174466-54-7Relevant academic research and scientific papers
Unprecedented directed oxidative cross-coupling of sulfahydantoins with aldehydes via a radical sulfonate-sulfinate conversion
Aubin, Yoann,Colacino, Evelina,Bouchouk, Djamel,Chataigner, Isabelle,Del Mar Sanchez,Martinez, Jean,Dewynter, Georges
supporting information; experimental part, p. 1560 - 1563 (2012/09/25)
An unexpected C-C cross-coupling radical oxidation involving aldehydes and glycine enolate equivalents such as activated mesyl-sulfahydantoins leading to β,β'-disubstituted aspartate semialdehydes (ASA) instead of the expected threonine analogues was obse
Synthesis and anticonvulsant activity of amino acid-derived sulfamides
Gavernet, Luciana,Elvira, Juan E.,Samaja, Gisela A.,Pastore, Valentina,Cravero, Mariana Sella,Enrique, Andrea,Estiu, Guillermina,Bruno-Blanch, Luis E.
experimental part, p. 1592 - 1601 (2010/02/16)
Sulfamides are promising functions for the design of new antiepileptic drugs (Bioorg. Med. Chem. 2007, 15, 1556-1567; 5604-5614). Following previous research in this line, a set of amino acid-derived sulfamides has been designed, synthesized, and tested a
Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II)
Dewynter, Georges,Aouf, Nourreddine,Regainia, Zine,Montero, Jean-Louis
, p. 993 - 1004 (2007/10/03)
A series of chiral sulfahydantoins have been synthesized by alkaline cyclization starting from N-sulfamylaminoacid methyl esters. Regioselective glycosylation of these pseudopyrimidic heterocycles was carried out with a benzyl protecting group on the N-su
