c2)cc1
Reaction #66368
N-(4-tert-butyl-phenyl)-3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-benzamide
Yield 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C(=O)OCC)c1ccc([N+](=O)[O-])cc1Br
Reaction #67469
diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #67470
solid
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(C2CC2)cc1
Reaction #91925
title compound
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(F)(F)F)c([N+](=O)[O-])cc1OCc1ccccc1
Reaction #161183
1-tert-butyl-2-(benzyloxy)-5-(trifluoromethyl)-4-nitrobenzene
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(F)(F)F)c(N)cc1O
Reaction #161184
5-Amino-2-tert-butyl-4-trifluoromethyl-phenol
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)C)c([N+](=O)[O-])c(O)c1O
Reaction #161202
4,6-di-tert-butyl-3-nitrobenzene-1,2-diol
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)C)c(O)c(O)c1N
Reaction #161203
4,6-di-tert-butyl-3-aminobenzene-1,2-diol
Yield 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(N)cc1NC(=O)c1c[nH]c2ccccc2c1=O
Reaction #161283
N-(5-amino-2-tert-butyl-phenyl)-4-oxo-1H-quinoline-3-carboxamide
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCNc2cc(NC(=O)c3c[nH]c4ccccc4c3=O)ccc21
Reaction #161290
N-(4,4-Dimethyl-1,2,3,4-tetrahydroquinolin-7-yl)-4-oxo-1H-quinoline-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(NC(=O)c2c[nH]c3ccccc3c2=O)cc1CN
Reaction #161292
N-[3-(Aminomethyl)-4-tert-butyl-phenyl]-4-oxo-1H-quinoline-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)C)c(NC(=O)c2c[nH]c3ccccc3c2=O)cc1O
Reaction #163977
N-(2,4-di-tert-butyl-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)C)c(NC(=O)c2c[nH]c3ccccc3c2=O)cc1O
Reaction #163978
N-(2,4-di-tert-butyl-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C(=O)OCC)c1ccc([N+](=O)[O-])cc1Br
Reaction #170939
diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170940
solid
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCCNc2cc(N)ccc21
Reaction #178084
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(NC(=O)c2ccc(-c3ncccc3Cl)cc2)cc1
Reaction #179243
DOI: 10.1039/C8SC04228D
CCCCCCCOc1cc2c(cc1N(CCC)c1ccc(C(=O)OCC)cc1)C(C)=CCC2(C)C
Reaction #195142
DOI: 10.1039/C8SC04228D
CC1(C)CCC(C)(C)c2cc(NC(=O)c3ccccc3)ccc21
Reaction #202191
DOI: 10.1039/C8SC04228D
CC(C(=O)O)c1ccc(Cl)c(CC(=O)O)c1
Reaction #203446
DOI: 10.1039/C8SC04228D
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