An unprecedent[4+3]cycloaddition of furoketenimines with furocarbenoids has been disclosed for the divergent and efficient synthesis of cycloheptafuran and cycloheptapyrrole scaffolds.Zinc chloride acted as promoters ...An unprecedent[4+3]cycloaddition of furoketenimines with furocarbenoids has been disclosed for the divergent and efficient synthesis of cycloheptafuran and cycloheptapyrrole scaffolds.Zinc chloride acted as promoters for both the formation of these two transient intermediates from isocyanides and ene-yne-ketones,and the subsequent construction of seven-membered ring.Three rings and five bonds were constructed successively in this three-component one-pot domino reaction.展开更多
A Cu-catalyzed chemoselective heterocyclization of o-cinnamoyl arylisocyanides with α-substituted tosylmethyl isocyanides is developed for the efficient synthesis benzopyrroloazepinones. An isocyanide insertion into ...A Cu-catalyzed chemoselective heterocyclization of o-cinnamoyl arylisocyanides with α-substituted tosylmethyl isocyanides is developed for the efficient synthesis benzopyrroloazepinones. An isocyanide insertion into the C–Cu bond of organocuprate intermediate is involved for the formation of the sevenmembered azepinone ring.展开更多
基金financial support from National Natural Science Foundation of China(Nos.22171168,22001152 and 22101159)Taishan Scholar Program of Shandong Province and the Natural Science Foundation of Shandong Province of China(No.ZR2020QB019)。
文摘An unprecedent[4+3]cycloaddition of furoketenimines with furocarbenoids has been disclosed for the divergent and efficient synthesis of cycloheptafuran and cycloheptapyrrole scaffolds.Zinc chloride acted as promoters for both the formation of these two transient intermediates from isocyanides and ene-yne-ketones,and the subsequent construction of seven-membered ring.Three rings and five bonds were constructed successively in this three-component one-pot domino reaction.
基金Financial support from the National Natural Science Foundation of China (Nos. 22001151, 22171168, 22101159)Taishan Scholar Program of Shandong Province and Shandong Provincial Natural Science Foundation (Nos. ZR2019QB004, ZR2020QB019) is gratefully acknowledged。
文摘A Cu-catalyzed chemoselective heterocyclization of o-cinnamoyl arylisocyanides with α-substituted tosylmethyl isocyanides is developed for the efficient synthesis benzopyrroloazepinones. An isocyanide insertion into the C–Cu bond of organocuprate intermediate is involved for the formation of the sevenmembered azepinone ring.