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CCCCC(NC(=O)OC)C(=O)OC
Reaction #312134
2-methoxycarbonylaminohexanoic acid methyl ester
Rendement 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
CCCCC(C(=O)OC)P(=O)(OCC)OCC
Reaction #395522
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC(Oc1ccc(F)c(C)c1)C(=O)OC
Reaction #749359
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCCC(Sc1ccc(F)c(C)c1)C(=O)OC
Reaction #765543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCCC(Nc1ccc(F)c(C)c1)C(=O)OC
Reaction #972682
title compound
Rendement 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCCCC(Oc1nc(OC)cc(OC)n1)C(=O)OC
Reaction #1160211
desired product
Rendement 73.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_11
CCCCC(Oc1ccccc1C(=O)OC)C(=O)OC
Reaction #1226583
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CCCCC(Oc1nc(OC)cc(OC)n1)C(=O)OC
Reaction #1325307
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCCCC(Oc1ccc(F)c(C)c1)C(=O)OC
Reaction #1448231
title compound
Rendement 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
CCCCC(Sc1ccc(F)c(C)c1)C(=O)OC
Reaction #1448232
title compound
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
CCCCC(Nc1ccc(F)c(C)c1)C(=O)OC
Reaction #1652930
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CCCCC(F)C(=O)OC
Reaction #1675593
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_06
CCCCC(Oc1ccccc1C(=O)OC)C(=O)OC
Reaction #1698236
Methyl 2-(1-methoxycarbonylpentoxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01