hydrogen peroxide

CN(C)NCCCC[C@@H](C(=O)OC(C)(C)C)[NH+]([O-])C(=O)OCc1ccccc1
Reaction #1272
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=COCn1cnc2c(C(=O)N(c3ccccc3)c3ccccc3)nc(NC(C)=O)nc21
Reaction #1653
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)Cc1ccc([C@H]2CC[C@@H](O)CC2)cc1
Reaction #1743
cis-4-(4-Dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1ccc(O)cn1
Reaction #1915
product
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(F)c[n+]1[O-]
Reaction #1952
title compound
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)Oc1c(O)c(F)nc(F)c1F
Reaction #1970
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCCCOC1CCCCO1
Reaction #2031
1-(Tetrahydopyran-2-yloxy)-4-pentyne
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(F)c(F)c1O
Reaction #2674
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)Cc1cccn1-c1ccccc1[N+](=O)[O-]
Reaction #3663
product
Ausbeute 10.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(S(C)=O)ccc1-c1nc2c[nH][nH]c(=O)c-2n1
Reaction #3945
2-(2-Methoxy-4-methylsulfinyl-phenyl)-5H-imidazo[4,5-d]pyridazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1cc(S(C)(=O)=O)ccc1-c1nc2c[nH][nH]c(=O)c-2n1
Reaction #3946
2-(2-Methoxy-4-methylsulfonyl-phenyl)-5H-imidazo[4,5-d]pyridazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1cc(CC2CO2)cc(C)c1OCC1CO1
Reaction #4243
4-(2,3-epoxypropyl)-2,6-dimethylphenyl glycidyl ether
Ausbeute 85.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CNc1nnc(NCCCOc2cccc(CN3CCCCC3)c2)s1
Reaction #4724
N-Methyl-N'-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]1,3,4-thiadiazole-2,5-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)c1ccc(OCCCCCO)cc1
Reaction #5105
5-p-t-butylphenoxy-1-pentanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)OCc1ncccc1C
Reaction #7239
2-acetoxymethyl-3-methyl-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)OCc1cc(C)cc(C)n1
Reaction #7242
2-acetoxymethyl-4,6-dimethylpyridine
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)C(=O)Nc1cnccc1O
Reaction #7873
N-(4-hydroxypyridin-3-yl)-2,2-dimethylpropanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)C(=O)OOC(=O)C(C)C
Reaction #8236
diisobutanoyl peroxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O[C@H]1Cc2c(O)cc(O)cc2O[C@H]1c1cc(O)c(O)c2c(O)c(=O)cc([C@H]3Oc4cc(O)cc(O)c4C[C@H]3O)cc12)c1cc(O)c(O)c(O)c1
Reaction #8611
theaflavin 3-gallate
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1c1cc(=O)c(O)c2c(O)c(O)cc([C@H]3Oc4cc(O)cc(O)c4C[C@H]3OC(=O)c3cc(O)c(O)c(O)c3)c2c1)c1cc(O)c(O)c(O)c1
Reaction #8612
theaflavin 3,3′-digallate
Ausbeute 10.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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