Utilize este identificador para referenciar este registo: https://hdl.handle.net/10316/107438
Título: Recent Advances in the Synthesis of Spiro‐β‐Lactams and Spiro‐δ‐Lactams
Autor: Alves, Nuno Guerreiro 
Alves, Américo J. S. 
Soares, Maria I. L. 
Pinho e Melo, Teresa M. V. D. 
Palavras-chave: β-lactams; δ-lactams; spiro-β-lactams; spiro-δ-lactams; penicillanates; spirocyclization
Data: 2021
Editora: Wiley Online Library
Projeto: info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB/00313/2020/PT/Coimbra Chemistry Center 
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP/00313/2020/PT/Coimbra Chemistry Center 
info:eu-repo/grantAgreement/FCT/POR_CENTRO/PD/BD/135287/2017/PT/Broadening the spectrum of spito-B-lactams antiviral activity: from new targets identification to the discovery of new compounds with anti-influenza activity. 
info:eu-repo/grantAgreement/FCT/OE/SFRH/BD/128910/2017/PT/Novel spiro-lactams as new antimicrobial agents 
Título da revista, periódico, livro ou evento: Advanced Synthesis & Catalysis
Volume: 363
Número: 10
Resumo: Spirocyclic molecules are widely recognized for their complex three-dimensional features and structural rigidity. Among this class of molecules, the spiro-lactams subclass stands out, being extensively explored due to its bioactivity and utility in a variety of scientific fields such as drug design and organic synthesis. Given the recognition of spirocyclic lactams’ broad potential, several efforts have been engaged on the pursuit of new synthetic strategies towards these molecules. The present review gathers advances on the synthesis of both spiro- β-lactams (spiroazetidin-2-ones) and spiro-δ-lactams (spiropiperidon-2-ones) reported since 2015. The work is divided into two distinct parts, each one dedicated to one of these types of spiro-lactam, with the approach used for building the spirocyclic system being extensively discussed, according to the method’s scope, efficiency, selectivity, and reaction mechanism.
URI: https://hdl.handle.net/10316/107438
ISSN: 1615-4150
1615-4169
DOI: 10.1002/adsc.202100013
Direitos: embargoedAccess
Aparece nas coleções:I&D CQC - Artigos em Revistas Internacionais

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