2-Halomethyleneoxetanes from 2-Methyleneoxetanes by Reaction with <i>N</i>-Halosuccinimides: Reactant Influences on Stereochemical Outcomes and Reaction Pathways

The first general synthesis of 2-halomethyleneoxetanes, realized by the reaction of 2-methyleneoxetanes with <i>N</i>-halosuccinimides (NXS), is reported. The relative diastereoselectivities of the transformations were dependent on the halogen of NXS, while alternative reaction outcomes were influenced by substituents on the oxetane. Quantum mechanical calculations and molecular dynamics simulations exploring the basis of the observed diastereoselectivities are described. These highly strained heterocycles underwent standard cross-coupling reactions, demonstrating their utility as synthetic intermediates.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-11-05
DOI
https://doi.org/10.1021/acs.joc.4c01877
Citations
4
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.83
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article

2-Halomethyleneoxetanes from 2-Methyleneoxetanes by Reaction with N-Halosuccinimides: Reactant Influences on Stereochemical Outcomes and Reaction Pathways

Amy R. Howell, José A. Gascón, Julia DiSapio, Dennis Sulwey
4 citations
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
0.83
article

2-Halomethyleneoxetanes from 2-Methyleneoxetanes by Reaction with N-Halosuccinimides: Reactant Influences on Stereochemical Outcomes and Reaction Pathways

Amy R. Howell, José A. Gascón, Julia DiSapio, Dennis Sulwey
article en
4 citations

Abstract

The first general synthesis of 2-halomethyleneoxetanes, realized by the reaction of 2-methyleneoxetanes with <i>N</i>-halosuccinimides (NXS), is reported. The relative diastereoselectivities of the transformations were dependent on the halogen of NXS, while alternative reaction outcomes were influenced by substituents on the oxetane. Quantum mechanical calculations and molecular dynamics simulations exploring the basis of the observed diastereoselectivities are described. These highly strained heterocycles underwent standard cross-coupling reactions, demonstrating their utility as synthetic intermediates.

The Journal of Organic ChemistryVol. 89(22)
University of Connecticut (US)
Openalex Percentile: Top 30%
Fluorine in Organic Chemistry
0.83
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2-Halomethyleneoxetanes from 2-Methyleneoxetanes by Reaction with <i>N</i>-Halosuccinimides: Reactant Influences on Stereochemical Outcomes and Reaction Pathways — Amy R. Howell, José A. Gascón, et al. · The Journal of Organic Chemistry (2024) | TGRS Research Map | TGRS