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1345280

O[C@@H]1CO[C@H]2[C@@H]1OC[C@@H]2O
Reaction #57372
isosorbide
Выход 42.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(=O)O[C@H]1CO[C@H]2[C@@H]1OC[C@H]2OC(=O)CCCCCCC
Reaction #90211
Isosorbide Dicaprylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCOc1ccc(C=Cc2ccc(COC3COC4C(O)COC34)cc2)cc1
Reaction #205153
DOI: 10.1039/C8SC04228D
CCCCc1nc(Cl)c(C(=O)OCP(=O)(OCC)OCC)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #267555
DOI: 10.1039/C8SC04228D
CCOc1nc2cccc(C(=O)OC(C)(C)OC(=O)O[C@H]3COC4C3OC[C@H]4O[N+](=O)[O-])c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #309711
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(Cl)c(C(=O)O[C@H](C)OC(=O)O[C@H]2CO[C@H]3[C@@H]2OC[C@H]3O[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #309712
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(Cl)c(C(=O)O[C@H]2CO[C@H]3[C@@H]2OC[C@H]3O[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #309713
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(OC)O[C@H]1CO[C@H]2[C@@H]1OC[C@H]2O[N+](=O)[O-]
Reaction #309718
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(O)O[C@H]1CO[C@H]2[C@@H]1OC[C@H]2O[N+](=O)[O-]
Reaction #309719
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(OCCl)O[C@H]1CO[C@H]2[C@@H]1OC[C@H]2O[N+](=O)[O-]
Reaction #309720
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(Cl)c(C(=O)OCOP(=O)(OC)O[C@H]2CO[C@H]3[C@@H]2OC[C@H]3O[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #309721
[(methoxy{[(3S,3aS,6R,6aS)-6-(nitrooxy)hexahydrofuro[3,2-b]furan-3-yl]oxy}phosphoryl)oxy]methyl 2-butyl-4-chloro-1-{[2′-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-imidazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(Cl)c(C(=O)OCOP(=O)(OC)O[C@H]2CO[C@H]3[C@@H]2OC[C@H]3O[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #309722
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(Cl)c(C(=O)OCP(=O)(OCC)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #309723
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(Cl)c(C(=O)OCP(=O)(OCC)OCC)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #309724
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1O[C@H]2[C@H](OC[C@H]2OC(=O)c2ccccc2)[C@H]1OC
Reaction #331709
methyl 3,6-anhydro-2-O-methyl-5-O-(phenylcarbonyl)-β-D-glucofuranoside
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1O[C@H]2[C@H](OC[C@H]2O)[C@H]1OC
Reaction #331710
methyl 3,6-anhydro-2-O-methyl-β-D-glucofuranoside
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1O[C@H]2[C@H](OC[C@H]2OS(C)(=O)=O)[C@H]1OC
Reaction #331711
methyl 3,6-anhydro-2-O-methyl-5-O-(methylsulfonyl)-β-D-glucofuranoside
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Nc3ccc(Br)c(Cl)c3)ncnc2cc1O[C@H]1CO[C@@H]2[C@@H](OC)[C@H](OC)O[C@@H]21
Reaction #331712
methyl 3,6-anhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6-(methyloxy)quinazolin-7-yl]-2-O-methyl-α-L-idofuranoside
Выход 28.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1OC2C(OS(C)(=O)=O)COC2C1OC
Reaction #382996
DOI: 10.1039/C8SC04228D
COC1OC2C(OC(=O)c3ccccc3)COC2C1OC
Reaction #385032
DOI: 10.1039/C8SC04228D
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