(2,3,3-trimethyl-3-H-indol-5-yl)-acetic acid

CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #77177
(3,3-dihydroxymethyl-2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #312576
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #317257
(3,3-dihydroxymethyl-2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #434781
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #518083
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #519711
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #521024
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #565299
(3,3-dihydroxymethyl-2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #582504
(3,3-dihydroxymethyl-2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #586087
(3,3-dihydroxymethyl-2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #654810
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #654811
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #654812
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #721752
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #722954
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #1355835
(3,3-dihydroxymethyl-2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_04
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #1472984
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_07
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #1472985
(3,3-dihydroxymethyl2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_07
CC1=[N+](C)c2ccc(CC(=O)O)cc2C1(C)C.[I-]
Reaction #1531955
product
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
O=C(O)Cc1ccc2c(c1)CC=[N+]2Cc1cc([N+](=O)[O-])cc([N+](=O)[O-])c1.[Br-]
Reaction #1531956
solid
Rendimiento 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
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