Metal- and Solvent-Free Synthesis of m-Terphenyls by an Iodine-Catalyzed Tandem Formal [3+3]-Cycloaddition/Oxidation

被引:7
|
作者
Pavithra, Thangavel [1 ]
Karthiyayini, Gnanaoli [1 ]
Nagarajan, Subbiah [2 ]
Sridharan, Vellaisamy [3 ]
Maheswari, C. Uma [1 ]
机构
[1] SASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur 613401, India
[2] Natl Inst Technol Warangal, Dept Chem, Warangal 506004, Andhra Pradesh, India
[3] Cent Univ Jammu, Dept Chem & Chem Sci, Jammu 181143, Jammu & Kashmir, India
关键词
terphenyls; chalcones; enamine esters; cycloaddition; iodine catalysis; oxidation; ONE-POT SYNTHESIS; CROSS-COUPLING REACTIONS; MOLECULAR-IODINE; EXPEDITIOUS SYNTHESIS; PRINS-CYCLIZATION; REGIOSELECTIVE SYNTHESIS; OXIDATIVE CONDENSATION; VERSATILE REAGENT; DERIVATIVES; BENZANNULATION;
D O I
10.1055/a-1903-5174
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A tandem formal [3+3]-cycloaddition/oxidation between chalcones and beta-enamine esters, employing iodine as a catalyst, was developed for the construction of various substituted m-terphenyls. A wide range of chalcones and beta-enamine esters were tested under metal- and solvent-free conditions for the synthesis of substituted m-terphenyls in good to excellent yields in the presence of sulfur as an oxidant. This reaction proceeds with the formation of four new bonds and one new ring, with a high atom economy.
引用
收藏
页码:807 / 814
页数:8
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