Microwave-enhanced alpha-functionalisation of tetramates

Microwave-enhanced alpha-functionalisation of tetramates

Bicyclic tetramic acids may be efficiently allylated or arylated either directly or via the corresponding triflate, using a microwave-enhanced protocol; under these conditions, the yield and diastereoselectivity are very high. © Georg Thieme Verlag Stuttgart.

Bibliográfalaš dieđut
Váldodahkkit:	Moloney, M, Yaqoob, M
Materiálatiipa:	Journal article
Giella:	English
Almmustuhtton:	2008

Geahča maid

Functionalised bicyclic tetramates derived from cysteine as antibacterial agents.
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Almmustuhtton: (2019)

Chemoselective formation and reaction of densely functionalised bicyclic tetramic acids and their biological activity
Dahkki: Moloney, M, et al.
Almmustuhtton: (2017)

Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives
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Novel chiral skeletons for drug discovery: antibacterial tetramic acids.
Dahkki: Holloway, C, et al.
Almmustuhtton: (2011)

Stereoselectivity in the reduction of bicyclic tetramates
Dahkki: Josa-Cullere;, L, et al.
Almmustuhtton: (2016)

Functionalised polymers by covalent surface modification
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Almmustuhtton: (2008)

Tetramic Acids as Scaffolds: Synthesis, Tautomeric and Antibacterial Behaviour
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Metal binding and its amelioration in tetramates
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Efficient enantioselective synthesis of tetramic acids and lactams from threonine
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A CONCISE APPROACH TO FUNCTIONALIZED, HOMOCHIRAL TETRAMIC ACIDS
Dahkki: Andrews, M, et al.
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Synthesis and antibacterial activity of monocyclic 3-carboxamide tetramic acids
Dahkki: Jeong, Y, et al.
Almmustuhtton: (2013)

Chiral bicyclic tetramates as non-planar templates for chemical library synthesis.
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Almmustuhtton: (2013)

Synthetic access to hydrophilic tetramate derivatives of cysteine
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Almmustuhtton: (2020)

Diastereoselective reduction of the tricarbonyl moiety in bicyclic tetramates giving pyroglutamates
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A chemical method for the convenient surface functionalisation of polymers.
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Synthesis and antibacterial activity of monocyclic 3-carboxamide tetramic acids
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Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids.
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Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids
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Aggregation-resistant alpha-synuclein tetramers are reduced in the blood of Parkinson’s patients
Dahkki: Laura de Boni, et al.
Almmustuhtton: (2024-06-01)

Functionalised bicyclic alcohols by enantioselective alpha-deprotonation-rearrangement of meso-epoxides
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2001)

Natural product inspired antibacterial tetramic acid libraries with dual enzyme inhibition
Dahkki: Jeong, Y, et al.
Almmustuhtton: (2012)

Highly functionalised pyroglutamates by intramolecular aldol reactions: Towards the pyroglutamate skeleton of oxazolomycin
Dahkki: Andrews, MD, et al.
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Spirocyclic tetramates by sequential Knoevenagel and [1,5]-prototropic shift
Dahkki: Josa-Culleré, L, et al.
Almmustuhtton: (2019)

Chemoselectivity and stereoselectivity of cyclisation pathways leading to bicyclic tetramates controlled by ring-chain tautomerisation in thiazolidines.
Dahkki: Panduwawala, T, et al.
Almmustuhtton: (2016)

Functionalised pyrrolidinones derived from (S)-pyroglutamic acid by cycloaddition reactions
Dahkki: Bailey, J, et al.
Almmustuhtton: (1997)

Palladium-catalysed alpha-arylation of esters and amides under microwave conditions
Dahkki: Bentz, E, et al.
Almmustuhtton: (2004)

Antibacterial mimics of natural products by side-chain functionalization of bicyclic tetramic acids
Dahkki: Josa-Cullere, L, et al.
Almmustuhtton: (2018)

Intramolecular aldol ring closures of cysteine derivatives leading to densely functionalised pyroglutamates
Dahkki: Almahli, H, et al.
Almmustuhtton: (2019)

Particulate polyaryletherketones with amine end functionalisation by a Friedel Crafts dispersion polymerisation
Dahkki: Smith, K, et al.
Almmustuhtton: (2016)

Diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin
Dahkki: Heaviside, E, et al.
Almmustuhtton: (2014)

Synthetic access to 3-substituted pyroglutamic acids from tetramate derivatives of serine, threonine, allo-threonine, and cysteine
Dahkki: Bagum, H, et al.
Almmustuhtton: (2019)

Molecular structure of soluble vimentin tetramers
Dahkki: Pieter-Jan Vermeire, et al.
Almmustuhtton: (2023-05-01)

Microfibre-Functionalised Silk Hydrogels
Dahkki: Jirada Kaewchuchuen, et al.
Almmustuhtton: (2023-12-01)

Synthetic access to 3,4-disubstituted pyroglutamates from tetramate derivatives from serine, allo-threonine and cysteine
Dahkki: Bagum, H, et al.
Almmustuhtton: (2019)

Functionalisation of Virus-Like Particles Enhances Antitumour Immune Responses
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Biocompatibility enhancement of graphene oxide‐silver nanocomposite by functionalisation with polyvinylpyrrolidone
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