Participa en 10 reacciones

119911

Cc1ccc(-c2ccc3c(c2)OC(C)(C)C3)cc1
Reaction #173722
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1cc2ccc(-c3ccc(C)cc3)cc2[nH]1
Reaction #273403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(OB(O)O)cc1
Reaction #653335
4-methylphenyl boric acid
Rendimiento 73.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
Cc1ccc(OB(O)O)cc1
Reaction #653337
4-methylphenyl boric acid
Rendimiento 73.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
Cc1ccc(-c2cc3c(cc2C(C)(C)C)-c2cc(C(C)(C)C)c(-c4ccc(C)cc4)cc2C3)cc1
Reaction #1137842
product
Rendimiento 165.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CCOC(=O)c1cc2ccc(-c3ccc(C)cc3)cc2[nH]1
Reaction #1256537
ethyl 6-(4-methylphenyl)-1H-indole-2-carboxylate
Rendimiento 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_09
Cc1ccc(-c2ccc3c(c2)CNCC3)cc1
Reaction #1256548
7-(4-methylphenyl)-1,2,3,4-tetrahydroisoquinoline
Rendimiento 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_09
Cc1ccc(-c2ccsc2[N+](=O)[O-])cc1
Reaction #1376254
product
Rendimiento 74.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_05
Cc1ccc(-c2ccc3c(c2)OC(C)(C)C3)cc1
Reaction #1937554
title compound
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
Cc1ccc(-c2ccc3c(c2)OC(C)(C)C3)cc1
Reaction #2150963
title compound
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10