部分構造検索

CCOC(CN)OCC

C=C(C)C(=O)OCCO
Reaction #5381
2-hydroxyethyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #47771
amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2cccc(C(F)(F)F)c2)cc1Nc1ncc[nH]1
Reaction #47772
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccccc2)cc1Nc1ncc[nH]1
Reaction #47775
N-[3-(1H-imidazol-2-ylamino)-4-methyl-phenyl]-benzamide
収率 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn2cccc2cn1
Reaction #53435
ethyl pyrrolo[1,2-a]pyrazine-3-carboxylate
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CNC(=O)c1ccncc1Nc1ccc(I)cc1F)OCC
Reaction #67866
N-(2,2-diethoxyethyl)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](O[C@@H]2[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](C)O[C@H]2O)[C@H](NC(=O)C(Cl)(Cl)Cl)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90567
318
収率 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)[C@H](NC(=O)C(Cl)(Cl)Cl)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90568
306
収率 79.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CN=C=N)OCC
Reaction #91502
N-(2,2-diethoxyethyl)carbodiimide
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CNC(=N)Nc1ccccc1)OCC
Reaction #91503
guanidine
収率 73.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CN=C=N)OCC
Reaction #157233
N-(2,2-diethoxyethyl)carbodiimide
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CNC(=N)Nc1ccccc1)OCC
Reaction #157234
guanidine
収率 73.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CNC(=O)c1ccncc1Nc1ccc(I)cc1F)OCC
Reaction #166031
N-(2,2-diethoxyethyl)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CC=CCC(NC(=O)c2nccc3ccccc23)C1=O)NC1CC(=O)OC1O
Reaction #179393
DOI: 10.1039/C8SC04228D
CCOC(CN1CCSc2sccc2C1=O)OCC
Reaction #179544
DOI: 10.1039/C8SC04228D
CC(C)(C)C(NC(=O)c1ccc(N)c(Cl)c1)C(=O)N1CCCC1C(=O)NC1CC(=O)OC1OCc1ccccc1
Reaction #190103
DOI: 10.1039/C8SC04228D
CCOC1OC(=O)CC1N=P(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #194847
DOI: 10.1039/C8SC04228D
CCOC(CN(Cc1cccc2scnc12)C(=O)C(N)Cc1ccc(OC(C)(C)C)cc1)OCC
Reaction #204143
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(C)NC(C=O)=C(C(=O)OCC)C1c1ccccc1C(F)(F)F
Reaction #213581
DOI: 10.1039/C8SC04228D
CS(=O)(=O)N1CC2CCCCC(NC(=O)c3ccccc3)C(=O)N2C(C(=O)NC2CC(=O)OC2O)C1
Reaction #242721
DOI: 10.1039/C8SC04228D
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