1365692-63-2Relevant academic research and scientific papers
Copper-free arylation of 3,3-disubstituted allylic halides with triazene-softened aryl Grignard reagents
Xu, Lijun,Liu, Zhubo,Dong, Weipeng,Song, Jinyu,Miao, Maozhong,Xu, Jianfeng,Ren, Hongjun
supporting information, p. 6333 - 6337 (2015/06/08)
A copper-free allylic arylation reaction between 3,3-disubstituted allylic halides and triazene-softened aryl Grignard reagents has been developed. This protocol presents a direct and efficient way to construct both α- or γ-isomers with high regioselectivity under environmentally benign conditions. Various functional groups can be tolerated in the reaction and the products are of high value for multiple synthetic applications. The α- and γ-isomers can be converted to the corresponding 3H-indole and indole derivatives in multigram scale respectively.
A simple and efficient synthesis of dibenzothiophene via BF 3·OEt2-promoted intramolecular annulation
Shang, Xiaobo,Chen, Wanzhi,Yao, Yingming
supporting information, p. 851 - 854 (2013/05/23)
A simple and efficient protocol promoted by BF3·OEt 2 for synthesizing functionalized dibenzothiophenes (DBTs) has been demonstrated. The annulation condition can tolerate a variety of functional groups. Georg Thieme Verlag Stuttgart · New York.
