lithium hydroxide trihydrate

O=C(O)CCc1c(C(=O)O)[nH]c2cc(Br)cc(Br)c12
Reaction #554605
3-(2-Carboxyethyl)-4,6-dibromo-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(O)CCc1c(C(=O)O)[nH]c2cc(Br)ccc12
Reaction #554606
3-(2-Carboxyethyl)-6-bromo-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(O)CCc1c(C(=O)O)[nH]c2cc(I)ccc12
Reaction #554607
3-(2-Carboxyethyl)-6-iodo-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(O)CCc1c(C(=O)O)[nH]c2cc(I)cc(I)c12
Reaction #554608
3-(2-Carboxyethyl)-4,6-diiodo-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(O)CCC1=C2C(=CC(Cl)=CC2(F)Cl)NC1C(=O)O
Reaction #554609
3-(2-Carboxyethyl)-4,6-dichloro-4-fluoro-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(O)CCc1c(C(=O)O)[nH]c2cc(-c3ccccc3)cc(-c3ccccc3)c12
Reaction #554611
3-(2-Carboxyethyl)-4,6-diphenyl-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(O)CCc1c(C(=O)O)[nH]c2cc(-c3ccccc3)ccc12
Reaction #554613
3-(2-Carboxyethyl)-6-phenyl-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(O)CCc1c(C(=O)O)[nH]c2cc(Br)cc(Br)c12
Reaction #2037859
3-(2-Carboxyethyl)-4,6-dibromo-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
O=C(O)CCc1c(C(=O)O)[nH]c2cc(Br)ccc12
Reaction #2037860
3-(2-Carboxyethyl)-6-bromo-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
O=C(O)CCc1c(C(=O)O)[nH]c2cc(I)ccc12
Reaction #2037861
3-(2-Carboxyethyl)-6-iodo-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
O=C(O)CCc1c(C(=O)O)[nH]c2cc(I)cc(I)c12
Reaction #2037862
3-(2-Carboxyethyl)-4,6-diiodo-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
O=C(O)CCC1=C2C(=CC(Cl)=CC2(F)Cl)NC1C(=O)O
Reaction #2037863
3-(2-Carboxyethyl)-4,6-dichloro-4-fluoro-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
O=C(O)CCc1c(C(=O)O)[nH]c2cc(-c3ccccc3)cc(-c3ccccc3)c12
Reaction #2037865
3-(2-Carboxyethyl)-4,6-diphenyl-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
O=C(O)CCc1c(C(=O)O)[nH]c2cc(-c3ccccc3)ccc12
Reaction #2037867
3-(2-Carboxyethyl)-6-phenyl-1H-indole-2-carboxylic acid
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03