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Showing papers by "J. Fraser Stoddart published in 1979"

Journal Article•DOI•
Tate and Lyle Lecture. From carbohydrates to enzyme analogues

[...]

J. Fraser Stoddart1•
AkzoNobel1
01 Jan 1979-Chemical Society Reviews

128 citations

Journal Article•DOI•
Chiral asymmetric crowns incorporating the 4,6-O-benzylidene derivatives of methyl α-D-mannopyranoside and methyl α-D-altropyranoside. The influence of stereochemistry upon complexation of organic cations

[...]

Roger B. Pettman1, J. Fraser Stoddart1•
University of Sheffield1
01 Jan 1979-Tetrahedron Letters

16 citations

Journal Article•DOI•
The complexing properties of chiral crown ethers incorporating 1,3:4,6-di-O-methylene-D-mannitol residues. A secondary dipole-induced dipole interaction.

[...]

Dale A. Laidler1, J. Fraser Stoddart1•
University of Sheffield1
01 Jan 1979-Tetrahedron Letters

15 citations

Journal Article•DOI•
Chiral symmetric crowns incorporating the 4,6-O-benzylidene derivatives of methyl α-D-glucopyranoside and methyl α-D-galactopyranoside. A configurational impediment to complexation of organic cations by 18-crown-6 derivatives

[...]

Dale A. Laidler1, J. Fraser Stoddart1, John B. Wolstenholme1•
University of Sheffield1
01 Jan 1979-Tetrahedron Letters

14 citations

Journal Article•DOI•
Complexation selectivity by chiral asymmetric crowns incorporating the 4,6-O-benzylidene derivatives of methyl β-D-glucopyranoside and methyl β-D-galactopyranoside. A secondary anomeric effect?

[...]

Roger B. Pettman1, J. Fraser Stoddart1•
University of Sheffield1
01 Jan 1979-Tetrahedron Letters

12 citations

Journal Article•DOI•
The complexing properties of a chiral 18-crown-6 derivative incorporating a 2,5-anhydro-d-mannitol residue. A constitutional and stereochemical means of enhancing complexation

[...]

J.Anthony Haslegrave1, J. Fraser Stoddart1, David John Dr. Thompson2•
University of Sheffield1, Imperial Chemical Industries2
01 Jan 1979-Tetrahedron Letters
TL;DR: In this article, an 18-crown-6 derivative incorporating a chiral diethyleneglycol unit in the shape of a 2,5-anhydro- D -mannitol residue formed extremely strong complexes with alkali metal, NH + 4, and RNH + 3 ions.

11 citations

Journal Article•DOI•
The synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution

[...]

David G. Andrews1, Peter R. Ashton1, Dale A. Laidler1, J. Fraser Stoddart1, John B. Wolstenholme1 •
University of Sheffield1
01 Jan 1979-Tetrahedron Letters
TL;DR: In this paper, the rationale behind designing and the approach to synthesising chiral crown ethers incorporating three trigonally-disposed carbohydrate residues is presented as a prelude to attaining chiral discrimination in the complexation of ( R )- and ( S )-α-phenylethylammonium perchlorate.

7 citations