NH2OH

CC(=NO)c1nccc2ccccc12
Reaction #1026
1-acetyl-isoquinoline oxime
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=NO)c1cc2ccccc2cn1
Reaction #1028
3-acetyl-isoquinoline oxime
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=NO)c1nccc(-c2ccccn2)n1
Reaction #1029
2-acetyl-4-(pyrid-2-yl)-pyrimidine oxime
Ausbeute 91.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Cc1ccccc1)NO
Reaction #10026
N-hydroxy-2-phenylacetamide
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(CCc1ccccc1)NO
Reaction #10027
N-hydroxy-3-phenylpropionamide
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #10028
hydroxamic acids
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N=C(NO)c1ccc(Oc2cc3[nH]c(-c4cnccn4)nc3cc2Oc2ccccc2F)cc1
Reaction #41656
compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=NO
Reaction #46155
1-hydroxyimino-3-phenyl-6-(3-phenylpropyloxy)-1H-indene-2-carboxylate ethyl ester
Ausbeute 9.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#CC1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=NO
Reaction #46168
1-hydroxy imino-3-phenyl-6-(3-phenylpropyloxy)-1H-indene-2-carbonitrile
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #47226
foam
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC[C@H](C)Oc1cc(Oc2ccc(C(=N)NO)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48835
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(NCC(=O)NO)cc(=O)oc2c1OC1CCCC1
Reaction #48916
2-(8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-ylamino)-N-hydroxyacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCN(CCC)C1CCc2cccc(-c3oncc3CC)c2C1
Reaction #50422
2-Di-n-propylamino-8-(4-ethylisoxazol-5-yl)-1,2,3,4-tetrahydronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
NC(=O)NCC(=O)NO
Reaction #51871
N-hydroxy-2-ureidoacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
NC(=O)NCC(=O)NO
Reaction #51872
N-hydroxy-2-ureidoacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(CN(CCC1CCCC1)C(=O)N1CCCC1C(=O)Nc1cccc(O)c1)NO
Reaction #51874
N-hydroxy-{N-[2-(cyclopentyl)ethyl]-N-[2-(3-hydroxyphenyl)aminocarbonylpyrrolidin-1-ylcarbonyl]-amino}acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(CSCc1ccc(Cl)cc1)NO
Reaction #55076
p-Chlorobenzylmercapto-acetohydroxamic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
ONC(=S)CCc1ccc(Cl)c(Cl)c1
Reaction #55080
stated product
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C(CC(=O)Nc1cccc2ccccc12)NO
Reaction #55094
α-Naphthylcarbamoylacetohydroxamic acid
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
ON=C(c1ccccc1)C(O)(c1ccccc1)c1ccccc1
Reaction #56367
alpha-phenylbenzoin oxime
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Seite 1Weiter