Synthesis of 16-membered ring macrolide antibiotics I. Stereoselective construction of the ‘right wing' of the carbomycins and leucomycins from -glucose

Autor:	M. R. Pavia, Kyriacos C. Nicolaou, S. P. Seitz
Rok vydání:	1979
Předmět:	Stereochemistry medicine.drug_class Organic Chemistry Backbone chain Leucomycins Ring (chemistry) Biochemistry Macrolide Antibiotics chemistry.chemical_compound chemistry D-Glucose Carbomycin A Right wing Drug Discovery medicine Stereoselectivity
Zdroj:	Tetrahedron Letters. 20:2327-2330
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(01)93964-4
Popis:	D-Glucose was converted to a backbone chain containing the appropriate functionalities and correct stereochemistry for the construction of the C1–C9 fragment of the 16-membered ring macrolide antibiotics carbomycin A and B and leucomycin A3.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::82bd4e6990974b0f3038feb9cb3cfef5 https://doi.org/10.1016/s0040-4039(01)93964-4 Zobrazit plný text záznamu