1233362-20-3Relevant academic research and scientific papers
Selective deprotection of phenolic polysulfonates
Chapman, Erin E.,Langler, Richard F.
, p. 19 - 26 (2010)
Nosylates of phenols can be selectively deprotected by thiocresol anions in DMSO. Successful deprotection can be accomplished in molecules containing aryl-appended halides, ethers, aldehydes, alkanesulfonates or arylsulfonates. Nosylate deprotection is accomplished by the CS bond rupture which is believed to proceed by nucleophilic aromatic substitution.
