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Access to 5-Substituted 3-Aminofuran/Thiophene-2-Carboxylates from Bifunctional Alkynenitriles
Advanced Synthesis & Catalysis ( IF 4.4 ) Pub Date : 2022-05-12 , DOI: 10.1002/adsc.202200305 Chandresh Kumari 1 , Avijit Goswami 2
Advanced Synthesis & Catalysis ( IF 4.4 ) Pub Date : 2022-05-12 , DOI: 10.1002/adsc.202200305 Chandresh Kumari 1 , Avijit Goswami 2
Affiliation
An atom-economical approach for the synthesis of 3-aminofurans/thiophenes via a conjugate addition of alcohols and thiols with electron withdrawing groups (EWGs) at α positions on alkynenitriles followed by a modified Thorpe-Ziegler cyclization have been reported. This operationally simple protocol offers a rapid access to a library of 3-aminofurans/thiophenes in moderate to good yields.
中文翻译:
从双功能炔腈中获得 5-取代的 3-氨基呋喃/噻吩-2-羧酸盐
已经报道了一种通过在炔腈上的 α 位共轭加成具有吸电子基团 (EWG) 的醇和硫醇,然后进行修饰的索普-齐格勒环化来合成 3-氨基呋喃/噻吩的原子经济方法。这种操作简单的协议可快速访问 3-氨基呋喃/噻吩库,产量适中至良好。
更新日期:2022-05-12
中文翻译:
从双功能炔腈中获得 5-取代的 3-氨基呋喃/噻吩-2-羧酸盐
已经报道了一种通过在炔腈上的 α 位共轭加成具有吸电子基团 (EWG) 的醇和硫醇,然后进行修饰的索普-齐格勒环化来合成 3-氨基呋喃/噻吩的原子经济方法。这种操作简单的协议可快速访问 3-氨基呋喃/噻吩库,产量适中至良好。