ozone

C[Si](C)(C)CCOC(=O)C(Cc1ccccc1C=O)N1C(=O)c2ccccc2C1=O
Reaction #2809
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)O[C@H](CC=O)C[C@H](CC#N)O1
Reaction #5783
(±)-cis-6-(2-oxoethyl)-2,2-dimethyl-1,3-dioxane-4-acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#CC[C@H]1C[C@@H](CC=O)OC2(CCCC2)O1
Reaction #5791
(±)-cis-9-(2-oxoethyl)-6,10-dioxaspiro[4.5]decane-7-acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#CC[C@H]1C[C@@H](CC=O)OC2(CCCCC2)O1
Reaction #5794
(±)-cis-4-(2-oxoethyl)-1,5-dioxaspiro[5.5]undecane-2-acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#CC[C@H]1C[C@@H](CC=O)OCO1
Reaction #5799
(±)-cis-6-(2-oxoethyl)-1,3-dioxane-4-acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)CC[C@@H](CCC=O)OC1CCCCO1
Reaction #6152
methyl 5-formyl-(R)-3[(tetrahydro-2H- pyran-2-yl)oxy]pentanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(NCC(F)(F)CN1CCOCC1)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6981
title compound
収率 51.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1CCC2(CCC(=O)C2C=O)CC1
Reaction #8856
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCCc2cccnc21
Reaction #46525
title compound
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=CCC1(c2ccc(F)cc2)c2c(ccc(F)c2F)NC(=O)N1CC(F)(F)F
Reaction #47966
[5,6-Difluoro-4-(4-fluorophenyl)-2-oxo-3-(2,2,2-trifluoroethyl)-1,2,3,4-tetrahydroquinazolin-4-yl]acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCN(CCC)C(=O)c1cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)[C@H]2C[C@@H](S(=O)(=O)CCC)CN2)cc(-c2ncco2)c1
Reaction #49250
sulfone
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1c(Cl)ccc2ccoc12
Reaction #51055
ethyl 6-chlorobenzofuran-7-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C/C(O)=C(/C(=O)OC(c1ccccc1)c1ccccc1)N1C(=O)C(NC(=O)COc2ccccc2)C1SSc1nc2ccccc2o1
Reaction #54376
2-[4-(Benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
C/C(O)=C(/C(=O)OC(c1ccccc1)c1ccccc1)N1C(=O)C(NC(=O)COc2ccccc2)C1SSc1nc2ccccc2s1
Reaction #54378
2-[4-(Benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin- 1-yl]-3-hydroxy-crotonic acid diphenylmethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
C=C(C)C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C(NC(=O)COc2ccccc2)C1SSc1nc2ccccc2s1
Reaction #54380
2-[4-(benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methylene-butyric acid 2,2,2-trichloroethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC(O)C1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(O)CS[C@H]12
Reaction #54847
benzhydryl 7-(1-hydroxyethyl)-3-hydroxy-3-cephem-4carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
—
Reaction #55630
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
—
Reaction #56742
hydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(C)OCC=O
Reaction #63006
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=CCCC(C(=O)NCCCc1ccccc1)N1C(=O)c2ccccc2C1=O
Reaction #65651
2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl-5-oxo-pentylamine
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
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