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High‐Throughput Ligand Screening Enables the Enantioselective Conjugate Borylation of Cyclobutenones to Access Synthetically Versatile Tertiary Cyclobutylboronates.
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- Angewandte Chemie, 2019, v. 131, n. 51, p. 18576, doi. 10.1002/ange.201909308
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- Article
Boronsäuren als bioorthogonale Sonden für zentrenselektives Protein‐Labeling.
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- Angewandte Chemie, 2018, v. 130, n. 40, p. 13210, doi. 10.1002/ange.201712611
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- Article
Diastereocontrolled Monoprotodeboronation of β‐Sulfinimido gem‐Bis(boronates): A General and Stereoselective Route to α,β‐Disubstituted β‐Aminoalkylboronates.
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- Angewandte Chemie, 2018, v. 130, n. 32, p. 10461, doi. 10.1002/ange.201804277
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- Article
Fast and Tight Boronate Formation for Click Bioorthogonal Conjugation.
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- Angewandte Chemie, 2016, v. 128, n. 12, p. 3977, doi. 10.1002/ange.201510321
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- Article
Catalytic enantioselective transformations of borylated substrates: Preparation and synthetic applications of chiral alkylboronates.
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- Pure & Applied Chemistry, 2012, v. 84, n. 11, p. 2263, doi. 10.1351/PAC-CON-12-02-04
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- Article
Boronic Acids as Bioorthogonal Probes for Site‐Selective Labeling of Proteins.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 40, p. 13028, doi. 10.1002/anie.201712611
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- Article
Diastereocontrolled Monoprotodeboronation of β‐Sulfinimido gem‐Bis(boronates): A General and Stereoselective Route to α,β‐Disubstituted β‐Aminoalkylboronates.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 32, p. 10304, doi. 10.1002/anie.201804277
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- Publication type:
- Article
Fast and Tight Boronate Formation for Click Bioorthogonal Conjugation.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 12, p. 3909, doi. 10.1002/anie.201510321
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- Article
Concise Synthesis and Antimalarial Activity of All Four Mefloquine Stereoisomers Using a Highly Enantioselective Catalytic Borylative Alkene Isomerization.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 31, p. 8069, doi. 10.1002/anie.201303931
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- Article
Combinatorial chemistry gives cell biology some muscle.
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- Nature Biotechnology, 2000, v. 18, n. 3, p. 261, doi. 10.1038/73684
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- Article
Suppressing Protodeboronation in Cu‐Mediated <sup>19</sup>F/<sup>18</sup>F‐Fluorination of Arylboronic Acids: A Mechanistically Guided Approach Towards Optimized PET Probe Development.
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- Chemistry - A European Journal, 2024, v. 30, n. 55, p. 1, doi. 10.1002/chem.202400906
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- Article
Concise Synthesis and Antimalarial Activity of All Four Mefloquine Stereoisomers Using a Highly Enantioselective Catalytic Borylative Alkene Isomerization.
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- Angewandte Chemie, 2013, v. 125, n. 31, p. 8227, doi. 10.1002/ange.201303931
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- Publication type:
- Article
Boronic Acid Catalysis as a Mild and Versatile Strategy for Direct Carbo- and Heterocyclizations of Free Allylic Alcohols.
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- Angewandte Chemie, 2012, v. 124, n. 25, p. 6291, doi. 10.1002/ange.201201620
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- Article
Recent Advances in the Luminescence of Arylboronic Acids and their Heteroatom Condensates.
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- ChemPhotoChem, 2022, v. 6, n. 6, p. 1, doi. 10.1002/cptc.202100219
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- Article
Direct nucleophilic and electrophilic activation of alcohols using a unified boron-based organocatalyst scaffold.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38228-8
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- Article
A Pipeline for Screening Small Molecules with Growth Inhibitory Activity against Burkholderia cenocepacia.
