Substructure Search

CCOC(CCO)OCC

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Reaction #4345
sugar alcohols
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@](C)(O)C[C@@H](C)CN(C)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #52549
Azithromycin monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1
Reaction #62962
nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](NC)[C@H]2O)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #65120
N-demethylerythromycin A
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](NC)[C@H]2O)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #65121
N-demethylerythromycin A
Yield 40.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@H]1O[C@H](O)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #82117
Allyl(5S)-5-hydroxy-2,3,4-tri-O-benzyl-α-D-xylopyranoside
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1O[C@H](CO)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #87464
((2R,3R,4S,5R)-6-allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yl)-methanol
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1O[C@H](CO)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #87484
((2R,3R,4S,5R)-6-allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yl)-methanol
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](Oc3c(-c4ccc(O)cc4)oc4cc(O[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)cc(O)c4c3=O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@H](O)[C@H]1O.[Ag]
Reaction #89802
Robinin silver
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](OCc5cn(O[C@@H]6O[C@H](CO)[C@@H](O[C@@H]7O[C@H](CO)[C@H](O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)nn5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #162031
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](OCc5cn(O[C@@H]6O[C@H](CO)[C@@H](O[C@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)nn5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #162032
off-white solid
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](NC)[C@H]2O)[C@](C)(O)C[C@@H](C)CN(C)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #164457
amine
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC(OC(C)=O)C1=CC(=O)OC1OC(=O)CCCCCCC
Reaction #187277
DOI: 10.1039/C8SC04228D
CC(=O)NC1C(OCc2ccccc2)OC(COCc2ccccc2)C(OS(C)(=O)=O)C1OCc1ccccc1
Reaction #193029
DOI: 10.1039/C8SC04228D
CC(=O)NC1C(OCc2ccccc2)OC(CO)C(O)C1OCc1ccccc1
Reaction #206361
DOI: 10.1039/C8SC04228D
CCS[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O
Reaction #216096
Ethyl 4-O-β-galactopyranosyl-1-thio-β-D-glucopyranoside
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CCOc1ccc(C(N)=O)cc1)OCC
Reaction #231419
DOI: 10.1039/C8SC04228D
CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(N(C)C)C2O)C(C)(O)CC(C)C(=O)C(C)C(O)C1(C)O
Reaction #276742
DOI: 10.1039/C8SC04228D
CC(=O)OCC1(COCc2ccccc2)OC(n2ccc(=O)[nH]c2=O)C(OC(C)=O)C1OCc1ccccc1
Reaction #291573
DOI: 10.1039/C8SC04228D
CN[C@@H]1[C@@H](O)[C@@H](O[C@@H]2[C@@H](O)[C@H](O[C@H]3O[C@H]([C@@H](C)O)[C@@H](O)[C@H](O)[C@H]3N)[C@@H](N)C[C@H]2N)OC[C@]1(C)O
Reaction #304603
G418
DOI: 10.6084/m9.figshare.5104873.v1
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