Autor:	Alain Olesker, Vincent Bailliez, Jeannine Cleophax, Renata M. de Figueiredo
Rok vydání:	2003
Předmět:	chemistry.chemical_compound Chemistry Levoglucosan Organic Chemistry Drug Discovery Organic chemistry Core (manufacturing) Biochemistry
Zdroj:	Tetrahedron Letters. 44:9151-9153
ISSN:	0040-4039
DOI:	10.1016/j.tetlet.2003.10.047
Popis:	The macrocyclic core of cycloviracin and glucolipsin has been synthesised in ten steps from levoglucosan and (S)-(−)-dimethyl malate. The limited number of steps to obtain this macrolide makes it a valuable procedure for the synthesis of analogues of cycloviracin and glucolipsin.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::d3c439aeac6a96813f62ce41afb746d5 https://doi.org/10.1016/j.tetlet.2003.10.047 Zobrazit plný text záznamu Full Text from ScienceDirect