Synthesis of dibenzoarsole derivatives from biarylborates via the twofold formation of C–As bonds using arsenium dication equivalents

IF 7.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Kazutoshi Nishimura, Hiroki Iwamoto, Yuji Nishii, Koji Hirano
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引用次数: 0

Abstract

A strategy for the generation of arsenium dication equivalents from readily available and easy-to-handle phenylarsine oxide and Tf2O has been developed. The in-situ-generated dication equivalent can react with biarylborates to directly produce the corresponding dibenzoarsoles, which are difficult to prepare by other means, via the successive formation of inter- and intramolecular C-As bonds. Furthermore, the unique oxygen atom insertion into the C–As bond in the dibenzoarsole is developed to form the corresponding [1,2]oxarsinine derivative.
用砷化等价物通过C-As键的双重形成从双芳基硼酸盐合成二苯甲油衍生物
已经开发了一种从现成且易于处理的氧化苯larsin和Tf2O生成砷化当量的策略。原位生成的阳离子等价物可以通过分子间和分子内C-As键的连续形成,与双芳基硼酸盐反应,直接生成其他方法难以制备的相应的二苯并甲醚。此外,二苯甲醚中独特的氧原子插入到C-As键中,形成相应的[1,2]草精氨酸衍生物。
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来源期刊
Chemical Science
Chemical Science CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
14.40
自引率
4.80%
发文量
1352
审稿时长
2.1 months
期刊介绍: Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.
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