2,2,2-Trifluoroethanol activated one-pot Mannich-like reaction of β-nitroenamines, secondary amines, and aromatic aldehydes-Reference-Cited by-同舟云学术

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2,2,2-Trifluoroethanol activated one-pot Mannich-like reaction of β-nitroenamines, secondary amines, and aromatic aldehydes

Published:2016-06 Issue:25 Volume:57 Page:2727-2731
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Han Li,Feng Yian,Luo Ming,Yuan Zihao,Shao Xusheng,Xu Xiaoyong,Li Zhong

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference58 articles.

1. Push–pull allenes-conjugation, (anti)aromaticity and quantification of the push–pull character

2. Synthesis of 4-Substituted 3,5-Dinitro-1,4-dihydropyridines by the Self-Condensation of β-Formyl-β-nitroenamine

3. Heterocyclic Ketene Aminals: Scaffolds for Heterocycle Molecular Diversity

4. Novel heterocyclic β-nitroenamines-based on a one-pot three-component reaction: a facile synthesis of fully substituted 1H-pyrrolo[1,2-a]-fused-1,3-diazaheterocycles

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3. Microwave-mediated approach to highly substituted nitropyrimidines via double Mannich reactions and their biological properties;Tetrahedron;2022-08

4. Nitroenediamines (EDAMs), and N-methyl-1-(methylthio)-2-nitroethenamine (NMSM) derivatives: scaffolds for heterocycle molecular diversity (update from 2012 to 2021);RSC Advances;2022

5. Reactions of Aldehydes and Ketones and Their Derivatives;Organic Reaction Mechanisms · 2016;2020-01-13

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