493018-08-9Relevant articles and documents
Facile synthesis of fused furanosyl β-amino acids from protected sugar lactones: Incorporation into a peptide chain
Taillefumier, Claude,Lakhrissi, Younes,Lakhrissi, Mohammed,Chapleur, Yves
, p. 1707 - 1711 (2002)
The synthesis of fused furanosyl β-amino esters from protected sugar lactones is described, using the combination of a Wittig type reaction and 1,4-addition of benzylamine on the resulting glycosylidenes. This sequence of reactions afford either N-glycosy
Anomeric spiroannelated 1,4-diazepine 2,5-diones from furano exo-glycals: Towards a new class of spironucleosides
Taillefumier, Claude,Thielges, Sabine,Chapleur, Yves
, p. 2213 - 2224 (2007/10/03)
The first synthesis of 1,4-diazepine 2,5-dione peptides containing a β-amino acid in which the β carbon is also the anomeric carbon of a furanoid sugar is described. These new anomeric spirosugars obtained with a stereoselective control in the D-gulo, D-m