Works by Fokin, Valery V.
Results: 46
Copper(I)-Catalyzed Cycloaddition of Organic Azides and 1-Iodoalkynes.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 43, p. 8018, doi. 10.1002/anie.200903558
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- Article
Iterative In Situ Click Chemistry Creates Antibody-like Protein-Capture Agents.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 27, p. 4944, doi. 10.1002/anie.200900488
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- Article
Ruthenium-Catalyzed Cycloaddition of Nitrile Oxides and Alkynes: Practical Synthesis of Isoxazoles.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 43, p. 8285, doi. 10.1002/anie.200801920
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- Article
Copper-Catalyzed Synthesis of N-Sulfonyl-1,2,3-triazoles: Controlling Selectivity.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 10, p. 1730, doi. 10.1002/anie.200604241
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- Article
Rapid Diversity-Oriented Synthesis in Microtiter Plates for In Situ Screening of HIV Protease Inhibitors.
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- ChemBioChem, 2003, v. 4, n. 11, p. 1246, doi. 10.1002/cbic.200300724
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- Article
Click chemistry-facilitated comprehensive identification of proteins adducted by antimicrobial 5-nitroimidazoles for discovery of alternative drug targets against giardiasis.
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- PLoS Neglected Tropical Diseases, 2020, v. 14, n. 4, p. 1, doi. 10.1371/journal.pntd.0008224
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- Article
Osmium-Catalyzed Dihydroxylation of Olefins in Acidic Media: Old Process, New Tricks.
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- Advanced Synthesis & Catalysis, 2002, v. 344, n. 3/4, p. 421, doi. 10.1002/1615-4169(200206)344:3/4<421::AID-ADSC421>3.0.CO;2-F
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- Article
From BACE1 Inhibitor to Multifunctionality of Tryptoline and Tryptamine Triazole Derivatives for Alzheimer's Disease.
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- Molecules, 2012, v. 17, n. 7, p. 8312, doi. 10.3390/molecules17078312
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- Article
Sulfuryl Fluoride Mediated Synthesis of Amides and Amidines from Ketoximes via Beckmann Rearrangement.
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- Chemistry - A European Journal, 2020, v. 26, n. 46, p. 10402, doi. 10.1002/chem.201905358
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- Article
Reversal of Tabun Toxicity Enabled by a Triazole‐Annulated Oxime Library—Reactivators of Acetylcholinesterase.
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- Chemistry - A European Journal, 2019, v. 25, n. 16, p. 4100, doi. 10.1002/chem.201805051
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- Article
Sulfuryl Fluoride Mediated Conversion of Aldehydes to Nitriles.
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- Chemistry - A European Journal, 2019, v. 25, n. 8, p. 1906, doi. 10.1002/chem.201805175
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- Article
Sulfonyl-1,2,3-Triazoles: Convenient Synthones for Heterocyclic Compounds.
- Published in:
- Angewandte Chemie, 2013, v. 125, n. 5, p. 1547, doi. 10.1002/ange.201206388
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- Article
Ring Expansion and Rearrangements of Rhodium(II) Azavinyl Carbenes.
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- Angewandte Chemie, 2012, v. 124, n. 52, p. 13231, doi. 10.1002/ange.201207820
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- Article
Halogen Exchange (Halex) Reaction of 5-Iodo-1,2,3-triazoles: Synthesis and Applications of 5-Fluorotriazoles.
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- Angewandte Chemie, 2012, v. 124, n. 47, p. 11961, doi. 10.1002/ange.201204979
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- Article
Click and Pick: Identification of Sialoside Analogues for Siglec-Based Cell Targeting.
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- Angewandte Chemie, 2012, v. 124, n. 44, p. 11176, doi. 10.1002/ange.201205831
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- Article
Practical Synthesis of Amides from In Situ Generated Copper(I) Acetylides and Sulfonyl AzidesWe thank the National Institutes of Health, the National Institute of General Medical Sciences (GM28384), the Skaggs Institute for Chemical Biology, and Pfizer, Inc. for financial support. We also thank Prof. K. B. Sharpless, Prof. M. G. Finn, and Dr. M. Whiting for valuable advice and stimulating discussions.
