Substructure Search

176141

CC1(C)O[C@H]2O[C@H]([C@H]3COC(C)(C)O3)[C@@H](O)[C@H]2O1
Reaction #53747
1,2:5,6-di-O-isopropylidene-α-D-allofuranose
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H]([C@H]3COC(C)(C)O3)[C@@H](O)[C@H]2O1
Reaction #53748
1,2:5,6-di-O-isopropylidene-α-D-allofuranose
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H]([C@H]3COC(C)(C)O3)[C@@H](O)[C@H]2O1
Reaction #53749
1,2:5,6-di-O-isopropylidene-α-D-allofuranose
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H]([C@H]3COC(C)(C)O3)[C@@H](O)[C@H]2O1
Reaction #53750
1,2:5,6-di-O-isopropylidene-α-D-allofuranose
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CSC(=S)O[C@@H]1[C@H]2OC(C)(C)O[C@H]2O[C@@H]1C1COC(C)(C)O1
Reaction #88967
O-[(3aR,5R,6S,6aR)-5-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-yl] methylsulfanylmethanethioate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC([C@@H]2C[C@H]3OC(C)(C)O[C@H]3O2)O1
Reaction #88968
(3aR,5S,6aR)-5-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxole
Yield 83.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H]([C@@H](O)CO)C[C@H]2O1
Reaction #88969
(1S)-1-[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol
Yield 62.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC([C@H]2O[C@@H]3OC(C)(C)O[C@@H]3C2=O)O1
Reaction #171206
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC2OC(C(O)CO)C(OCc3ccccc3)C2O1
Reaction #233552
DOI: 10.1039/C8SC04228D
CC1(C)O[C@H]2O[C@H]([C@H]3COC(C)(C)O3)[C@H](O)[C@H]2O1
Reaction #445310
1,2:5,6-di-O-isopropylidene-α-D-glucofuranose
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1[C@H]2OC3(CCCCC3)O[C@H]2O[C@@H]1C1COC2(CCCCC2)O1
Reaction #445311
1,2:5,6-di-O-cyclohexylidene-α-D-glucofuranose
Yield 77.8%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1[C@@H]2OC3(CCCCC3)O[C@H]2O[C@@H]1[C@H]1COC2(CCCCC2)O1
Reaction #445314
2,3:5,6-di-O-cyclohexylidene-α-D-mannofuranose
Yield 82.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H]([C@H]3COC(C)(C)O3)[C@H](O)[C@H]2O1
Reaction #549518
1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H]([C@H]3COC(C)(C)O3)[C@H](O)[C@H]2O1
Reaction #630096
1,2:5,6-di-O-isopropylidene-α-D-glucofuranose
Yield 144.8%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1[C@H]2OC3(CCCCC3)O[C@H]2O[C@@H]1C1COC2(CCCCC2)O1
Reaction #630097
1,2:5,6-di-O-cyclohexylidene-α-D-glucofuranose
Yield 66.4%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1[C@@H]2OC3(CCCCC3)O[C@H]2O[C@@H]1[C@H]1COC2(CCCCC2)O1
Reaction #630100
2,3:5,6-di-O-cyclohexylidene-α-D-mannofuranose
Yield 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(C2OC3OC(C)(C)OC3C2OCc2ccccc2)O1
Reaction #747050
semisolid
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H]([C@H](O)CO)[C@H](OCc3ccccc3)[C@H]2O1
Reaction #747051
30C
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H]([C@H]3COC(C)(C)O3)[C@H](O)[C@H]2O1
Reaction #930391
di-isopropylidene glucose
Yield 112.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)OC(=O)O[C@H]1[C@@H]2OC(C)(C)O[C@@H]2O[C@H]1[C@@H]1COC(C)(C)O1
Reaction #969569
1-chloroethyl (3aS,5S,6R,6aS)-5-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,2-d][1,3]dioxol-6-yl carbonate
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
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