N,N-bis(2-hydroxyethyl)-p-toluenesulfonamide

COc1ccc2cc(C(C)C(=O)OCCN(CCO)S(=O)(=O)c3ccc(C)cc3)ccc2c1
Reaction #244758
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc2cc([C@H](C)C(=O)OCCN(CCO)S(=O)(=O)c3ccc(C)cc3)ccc2c1
Reaction #502130
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
NS(=O)(=O)c1ccccc1
Reaction #569168
benzenesulfonamide
Rendimiento 85.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
COc1ccc2cc([C@H](C)C(=O)OCCN(CCO)S(=O)(=O)c3ccc(C)cc3)ccc2c1
Reaction #1449996
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
COc1ccc2cc([C@H](C)C(=O)OCCN(CCO)S(=O)(=O)c3ccc(C)cc3)ccc2c1
Reaction #1461249
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_01
Cc1ccc(S(=O)(=O)OCCN(CCOS(=O)(=O)c2ccc(C)cc2)S(=O)(=O)c2ccc(C)cc2)cc1
Reaction #1501627
N,O,O'-tritosyldiethanolamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_01
COc1ccc2cc([C@H](C)C(=O)OCCN(CCO)S(=O)(=O)c3ccc(C)cc3)ccc2c1
Reaction #1601961
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_07
COc1ccc2cc(C(C)C(=O)OCCN(CCO)S(=O)(=O)c3ccc(C)cc3)ccc2c1
Reaction #1646651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COc1ccc2cc([C@H](C)C(=O)OCCN(CCO)S(=O)(=O)c3ccc(C)cc3)ccc2c1
Reaction #1960817
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_11
NS(=O)(=O)c1ccccc1
Reaction #2028376
benzenesulfonamide
Rendimiento 85.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_12
NS(=O)(=O)c1ccccc1
Reaction #2347991
benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_12
NS(=O)(=O)c1ccccc1
Reaction #2391647
benzenesulfonamide
Rendimiento 85.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_08
COc1ccc2cc([C@H](C)C(=O)OCCN(CCO)S(=O)(=O)c3ccc(C)cc3)ccc2c1
Reaction #2442834
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07