2-(6-Hydroxynaphthalen-2-yl)-propionic acid

CC(=O)Oc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #179699
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C(=O)O)c1ccc2cc(OCc3ccc4ccccc4n3)ccc2c1
Reaction #335359
oil
収率 151.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CC(C(=O)O)c1ccc2cc(OCc3ccccc3)ccc2c1
Reaction #335360
white crystals
収率 38.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CC(C(=O)O)c1ccc2cc(OCc3csc(-c4ccccc4)n3)ccc2c1
Reaction #335361
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCCCOc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #335362
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCOc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #335363
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCCOc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #335364
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCCCCCCCCCOc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #335365
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CC(C(=O)O)c1ccc2cc(OCC=C(Cl)Cl)ccc2c1
Reaction #335366
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
COC(=O)C(C)c1ccc2cc(O)ccc2c1
Reaction #645210
product
収率 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
COC(=O)C(C)c1ccc2cc(O)ccc2c1
Reaction #725882
6
収率 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CCCCCCOc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #923247
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(=O)Oc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #927223
6-acetoxy-2-naphthyl-α-methylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_06
CC(C(=O)O)c1ccc2cc(OCc3ccc4ccccc4n3)ccc2c1
Reaction #1020451
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC(C(=O)O)c1ccc2cc(OCc3ccc4ccccc4n3)ccc2c1
Reaction #1175086
oil
収率 151.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
CC(C(=O)O)c1ccc2cc(OCc3ccccc3)ccc2c1
Reaction #1175087
white crystals
収率 38.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
CC(C(=O)O)c1ccc2cc(OCc3csc(-c4ccccc4)n3)ccc2c1
Reaction #1175088
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
CCCCCCOc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #1175089
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
CCCCOc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #1175090
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
CCCCCOc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #1175091
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
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