参与 242 个反应

CCON.Cl

CCON=C(CC)C1=C(O)CC(c2c(C)cc(C)c([N+](=O)[O-])c2C)CC1=O
Reaction #64040
2-[1-(ethoxyimino)propyl]-3-hydroxy-5-(2,4,6-trimethyl-3-nitrophenyl)cyclohex-2-en-1one
收率 83.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCON=C(CC)C1=C(O)CC(c2c(C)c([N+](=O)[O-])c(C)c([N+](=O)[O-])c2C)CC1=O
Reaction #64041
2-[1-(ethoxyimino)propyl]-3-hydroxy-5-(2,4,6-trimethyl-3,5-dinitrophenyl)cyclohex-2-en-1-one
收率 39.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCON=C(CC)C1=C(O)CC(c2c(C)cc(C)c(S(N)(=O)=O)c2C)CC1=O
Reaction #64044
2-[1-(ethoxyimino)propyl]-3-hydroxy-5-(2,4,6-trimethyl-3-sulfamoylphenyl)cyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCON=C(CC)C1=C(O)CC(c2c(C)cc(C)c(S(=O)(=O)N(C)C)c2C)CC1=O
Reaction #64045
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(2,4,6-trimethyl-3-dimethylsulfamoylphenyl)cyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCON=C(CC)C1=C(O)CC(c2c(C)ccc(S(=O)(=O)N(C)C)c2C)CC1=O
Reaction #64046
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(2,6-dimethyl-3-dimethylsulfamoylphenyl)cyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCC(=NOCC)C1=C(O)CC(c2c(C)cc(C)c(N)c2C)CC1=O
Reaction #64048
2-[1-(ethoxyimino)butyl]-3-hydroxy-5-(3-amino-2,4,6-trimethylphenyl)cyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCC(=NOCC)C1=C(O)CC(c2c(C)cc(C)c(CO)c2C)CC1=O
Reaction #64058
2-[1-(Ethoxyimino)butyl]-3-hydroxy-5-(3-hydroxymethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCCSCc1c(C)cc(C)c(C2CC(=O)C(C(CCC)=NOCC)=C(O)C2)c1C
Reaction #64059
5-[3-(n-Butylthiomethyl)-2,4,6-trimethylphenyl]-2-[1-(ethoxyimino)butyl]-3-hydroxycyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCON=C(CC)C1=C(O)CC(c2c(C)cc(O)cc2C)CC1=O
Reaction #64061
5-(2,6-Dimethyl-4-hydroxyphenyl)-2-[1-(ethoxyimino)propyl]-3-hydroxycyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCC(=NOCC)C1=C(O)CC(c2c(C)c(C)c(C)c(C)c2S(C)(=O)=O)CC1=O
Reaction #64064
2-[1-(Ethoxyimino)butyl]-3-hydroxy-5-(6-methylsulfonyl-2,3,4,5-tetramethylphenyl)cyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCONC(=O)c1ccncc1Nc1ccc(Br)cc1C
Reaction #67780
desired product
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCONC(=O)c1ccncc1Nc1ccc(I)cc1C
Reaction #67781
desired product
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCON=C(C)c1ccc2c(c1)ncn2-c1cccc(C2=CCCN(C)C2)c1
Reaction #78096
5-acetyl-1-[3-(1-methyl-1,2,3,6-tetrahydropyrid-5-yl)phenyl]benzimidazole O-ethyl oxime
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCON=C(CBr)c1ncc(Cl)cc1Cl
Reaction #84255
desired product
收率 87.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCON=C(CN1C(=O)c2ccccc2C1=O)c1ncc(C(F)(F)F)cc1Cl
Reaction #84279
desired product
收率 46.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCON=C(CNC(=O)c1ccccc1C(F)(F)F)c1ncc(Br)cc1Br
Reaction #84317
desired product
收率 89.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCONC(=O)c1ccncc1Nc1ccc(Br)cc1C
Reaction #165945
desired product
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCONC(=O)c1ccncc1Nc1ccc(I)cc1C
Reaction #165946
desired product
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCONC(=O)c1ccc2[nH]ncc2c1Nc1ccc(I)cc1F
Reaction #166248
title compound
收率 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #170239
solid
收率 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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