N-acetylglycine

CC1=NC(=Cc2ccc(C#N)cc2)C(=O)O1
Reaction #7296
4-(2-Methyl-5-oxooxazol-4-ylidenemethyl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1=N/C(=C\c2cccnc2)C(=O)O1
Reaction #7298
2-Methyl-4-[pyridin-3-yl-(Z)-methylene]-4H-oxazol-5-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
[N-]=[N+]=Nc1cc2ccc(O)cc2oc1=O
Reaction #47731
3-azido-7-hydroxycoumarin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cccc(CC(=O)C(=O)O)c1
Reaction #55493
3-methoxyphenylpyruvic acid
Ausbeute 34.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC(=O)NC(=Cc1cccnc1)C(=O)O
Reaction #55496
2-acetamido-3-(3-pyridyl)acrylic acid
Ausbeute 23.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
COc1ccc(Cc2cc(Oc3c(C)cc(C=C4N=C(C)OC4=O)cc3C)ccc2OC)cn1
Reaction #63564
2-methyl-4-(3,5-dimethyl-4-(4-methoxy-3-(6-methoxy-3-pyridylmethyl)-phenoxy)-benzal)-5-oxazolone
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC(=O)NCC(=O)Nc1ccc(SCc2ccccc2)c(/C=C/C2=NCCN(C)c3ccccc32)c1.Cl.Cl
Reaction #76609
(E)-2-acetamido-4′-benzylthio-3′-[2-(2,3-dihydro-1-methyl-1H-1,4-benzodiazepin-5-yl)vinyl]acetanilide dihydrochloride
Ausbeute 30.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)/C(NC(C)=O)=C(/C)N(C)C
Reaction #162660
(E)-ethyl 2-acetamido-3-(dimethylamino)but-2-enoate
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)NCC(=O)N1CCC(N(C)C(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(c2ccc(Cl)c(Cl)c2)C1
Reaction #177161
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)N(CC(=O)O)CC(=O)O
Reaction #185408
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)N(CC(=O)O)CC(=O)O
Reaction #186837
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)C(=O)Cc1cc([N+](=O)[O-])ccc1Oc1ccc(F)cc1
Reaction #197232
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)NCC(=O)NCCc1c[nH]c2ccccc12
Reaction #211994
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)NCC(=O)N1CCC(n2cc(Nc3ncc(Cl)c(NC4C5C=CC(C5)C4C(N)=O)n3)cn2)CC1
Reaction #213233
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc2c(c3c1OC(C)(C)C3)C(c1cccc(-c3ccc(NC(=O)CNC(C)=O)cc3)c1)=NC(C)(C)C2
Reaction #252997
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCc1cc(C=C2N=C(C)OC2=O)ccc1OC(C)=O
Reaction #346794
2-Methyl-4-(4-acetoxy-3-allyl-benzylidene)-5-(4H)-oxazolone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
COc1cc(C=C2N=C(C)OC2=O)ccc1OC(C)=O
Reaction #346799
2-methyl-4-(3-methoxy-4-acetoxy-benzylidene)-5(4H)-oxazolone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
COC(=O)C(=Cc1cccc(Br)c1)NC(C)=O
Reaction #364482
methyl m-bromo-α-acetamidocinnamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(=O)N(CC(=O)O)CC(=O)O
Reaction #374631
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)NCC(=O)N1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #377781
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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