A stereoselective approach to the synthesis of pseudodistomin D

Autor:	Mansour Haddad, Han Min Tong, Marc Larchevêque
Rok vydání:	2005
Předmět:	Stereochemistry Organic Chemistry Intramolecular cyclization Total synthesis Pseudodistomin D Ring (chemistry) Biochemistry chemistry.chemical_compound chemistry Intramolecular force Drug Discovery Michael reaction Stereoselectivity Piperidine
Zdroj:	Tetrahedron Letters. 46:6015-6017
ISSN:	0040-4039
DOI:	10.1016/j.tetlet.2005.07.014
Popis:	A stereoselective total synthesis of the core unit of pseudodistomin D, starting from l -serine, is described. The key step is a stereoselective intramolecular Michael reaction in which the piperidine ring is formed with the obtention of 1 .
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::7d638a638eb1c8e056a3889bf0c02da9 https://doi.org/10.1016/j.tetlet.2005.07.014 Zobrazit plný text záznamu Full Text from ScienceDirect