Autor:	C. A. Slinn, Antony J. Fairbanks, Richard J. Tennant-Eyles, H. S. Yeates, S. C. Ennis
Rok vydání:	2001
Předmět:	chemistry.chemical_compound chemistry Stereochemistry Intramolecular force Organic Chemistry Drug Discovery Two step Stereoselectivity N-iodosuccinimide Biochemistry Enol
Zdroj:	Tetrahedron. 57:4221-4230
ISSN:	0040-4020
DOI:	10.1016/s0040-4020(01)00308-8
Popis:	Enol ethers may be accessed via Tebbe methylenation of either 2- O acetates or para -methoxybenzoates. N -Iodosuccinimide may then be employed to achieve both tethering and thioglycoside activation allowing the stereoselective synthesis of α-glucosides and β-mannosides, either in a one or two step procedure.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::10868b98a4417373e5fb36c80d33f45f https://doi.org/10.1016/s0040-4020(01)00308-8 Zobrazit plný text záznamu Full Text from ScienceDirect