论文信息 - Oxetane cis- and trans-β-amino-acid scaffolds from l-rhamnose by efficient SN2 reactions in oxetane rings; pseudoenantiomeric analogues of the antibiotic oxetin - 字舞流文

Oxetane cis- and trans-β-amino-acid scaffolds from l-rhamnose by efficient SN2 reactions in oxetane rings; pseudoenantiomeric analogues of the antibiotic oxetin

C. Taillefumier | G. Fleet | S. F. Jenkinson | D. Angus | J. H. Jones | Stephen W. Johnson

[1] W. DeGrado,et al. beta-Peptides: from structure to function. , 2001, Chemical reviews.

[2] J. Goodman,et al. 10-Helical conformations in oxetane β-amino acid hexamers , 2001 .

[3] T. Claridge,et al. cis - and trans -3-Azido-oxetane-2-carboxylate scaffolds: hexamers of oxetane cis -β-amino acids , 2001 .

[4] D. Watkin,et al. Two epimerisations in the formation of oxetanes from l-rhamnose: towards oxetane-containing peptidomimetics , 2000 .

[5] M. Deninno,et al. A method for the selective reduction of carbohydrate 4,6-O-benzylidene acetals , 1995 .

[6] S. Ōmura,et al. Oxetin, a new antimetabolite from an actinomycete. Fermentation, isolation, structure and biological activity. , 1984, The Journal of antibiotics.