(5S)-1,1-diethoxy-5-t-butyldiphenylsilyloxy-hex-3-en-2-one: A new functionalized versatile chiral building block

Autor:	Yves Le Floc'h, René Grée, Hervé Dumartin
Rok vydání:	1994
Předmět:	Stereochemistry Chemistry Organic Chemistry Acetal Biochemistry Combinatorial chemistry chemistry.chemical_compound Block (telecommunications) Drug Discovery Wittig reaction Chemical reduction Aliphatic compound Lactaldehyde Enone
Zdroj:	Tetrahedron Letters. 35:6681-6684
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(00)73467-8
Popis:	The title enone 3 is easily prepared from protected lactaldehyde. Highly diastereoselective reduction of 3 is only obtained with CBS reagents.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::310b6ee692dd6befc28625ebdae03d50 https://doi.org/10.1016/s0040-4039(00)73467-8 Zobrazit plný text záznamu