methyl 2-chloropropionate

COC(=O)C(C)Oc1ccc(NC(C)=O)cc1
Reaction #170961
8
Выход 27257.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(C)Oc1ccc([N+](=O)[O-])cc1
Reaction #170967
14
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(Oc1cccc(F)c1)C(=O)O
Reaction #362621
2-(3' -fluorophenoxy)propionic acid
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CCOC(=O)c1ccc(Cl)cc1OC(C)C(=O)OC
Reaction #376473
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)C(C)Oc1ccc(F)c(N)c1
Reaction #379129
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCc1ccc(CN2CCOCC2)c(OC(C)C(=O)OC)c1
Reaction #456629
methyl 2-[2-(morpholin-4-ylmethyl)-5-ethylphenoxy]propanoate
Выход 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
COC(=O)C(C)Oc1ccc(NC(C)=O)cc1
Reaction #589016
8
Выход 27257.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)C(C)Oc1ccc([N+](=O)[O-])cc1
Reaction #589019
14
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)C1(C)OC12CCCC2
Reaction #668891
methyl 2-methyl-1-oxaspiro[2.4]heptane-2-carboxylate
Выход 56.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
COC(=O)C(C)Oc1ccc2cc(C(C)C(=O)OC)ccc2c1
Reaction #725883
8
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
COC(=O)C(C)Oc1ccc(CNC(=O)CCCCC=CC(C)C)cc1OC
Reaction #725886
11
Выход 31.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
COC(=O)C(C)Oc1ccc(NC(C)=O)cc1
Reaction #725890
16
Выход 27257.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
COC(=O)C(C)Oc1ccccc1O
Reaction #753325
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)C(C)Oc1ccc(F)c2nc(C3CC3)c(Cc3ccc(-n4cccn4)cc3)c(C)c12
Reaction #773823
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)C1(C)OC12CCCC2
Reaction #781459
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)C(C)Oc1ccc([N+](=O)[O-])cc1
Reaction #922713
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(=O)C(C)Oc1ccc(NC(C)=O)cc1
Reaction #925217
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COc1cc2c(cc1OC)NC(C)C(=O)N2
Reaction #927744
6,7-Dimethoxy-3-methyl-3,4-dihydroquinoxalin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
COC(=O)C(C)Oc1ccc(CNC(=O)CCCCC=CC(C)C)cc1OC
Reaction #1030033
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COC(=O)C(C)Oc1ccc(C(C)=O)cc1
Reaction #1172511
methyl 2-(4-acetylphenoxy)propanoate
Выход 80.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_04
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