anti-Selective enolboration–aldolization of propanoic acid

Autor:	P. Veeraraghavan Ramachandran, Barnabas Otoo, Prem B. Chanda
Rok vydání:	2014
Předmět:	chemistry.chemical_classification chemistry.chemical_compound Propanoic acid chemistry Base (chemistry) Reagent Organic Chemistry Drug Discovery Organic chemistry Keto–enol tautomerism Biochemistry Triethylamine
Zdroj:	Tetrahedron Letters. 55:1289-1291
ISSN:	0040-4039
DOI:	10.1016/j.tetlet.2013.12.048
Popis:	A systematic examination of enolboration–aldolization of propanoic acid has led to an efficient synthesis of anti -β-hydroxy-α-methyl carboxylic acids in consistently high yields and diastereoselectivities by using B -bromodicyclohexylborane as the enolization reagent and triethylamine as the base.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::b25cc14e76833633dec4dc62dacd84b5 https://doi.org/10.1016/j.tetlet.2013.12.048 Zobrazit plný text záznamu Full Text from ScienceDirect