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Conformational analysis of N-aryl-N-(2-azulenyl)acetamides
Tetrahedron Letters ( IF 1.8 ) Pub Date : 2018-09-20 , DOI: 10.1016/j.tetlet.2018.09.053
Ai Ito , Takamasa Amaki , Ayako Ishii , Kazuo Fukuda , Ryu Yamasaki , Iwao Okamoto

Aromatic amides bearing 2-azulenyl group on the amide nitrogen were synthesized and their structures were investigated. The π-electron density of the N-aryl group was found to influence the cis-trans conformational preferences of these compounds in solution. X-ray crystallography revealed that the plane of the 2-azulenyl ring has a strong tendency to lie coplanar with the amide plane when the azulene group is located on the same side as the amide oxygen atom.



中文翻译:

N-芳基-N-(2-氮烯基)乙酰胺的构象分析

合成了在酰胺氮上带有2-氮杂烯基的芳族酰胺,并对其结构进行了研究。发现N-芳基的π电子密度影响溶液中这些化合物的-构象偏好。X射线晶体学表明,当氮杂基团与酰胺氧原子位于同一侧时,2-氮杂烯基环的平面具有很强的与酰胺平面共面的倾向。

更新日期:2018-09-20
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