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- Angewandte Chemie, 2006, v. 118, n. 19, p. 3226, doi. 10.1002/ange.200503805
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- Article
Copper-Catalyzed Reaction Cascade: Direct Conversion of Alkynes into N-Sulfonylazetidin-2-iminesWe thank the National Institutes of Health, the National Institute of General Medical Sciences (GM28384), the Skaggs Institute for Chemical Biology, and Pfizer, Inc. for financial support. We also thank Prof. K. B. Sharpless for valuable advice and stimulating discussions.
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- Angewandte Chemie, 2006, v. 118, n. 19, p. 3229, doi. 10.1002/ange.200503936
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- Article
Inhibitors of HIV-1 Protease by Using In Situ Click ChemistryWe thank the National Institute of General Medical Sciences, the National Institutes of Health (GM048870), the Skaggs Institute for Chemical Biology, and the W. M. Keck Foundation (K.B.S.) for financial support.
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- Angewandte Chemie, 2006, v. 118, n. 9, p. 1463, doi. 10.1002/ange.200502161
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- Article
Titelbild: “On Water”: Unique Reactivity of Organic Compounds in Aqueous Suspension (Angew. Chem. 21/2005).
- Published in:
- Angewandte Chemie, 2005, v. 117, n. 21, p. 3219, doi. 10.1002/ange.200590069
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- Publication type:
- Article
“On Water”: Unique Reactivity of Organic Compounds in Aqueous SuspensionWe thank Dr. Vladislav Litosh for carrying out preliminary work. Support from the National Institutes of Health, National Institute of General Medical Sciences (GM 28384), the National Science Foundation (CHE9985553), the Skaggs Institute for Chemical Biology, and the W. M. Keck Foundation is gratefully acknowledged. S.N. thanks the Skaggs Institute for a postdoctoral fellowship. We also thank Dr. Suresh Suri, Edwards Air Force Base, California, for a generous gift of quadricyclane. We urge our fellow chemists to float their problematic reactions on water and to send observations of success or failure to us at onwater@scripps.edu for public dissemination with attribution.
- Published in:
- Angewandte Chemie, 2005, v. 117, n. 21, p. 3339, doi. 10.1002/ange.200462883
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- Publication type:
- Article
Mechanism of the Ligand-Free CuI-Catalyzed Azide–Alkyne Cycloaddition ReactionWe thank the Skaggs Institute for Chemical Biology for support of this work.
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- Angewandte Chemie, 2005, v. 117, n. 15, p. 2250, doi. 10.1002/ange.200461496
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- Publication type:
- Article
Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and AlkynesWe thank the National Institute of General Medical Sciences, the National Institutes of Health (GM 28284), the National Science Foundation (CHE-9985553), the W. M. Keck Foundation, the Skaggs Institute for Chemical Biology, the MRSEC Program of the National Science Foundation (award no. DMR-0213618 for the Center for Polymeric Interfaces and Macromolecular Assemblies), the NIRT Program of the National Science Foundation (grant no. 0210247), IBM Corporation, DOE-BES, and NSF International/DAAD for financial support. We are also grateful to Prof. M. G. Finn for helpful discussions.
- Published in:
- Angewandte Chemie, 2004, v. 116, n. 30, p. 4018, doi. 10.1002/ange.200454078
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- Publication type:
- Article
Titelbild: Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and Alkynes (Angew. Chem. 30/2004).
- Published in:
- Angewandte Chemie, 2004, v. 116, n. 30, p. 3951, doi. 10.1002/ange.200490100
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- Publication type:
- Article
Ruthenium-Catalyzed Cycloadditions of 1-Haloalkynes with Nitrile Oxides and Organic Azides: Synthesis of 4-Haloisoxazoles and 5-Halotriazoles.
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- Chemistry - A European Journal, 2014, v. 20, n. 35, p. 11101, doi. 10.1002/chem.201402559
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- Article
SuFEx-Based Synthesis of Polysulfates.
