61784-07-4Relevant academic research and scientific papers
Preparation of diamino pseudodisaccharide derivatives from 1,6-anhydro-β-d-hexopyranoses via aziridine-ring cleavage
Kroutil, Jiri,Budesinsky, Milos
, p. 147 - 153 (2007/10/03)
Twelve positional isomers of diamino pseudodisaccharide derivatives with gluco-gluco configuration have been prepared using aziridine-ring cleavage of epimino derivatives of 1,6-anhydro-β-d-hexopyranoses of the d-allo, d-manno, and d-galacto configuration
Selective N-debenzylation of benzylamino derivatives of 1,6-anhydro-β-D-hexopyranoses
Kroutil, Jiri,Trnka, Tomas,Cerny, Miloslav
, p. 1681 - 1683 (2007/10/03)
(matrix presented) When the series of 2-, 3-, and 4-(benzylamino)-2-, 3-, and 4-deoxy derivatives of 1,6-anhydro-β-D-hexopyranoses in the D-gluco, D-lyxo, and D-arabino configurations were reacted with diisopropyl azodicarboxylate, N-benzyl groups were selectively cleaved in the presence of O-benzyl groups. The yields ranged from 51 to 97percent. The debenzylation of some aliphatic benzylamines is also discussed.