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- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128587
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- Article
Direct Boronic Acid Promoted Amidation of Carboxylic Acids with Poorly Nucleophilic Amines.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 41, p. 1, doi. 10.1002/ejoc.202201050
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- Article
Phenoxy‐Dialkoxy Borates as a New Class of Readily Prepared Preactivated Reagents for Base‐Free Cross‐Coupling.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 38, p. 6566, doi. 10.1002/ejoc.201900993
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- Article
Direct Sulfonamidation of Primary and Secondary Benzylic Alcohols Catalyzed by a Boronic Acid/Oxalic Acid System.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 38, p. 5729, doi. 10.1002/ejoc.201700621
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- Article
Chiral α-substituted allylboronates in a one-pot three-component asymmetric allylic alkylation/carbonyl allylation reaction sequence — Applications to the syntheses of (+)-(3R,5R)-3-hydroxy-5-decanolide and (–)-massoialactone.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 5, p. 650, doi. 10.1139/V09-036
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- Article
Nano-Delivery of a Novel Inhibitor of Polynucleotide Kinase/Phosphatase (PNKP) for Targeted Sensitization of Colorectal Cancer to Radiation-Induced DNA Damage.
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- Frontiers in Oncology, 2021, v. 11, p. 1, doi. 10.3389/fonc.2021.772920
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- Article
Divergent Synthesis of 1,2,3,4‐Tetrasubstituted Cyclobutenes from a Common Scaffold: Enantioselective Desymmetrization by Dual‐Catalyzed Photoredox Cross‐Coupling.
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- Angewandte Chemie, 2023, v. 135, n. 49, p. 1, doi. 10.1002/ange.202313503
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- Article
Synthesis of chiral heterocycles by ligand-controlled regiodivergent and enantiospecific Suzuki Miyaura cross-coupling.
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- Nature Communications, 2014, v. 5, n. 11, p. 5474, doi. 10.1038/ncomms6474
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- Article
Divergent Synthesis of 1,2,3,4‐Tetrasubstituted Cyclobutenes from a Common Scaffold: Enantioselective Desymmetrization by Dual‐Catalyzed Photoredox Cross‐Coupling.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 49, p. 1, doi. 10.1002/anie.202313503
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- Publication type:
- Article
High‐Throughput Ligand Screening Enables the Enantioselective Conjugate Borylation of Cyclobutenones to Access Synthetically Versatile Tertiary Cyclobutylboronates.
- Published in:
- Angewandte Chemie International Edition, 2019, v. 58, n. 51, p. 18405, doi. 10.1002/anie.201909308
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- Publication type:
- Article
Boronic Acid Catalysis for Mild and Selective [3+2] Dipolar Cycloadditions to Unsaturated Carboxylic Acids.
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- Chemistry - A European Journal, 2010, v. 16, n. 18, p. 5454, doi. 10.1002/chem.200903484
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- Article
Catalytic Enantioselective Three-Component Hetero-[4+2] Cycloaddition/Allylboration Approach to α-Hydroxyalkyl Pyrans: Scope, Limitations, and Mechanistic Proposal.
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- Chemistry - A European Journal, 2006, v. 12, n. 11, p. 3132
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- Article
Modular Solid-Phase Synthetic Approach To Optimize Structural and Electronic Properties of Oligoboronic Acid Receptors and Sensors for the Aqueous Recognition of Oligosaccharides.
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- Chemistry - A European Journal, 2004, v. 10, n. 1, p. 92, doi. 10.1002/chem.200305400
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- Article
A Three-Component Reaction for Diversity-Oriented Synthesis of Polysubstituted Piperidines: Solution and Solid-Phase Optimization of the First Tandem Aza[4+2]/Allylboration.
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- Chemistry - A European Journal, 2003, v. 9, n. 2, p. 466, doi. 10.1002/chem.200390049
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- Article
Multistep Phase-Switch Synthesis by Using Liquid-Liquid Partitioning of Boronic Acids: Productive Tags with an Expanded Repertoire of Compatible Reactions.
