Author： Charrier Florian Husson Jérôme Guyard Laurent
Publisher： MDPI
E-ISSN： 1422-8599|2017|2|M940-M940
ISSN： 1422-8599
Source： Molbank, Vol.2017, Iss.2, 2017-04, pp. : M940-M940
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
A new member of the 2-acetylpyridine family has been prepared and characterized. Its synthesis is a two-step process starting from a pyridyl-alcohol in which the ketone moiety is protected as a cyclic acetal. Alkylation of the alcohol followed by hydrolysis of the acetal afforded the title compound in 52% overall yield.
Related content
1‐[5‐(3,6‐Dichloropyridin‐2‐yl)‐2,2‐dimethyl‐1,3,4‐oxadiazol‐3‐yl]ethanone
Acta Crystallographica Section E, Vol. 62, Iss. 10, 2006-10 ,pp. :
Access to resources
Recommend
Acta Crystallographica Section E, Vol. 63, Iss. 8, 2007-08 ,pp. :
1‐(5‐Methyl‐3‐phenylisoxazol‐4‐yl)ethanone
Acta Crystallographica Section E, Vol. 63, Iss. 6, 2007-06 ,pp. :
1‐[1‐(4‐Fluorophenyl)‐2‐methyl‐5‐phenyl‐1H‐pyrrol‐3‐yl]ethanone
Acta Crystallographica Section E, Vol. 62, Iss. 6, 2006-06 ,pp. :