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- W234373182 abstract "INTRODUCTION Aza-bicycles are an important scafold because a great number of biological active alkaloids and synthetic analogous belong to this class. 1 Employing enaminones in order to obtain these compounds is strategic, once enaminones are obtained in good yields and can be used to prepare diverse heterocycles. This work evaluates the bicomponent aza-annulation [3+3] reaction between enaminones and Meldrum’s acid derivatives, as well as the trimolecular [3+2+1] and the tetramolecular [3+1+1+1] multicomponent reactions. 2,3" @default.
- W234373182 created "2016-06-24" @default.
- W234373182 creator A5002319379 @default.
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- W234373182 date "2013-09-01" @default.
- W234373182 modified "2023-09-24" @default.
- W234373182 title "Aza-bicycles Synthesis Through Formal Aza [3+3], [3+2+1] and [3+1+1+1] Cycloadditions Between Enaminones, Aldehydes and Meldrum’s Acid Derivatives." @default.
- W234373182 doi "https://doi.org/10.5151/chempro-14bmos-r0056-1" @default.
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