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1272989

OC[C@H]1O[C@@H](n2c(Cl)nc3cc(Cl)c(Cl)cc32)[C@H](O)[C@@H]1O
Reaction #6441
2,5,6-Trichloro-1-(β-D-ribofuranosyl)benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6879
material
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1O[C@H](COCc2ccc(Cl)cc2Cl)[C@@H](OCc2ccc(Cl)cc2Cl)[C@H]1O
Reaction #10255
1-O-methyl-3,5-bis-O-(2,4-dichlorobenzyl)-β-D-ribofuranose
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2CCC(OC)O2)cc(OC)c1OC
Reaction #50766
2-(3,4,5-trimethoxyphenyl)-5 -methoxytetrahydrofuran
収率 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1nc2ccc(S(=O)(=O)NC(OC3CCCC3)[C@H](O)[C@H](Cc3ccccc3)NC(=O)O[C@@H]3CO[C@@H]4OCC[C@@H]43)cc2[nH]1
Reaction #57450
(3S,3aR,6aS)Hexahydrofuro[2,3-b]furan-3-yl-N-((1S,2R)-1-benzyl-3-(cyclopentyloxy)(2-[(methylsulfonyl)amino]benzimidazol-5-ylsulfonyl)amino-2-hydroxypropyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1nc2ccc(S(=O)(=O)NC(OC3CCCC3)[C@H](O)[C@H](Cc3ccccc3)NC(=O)O[C@H]3CO[C@H]4OCC[C@H]43)cc2[nH]1
Reaction #57451
(3R,3aS,6aR)Hexahydrofuro[2,3-b]furan-3-yl-N-((1S,2R)-1-benzyl-3-(cyclopentyloxy)(2-[(methylsulfonyl)amino]benzimidazol-5-ylsulfonyl)amino-2-hydroxypropyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)ON(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CO[C@H]2OCC[C@H]21)S(=O)(=O)c1ccc2c(c1)OCO2
Reaction #57490
(3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(1-ethylpropoxy)amino]-1-benzyl-2-hydroxypropylcarbamate
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)ON(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CO[C@H]2OCC[C@H]21)S(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #57491
(3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-1-benzyl-3-{(1-ethylpropoxy)[(4-nitrophenyl)sulfonyl]amino}-2-hydroxypropylcarbamate
収率 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)ON(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CO[C@H]2OCC[C@H]21)S(=O)(=O)c1cccc([N+](=O)[O-])c1
Reaction #57493
(3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-1-benzyl-3-{(1-ethylpropoxy)[(3-nitrophenyl)sulfonyl]amino}-2-hydroxypropylcarbamate
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)ON(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CO[C@H]2OCC[C@H]21)S(=O)(=O)c1ccc(OCc2ccccc2)cc1
Reaction #57495
(3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-1-benzyl-3-[{[4-(benzyloxy)phenyl]sulfonyl}(1-ethylpropoxy)amino]-2-hydroxypropylcarbamate
収率 74.1%DOI: 10.6084/m9.figshare.5104873.v1
COC1O[C@H](COCc2ccc(Cl)cc2Cl)[C@@H](OCc2ccc(Cl)cc2Cl)[C@H]1O
Reaction #59248
3,5-bis-O-(2,4-dichlorobenzyl)-1-O-methyl-D-ribofuranose
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C(=O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H]1O[C@@H](CC(=O)OO)[C@H](C)C[C@@H]1C)[C@H]1O[C@](C)([C@]2(O)O[C@](CC)([C@@H](O)CC)C[C@H]2C)C[C@@H]1C
Reaction #62575
lysocellin
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1O[C@H]2[C@H](OC(=O)[C@H]2O)[C@H]1O
Reaction #64339
methyl β-D-glucofuranosidurono-6, 3-lactone
収率 19.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH][nH]c(=O)c2c(O)c(-c3ccccc3)ncc12
Reaction #65738
8-Hydroxy-7-phenylpyrido[3,4-d]pyridazine-1, 4(2H, 3H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(O)OC[C@H]1O[C@@](COS(=O)(=O)O)(O[C@H]2O[C@H](COS(=O)(=O)O)[C@@H](OS(=O)(=O)O)[C@H](OS(=O)(=O)O)[C@H]2OS(=O)(=O)O)[C@@H](OS(=O)(=O)O)[C@@H]1OS(=O)(=O)O
Reaction #81382
Sucrose octasulfate
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])OC[C@H]1O[C@@](COS(=O)(=O)[O-])(O[C@H]2O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](OS(=O)(=O)[O-])[C@H]2OS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@@H]1OS(=O)(=O)[O-].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+]
Reaction #81383
Potassium sucrose octasulfate
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])OC[C@H]1O[C@@](COS(=O)(=O)[O-])(OC2O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](OS(=O)(=O)[O-])[C@H]2OS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@@H]1OS(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]
Reaction #81384
Sodium sucrose octasulfate
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2ccccc2nnn1CC[C@@H]1[C@H](O)[C@H](O)O[C@@H]1CCc1ccc(-c2cncnc2)cc1
Reaction #171180
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=CO[C@H](CCc1ccc(-c2cncnc2)cc1)[C@H](CCn1nnc2ccccc2c1=O)C(=O)O
Reaction #171181
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(CC[C@H]3O[C@@H](O)[C@@H](O)[C@H]3CCn3nnc4ccccc4c3=O)cc2)cn1
Reaction #171184
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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