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CCOCC(=O)O

O=C1CCCCCO1.O=C1COCCO1
Reaction #2356
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2357
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2358
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2359
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
CC(OC1C(Cl)=C(OC2=C(Cl)C(OC(C)C(=O)O)C(c3ccccc3C(F)(F)F)([N+](=O)[O-])C=C2)C=CC1(c1ccccc1C(F)(F)F)[N+](=O)[O-])C(=O)O
Reaction #55593
2-chloro-α,α,α-trifluoro-p-tolyl-3-(1-carboxyethoxy)-4-nitrophenyl ether
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)OC1C(Cl)=C(OC2=C(Cl)C(OC(C)CO)C(c3ccccc3C(F)(F)F)([N+](=O)[O-])C=C2)C=CC1(c1ccccc1C(F)(F)F)[N+](=O)[O-]
Reaction #55607
2-chloro-α,α,α-trifluoro-p-tolyl-3-(1-hydroxymethylethoxy)-4-nitrophenyl ether
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCOC(C(=O)OCc2ccccc2)C1
Reaction #70519
title compound
Выход 58.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCOC(C(=O)O)C1
Reaction #70520
title compound
Выход 24.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@H](OCc1ccccc1)C(=O)O)OCc1ccccc1
Reaction #72436
(S)-2-benzyloxy-4-benzyloxycarbonylaminobutyric acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@@H](OCc1ccccc1)C(=O)O)OCc1ccccc1
Reaction #72437
title compound
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCN(CCc1ccc(CC(OCC)C(=O)O)cc1)C(=O)C1(c2ccc(C)cc2)CC1
Reaction #76080
2-ethoxy-3-(4-{2-[heptyl-(1-p-tolyl-cyclopropanecarbonyl)-amino]-ethyl}-phenyl)-propionic acid
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COCc1cccc(-c2ccccc2O[C@@H]2O[C@@H](C)[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]2OC(C)=O)c1
Reaction #82472
ethyl 3-(2-(2,3,4-tri-O acetyl-α-L-fucopyranosyloxy)phenyl)benzyloxyacetate
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC1C(Cl)=C(OC2=C(Cl)C(OC(C)C(=O)O)C(c3ccccc3C(F)(F)F)([N+](=O)[O-])C=C2)C=CC1(c1ccccc1C(F)(F)F)[N+](=O)[O-])C(=O)O
Reaction #93605
2-chloro-α,α,α-trifluoro-p-tolyl-3-(1-carboxyethoxy)-4 -nitrophenyl ether
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)OC1C(Cl)=C(OC2=C(Cl)C(OC(C)CO)C(c3ccccc3C(F)(F)F)([N+](=O)[O-])C=C2)C=CC1(c1ccccc1C(F)(F)F)[N+](=O)[O-]
Reaction #93619
2-chloro-α,α,α-trifluoro-p-tolyl-3-(1-hydroxymethylethoxy)-4-nitrophenyl ether
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CO
Reaction #161325
glycolic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(OCc1nn(C(=O)c2ccccc2)c2ccccc12)C(=O)O
Reaction #163298
2-[(1-benzoyl-1H-indazol-3-yl)methoxy]-2-methylpropanoic acid
Выход 22.7%DOI: 10.6084/m9.figshare.5104873.v1
OCC1CN(Cc2ccccc2)CCO1
Reaction #169944
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N2CCN(C3=Nc4c(F)cccc4C(CC(=O)O)N3c3cc(C(F)(F)F)ccc3OC)CC2)c1
Reaction #173972
DOI: 10.1039/C8SC04228D
CCOC(Cc1ccc(OCc2nc(-c3ccccc3)oc2C)cc1Cl)C(=O)O
Reaction #176606
DOI: 10.1039/C8SC04228D
CCOC(=O)C(O)c1ccc(Cl)c(NC(=O)c2ccc(OCC3CN(C)c4ccccc4O3)cc2Cl)c1
Reaction #178457
DOI: 10.1039/C8SC04228D
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