Substructure Search

CCCC(C)CO

CC(C)CC1Cc2c(Br)cccc2C1O
Reaction #1359
desired product
Yield 96.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1Cc2c(Br)cccc2C1O[Si](C)(C)C
Reaction #1360
desired product
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[C@H]1/C(=C/CO)O[C@@H]2CC(=O)N21.[K+]
Reaction #3722
potassium clavulanate
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)C(=CCN1CCN(C)CC1)c1ccccc1CO2
Reaction #5138
methyl 11-[2-(4-methyl-1-piperazinyl)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7116
crude product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7117
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CCCCC[C@@H]1N
Reaction #7118
cis-2-aminocycloheptanecarboxylic acid methyl ester
Yield 61.8%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@H]1N
Reaction #7119
(1S,2R)-2-aminocyclohexanecarboxylic acid amide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCC[C@@H]1N
Reaction #7120
cis-2-aminocyclohexanecarboxylic acid amide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCCC[C@@H]1N
Reaction #7121
cis-2-aminocycloheptanecarboxylic acid amide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1CC1C(=O)O
Reaction #42330
2-butylcyclopropanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COCCCc1nc(C(F)F)ccc1C(=O)OC1=CC(=O)C2CCC1C2
Reaction #48277
6-Difluoromethyl-2-(3-methoxy-propyl)-nicotinic acid 4-oxo-bicyclo[3.2.1]oct-2-en-2-yl ester
Yield 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCC1Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #49744
N-{2-fluoro-4-chloro-5-(2-methylcyclopentyl)oxyphenyl}-3,4,5,6-tetrahydrophthalimide
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCC1Oc1cc(N)c(F)cc1Cl
Reaction #49761
2-fluoro-4-chloro-5-(2-methylcyclopentyl)oxyaniline
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C)(C)C(=O)OC
Reaction #57046
ester
Yield 100.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(C)C(=O)O
Reaction #63993
2-methylheptanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(C)C(=O)Cl
Reaction #63994
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](O)[C@H](Nc2ncc3cc(-c4c(Cl)c(OC)cc(OC)c4Cl)ccc3n2)C1
Reaction #84666
(1S,3R,4R)-methyl 3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)-4-hydroxycyclopentanecarboxylate
Yield 67.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)N[C@H]3CCC[C@H]3C(=O)O)cc2F)C1
Reaction #88192
(1R,2S)-2-(6-((R)-3-(2-ethoxyphenoxy)piperidin-1-yl)-5-fluoronicotinamido)cyclopentane-1-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)N[C@H]3CCC[C@H]3C(=O)O)cn2)C1
Reaction #88193
(1R,2S)-2-(2-((R)-3-(2-ethoxyphenoxy)piperidin-1-yl)pyrimidine-5-carboxamido)cyclopentane-1-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
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