Organocatalytic Cascade Reactions for the Synthesis and Diversification of Privileged Structures
Open Access
- 14 November 2024
- conference paper
- Published by MDPI AG in Chemistry Proceedings
- Vol. 16 (1) , 72
Abstract
Herein, we present the development of new organocatalytic cascade reactions for the synthesis and diversification of privileged structures, using trienamine activation as a key step. An important feature of this process is that once it is completed, it is possible to generate new reactive species within the same molecule. In this sense, a series of consecutive reactions can be carried out, incorporating dienophiles with a nucleophilic addition functionality. As a result, complex and diverse compounds can be accessed through simple starting materials.Keywords
Funding Information
- Ciencia Básica y de Frontera 2023–2024 (BF2023-2024-266, 150/2024, 090/2024)
- DAIP-UG (BF2023-2024-266, 150/2024, 090/2024)
This publication has 3 references indexed in Scilit:
- Organocatalytic Cascade Reactions for the Diversification of Thiopyrano‐Piperidone Fused Rings Utilizing Trienamine ActivationChemistry – A European Journal, 2020
- Aminocatalytic Privileged Diversity‐Oriented Synthesis (ApDOS): An Efficient Strategy to Populate Relevant Chemical SpacesEuropean Journal of Organic Chemistry, 2018
- Organocatalytic cascade reactions: diversity-oriented synthesis for the construction of hydroisoquinoline scaffoldsChemical Communications, 2014