One-pot synthesis of spiropyrroloquinoline-isoindolinone and their aza-analogs via the Ugi-4CR/metal-free intramolecular bis-annulation process

被引:37
作者
Ghandi, Mehdi [1 ]
Zarezadeh, Nahid [1 ]
Abbasi, Alireza [1 ]
机构
[1] Univ Tehran, Coll Sci, Sch Chem, Tehran, Iran
关键词
C-H ACTIVATION; DIASTEREOSELECTIVE DOMINO CYCLIZATION; RUTHENIUM-CATALYZED CYCLIZATION; DIVERSE HETEROCYCLIC SCAFFOLDS; HIGHLY EFFICIENT SYNTHESIS; UGI 4CC/S-N CYCLIZATION; MULTICOMPONENT REACTIONS; 3-SUBSTITUTED ISOINDOLINONES; STEREOSELECTIVE-SYNTHESIS; ASYMMETRIC-SYNTHESIS;
D O I
10.1039/c5ob01095k
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This presentation discloses a one-pot synthesis of a series of spiropyrroloquinoline isoindolinone and spiropyrroloquinoline aza-isoindolinone scaffolds. The reaction proceeds by the combination of a Ugi four-component reaction (4CR) and two intramolecular cyclizations under metal-free conditions. The proof of the structures relies on analytical investigation and X-ray crystallography.
引用
收藏
页码:8211 / 8220
页数:10
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