Sulfur- and DABCO-Promoted Reaction between Alkylidene Rhodanines and Isothiocyanates: Access to Aminoalkylidene Rhodanines

被引:4
|
作者
Farajpour, Behnaz [1 ]
Alizadeh, Gul Bahar [1 ]
Majedi, Soma [2 ]
Moradkhani, Fatemeh [3 ]
Majedi, Serveh [4 ]
Notash, Behrouz [5 ]
Hosseindoust, Benyamin [1 ]
Shiri, Morteza [1 ]
机构
[1] Alzahra Univ, Fac Chem, Dept Organ Chem, Tehran 1993893973, Iran
[2] Tishk Int Univ, Appl Sci Fac, Med Anal Dept, Erbil 46001, Kurdistan Regio, Iraq
[3] Univ Tehran Med Sci, Fac Pharm, Pharmaceut Sci Res Ctr, Dept Med Chem, Tehran P94V 8MF, Iran
[4] Payame Noor Univ, Dept Chem, Tehran RG23 F4X, Iran
[5] Shahid Beheshti Univ, Dept Inorgan Chem, Tehran 1983969411, Iran
来源
ACS OMEGA | 2024年 / 9卷 / 24期
基金
美国国家科学基金会;
关键词
DIASTEREOSELECTIVE SYNTHESIS; MICHAEL ADDITION; ONE-POT; CONDENSATION; DERIVATIVES; CONSTRUCTION; PYRAZOLONES; EFFICIENT; KETONES; DESIGN;
D O I
10.1021/acsomega.4c03341
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, an efficient sulfur- and DABCO-promoted reaction for the synthesis of aminoalkylidene rhodanines from available alkylidene rhodanines and isothiocyanates is reported. A tandem process including sulfurative annulation/ring-opening by liberation of a CS2 molecule/olefination allows the synthesis of aminoalkylidene rhodanines with acceptable functional group tolerance. Chemo- and stereoselectivity, operational simplicity, and synthetically useful yields are some highlighted advantages of these transformations.
引用
收藏
页码:26607 / 26615
页数:9
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