1040413-86-2Relevant academic research and scientific papers
Synthesis of chiral Nβ-protected amino diselenides from the corresponding amino alkyl iodides using NaBH2Se3 as a selenating reagent and their conversion to seleninic acids
Panguluri, Nageswara Rao,Panduranga, Veladi,Prabhu, Girish,Vishwanatha,Sureshbabu, Vommina V.
, p. 51807 - 51811 (2015)
A convenient approach has been presented for the synthesis of Nβ-protected amino diselenides from the corresponding amino alkyl iodides using in situ generated NaBH2Se3 as an efficient selenating reagent. All the diselenid
Biomimetic seleninates and selenonates
Abdo, Mohannad,Knapp, Spencer
supporting information; body text, p. 9234 - 9235 (2009/02/02)
The synthesis of a variety of pyranose-, nucleoside-, (amino acid)-, and polyhydric-based seleninic and selenonic acids by DMDO oxidation of the corresponding selenoesters is reported, as well as some unusual coupling reactions of the seleninate and selenonate functionality with biological nucleophilic groups (sulfhydryl, indole, phenol, imidazole, carboxamide) that are found in proteins and enzyme active sites. Copyright