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- Angewandte Chemie, 2010, v. 122, n. 16, p. 2945, doi. 10.1002/ange.200906710
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- Article
Totalsynthese von Vinigrol: Komplexität durch Fragmentierung.
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- Angewandte Chemie, 2010, v. 122, n. 13, p. 2336, doi. 10.1002/ange.200906826
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- Article
Design, Synthesis, and Screening of a Library of Peptidyl Bis(Boroxoles) as Oligosaccharide Receptors in Water: Identification of a Receptor for the Tumor Marker TF-Antigen Disaccharide.
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- Angewandte Chemie, 2010, v. 122, n. 8, p. 1534, doi. 10.1002/ange.200906620
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- Article
Catalytic Enantioselective and Catalyst-Controlled Diastereofacial-Selective Additions of Allyl- and Crotylboronates to Aldehydes Using Chiral Brønsted AcidsAcknowledgement for financial support is given to the Natural Sciences and Engineering Research Council (NSERC) of Canada (Discovery Grant to D.G.H.), the Donors of the American Chemical Society Petroleum Research Funds (PRF-AC Grant to D.G.H.), and the University of Alberta. V.R. thanks the Alberta Ingenuity Foundation for a Graduate Scholarship. The authors are grateful to Glen Bigam and Mark Miskolzie for help in the variable-temperature NMR studies.
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- Angewandte Chemie, 2006, v. 118, n. 15, p. 2486, doi. 10.1002/ange.200504432
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- Article
Three-Component Sequential Aza[4+2] Cycloaddition/Allylboration/Retro-Sulfinyl-Ene Reaction: A New Stereocontrolled Entry to Palustrine Alkaloids and Other 2,6-Disubstituted Piperidines ( Financial support for this research by the Natural Sciences and Engineering Research Council (NSERC) of Canada (Discovery Grant to D.G.H.) and the University of Alberta is gratefully acknowledged. B.B.T. thanks the Canadian Institutes for Health Research (CIHR) for a graduate scholarship. The authors thank Melissa Chee for help in the preparation of intermediates. )
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- Angewandte Chemie, 2004, v. 116, n. 15, p. 2035, doi. 10.1002/ange.200353152
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- Article
Aktivierung von Bor- und Siliciumreagentien bei stereokontrollierten Allylierungen.
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- Angewandte Chemie, 2003, v. 115, n. 39, p. 4880, doi. 10.1002/ange.200301632
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- Article
Synthetic Studies Towards the Core Tricyclic Ring System of Pradimicin A.
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- European Journal of Organic Chemistry, 2012, v. 2012, n. 22, p. 4153, doi. 10.1002/ejoc.201200294
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- Publication type:
- Article
Catalytic Enantioselective and Catalyst-Controlled Diastereofacial-Selective Additions of Allyl- and Crotylboronates to Aldehydes Using Chiral Brønsted AcidsAcknowledgement for financial support is given to the Natural Sciences and Engineering Research Council (NSERC) of Canada (Discovery Grant to D.G.H.), the Donors of the American Chemical Society Petroleum Research Funds (PRF-AC Grant to D.G.H.), and the University of Alberta. V.R. thanks the Alberta Ingenuity Foundation for a Graduate Scholarship. The authors are grateful to Glen Bigam and Mark Miskolzie for help in the variable-temperature NMR studies.
