Expanding the Chemical Space of Electrophilic β-Glycosyl β-Lactams through Photoinduced Diastereoselective Functionalization-Reference-Cited by-同舟云学术

Expanding the Chemical Space of Electrophilic β-Glycosyl β-Lactams through Photoinduced Diastereoselective Functionalization

Published:2024-06-20 Issue:26 Volume:26 Page:5500-5505
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Tordato Éverton A.¹,Gonçalves Renan O.¹,Baldassari Lucas L.¹²,Jiménez Claudio A.³^ORCID,Lüdtke Diogo S.²^ORCID,Paixão Márcio W.¹^ORCID

Affiliation:

1. Laboratory for Sustainable Organic Synthesis and Catalysis - Chemistry Department − Federal University of São Carlos − UFSCar, São Carlos, São Paulo 13565-905, Brazil

2. Institute of Chemistry, Federal University of Rio Grande do Sul - UFRGS, Porto Alegre, Rio Grande do Sul 91501-970, Brazil

3. Department of Organic Chemistry, Faculty of Chemical Sciences, Universidad de Concepción, Concepción 4130000, Chile

Funder

Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico

Funda??o de Amparo ? Pesquisa do Estado do Rio Grande do Sul

Funda??o de Amparo ? Pesquisa do Estado de S?o Paulo

Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior

Instituto Nacional de Ci?ncia e Tecnologia de Cat?lise em Sistemas Moleculares e Nanoestruturados

Agencia Nacional de Investigaci?n y Desarrollo

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01844

Reference42 articles.

1. β-Lactams as Versatile Synthetic Intermediates for the Preparation of Heterocycles of Biological Interest

2. β-Lactams: Versatile Building Blocks for the Stereoselective Synthesis of Non-β-Lactam Products

3. Advances in the Use of Enantiopure β-Lactams for the Synthesis of Biologically Active Compounds of Medicinal Interests

4. The Never-Ending Story of β-Lactams: Use as Molecular Scaffolds and Building Blocks

5. From?-lactams to?- and?-amino acid derived peptides