carbonate

CC(=O)O[C@H]1C=C[C@@H](O)C1
Reaction #2655
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3860
yellow oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(O)c1ccccc1-c1c2ccc(=O)cc-2oc2cc(O)ccc12
Reaction #4260
Fluorescein
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCOC(=O)CCC(C)Oc1ccc(Oc2ccc(Cl)cc2F)cc1
Reaction #4556
ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cn1c(=O)c2[nH]cnc2n(C)c1=O
Reaction #4988
theophylline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)OC(=O)OCC
Reaction #5845
diethyl pyrocarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(O)C(=O)O.O=C(O)O
Reaction #7552
carbonate oxalate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21
Reaction #42631
biotin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21
Reaction #42632
biotin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(CN4CCCC(F)C4)cc3)n[nH]2)cc(OC)c1
Reaction #45020
title compound
Yield 16.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(COc2cc(N)[nH]n2)cc(OC)c1
Reaction #45078
5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amine
Yield 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(-c2csc3c(C(=O)NC4CCN(C(C)=O)C4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45490
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1cc(F)cnc1N
Reaction #48373
title compound
Yield 92.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(C)OC(CC=C(C)C)C(C)CCO
Reaction #55930
3,7-dimethyl-4-[(1-ethoxyethoxy)]-6-octen-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC[C@@H]1c2nncn2-c2cnc(NC)nc2N1C1CCCC1
Reaction #67622
title compound
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1ccc(-c2ccc(Nc3nnc(Cc4ccncc4)c4ccccc34)cc2)cc1
Reaction #78169
Title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cl.O=C(CC1CN2CCC1CC2)Nc1cc2ccc(Br)cc2s1
Reaction #84052
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cl.O=C(CC1CN2CCC1CC2)Nc1ccc2cccnc2c1
Reaction #84053
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=CC[C@@H]1C[C@H]1OC(=O)N[C@H](C(=O)O)C(C)(C)C.C[C@H](N)c1ccccc1
Reaction #88820
VII
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
—
Reaction #89597
polycarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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