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- Angewandte Chemie, 2014, v. 126, n. 36, p. 9620, doi. 10.1002/ange.201403758
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- Publication type:
- Article
Catalytic Asymmetric Transannulation of N H-1,2,3-Triazoles with Olefins.
- Published in:
- Angewandte Chemie, 2014, v. 126, n. 13, p. 3520, doi. 10.1002/ange.201306706
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- Publication type:
- Article
Copper(I)-Catalyzed Cycloaddition of Bismuth(III) Acetylides with Organic Azides: Synthesis of Stable Triazole Anion Equivalents.
- Published in:
- Angewandte Chemie, 2013, v. 125, n. 49, p. 13275, doi. 10.1002/ange.201306192
- By:
- Publication type:
- Article
Copper-Catalyzed Reaction Cascade: Direct Conversion of Alkynes into N-Sulfonylazetidin-2-iminesWe thank the National Institutes of Health, the National Institute of General Medical Sciences (GM28384), the Skaggs Institute for Chemical Biology, and Pfizer, Inc. for financial support. We also thank Prof. K. B. Sharpless for valuable advice and stimulating discussions.
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 19, p. 3157, doi. 10.1002/anie.200503936
- By:
- Publication type:
- Article
Practical Synthesis of Amides from In Situ Generated Copper(I) Acetylides and Sulfonyl AzidesWe thank the National Institutes of Health, the National Institute of General Medical Sciences (GM28384), the Skaggs Institute for Chemical Biology, and Pfizer, Inc. for financial support. We also thank Prof. K. B. Sharpless, Prof. M. G. Finn, and Dr. M. Whiting for valuable advice and stimulating discussions.
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 19, p. 3154, doi. 10.1002/anie.200503805
- By:
- Publication type:
- Article
Inhibitors of HIV-1 Protease by Using In Situ Click ChemistryWe thank the National Institute of General Medical Sciences, the National Institutes of Health (GM048870), the Skaggs Institute for Chemical Biology, and the W. M. Keck Foundation (K.B.S.) for financial support.
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1435, doi. 10.1002/anie.200502161
- By:
- Publication type:
- Article
Cover Picture: “On Water”: Unique Reactivity of Organic Compounds in Aqueous Suspension (Angew. Chem. Int. Ed. 21/2005).
- Published in:
- Angewandte Chemie International Edition, 2005, v. 44, n. 21, p. 3157, doi. 10.1002/anie.200590069
- By:
- Publication type:
- Article
“On Water”: Unique Reactivity of Organic Compounds in Aqueous SuspensionWe thank Dr. Vladislav Litosh for carrying out preliminary work. Support from the National Institutes of Health, National Institute of General Medical Sciences (GM 28384), the National Science Foundation (CHE9985553), the Skaggs Institute for Chemical Biology, and the W. M. Keck Foundation is gratefully acknowledged. S.N. thanks the Skaggs Institute for a postdoctoral fellowship. We also thank Dr. Suresh Suri, Edwards Air Force Base, California, for a generous gift of quadricyclane. We urge our fellow chemists to float their problematic reactions on water and to send observations of success or failure to us at onwater@scripps.edu for public dissemination with attribution.
- Published in:
- Angewandte Chemie International Edition, 2005, v. 44, n. 21, p. 3275, doi. 10.1002/anie.200462883
- By:
- Publication type:
- Article
Mechanism of the Ligand-Free CuI-Catalyzed AzideAlkyne Cycloaddition ReactionWe thank the Skaggs Institute for Chemical Biology for support of this work.
- Published in:
- Angewandte Chemie International Edition, 2005, v. 44, n. 15, p. 2210, doi. 10.1002/anie.200461496
- By:
- Publication type:
- Article
Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and AlkynesWe thank the National Institute of General Medical Sciences, the National Institutes of Health (GM 28284), the National Science Foundation (CHE-9985553), the W. M. Keck Foundation, the Skaggs Institute for Chemical Biology, the MRSEC Program of the National Science Foundation (award no. DMR-0213618 for the Center for Polymeric Interfaces and Macromolecular Assemblies), the NIRT Program of the National Science Foundation (grant no. 0210247), IBM Corporation, DOE-BES, and NSF International/DAAD for financial support. We are also grateful to Prof. M. G. Finn for helpful discussions.
