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Allyl and 2-Cyclopropylethyl Rearrangements in the Reaction of 1-Alkenylaluminums with Diiodomethane/Triethylaluminum Reagent
Synlett ( IF 2 ) Pub Date : 2017-11-28 , DOI: 10.1055/s-0036-1591731
Ilfir Ramazanov , Alsu Yaroslavova , Niyaz Yaubasarov , Usein Dzhemilev

The reaction of diiodomethane and triethylaluminum with substituted 1-alkenylaluminums obtained by the Zr-catalyzed carbo- or cycloalumination of mono- or dialkyl-substituted alkynes resulted in the selective formation of di- and tetrasubstituted cyclopropanes. 1-Alkenylaluminums prepared from substituted propargylamines reacted with diiodomethane and triethylaluminum to give substituted allylamines. A plausible mechanism for the reaction of the 1-alkenylaluminums with diiodomethane/triethylaluminum is proposed.

中文翻译:

1-烯基铝与二碘甲烷/三乙基铝试剂反应中的烯丙基和2-环丙基乙基重排

二碘甲烷和三乙基铝与通过 Zr 催化的单或二烷基取代炔烃的碳或环铝化反应获得的取代 1-链烯基铝的反应导致选择性形成二和四取代的环丙烷。由取代的炔丙胺制备的 1-烯基铝与二碘甲烷和三乙基铝反应得到取代的烯丙胺。提出了 1-链烯基铝与二碘甲烷/三乙基铝反应的合理机制。
更新日期:2017-11-28
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