N-methylhydroxylamine

C#CCC1C(=O)N(C)OC1c1ccccc1
Reaction #907
2-methyl-5-phenyl-4-propargylisoxazolin-3-one
收率 34.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCn1nc(C)cc1Nc1cc(Nc2ccccc2C(=O)N(C)O)c(Cl)cn1
Reaction #90803
2-({5-Chloro-2-[(1-ethyl-3-methyl-1H-pyrazol-5-yl)amino]-4-pyridinyl}amino)-N-hydroxy-N-methylbenzamide
收率 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CN(O)C(=O)c1ccc(CCCc2ccccc2OCc2ccccc2)cc1
Reaction #174158
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(O)C(=O)c1cccc([N+](=O)[O-])c1Cl
Reaction #182752
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(O)C(=O)c1cc2c(COC3CCOCC3)cn(Cc3ccc(F)cc3)c2cn1
Reaction #188182
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C(Cn2cncn2)=[N+](C)[O-])cc1
Reaction #195605
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(O)C(=O)c1cc2c(CN3CCNC(=O)C3)cn(Cc3ccc(F)cc3)c2cn1
Reaction #225675
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=CC(=O)N(C)O)c1ccn(-c2c(C)cccc2C)c1
Reaction #227562
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(O)C(=N)c1c(F)cccc1F
Reaction #230997
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(O)C(=O)Nc1ccc(Cl)c(C(F)(F)F)c1
Reaction #235066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(O)CCCc1ccc2c(c1)C(=O)c1ccccc1CO2
Reaction #254452
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCC(=O)N(C)O
Reaction #258264
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(O)C(=O)CCCCCCCCCCBr
Reaction #261188
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(c1nn(-c2c(Cl)cc(C(F)(F)F)cc2Cl)c(N)c1S(C)=O)=[N+](C)[O-]
Reaction #261377
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C[N+]([O-])=Cc1ccc(C#N)cc1
Reaction #268648
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(O)C(=O)c1cc2c(COCC3COC(C)(C)O3)cn(Cc3ccc(F)cc3)c2cn1
Reaction #287648
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(O)CC1=C(n2ccccc2=O)c2cc([N+](=O)[O-])ccc2OC1(C)C
Reaction #288615
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc([N+](=O)[O-])c(NC(C)C(=O)N(C)O)c([N+](=O)[O-])c1
Reaction #298531
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(OCc1cn(Cc2ccc(F)cc2)c2cnc(C(=O)N(C)O)cc12)c1ccccc1
Reaction #301667
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(O)C(=O)Nc1ccc([N+](=O)[O-])c(C(F)(F)F)c1
Reaction #370750
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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