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 15, p. 2426, doi. 10.1002/anie.200504432
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- Publication type:
- Article
Three-Component Sequential Aza[4+2] Cycloaddition/Allylboration/Retro-Sulfinyl-Ene Reaction: A New Stereocontrolled Entry to Palustrine Alkaloids and Other 2,6-Disubstituted Piperidines ( Financial support for this research by the Natural Sciences and Engineering Research Council (NSERC) of Canada (Discovery Grant to D.G.H.) and the University of Alberta is gratefully acknowledged. B.B.T. thanks the Canadian Institutes for Health Research (CIHR) for a graduate scholarship. The authors thank Melissa Chee for help in the preparation of intermediates. )
- Published in:
- Angewandte Chemie International Edition, 2004, v. 43, n. 15, p. 2001, doi. 10.1002/anie.200353152
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- Publication type:
- Article
Recent Advances in the Activation of Boron and Silicon Reagents for Stereocontrolled Allylation Reactions.
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- Angewandte Chemie International Edition, 2003, v. 42, n. 39, p. 4732, doi. 10.1002/anie.200301632
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- Article
N, N-Diethanolaminomethyl Polystyrene: An Efficient Solid Support to Immobilize Boronic Acids.
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- Angewandte Chemie International Edition, 1999, v. 38, n. 20, p. 3064, doi. 10.1002/(SICI)1521-3773(19991018)38:20<3064::AID-ANIE3064>3.0.CO;2-T
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- Article
Diazaboryl‐naphthyl‐ketone: A New Scaffold with Bright Fluorescence, Aggregation‐Induced Emission, and Application in the Quantitation of Trace Boronic Acids in Drug Intermediates.
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- Chemistry - A European Journal, 2020, v. 26, n. 63, p. 14324, doi. 10.1002/chem.202003248
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- Article
Synthesis and Applications of β‐Aminoalkylboronic Acid Derivatives.
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- Advanced Synthesis & Catalysis, 2021, v. 363, n. 9, p. 2209, doi. 10.1002/adsc.202000690
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- Article
C-C bond formation: Rethinking cross-coupling.
- Published in:
- Nature Chemistry, 2014, v. 6, n. 7, p. 561, doi. 10.1038/nchem.1983
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- Article
Enantioselective preparation and chemoselective cross-coupling of 1,1-diboron compounds.
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- Nature Chemistry, 2013, v. 5, n. 7, p. 634, doi. 10.1038/nchem.1679
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- Article
Enantioselective preparation and chemoselective cross-coupling of 1,1-diboron compounds.
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- Nature Chemistry, 2011, v. 3, n. 11, p. 894, doi. 10.1038/nchem.1150
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- Article
Reaction Optimization, Scalability, and Mechanistic Insight on the Catalytic Enantioselective Desymmetrization of 1,1-Diborylalkanes via Suzuki-Miyaura Cross-Coupling.
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- Chemistry - A European Journal, 2015, v. 21, n. 52, p. 19186, doi. 10.1002/chem.201406680
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- Publication type:
- Article
A Surprising Substituent Effect Provides a Superior Boronic Acid Catalyst for Mild and Metal-Free Direct Friedel–Crafts Alkylations and Prenylations of Neutral Arenes.
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- Chemistry - A European Journal, 2015, v. 21, n. 11, p. 4218, doi. 10.1002/chem.201500020
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- Publication type:
- Article
Boronic Acid Catalysis as a Mild and Versatile Strategy for Direct Carbo- and Heterocyclizations of Free Allylic Alcohols.
- Published in:
- Angewandte Chemie International Edition, 2012, v. 51, n. 25, p. 6187, doi. 10.1002/anie.201201620
- By:
- Publication type:
- Article
Multistep Phase-Switch Synthesis by Using Liquid-Liquid Partitioning of Boronic Acids: Productive Tags with an Expanded Repertoire of Compatible Reactions.
- Published in:
- Angewandte Chemie International Edition, 2010, v. 49, n. 16, p. 2883, doi. 10.1002/anie.200906710
- By:
- Publication type:
- Article
Fragmentation Enables Complexity in the First Total Synthesis of Vinigrol.
- Published in:
- Angewandte Chemie International Edition, 2010, v. 49, n. 13, p. 2286, doi. 10.1002/anie.200906826
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- Publication type:
- Article