SALICYLIC ACID AS AN EFFICIENT CATALYST FOR THE DIASTEREOSELECTIVE SYNTHESIS OF DISPIROHYDROQUINOLINES VIA A ONE-POT DOMINO EIGHT-COMPONENT REACTION

被引：7

作者：

Salahi, Sajjad ^{[1
]}

Hazeri, Nourallah ^{[1
]}

Maghsoodlou, Malek Taher ^{[1
]}

Lashkari, Mojtaba ^{[2
]}

Torbati, Niloufar Akbarzadeh ^{[1
]}

Garcia-Granda, Santiago ^{[3
]}

Torre-Fernandez, Laura ^{[3
]}

机构：

[1] Univ Sistan & Baluchestan, Fac Sci, Dept Chem, POB 98135-674, Zahedan, Iran

[2] Velayat Univ, Fac Sci, Iranshahr, Iran

[3] Univ Oviedo, Dept Phys & Analyt Chem, CINN, Oviedo, Spain

来源：

JOURNAL OF THE CHILEAN CHEMICAL SOCIETY | 2018年 / 63卷 / 04期

关键词：

Aromatic aldehydes; Aromatic amines; Meidrum's acid; Dispiro compounds; MULTICOMPONENT REACTIONS; ACETYLENIC ESTERS; ALKYL ISOCYANIDES; TETRAHYDROQUINOLINES; CONSTRUCTION; DERIVATIVES; SEQUENCE;

D O I：

10.4067/S0717-97072018000404159

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Salicylic acid was used as an efficient catalyst for the diastereoselective synthesis of dispirohydroquinoline-bis (Meldrim's acid) derivatives via a one-pot domino eight-component reaction of arylamines, aromatic aldehydes and Meldrum's acid in CH3CN at room temperature. The remarkable advantages offered by this method are inexpensive catalyst, good yields, simple and easy work-up procedure. The characterization of products was done by IR, mass, H-1 NMR, C-13 NMR spectroscopy, and elemental analyses. The stereoselectivity of compounds was confirmed with crystallography and NMR spectroscopy.

引用

页码：4159 / 4164

页数：6

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