Lewis acid mediated cyclization of ortho-allyl substituted homochiral anthraquinone dioxolanes

Autor:	Paul D. Woodgate, Peter S. Rutledge, Richard C. Cambie, S. E. Holroyd
Rok vydání:	1993
Předmět:	Organic Chemistry Acetal chemistry.chemical_element Hydroxyanthraquinone Biochemistry Anthraquinone Chloride Quinone chemistry.chemical_compound chemistry Drug Discovery medicine Organic chemistry Lewis acids and bases Phenols Tin medicine.drug
Zdroj:	Tetrahedron Letters. 34:697-698
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(00)61656-8
Popis:	Tin(IV) chloride N,N-dimethylformamide and titanium(IV) chloride mediated cyclizations of ortho -allyl-substituted homochiral hydroxyanthraquinone acetals results in high diastereoselection in the generation of two stereocentres.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::d9e064b8d338a855a0b8422b13852906 https://doi.org/10.1016/s0040-4039(00)61656-8 Zobrazit plný text záznamu