dimethyl acetylenedicarboxylate

COC(=O)c1nc2cc(Cl)ccc2c(O)c1C(=O)OC
Reaction #3196
dimethyl 7-chloro-4-hydroxyquinoline-2,3-dicarboxylate
Ausbeute 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1nc2cccc(Cl)c2c(O)c1C(=O)OC
Reaction #3198
dimethyl 5-chloro-4-hydroxyquinoline-2,3-dicarboxylate
Ausbeute 80.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1nc2cc(Cl)cc(Cl)c2c(O)c1C(=O)OC
Reaction #3201
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1nc2cccc(C)c2c(O)c1C(=O)OC
Reaction #3202
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1nc2cccc(OC)c2c(O)c1C(=O)OC
Reaction #3211
desired compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)/C=C(\Nc1ccccc1C#N)C(=O)OC
Reaction #3214
solid
Ausbeute 44.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C1=Nc2c(cc(Cl)c(C)c2Cl)C(=O)C1
Reaction #6774
2-(methoxycarbonyl)-4-oxo-6,8-dichloro-7-methylquinoline
Ausbeute 90.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C1=Nc2cc(C)c(Cl)cc2C(=O)C1
Reaction #6776
2-methoxycarbonyl-6-chloro-7-methyl-4-oxoquinoline
Ausbeute 81.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc2c(c1)ccc1ccccc12
Reaction #50907
phenanthrene
Ausbeute 61.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
c1ccc2ccccc2c1
Reaction #50909
naphthalene
Ausbeute 142.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
N#Cc1cc(Br)cnc1F
Reaction #84137
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)C=C(Nc1ccsc1)C(=O)OC
Reaction #202347
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C=C(C(=O)OC)N1CC1c1ccc2c(c1)OCO2
Reaction #205274
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C1=C(C(=O)OC)CC(C)=C(C)C1
Reaction #215948
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COC(=O)C=C(ON=C(N)C(CCCC(C)O)N(C)C(=O)OC(C)(C)C)C(=O)OC
Reaction #240354
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C=C(Nc1ccc([N+](=O)[O-])cc1)C(=O)OC
Reaction #250553
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C=C(NN)C(=O)OC
Reaction #252689
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C=C(Oc1ccc(C(C)(C)C)cc1C(C)(C)C)C(=O)OC
Reaction #280894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C=C(Nc1c[nH]c(=O)[nH]c1=O)C(=O)OC
Reaction #291047
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C=C(ON=C(N)C1CC(F)CN1C(=O)OCc1ccccc1)C(=O)OC
Reaction #300079
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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