Поиск подструктуры

C=CC(=O)OCCO

C=CC(=O)OCCOCCN1C(=O)C2CCCCC2C1=O
Reaction #3165
orange-red liquid
Выход 59.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)OCC1CNC(=O)O1
Reaction #3168
5-Acryloyloxymethyl-oxazolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CSCCOC(=O)C1=C(C)NC(C)=C(C(=O)OCCOc2ccc(NC(C)=O)cc2)C1c1cccc([N+](=O)[O-])c1
Reaction #4676
2-(4-acetylaminophenoxy)ethyl 2,6-dimethyl-5-(2-methylthioethoxycarbonyl)-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCSCCOC(=O)C1=C(C)NC(C)=C(C(=O)OCCOc2ccc(NC(C)=O)cc2)C1c1cccc([N+](=O)[O-])c1
Reaction #4678
2-(4-acetylaminophenoxy)ethyl 2,6-dimethyl-5-(2-ethylthioethoxycarbonyl)-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(C)NC(C)=C(C(=O)OCCOC(=O)c2ccc(NC(C)=O)cc2)C1c1cccc([N+](=O)[O-])c1
Reaction #4683
2-(4-acetylaminobenzoyloxy)ethyl 2,6-dimethyl-5-methoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOCCOCCOc1cccc(N)c1
Reaction #5145
2-(2-(2-(3-aminophenoxy)ethoxy)ethoxy)ethyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC(=O)C[C@@H](CC#N)O[Si](C)(C)C(C)(C)C
Reaction #5779
(R)-1,1-dimethylethyl 6-cyano-5-[(1,1-dimethylethyl)dimethylsilyl]oxy-3-oxohexanoate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6499
2-ethoxalyloxyethyl methacrylate
Выход 76.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6500
2-ethoxalyloxyethyl methacrylate
Выход 76.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6501
2-ethoxalyloxyethyl methacrylate
Выход 56.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6502
2-ethoxalyloxyethyl methacrylate
Выход 73.2%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(Oc2ccc3c(c2)nc(Nc2cccc(-c4cn(Cc5ccccc5)nn4)c2)n3C)ccn1
Reaction #41788
4-{2-(3-(1-Benzyl-1H-[1,2,3]triazol-4-yl)-phenyl amino]-1-methyl-1H-benzoimidazol-5-yloxy}-pyridine-2-carboxylic acid methyl amide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cn(Cc2ccccc2)nn1)C(=O)OCc1ccccc1
Reaction #46653
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cn(Cc2ccccc2)nn1)C(=O)OCc1ccccc1
Reaction #49143
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OC(C)(C)C
Reaction #49695
tert-butyl propanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OC(C)(C)C
Reaction #49696
tert-butyl propanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OC(C)(C)C
Reaction #49697
tert-butyl propanoate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc2c(c(=O)[nH]1)NC(CNc1ccc(C(=O)N[C@@H](CCC(=O)O)C(=O)O)cc1)CN2
Reaction #54546
tetrahydrofolic acid
Выход 0.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)/C=C/c1ccc(O)c(O)c1
Reaction #56616
caffeic acid
DOI: 10.6084/m9.figshare.5104873.v1
CNCCCN1c2ccccc2CCc2ccccc21
Reaction #57129
desipramine
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее