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Direct and cost-efficient hyperpolarization of long-lived nuclear spin states on universal 15N2-diazirine molecular tags
TLDR
This work uses a recently developed method, SABRE-SHEATH, to directly hyperpolarize 15N 2 magnetization and long-lived 15N2 singlet spin order, with signal decay time constants of 5.8 and 23 minutes, respectively.
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Generalizing, Extending, and Maximizing Nitrogen-15 Hyperpolarization Induced by Parahydrogen in Reversible Exchange
TLDR
The heteronuclear variant introduced as SABRE-SHEATH (SABRE in SHield Enables Alignment Transfer to Heteronuclei) and nitrogen-15 targets in particular are focused on, showing that 15N-SABRE works more efficiently and on a wider range of substrates than 1H-SA BRE, greatly generalizing the SABre approach.
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Synthesis of ortho-haloaminoarenes by aryne insertion of nitrogen-halide bonds.
A rapid and general access to ortho-haloaminoarenes has been developed by aryne insertion into N-chloramine, N-bromoamine, and N-iodoamine bonds via two complementary protocols harnessing…
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Diazirines as Potential Molecular Imaging Tags: Probing the Requirements for Efficient and Long-Lived SABRE-Induced Hyperpolarization.
TLDR
The generality of this approach is shown by illustrating that the diazirine tag alone is sufficient for achieving excellent signal enhancements with long-lasting polarization, and reveals the critical role of Lewis basic additives, including water, on achieving SABRE-promoted hyperpolarization.
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Histone Acetylation and Deacetylation
TLDR
The acetylation and deacetylation of the N-terminal tails of histones (the core protein component of chromatin) represents an important epigenetic mechanism which affects chromatin structure and, ultimately genomic response, via gene expression.
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Luminescent Cu4I4-Cu3(Pyrazolate)3 Coordination Frameworks: Postsynthetic Ligand Substitution Leads to Network Displacement and Entanglement.
TLDR
This work has successfully implemented the single-site substitution of Cu4I4-based coordination frameworks by taking advantage of the solvent-assisted ligand substitution strategy recently developed in metal-organic framework (MOF) chemistry.
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Copper-Catalyzed Alkene Aminoazidation as a Rapid Entry to 1,2-Diamines and Installation of an Azide Reporter onto Azahetereocycles.
  • Kun Shen, Qiu Wang
  • Chemistry, Biology
    Journal of the American Chemical Society
  • 5 September 2017
TLDR
A copper-catalyzed aminoazidation of unactivated alkenes is achieved for the synthesis of versatile unsymmetrical 1,2-diamine derivatives, providing an efficient strategy to introduce azide, one of the most useful chemical reporters, onto a broad range of bioactive azaheterocycles, offering new opportunities in bioorthogonal chemistry and biological studies.
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Selective α-amination and α-acylation of esters and amides via dual reactivity of O-acylhydroxylamines toward zinc enolates.
TLDR
Introduction of a copper catalyst into the system shifts the reactivity entirely, yielding α-amination products exclusively, and treatment of zinc enolates with O-acylhydroxylamines provides solely 1,3-dicarbonyl compounds under mild conditions.
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Copper-catalyzed electrophilic amination of heteroarenes and arenes by C-H zincation.
TLDR
Direct amination of heteroarenes and arenes has been achieved in a one-pot CH zincation/copper-catalyzed electrophilic amination procedure, demonstrating its great potential for the synthesis of important and complex amines.
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Copper-Catalyzed Amino Lactonization and Amino Oxygenation of Alkenes Using O-Benzoylhydroxylamines.
A copper-catalyzed amino lactonization of unsaturated carboxylic acids has been achieved as well as the analogous intermolecular three-component amino oxygenation of olefins. The transformation…
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