First stereoselective total synthesis of pectinolide C and total synthesis of pectinolide A

Autor:	Sukant Kishore Das, J. S. Yadav, Gowravaram Sabitha, Praveen AnkiReddy
Rok vydání:	2013
Předmět:	chemistry.chemical_classification chemistry Stereochemistry Organic Chemistry Drug Discovery Organic chemistry Total synthesis Stereoselectivity Biochemistry Aldehyde
Zdroj:	Tetrahedron Letters. 54:1097-1099
ISSN:	0040-4039
DOI:	10.1016/j.tetlet.2012.12.039
Popis:	The first stereoselective synthesis of pectinolide C and synthesis of pectinolide A, from easily accessible 1-hexyne and d -mannitol are reported in a convergent manner. The salient features include acetylenic addition to the chiral aldehyde and Still–Gennari olefination.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::2207515eba64d0963ac8f47d592b9a50 https://doi.org/10.1016/j.tetlet.2012.12.039 Zobrazit plný text záznamu Full Text from ScienceDirect