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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 >REACTION OF 3-AROYLAZIRIDINES WITH DIPHENYLCYCLOPROPENONE AND SUBSEQUENT STEREOSPECIFIC 1,3-DIPOLAR CYCLOADDITION OF THE ADDUCTS WITH DIMETHYL 1-CYCLOBUTENE 1,2-DICARBOXYLATE
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REACTION OF 3-AROYLAZIRIDINES WITH DIPHENYLCYCLOPROPENONE AND SUBSEQUENT STEREOSPECIFIC 1,3-DIPOLAR CYCLOADDITION OF THE ADDUCTS WITH DIMETHYL 1-CYCLOBUTENE 1,2-DICARBOXYLATE

机译:3-芳基氮丙啶与二苯并环戊烯酮的反应以及随后的立体特定的1,3-二烯丙基环戊二烯1,2-二羧酸二丁酯的加成反应

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摘要

Reaction of 3-aroylaziridines with diphenylcyclopropenone provides anhydro-3-hydroxy-2,4-diphenyl-6-arylpyrlium hydroxides that undergo stereospecific 1,3-dipolar cycloaddition with dimethyl l-cyclobutene 1,2-dicarboxylate to give the corresponding exo- and endo-adducts depending on the substituents of the 6-phenyl group. [References: 40]
机译:3-芳基氮丙啶与二苯基环丙烯酮的反应提供了脱水-3-羟基-2,4-二苯基-6-芳基py氢氧化物,该立体氢氧化物经历了立体有规的1,3-偶极环加成反应,并与1-环丁烯二甲酯1,2-二羧酸二甲酯形成相应的外-和-内加成物取决于6-苯基的取代基。 [参考:40]

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