首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >Short Step Syntheses of Indolo[2,3-a]Carbazoles Carring an Alkyl, Allyl, or a Glycosyl Group at the 11-Position and a Novel 6,7-Dihydro-13H-Cyclopentano[mn]Indolo[3,2-c]Acridine Derivative
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Short Step Syntheses of Indolo[2,3-a]Carbazoles Carring an Alkyl, Allyl, or a Glycosyl Group at the 11-Position and a Novel 6,7-Dihydro-13H-Cyclopentano[mn]Indolo[3,2-c]Acridine Derivative

机译:在11位上带有烷基,烯丙基或糖基的吲哚[2,3-a]咔唑和新型6,7-二氢-13H-环戊烷[mn] Indolo [3,2-c]的短步合成A啶衍生物

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摘要

Novel 1-alkyl-, 1-allyl-, and 1-#beta#-glycosyl-2,2'-biindolyls are prepared. Their Diels-Alder reaction produced 11-alkyl-, 11-alkyl-, and 11-#beta#-glycosylindolo[2,3-a]carbazoles. Formation of a novel 6,7-dihydro-13H-cyclopentno[mn]indolo[3,2-c]acridine derivative is also reported.
机译:制备新的1-烷基-,1-烯丙基-和1-#β#-糖基-2,2'-联吲哚基。他们的Diels-Alder反应生成11-烷基-,11-烷基-和11-ββ-糖基吲哚并[2,3-a]咔唑。还报道了新型6,7-二氢-13H-环戊基[mn]吲哚并[3,2-c] ac啶衍生物的形成。

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