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CC(=O)OCCC(C)C

CC(=O)OCC(=O)[C@@]1(O[Si](C)(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42650
title compound
Выход 103.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42651
title compound
Выход 73.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](C(=O)OC(C)(C)C)[C@H](O)COC(C)=O
Reaction #48321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](C(=O)OC(C)(C)C)[C@@H](COC(C)=O)O[Si](C)(C)C(C)(C)C
Reaction #48322
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@](O)(CC)C(=O)O[C@@H]1C[C@H](C)CC[C@H]1C(C)(C)c1ccccc1
Reaction #58772
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)O[C@]1(C(=O)C(O)OC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #81347
(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methyl-butyric acid [11β,21-dihydroxy-3,20-dioxo-9-fluoro-16β-methyl-17-valeroyloxy-pregna -1,4-dien-21-yl] ester
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@H]1[C@@H](Cc2ccc(C(F)(F)F)cc2)COC[C@H](NC(=O)c2nccc(OC)c2OCOC(=O)COCC)C(=O)O[C@H]1C
Reaction #87243
((4-methoxy-2-(((3S,7S,8R,9S)-9-methyl-2-oxo-8-propoxy-7-(4-(trifluoromethyl)benzyl)-1,5-dioxonan-3-yl)carbamoyl)pyridin-3-yl)oxy)methyl 2-ethoxyacetate
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(=O)OCC(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #92988
above-identified compound
Выход 77.5%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CCC(C)C
Reaction #92989
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CCCC(=O)O
Reaction #92999
above-identified compound
Выход 56.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C)C(=O)OCC(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #93002
above-identified compound
Выход 19.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(=O)OCC(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #93005
above-identified compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)C1CCCCC1
Reaction #93007
above-identified compound
Выход 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CCC1CCCCC1
Reaction #93008
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(OC(=O)c2ccc(O)o2)C(C)CC2C3CC(F)C4=CC(=O)C=CC4(C)C34OC4CC21C
Reaction #185648
DOI: 10.1039/C8SC04228D
CCOC(=O)C(OC(=O)c1ccc(C(F)(F)F)cc1)C(=O)C(C)C
Reaction #185993
DOI: 10.1039/C8SC04228D
CC(C)CC12CCC3C4CCC(=O)C=C4CCC3C1CCC2OC(=O)CCc1ccccc1
Reaction #187524
DOI: 10.1039/C8SC04228D
CC1(C)CCCC2(C)OC(=O)CC12
Reaction #204097
DOI: 10.1039/C8SC04228D
C=CCOCc1cc(-n2ncc3c2C=C2CCC4C(C(O)CC5(C)C4CCC5(OC(=O)c4ccco4)C(=O)NC)C2(C)C3)ccc1F
Reaction #211598
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2(C)C(=O)CCC2C2CCC3=CC(=O)C=CC3(C)C12F
Reaction #212457
DOI: 10.1039/C8SC04228D
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