90762-85-9Relevant academic research and scientific papers
De novo synthesis of the trisaccharide subunit of landomycins A and E
Zhou, Maoquan,O'Doherty, George A.
supporting information; experimental part, p. 2283 - 2286 (2009/05/11)
(Chemical Equation Presented) A highly enantio- and diastereoselective synthesis of α-L-rhodinose, β-D-olivose as well as the trisaccharide portion of landomycin A from achiral acetyl furan has been developed. The key transformations include the palladium
Preparation of α- and β-Linked Disaccharides of 2,6-Dideoxy-D-arabino-hexose. Synthesis of Bamflalactone
Lundt, Inge,Thiem, Joachim,Prahst, Archibald
, p. 3063 - 3069 (2007/10/02)
1,4-α-Linked disaccharides of 2,6-dideoxy-D-arabino-hexose are prepared from the selectively protected 2,6-dideoxy sugars 3 or 4 and the 1,5-anhydrohex-1-enitol (9) by using the N-iodosuccinimide (NIS) method or from the deoxy sugar 6 and the acetylated 2
