silver carbonate

CCCCCCCCCCCCCCCCCCc1cc2nc3ccc(O[C@@H]4O[C@H](COC(C)=O)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@H]4OC(C)=O)cc3oc-2cc1=O
Reaction #4976
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)OC[C@H]1O[C@@H](Oc2n[nH]c(C)c2Cc2ccc(OC(C)C)cc2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #6737
4-[(4-isopropoxyphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCSc1ccc(Cc2c(O[C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]3OC(C)=O)n[nH]c2C)cc1
Reaction #6751
4-[(4-ethylthiophenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole
Ausbeute 37.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)OC[C@H]1O[C@@H](Oc2n[nH]c(C)c2Cc2ccc(C=C3CC3)cc2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #7454
5-methyl-4-{[4-(cyclopropylidenemethyl)phenyl]methyl}-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole
Ausbeute 16.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)OC[C@H]1O[C@@H](Oc2n[nH]c(C)c2Cc2ccc(OC(C)C)cc2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #7483
4-[(4-isopropoxyphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC#COc1ccncc1
Reaction #55319
4-(propynyloxy)pyridine
Ausbeute 3.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC(=O)OC[C@H]1O[C@@H](Oc2n[nH]c(C)c2Cc2ccc(OC(C)C)cc2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #61392
4-[(4-isopropoxy-phenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)OC[C@H]1O[C@@H](Oc2ncccc2C2CCCN2C)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #65729
(±)-3-(1-methyl-2-pyrrolidinyl)-2-pyridyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Fc1cc2ccnc(OCc3ccccc3)c2cc1Cl
Reaction #66723
title compound 1
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc2c(OCc3ccccc3)nccc2cc1F
Reaction #66724
( 2 )
Ausbeute 15.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ncc(Br)cc1OC(F)F
Reaction #67634
5-bromo-3-(difluoromethoxy)-2-methoxypyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CSc1sc2c(NC(=O)OC(C)(C)C)c(C)nn2c1Br
Reaction #69535
title compound
Ausbeute 47.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1ccc(-c2ncc(-c3cnc(-c4ccccc4)o3)cn2)cc1
Reaction #70582
title compound
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Fc1cc2ccnc(OCc3ccccc3)c2cc1Cl
Reaction #73460
title compound ( 38 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ncccc1Br
Reaction #76783
title compound
Ausbeute 62.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(OCc2ccccc2)c(C(=O)O)n1
Reaction #77709
3-BENZYLOXY-6-METHOXYPICOLINIC ACID
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ncccc1Br
Reaction #77880
title compound
Ausbeute 62.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
—
Reaction #87056
0.025
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1ccc(C2CC2)c(OC)n1
Reaction #157687
ethyl 5-cyclopropyl-6-methoxypyridine-2-carboxylate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1ccc(Cl)c(OC)n1
Reaction #157714
ethyl 5-chloro-6-methoxypyridine-2-carboxylate
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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