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CC(=O)OC[C@H]1O[C@@H](N=[N+]=[N-])[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1O[C@H]1O[C@H](COC(C)=O)[C@@H](O[C@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #162028
azide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](n2cc(CO[C@H]3CC[C@@]4(C)C(CC[C@H]5[C@@H]6CC[C@H]([C@H](C)CCCC(C)C)[C@@]6(C)CC[C@@H]54)C3)nn2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1O[C@H]1O[C@H](COC(C)=O)[C@@H](O[C@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #162029
triazole
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](O[C@H]2O[C@H](COC(=O)c3ccccc3)[C@@H](O[C@H]3O[C@H](COC(=O)c4ccccc4)[C@@H](O[C@H]4O[C@H](COC(=O)c5ccccc5)[C@@H](OC(=O)c5ccccc5)[C@H](OC(=O)c5ccccc5)[C@H]4OC(=O)c4ccccc4)[C@H](OC(=O)c4ccccc4)[C@H]3OC(=O)c3ccccc3)[C@H](OC(=O)c3ccccc3)[C@H]2OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1
Reaction #162030
amine
收率 101.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC[C@H]1O[C@@H](N=C=S)[C@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H]1O[C@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](O[C@H]2O[C@H](COC(=O)c3ccccc3)[C@@H](OC(=O)c3ccccc3)[C@H](OC(=O)c3ccccc3)[C@H]2OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1)c1ccccc1
Reaction #162040
white solid
收率 64.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC1OC(NC(=S)Nc2nc3ccccc3[nH]2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #173508
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(NC(=S)Nc2cc(=O)n(C)c(=O)n2C)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #178414
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(n2ccc(=O)[nH]c2=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #184824
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(NC(=S)Nc2nc3ccccc3s2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #192919
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCNC1OC(CO)C(O)C(O)C1O
Reaction #212646
DOI: 10.1039/C8SC04228D
NC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O
Reaction #224666
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(N=C=S)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #225835
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(NC(=O)CCCCCCNC(=O)OCc2ccccc2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #228323
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCNC1OC(CO)C(O)C(O)C1O
Reaction #232402
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(n2cc(C=O)c3c(F)cccc32)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #253551
DOI: 10.1039/C8SC04228D
CCOc1ccc(C(=O)c2cn(C3OC(COC(C)=O)C(OC(C)=O)C(OC(C)=O)C3OC(C)=O)c3cccc(F)c23)cc1
Reaction #265776
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(n2cc(C(=O)c3ccc(I)cc3)c3c(Cl)cccc32)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #275467
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(n2cc(C(O)c3ccc(C(F)F)cc3)c3c(F)cccc32)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #278926
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(n2cc(Cc3ccc(Br)cc3)c3c(C)cccc32)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #286648
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCN(C(=O)CCCCCCCCCCC)C1OC(CO)C(O)C(O)C1O
Reaction #292394
DOI: 10.1039/C8SC04228D
CCc1ccc(Cc2c(C)nn([C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c2C)cc1
Reaction #308179
3,5-dimethyl-4-(4-ethylphenylmethyl)-1-(β-D-glucopyranosyl)pyrazole
收率 78.6%DOI: 10.6084/m9.figshare.5104873.v1
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