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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Convenient synthesis of isoxazolines via tandem isomerization of allyl compounds to vinylic derivatives and 1,3-dipolar cycloaddition of nitrile oxides to the vinylic compounds
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Convenient synthesis of isoxazolines via tandem isomerization of allyl compounds to vinylic derivatives and 1,3-dipolar cycloaddition of nitrile oxides to the vinylic compounds

机译:通过将烯丙基化合物串联异构化为乙烯基衍生物,以及将腈氧化物与乙烯基化合物进行1,3-偶极环加成反应,方便地合成异恶唑啉

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摘要

A novel effective method for the synthesis of new isoxazolines via tandem isomerization of QCH(X)CH=CH(Y) to QC(X)=CHCH2(Y) (Q= RO, RS, R2N, R3Si, etc.; X = H, R, OR; Y = H, R; R = alkyl, aryl) catalyzed by ruthenium complexes and 1,3-dipolar cycloaddition of the latter compounds to arenenitrile oxides is presented. The cycloaddition of QCH(X)CH=CH(Y) to 2,6-dichlorobenzonitrile oxide is also described. The regio- and stereoselectivity of the cycloaddition of nitrile oxide to allyl and 1-propenyl (vinylic in general) compounds is discussed.
机译:通过将QCH(X)CH = CH(Y)串联异构化为QC(X)= CHCH2(Y)(Q = RO,RS,R2N,R3Si等; X = H,R,OR; Y = H,R; R =烷基,芳基)由钌配合物催化,并且提出了后者化合物的1,3-偶极环加成至芳族腈氧化物。还描述了QCH(X)CH = CH(Y)与2,6-二氯苄腈氧化物的环加成。讨论了氮氧化物与烯丙基和1-丙烯基(通常为乙烯基)化合物的环加成反应的区域选择性和立体选择性。

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