Por favor, use este identificador para citar o enlazar a este item:
http://hdl.handle.net/10261/156412
COMPARTIR / EXPORTAR:
SHARE BASE | |
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE | |
Título: | Multicomponent reactions in the synthesis of target molecules |
Autor: | Radtke, Lea; Marqués-López, Eugenia CSIC ORCID; Herrera, Raquel P. CSIC ORCID | Palabras clave: | Dihydropyrimidine Spiro compound Fused polyheterocycle Asymmetric catalysis Indole Heterocycle Target molecule Natural product Multicomponent reactions Drug discovery |
Fecha de publicación: | 2015 | Editor: | John Wiley & Sons | Citación: | Multicomponent Reactions: Concepts and Applications for Design and Synthesis (Cap.6): 198-246 (2015) | Resumen: | Multicomponent 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. | URI: | http://hdl.handle.net/10261/156412 | DOI: | 10.1002/9781118863992.ch6 | Identificadores: | doi: 10.1002/9781118863992.ch6 isbn: 9781118016008 |
Aparece en las colecciones: | (ISQCH) Libros y partes de libros |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
---|---|---|---|---|
accesoRestringido.pdf | 15,38 kB | Adobe PDF | Visualizar/Abrir |
CORE Recommender
Page view(s)
416
checked on 19-abr-2024
Download(s)
102
checked on 19-abr-2024
Google ScholarTM
Check
Altmetric
Altmetric
NOTA: Los ítems de Digital.CSIC están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.