Synthesis of 2-Alkenyl- and 2-Alkynyl-benzo[b]phospholes by Using Palladium-Catalyzed Cross-Coupling Reactions

被引:29
|
作者
Matano, Yoshihiro [1 ]
Hayashi, Yukiko [2 ]
Suda, Kayo [3 ]
Kimura, Yoshifumi [4 ]
Imahori, Hiroshi [2 ,5 ]
机构
[1] Niigata Univ, Fac Sci, Dept Chem, Nishi Ku, Niigata 9502181, Japan
[2] Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishikyo Ku, Kyoto 6158510, Japan
[3] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Kyoto 6068502, Japan
[4] Doshisha Univ, Fac Sci & Engn, Dept Mol Chem & Biochem, Kyotanabe 6100394, Japan
[5] Kyoto Univ, Inst Integrated Cell Mat Sci WPI ICeMS, Nishikyo Ku, Kyoto 6158510, Japan
关键词
OPTOELECTRONIC PROPERTIES; PHOTOPHYSICAL PROPERTIES; MEDIATED CYCLIZATION; STRUCTURE-PROPERTY; BUILDING-BLOCK; PI; PHOSPHINDOLES; LUMINESCENT; PHOSPHONIUM; STILBENES;
D O I
10.1021/ol401994e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Heck, Stille, and Sonogashira reactions of 2-bromobenzo[b]phosphole P-oxide afforded a series of 2-alkenyl- and 2-alkynyl-benzo[b]phosphole P-oxides. The charge-transfer character of the new benzo[b]phosphole pi-systems in the excited state is enhanced by the terminal electron-donating substituents. Furthermore, the C-Sn cross-coupling of the bromide was applied to the facile synthesis of a new Stille-coupling precursor, 2-stannylbenzo[b]phosphole.
引用
收藏
页码:4458 / 4461
页数:4
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