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37423

O=c1ccc2cc(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(OCc3ccccc3)cc2o1
Reaction #2785
7-benzyloxy-6-D-glucopyranosyloxycoumarin
収率 86.4%DOI: 10.6084/m9.figshare.5104873.v1
OB(O)c1cc(F)ccc1OC1CCCCO1
Reaction #41917
5-Fluoro-2-(tetrahydropyran-2-yloxy)benzeneboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
OB(O)c1ccc(F)cc1OC1CCCCO1
Reaction #41919
4-Fluoro-2-(tetrahydropyran-2-yloxy)benzeneboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(Br)c(Br)cnn1-c1ccc(OC2CCCCO2)cc1
Reaction #43326
title compound
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1C[C@](C)(O)Cc2cc3c(c(O)c21)C(=O)c1c(O)cc2c(c1C3=O)OC1OC2(C)[C@H](O)[C@@H](N(C)C)[C@@H]1O
Reaction #64004
7-0-methylnogarol
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2[nH]ccc2c1
Reaction #64078
indole
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OC2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1
Reaction #68735
Para-nitrophenyl glucopyranoside
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2oc3c(CC=C(C)C)c(O)cc(O)c3c(=O)c2O[C@@H]2O[C@H](C)[C@@H](O)[C@H](O)[C@@H]2O)cc1
Reaction #68769
icariside II
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(-c2ccccc2O[C@@H]2O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]2O)c1
Reaction #82477
methyl 3-(2-(α-L-fucopyranosyloxy)phenyl)benzoate
収率 88.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H]2CC(=O)c3c(O)cc(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)cc3O2)cc1O.[Ag]
Reaction #89803
Hesperidin silver
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(=O)c3c(O)cc(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)cc3o2)cc1O.[Pd]
Reaction #89804
Diosmin palladium
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H]1O[C@@H](Oc2ccc([N+](=O)[O-])cc2)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #92786
pNPG
DOI: 10.6084/m9.figshare.5104873.v1
COCOCCc1ccc(Cc2ccc(OC)cc2OC2OC(COC(C)=O)C(OC(C)=O)C(OC(C)=O)C2OC(C)=O)cc1
Reaction #182418
DOI: 10.1039/C8SC04228D
CCCCC(c1ccc(OC2CCCCO2)cc1)N(C(=O)CCc1ccccc1)c1ccc(OCCN2CCCC2)cc1
Reaction #188542
DOI: 10.1039/C8SC04228D
COc1cc(OC2CCCCO2)ccc1CN(C(=O)C1CCCCC1)c1ccc(OCCN2CCCC2)cc1
Reaction #194916
DOI: 10.1039/C8SC04228D
O=c1c(Br)c(Br)cnn1-c1ccc(OC2CCCCO2)cc1
Reaction #202401
DOI: 10.1039/C8SC04228D
O=C1CC(c2ccc(O)cc2)Oc2cc(O)cc(O)c21
Reaction #203809
DOI: 10.1039/C8SC04228D
c1ccc(OC2CCCCO2)cc1
Reaction #216990
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1nc(-c2ccc(OC3CCCCO3)cc2)cnc1N
Reaction #230882
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2cc(OC)ccc2F)c(OC2CCCCO2)c1
Reaction #232093
DOI: 10.1039/C8SC04228D
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