ethyl 2-chloro-2-oxoacetate

C=Cc1ccc(CCOC(=O)C(=O)OCC)cc1
Reaction #6503
aimed compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)C(=O)C(CC)NC(C)=O
Reaction #7632
Ethyl 3-(acetylamino)-2-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(=O)C(CC)NC(=O)C1CCCC1
Reaction #7645
Ethyl 3-[(cyclopentylcarbonyl)amino]-2-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(=O)N[C@@H](C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1cccc(OC)c1
Reaction #41366
Ethyl[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]carbamoylformate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(=O)C(NC(=O)C1CCC1)c1cccc(OCc2ccccc2)c1
Reaction #46253
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(=O)N1CCc2ccccc21
Reaction #80737
N-ethoxalylindoline
Ausbeute 108.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)C(=O)N1C2=CC=CCC2CCC1CO[Si](C)(C)C
Reaction #80765
N-ethoxalyl-2-trimethylsilyloxymethyltetrahydroquinoline
Ausbeute 106.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)C(=O)NCC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80773
title compound
Ausbeute 21.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1nc(-c2ccc([N+](=O)[O-])cc2)no1
Reaction #82821
5-ethoxycarbonyl-3-(4-nitrophenyl)-1,2,4-oxadiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1ncc(-c2ccccc2)o1
Reaction #86833
ethyl 5-phenyloxazole-2-carboxylate
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)C(=O)NCCc1c[nH]c2ccc(Cl)cc12
Reaction #86843
2-(2-(5-chloro-1H-indol-3-yl)ethylamino)-2-oxoacetic acid
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)C(=O)N[C@H](CO)Cc1ccccc1
Reaction #86845
(S)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acid
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)C(=O)N[C@@H](CO)Cc1ccccc1
Reaction #86847
(R)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acid
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)C(=O)c1cccn1CCOC(C)=O
Reaction #95388
ethyl 1-(2-acetoxyethyl)pyrrole-2-glyoxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)C(=O)NCC(C)O
Reaction #156269
title compound
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C[C@@H](Cc1ccc(-c2cccc(Cl)c2)cc1)NC(=O)C(=O)OCC
Reaction #158072
(R)-ethyl 4-(3′-chlorobiphenyl-4-yl)-3-(2-ethoxy-2-oxoacetamido)butanoate
Ausbeute 83.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(=O)N1CC=C(c2ccc(-c3cnc(Nc4cccc(Cl)c4)o3)cc2)CC1
Reaction #163224
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(=O)N1CCC(c2ccc(-c3ccc(Nc4ccc(C(F)(F)F)nc4)nc3)cc2)CC1
Reaction #163232
title compound
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(=O)NNC(=O)c1nc(-c2ccc(S(=O)(=O)C(C)C)cc2)cnc1N
Reaction #165837
product
Ausbeute 58.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(=O)c1ccc(SC2CC2)c(Br)c1
Reaction #178453
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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