Argitalpenak (17) Davide Bello argitalpenak

2021

  1. Advances in chemical probing of protein: O -GlcNAc glycosylation: Structural role and molecular mechanisms

    Chemical Society Reviews, Vol. 50, Núm. 18, pp. 10451-10485

  2. DNDI-6148: A Novel Benzoxaborole Preclinical Candidate for the Treatment of Visceral Leishmaniasis

    Journal of Medicinal Chemistry, Vol. 64, Núm. 21, pp. 16159-16176

  3. Isolation of 5′-O-sulfamyladenosine and related 3′-O-β-glucosylated adenosines from the nucleocidin producerStreptomyces calvus

    RSC Advances, Vol. 11, Núm. 10, pp. 5291-5294

  4. Multiple unbiased approaches identify oxidosqualene cyclase as the molecular target of a promising anti-leishmanial

    Cell Chemical Biology, Vol. 28, Núm. 5, pp. 711-721.e8

2019

  1. Acetyl Coenzyme A Analogues as Rationally Designed Inhibitors of Citrate Synthase

    ChemBioChem, Vol. 20, Núm. 9, pp. 1174-1182

  2. Two 3′-: O-β-glucosylated nucleoside fluorometabolites related to nucleocidin in Streptomyces calvus

    Chemical Science, Vol. 10, Núm. 41, pp. 9501-9505

2015

  1. Fluorovinyl Thioethers as Putative Steric and Electronic Thioester Enolate Mimetics: Chemoselective HF Addition to Acetylene Thioethers

    Australian Journal of Chemistry, Vol. 68, Núm. 1, pp. 72-79

  2. Hydrofluorination of alkynes catalysed by gold bifluorides

    ChemCatChem, Vol. 7, Núm. 2, pp. 240-244

  3. Lewis acid-promoted hydrofluorination of alkynyl sulfides to generate α-fluorovinyl thioethers

    Beilstein Journal of Organic Chemistry, Vol. 11, pp. 1902-1909

2013

  1. Fluorinated 5- and 7-membered carbacycle motifs by reaction of difluorocarbene with acetylene ethers

    Chemical Communications, Vol. 49, Núm. 22, pp. 2189-2191

2012

  1. Densely substituted unnatural l- and d-prolines as catalysts for highly enantioselective stereodivergent (3 + 2) cycloadditions and aldol reactions

    Chemical Science, Vol. 3, Núm. 5, pp. 1486-1491

2011

  1. Development of inositol-based antagonists for the D-myo-inositol 1,4,5-trisphosphate receptor

    Chemical Communications, Vol. 47, Núm. 1, pp. 242-244

  2. Erratum: Boron-based dipolar multicomponent reactions: Simple generation of substituted aziridines, oxazolidines and pyrrolidines (Chemistry - A European Journal (2010) 16 (7904-7915) DOI: 10.1002/chem.201000349)

    Chemistry - A European Journal

2010

  1. Boron-based dipolar multicomponent reactions: Simple generation of substituted aziridines, oxazolidines and pyrrolidines

    Chemistry - A European Journal, Vol. 16, Núm. 26, pp. 7904-7915

  2. Mechanistic variations of the Povarov multicomponent reaction and related processes

    Current Organic Chemistry, Vol. 14, Núm. 4, pp. 332-356

  3. Streamlined access to functionalized chromenes and quinolines using domino reactions of salicylic aldehydes and methyl 4-chloro-2-butynoate

    European Journal of Organic Chemistry, pp. 5373-5379

2007

  1. Synthesis and biological action of novel 4-position-modified derivatives of D-myo-inositol 1,4,5-trisphosphate

    Journal of Organic Chemistry, Vol. 72, Núm. 15, pp. 5647-5659