874341-17-0Relevant academic research and scientific papers
1,3-Dipolar cycloaddition reaction of a d-galactose derived nitrone with allyl alcohol: synthesis of polyhydroxylated perhydroazaazulene alkaloids
Bande, Omprakash P.,Jadhav, Vrushali H.,Puranik, Vedavati G.,Dhavale, Dilip D.
, p. 1176 - 1182 (2007)
Diastereofacial intermolecular 1,3-dipolar cycloaddition of d-galactose derived nitrone with allyl alcohol followed by tosylation afforded, in a 1:1 ratio endo- and exo-isooxazolidines 4a and 4b with complete diastereoselectivity at the nitrone carbon. Th
A short and highly stereoselective route to polyhydroxy-perhydroazaazulenes via a C-(D-galacto-pentopyranos-5-yl)isoxazolidine
Torres-Sanchez, Ma Isabel,Borrachero, Pastora,Cabrera-Escribano, Francisca,Gomez-Guillen, Manuel,Angulo-Alvarez, Manuel,Dianez, Ma Jesus,Estrada, Ma Dolores,Lopez-Castro, Amparo,Perez-Garrido, Simeon
, p. 3897 - 3907 (2007/10/03)
A short and efficient route to enantiomerically pure hexahydroxy- and pentahydroxy-perhydroazaazulenes, ring-homologues of castanospermine, starting from the sole isoxazolidine derivative obtained in the 1,3-dipolar cycloaddition of a D-galactose-derived
