Synthesis of Cyclic 1-Alkenylboronates via Zr-Mediated Double Functionalization of Alkynylboronates and Sequential Ru-Catalyzed Ring-Closing Olefin Metathesis

被引:17
|
作者
Nishihara, Yasushi [1 ,2 ]
Suetsugu, Masato [1 ]
Saito, Daisuke [1 ]
Kinoshita, Megumi [1 ]
Iwasaki, Masayuki [1 ]
机构
[1] Okayama Univ, Div Earth Life & Mol Sci, Grad Sch Nat Sci & Technol, Kita Ku, Okayama 7008530, Japan
[2] Japan Sci & Technol Agcy, Kawaguchi, Saitama 3320012, Japan
关键词
DISCOTIC LIQUID-CRYSTALS; METAL-PROMOTED CYCLIZATION; CROSS-COUPLING REACTIONS; STEREOSELECTIVE-SYNTHESIS; TRANSITION-METAL; BOND FORMATION; ASYMMETRIC 1,4-ADDITION; PHENOL DERIVATIVES; TERMINAL ALKYNES; NEW-GENERATION;
D O I
10.1021/ol400896u
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Synthesis of novel cyclic 1-alkenylboronates is accomplished through the zirconium-mediated regio- and stereoselective double functionalization of 1-alkynylboronates and the subsequent ruthenium-catalyzed ring-closing metathesis (RCM). The obtained substituted cyclic 1-alkenylboronates are transformed into o-terphenyl and triphenylene derivatives.
引用
收藏
页码:2418 / 2421
页数:4
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