glucose

COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1526
(2S,3S)-1-chloro-3-methoxycarbonylamino-4-phenyl-2-butanol
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N[C@H](Cc1ccccc1)C(=O)O
Reaction #2054
D-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N[C@H]1C(O)O[C@H](COP(=O)(O)O)[C@@H](O)[C@@H]1O
Reaction #10221
Glucosamine-6-Phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)C[C@H](O)C[C@H](O)COC(=O)c1ccccc1
Reaction #10226
(3R,5S)-6-benzoyloxy-3,5-dihydroxyhexanoic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)C[C@H](O)C[C@H](O)COC(=O)c1ccccc1
Reaction #10227
(3R,5S)-6-benzoyloxy-3,5-dihydroxyhexanoic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)C(=O)Nc1cnc([C@H](O)CO)cn1
Reaction #40279
(S)—N-[5-(1,2-dihydroxy-ethyl)-pyrazin-yl]-2,2-dimethyl-propionamide
Ausbeute 105.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1.O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #46041
NAD Glucose
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #56009
methyl-alpha-D-glucopyranoside
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CNCCCN1c2ccccc2CCc2ccccc21
Reaction #57129
desipramine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N[C@@H](CCC(=O)O)C(=O)O
Reaction #58019
L-glutamic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #66034
H+
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(-c2oc3c(CC=C(C)C)c(O)cc(O)c3c(=O)c2O[C@@H]2O[C@H](C)[C@@H](O)[C@H](O)[C@@H]2O)cc1
Reaction #68769
icariside II
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
—
Reaction #82997
polyunsaturated fatty acid
Ausbeute 26.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
—
Reaction #82998
polyunsaturated fatty acid
Ausbeute 8.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].[C].[Li+].[V+5]
Reaction #87213
lithium vanadium phosphate carbon
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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.v1uspto-grants-1986_09
[Os]
Reaction #95999
osmium
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](O)[C@H]1O
Reaction #96221
ATP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
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