Literature DB >> 33459485

Mild C-C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles.

Hai Huang1, Tianyu Zhang1, Jianwei Sun1,2.   

Abstract

Mild oxetane opening by soft carbon nucleophiles has been developed for efficient C-C bond formation. In the presence of LiNTf2 or TBSNTf2 as catalyst, silyl ketene acetals were found to be effective nucleophiles to generate a wide range of highly oxygenated molecules, which are key substructure in natural products like polyketides. Furthermore, intramolecular oxetane opening by a styrene-based carbon nucleophile via a Prins-type process was also achieved with Sc(OTf)3 as catalyst, leading to efficient formation of the useful 2,3-dihydrobenzo[b]oxepine skeleton.
© 2020 Wiley-VCH GmbH.

Entities:  

Keywords:  C−C bond formation; Lewis acids; oxetane; ring opening; strained molecules

Year:  2020        PMID: 33459485     DOI: 10.1002/anie.202013062

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  3 in total

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2.  Unexpected Isomerization of Oxetane-Carboxylic Acids.

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3.  Bioinspired Cobalt-Catalysis Enables Generation of Nucleophilic Radicals from Oxetanes.

Authors:  Aleksandra Potrząsaj; Michał Ociepa; Wojciech Chaładaj; Dorota Gryko
Journal:  Org Lett       Date:  2022-03-25       Impact factor: 6.005

  3 in total

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