304649-53-4Relevant academic research and scientific papers
Sultone opening with [18F]fluoride: An efficient 18F-labelling strategy for PET imaging
Schmitt, Sebastien,Bouteiller, Cedric,Barre, Louisa,Perrio, Cecile
supporting information; experimental part, p. 11465 - 11467 (2011/11/13)
Sultones were subject to ring opening by nucleophilic attack with [ 18F]fluoride to afford easily purified 18F-labelled hydrophilic sulfonated products in high yields. A two-step sequence including radiofluorination and coupling to l
Pharmacophoric 2-hydroxyalkyl benzenesulfonamide: A single-step synthesis from benzenesulfonamide via hemiaminal
Singh, Sunil K.,Shivaramakrishna,Saibaba,Rao, K. Srinivas,Ganesh, K. Ravi,Vasudev,Kumar, P. Praveen,Babu, J. Moses,Vyas,Rao, Y. Koteswar,Iqbal
, p. 456 - 462 (2008/02/07)
ortho-Acylation attempt of benzenesulfonamide afforded the corresponding hemiaminal as major product. The in situ reduction of the reaction mixture, reported herein, directly provided 2-hydroxyalkyl benzenesulfonamide, an important pharmacophoric element
