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A dynamic supramolecular polyurethane network whose mechanical properties are kinetically controlled

Polymer (Guilford), 2017-12, Vol.133, p.143-150

2017

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Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis

Scientific reports, 2018-04, Vol.8 (1), p.6541-16, Article 6541

2018

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Synthesis of azetidines and pyrrolidines via iodocyclisation of homoallyl amines and exploration of activity in a zebrafish embryo assay

Organic & biomolecular chemistry, 2013-08, Vol.11 (31), p.5083-5093

2013

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Palladium and Platinum 2,4- cis -amino Azetidine and Related Complexes

Frontiers in chemistry, 2018-06, Vol.6, p.211-211

2018

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Metabolism and Bioactivation: It’s Time to Expect the Unexpected: Miniperspective

Journal of medicinal chemistry, 2020-06, Vol.63 (12), p.6303-6314

2020

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A Thermoreversible Supramolecular Polyurethane with Excellent Healing Ability at 45 °C

Macromolecules, 2015-09, Vol.48 (17), p.6132-6141

2015

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Effect of temperature and strain rate on the compressive behaviour of supramolecular polyurethane

EPJ Web of Conferences, 2015, Vol.94, p.1046

2015

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Metabolism and Bioactivation: It's Time to Expect the Unexpected

Journal of medicinal chemistry, 2020-06

2020

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Base and solvent dependency of an oxidative retro-alkylation of secondary and tertiary benzylamines

RSC advances, 2013-01, Vol.3 (16), p.5370

2013

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Diastereoselective Preparation of Azetidines and Pyrrolidines

Organic letters, 2010-11, Vol.12 (21), p.5044-5047

2010

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High-resolution within-sewer SARS-CoV-2 surveillance facilitates informed intervention

Water research (Oxford), 2021-10, Vol.204, p.117613-117613, Article 117613

2021

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An adhesive elastomeric supramolecular polyurethane healable at body temperature

Chemical science (Cambridge), 2016-01, Vol.7 (7), p.4291-4300

2016

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Self-immolative systems for the disclosure of reactive electrophilic alkylating agents

Chemical communications (Cambridge, England), 2019-05, Vol.55 (36), p.5219-5222

2019

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Self-immolative systems for the disclosure of reactive electrophilic alkylating agentsElectronic supplementary information (ESI) available: Detailed experimental procedures and spectroscopic data for disclosure molecules 1-3. NMR spectra and kinetic curves for alkylation/β-elimination reactions. NMR spectrum of the degradation study for the disclosure molecule 3. UV-visible spectrum for disclosure molecule 3 and UV-visible spectra for alkylation/β-elimination reactions using disclosure molecule

2019-04

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Azetidines Kill Multidrug-Resistant Mycobacterium tuberculosis without Detectable Resistance by Blocking Mycolate Assembly

Journal of medicinal chemistry, 2024-02, Vol.67 (4), p.2529-2548

2024

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A systematic study of the effect of the hard end-group composition on the microphase separation, thermal and mechanical properties of supramolecular polyurethanes

Polymer (Guilford), 2016-12, Vol.107, p.368-378

2016

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An adhesive elastomeric supramolecular polyurethane healable at body temperatureElectronic supplementary information (ESI) available: Synthesis and experimental details, spectroscopic and crystallographic data, binding constant determination, differential scanning calorimetric data, rheological data and stress-strain profiles. See DOI: 10.1039/c5sc04864h

2016-06

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An adhesive elastomeric supramolecular polyurethane healable at body temperature† †Electronic supplementary information (ESI) available: Synthesis and experimental details, spectroscopic and crystallographic data, binding constant determination, differential scanning calorimetric data, rheological data and stress–strain profiles. See DOI: 10.1039/c5sc04864h

Chemical science (Cambridge), 2016-03, Vol.7 (7), p.4291-4300

2016

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Synthesis of azetidines and pyrrolidines: towards medicinal chemistry and organocatalysis applications

Feula, Antonio

2013

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Synthesis of azetidines and pyrrolidines via iodocyclisation of homoallyl amines and exploration of activity in a zebrafish embryo assayElectronic supplementary information (ESI) available: General and experimental chemical procedures, biological procedures and statistics and X-ray crystallographic information are available. CCDC 936733. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c3ob41007b

2013-08

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Synthesis of azetidines and pyrrolidines viaiodocyclisation of homoallyl amines and exploration of activity in a zebrafish embryo assay

Organic & biomolecular chemistry, 2013-08, Vol.11 (31), p.5083-5093

2013

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A dynamic supramolecular polyurethane network whose mechanical properties are kinetically controlled

Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis

Synthesis of azetidines and pyrrolidines via iodocyclisation of homoallyl amines and exploration of activity in a zebrafish embryo assay

Palladium and Platinum 2,4- cis -amino Azetidine and Related Complexes

Metabolism and Bioactivation: It’s Time to Expect the Unexpected: Miniperspective

A Thermoreversible Supramolecular Polyurethane with Excellent Healing Ability at 45 °C

Effect of temperature and strain rate on the compressive behaviour of supramolecular polyurethane

Metabolism and Bioactivation: It's Time to Expect the Unexpected

Base and solvent dependency of an oxidative retro-alkylation of secondary and tertiary benzylamines

Diastereoselective Preparation of Azetidines and Pyrrolidines

High-resolution within-sewer SARS-CoV-2 surveillance facilitates informed intervention

An adhesive elastomeric supramolecular polyurethane healable at body temperature

Self-immolative systems for the disclosure of reactive electrophilic alkylating agents

Azetidines Kill Multidrug-Resistant Mycobacterium tuberculosis without Detectable Resistance by Blocking Mycolate Assembly

A systematic study of the effect of the hard end-group composition on the microphase separation, thermal and mechanical properties of supramolecular polyurethanes

Effectiveness of building-level sewage surveillance during both community-spread and sporadic-infection phases of SARS-CoV-2 in a university campus population

Synthesis of azetidines and pyrrolidines: towards medicinal chemistry and organocatalysis applications

Synthesis of azetidines and pyrrolidines viaiodocyclisation of homoallyl amines and exploration of activity in a zebrafish embryo assay

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