Literature DB >> 28094945

PdII/AgI-Catalyzed Room-Temperature Reaction of γ-Hydroxy Lactams: Mechanism, Scope, and Antistaphylococcal Activity.

Manali Dutta1, Santi M Mandal2, Rupa Pegu1, Sanjay Pratihar1.   

Abstract

The present work reports a PdII/AgI-promoted amidoalkylation reaction involving various γ-hydroxy lactams and C/O/S nucleophiles at room temperature. The dual mode of activation of both the electrophile and nucleophile by in situ generated catalytically active cationic PdII species facilitates the reaction at room temperature. Among the synthesized isoindoline derivatives, three compounds are found to be active against vancomycin and methicillin-resistant S. aureus strain with appreciable MIC values.

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Year:  2017        PMID: 28094945     DOI: 10.1021/acs.joc.6b02378

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Nickel-Catalyzed Amidoalkylation Reaction of γ-Hydroxy Lactams: An Access to 3-Substituted Isoindolinones.

Authors:  Shuo Zhang; Xinhua Shi; Jichao Li; Zitong Hou; Zihe Song; Xiaofeng Su; Dan Peng; Feng Wang; Yitao Yu; Guilong Zhao
Journal:  ACS Omega       Date:  2019-11-05

2.  An Oxidation Study of Phthalimide-Derived Hydroxylactams.

Authors:  Bernard L Adjei; Frederick A Luzzio
Journal:  Molecules       Date:  2022-01-15       Impact factor: 4.411

  2 in total

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