gluconolactone

O=C([O-])CC(O)(CC(=O)O)C(=O)O.[Na+]
Reaction #64831
monosodium citrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C([O-])CC(O)(CC(=O)O)C(=O)O.[Na+]
Reaction #64832
monosodium citrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
OCc1cccc2ccccc12
Reaction #74461
1-naphthalenemethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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.v1uspto-grants-2013_09
CCCCCCCCCCCCOC(=O)[C@H](C)N
Reaction #83174
dodecyl alaninate
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #83175
D-gluconamide
المردود 215.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC[C@H](C)[C@H](N)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCc1ccccc1.O=C(O)[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #343644
GlcA Ile-Phe-OBzl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
O=[N+]([O-])c1ccc(O)cc1
Reaction #498288
p-nitrophenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
O=[N+]([O-])c1ccc(O)cc1
Reaction #498289
p-nitrophenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CCCCCCCCCCCCOC(=O)CN
Reaction #528294
dodecyl glycinate
المردود 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CCCCCCCCCCCCOC(=O)[C@H](C)N
Reaction #528295
dodecyl alaninate
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #528296
D-gluconamide
المردود 215.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.NCCc1ccc(O)c(O)c1
Reaction #657295
dopamine gluconamide
المردود 48.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
COc1ccc(Cc2cc(C3(O)O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)c3c(c2Br)CCC3)cc1
Reaction #663484
crude intermediate 16
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CCOc1ccc(Cc2cc(C3(OC)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)cc(OC)c2Cl)cc1
Reaction #663522
(3R,4S,5S,6R)-2-(4-Chloro-3-(4-ethoxybenzyl)-5-methoxyphenyl)-6-(hydroxymethyl)-2-methoxytetrahydro-2H-pyran-3,4,5-triol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
C1=CC2CCC1C2.O=C(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #693733
Norbornene-Gluconate
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.NCCc1ccc(O)c(O)c1
Reaction #710550
dopamine gluconamide
المردود 48.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
C[Si](C)(C)OC[C@H]1OC(=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C
Reaction #715933
product
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
C=C(C)C(=O)O.C=Cc1ccccc1C=C
Reaction #821344
Divinylbenzene Methacrylic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=C(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #937873
D-gluconic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_01
الصفحة 1التالي