Tetrahedron letters

The stereoselective synthesis of cyclomaltopentaose. A novel cyclodextrin homologue with DP five

T Nakagawa, K Ueno, M Kashiwa, J Watanabe

Index: Tetrahedron Letters, , vol. 35, # 12 p. 1921 - 1924

Full Text: HTML

Citation Number: 53

Abstract

... Please enable JavaScript to use all the features on this page. Tetrahedron Letters. Volume 35, Issue 12, 21 March 1994, Pages 1921–1924. Cover image Cover image. The stereoselective synthesis of cyclomaltopentaose. A novel cyclodextrin homologue with DP five. ...

Related Articles:

Regioselective lipase-catalysed acylation of 4, 6-O-benzylidene-α-and-β-d-pyranoside derivatives displaying a range of anomeric substituents

[Tetrahedron, , vol. 54, # 49 p. 14925 - 14946]

High-yield total synthesis of (−)-strictinin through intramolecular coupling of gallates

[Journal of Organic Chemistry, , vol. 78, # 9 p. 4319 - 4328]

'Naked'and Hydrated Conformers of the Conserved Core Pentasaccharide of N-linked Glycoproteins and Its Building Blocks

[Journal of the American Chemical Society, , vol. 135, # 45 p. 16895 - 16903]

More Articles...