- Published in:
- Angewandte Chemie International Edition, 2004, v. 43, n. 30, p. 3928, doi. 10.1002/anie.200454078
- By:
- Publication type:
- Article
Cover Picture: Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and Alkynes (Angew. Chem. Int. Ed. 30/2004).
- Published in:
- Angewandte Chemie International Edition, 2004, v. 43, n. 30, p. 3863, doi. 10.1002/anie.200490100
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- Publication type:
- Article
A Stepwise Huisgen Cycloaddition Process: Copper( I)-Catalyzed Regioselective 'Ligation' of Azides and Terminal Alkynes.
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- Angewandte Chemie International Edition, 2002, v. 41, n. 14, p. 2596, doi. 10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
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- Article
A New Approach to Osmium-Catalyzed Asymmetric Dihydroxylation and Aminohydroxylation of Olefins.
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- Angewandte Chemie International Edition, 2002, v. 41, n. 3, p. 472, doi. 10.1002/1521-3773(20020201)41:3<472::AID-ANIE472>3.0.CO;2-7
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- Article
A Practical and Highly Efficient Aminohydroxylation of Unsaturated Carboxylic Acids.
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- Angewandte Chemie International Edition, 2001, v. 40, n. 18, p. 3455, doi. 10.1002/1521-3773(20010917)40:18<3455::AID-ANIE3455>3.0.CO;2-I
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- Article
Synthesis of Indole-Derived Allocolchicine Congeners through Pd-Catalyzed Intramolecular C-H Arylation Reaction.
- Published in:
- European Journal of Organic Chemistry, 2014, v. 2014, n. 29, p. 6481, doi. 10.1002/ejoc.201402850
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- Publication type:
- Article
SuFEx-Based Synthesis of Polysulfates.
- Published in:
- Angewandte Chemie International Edition, 2014, v. 53, n. 36, p. 9466, doi. 10.1002/anie.201403758
- By:
- Publication type:
- Article
Catalytic Asymmetric Transannulation of N H-1,2,3-Triazoles with Olefins.
- Published in:
- Angewandte Chemie International Edition, 2014, v. 53, n. 13, p. 3452, doi. 10.1002/anie.201306706
- By:
- Publication type:
- Article
Copper(I)-Catalyzed Cycloaddition of Bismuth(III) Acetylides with Organic Azides: Synthesis of Stable Triazole Anion Equivalents.
- Published in:
- Angewandte Chemie International Edition, 2013, v. 52, n. 49, p. 13037, doi. 10.1002/anie.201306192
- By:
- Publication type:
- Article
Sulfonyl-1,2,3-Triazoles: Convenient Synthones for Heterocyclic Compounds.
- Published in:
- Angewandte Chemie International Edition, 2013, v. 52, n. 5, p. 1507, doi. 10.1002/anie.201206388
- By:
- Publication type:
- Article
Ring Expansion and Rearrangements of Rhodium(II) Azavinyl Carbenes.
- Published in:
- Angewandte Chemie International Edition, 2012, v. 51, n. 52, p. 13054, doi. 10.1002/anie.201207820
- By:
- Publication type:
- Article
Halogen Exchange (Halex) Reaction of 5-Iodo-1,2,3-triazoles: Synthesis and Applications of 5-Fluorotriazoles.
- Published in:
- Angewandte Chemie International Edition, 2012, v. 51, n. 47, p. 11791, doi. 10.1002/anie.201204979
- By:
- Publication type:
- Article
Click and Pick: Identification of Sialoside Analogues for Siglec-Based Cell Targeting.
- Published in:
- Angewandte Chemie International Edition, 2012, v. 51, n. 44, p. 11014, doi. 10.1002/anie.201205831
- By:
- Publication type:
- Article