Teilstruktursuche

O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO

OC1(c2cc3c(CCc4ccccc4)cccc3s2)O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #43684
2,3,4,6-tetra-O-benzyl-1-[4-(2-phenylethyl)benzo[b]-thiophene-2-yl]-D-glucopyranose
Ausbeute 86.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Cc2cccc3cc(C4(O)O[C@H](COCc5ccccc5)[C@@H](OCc5ccccc5)[C@H](OCc5ccccc5)[C@H]4OCc4ccccc4)sc23)cc1
Reaction #43688
title compound
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CC(O)(CC(=O)O)C(=O)O.[Na+]
Reaction #64831
monosodium citrate
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CC(O)(CC(=O)O)C(=O)O.[Na+]
Reaction #64832
monosodium citrate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1O[C@H](OCC(Cl)(Cl)Cl)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #68717
1-O-trichloroethyl-2,3,4-tri-O-acetyl-α-D-glucopyranuronic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
OCc1cccc2ccccc12
Reaction #74461
1-naphthalenemethanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2(O)O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #74490
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCOC(=O)[C@H](C)N
Reaction #83174
dodecyl alaninate
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #83175
D-gluconamide
Ausbeute 215.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COCC2(COCc3ccc(OC)cc3)OC(=O)[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)cc1
Reaction #87466
(3R,4S,5S)-3,4,5-tris-benzyloxy-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-one
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc(C3(O)OC(COCc4ccc(OC)cc4)(COCc4ccc(OC)cc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)C3OCc3ccccc3)ccc2Cl)cc1
Reaction #87467
(4S,5S)-3,4,5-tris-benzyloxy-2-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-ol
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(c2ccc(Cl)c(Cc3ccc(O)cc3)c2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #87468
product
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COCC2(COCc3ccc(OC)cc3)OC(=O)[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)cc1
Reaction #87486
(3R,4S,5S)-3,4,5-tris-benzyloxy-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-one
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc(C3(O)OC(COCc4ccc(OC)cc4)(COCc4ccc(OC)cc4)C(OCc4ccccc4)C(OCc4ccccc4)C3OCc3ccccc3)ccc2Cl)cc1
Reaction #87487
3,4,5-tris-benzyloxy-2-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-ol
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(c2ccc(Cl)c(Cc3ccc(O)cc3)c2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #87488
product
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CSC.N.N.O=C(O)C(O)C(O)C(O)C(O)C(=O)O
Reaction #90712
Mucic Acid Diamine DMS
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCOC(=O)[C@@H](O)[C@H](O)[C@H](O)[C@@H](O)C(=O)OCCCCCCC
Reaction #90847
diheptyl galactarate
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
CCCCCCCC/C=C\CCCCCCCC(=O)O.O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #93700
glucose oleate
Ausbeute 115.4%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter