Synthesis of the C13-C23 Segment of Tedanolide

Autor:	Markus Kalesse, Gunnar Ehrlich
Rok vydání:	2005
Předmět:	Tedanolide chemistry.chemical_compound Natural product chemistry Aldol reaction Stereochemistry Organic Chemistry Carbon skeleton Organic chemistry Total synthesis General Medicine
Zdroj:	Synlett. :655-657
ISSN:	1437-2096 0936-5214
DOI:	10.1055/s-2005-862391
Popis:	The synthesis of the C13-C23 segment of tedanolide is described making use of orthogonal protecting groups in the construction of the carbon skeleton and for the selective liberation of hydroxyl groups in the endgame of the total synthesis.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dd290078ce52018bdb1fc57777c3a29 https://doi.org/10.1055/s-2005-862391 Zobrazit plný text záznamu