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

Autor:	Dale A. Laidler, Peter R. Ashton, J. Fraser Stoddart, David G. Andrews, John B. Wolstenholme
Rok vydání:	1979
Předmět:	Perchlorate chemistry.chemical_compound chemistry Stereochemistry Organic Chemistry Drug Discovery Receptor molecule Crown (botany) Organic chemistry Carbohydrate Biochemistry
Zdroj:	Tetrahedron Letters. 20:2629-2632
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(01)86369-3
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::bfe00a7c6de859d23e0c5bc83b20d71d https://doi.org/10.1016/s0040-4039(01)86369-3 Zobrazit plný text záznamu