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Título

Multicomponent reactions in the synthesis of target molecules

AutorRadtke, Lea; Marqués-López, Eugenia CSIC ORCID; Herrera, Raquel P. CSIC ORCID
Palabras claveDihydropyrimidine
Spiro compound
Fused polyheterocycle
Asymmetric catalysis
Indole
Heterocycle
Target molecule
Natural product
Multicomponent reactions
Drug discovery
Fecha de publicación2015
EditorJohn Wiley & Sons
CitaciónMulticomponent Reactions: Concepts and Applications for Design and Synthesis (Cap.6): 198-246 (2015)
ResumenMulticomponent reactions are a powerful tool in the synthesis of complex target molecules because multiple bonds are effectively built up in one step from relatively simple building blocks. They introduce molecular diversity in only one step and do so in a highly efficient and convergent manner. Heterocycles are structural motifs that are often found in bioactive molecules or drugs, therefore the high yielding and fewer steps synthesis of these compounds is of great interest for Medicinal Chemistry. Here, we will discuss some multicomponent strategies to synthesize heterocycles like indoles, pyrroles, spiro-type polyheterocycles, fused polyheterocycles, dihydropyrimidines, thiazines, as well as amino acids.
URIhttp://hdl.handle.net/10261/156412
DOI10.1002/9781118863992.ch6
Identificadoresdoi: 10.1002/9781118863992.ch6
isbn: 9781118016008
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