Novel synthesis of alkoxy substituted oxa[9]helicenes by the reaction of helical quinone with alcohols

Autor:	Hidenori Ubukata, Takao Kimura, Mohammad Salim, Michinori Karikomi
Rok vydání:	2011
Předmět:	Organic Chemistry Alcohol biochemical phenomena metabolism and nutrition Biochemistry Chemical synthesis Quinone chemistry.chemical_compound Helicene chemistry Furan Drug Discovery Alkoxy group Organic chemistry Brønsted–Lowry acid–base theory
Zdroj:	Tetrahedron Letters. 52:6591-6593
ISSN:	0040-4039
DOI:	10.1016/j.tetlet.2011.09.126
Popis:	The reaction of helical quinone with alcohols in the presence of Bronsted acid such as para -toluenesulfonic acid ( p TSA) or HCl proceeded smoothly to produce the corresponding alkoxy substituted oxa[9]helicenes in good yields.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::765123fda75f7862982bd2c612f52d47 https://doi.org/10.1016/j.tetlet.2011.09.126 Zobrazit plný text záznamu Full Text from ScienceDirect