Works matching DE "MITSUNOBU reaction"
Results: 130
An Efficient and Scalable "Second Generation" Total Synthesis of the Marine Polyketide Limaol Endowed with Antiparasitic Activity.
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- Chemistry - A European Journal, 2024, v. 30, n. 40, p. 1, doi. 10.1002/chem.202401429
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Alkoxyphosphorane/Borane Cooperative Alkylations: A Frustrated Lewis Pair Version of the Mitsunobu Reaction.
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- Chemistry - A European Journal, 2023, v. 29, n. 23, p. 1, doi. 10.1002/chem.202300264
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Electrochemical Azo‐free Mitsunobu‐type Reaction.
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- Angewandte Chemie, 2024, v. 136, n. 20, p. 1, doi. 10.1002/ange.202402878
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Catalytic Asymmetric β‐Oxygen Elimination**.
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- Angewandte Chemie, 2022, v. 134, n. 22, p. 1, doi. 10.1002/ange.202114044
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Catalytic Enantioconvergent Allenylation of Aldehydes with Propargyl Halides.
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- Angewandte Chemie, 2022, v. 134, n. 10, p. 1, doi. 10.1002/ange.202117114
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Generation of Oxyphosphonium Ions by Photoredox/Cobaloxime Catalysis for Scalable Amide and Peptide Synthesis in Batch and Continuous‐Flow.
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- Angewandte Chemie, 2022, v. 134, n. 5, p. 1, doi. 10.1002/ange.202112668
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Spatially Resolved Covalent Functionalization Patterns on Graphene.
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- Angewandte Chemie, 2019, v. 131, n. 5, p. 1338, doi. 10.1002/ange.201810119
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Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium.
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- Communications Chemistry, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42004-019-0249-6
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Chiral 1,4-aminoalkylphenols for enantioselective diethylzinc addition to aldehydes.
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- Turkish Journal of Chemistry, 2019, v. 43, n. 2, p. 612, doi. 10.3906/kim-1810-78
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Chemoenzymatic Stereoselective Synthesis of trans -Flavan-4-ols via Lipase-Catalyzed Kinetic Resolutions.
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- Catalysts (2073-4344), 2021, v. 11, n. 11, p. 1296, doi. 10.3390/catal11111296
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Self‐assembly of chiral diketopyrrolopyrrole chromophores giving supramolecular chains in monolayers and twisted microtapes.
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- Chirality, 2023, v. 35, n. 5, p. 281, doi. 10.1002/chir.23539
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Synthesis and Evaluation of Two Coumarin-Type.
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- Chirality, 2013, v. 25, n. 12, p. 957, doi. 10.1002/chir.22240
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Analysing a billion reactions with the RInChI.
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- Pure & Applied Chemistry, 2022, v. 94, n. 6, p. 643, doi. 10.1515/pac-2021-2008
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Synthesis of glucopyranos-6′-yl purine and pyrimidine isonucleosides as potential cholinesterase inhibitors. Access to pyrimidine-linked pseudodisaccharides through Mitsunobu reaction.
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- Pure & Applied Chemistry, 2016, v. 88, n. 4, p. 363, doi. 10.1515/pac-2016-0102
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Mitsunobu Functionalization of Poly(vinyl alcohol) Derivatives<sup>†</sup>.
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- Chinese Journal of Chemistry, 2023, v. 41, n. 6, p. 637, doi. 10.1002/cjoc.202200478
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Contents.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 10, p. 2645, doi. 10.1002/cjoc.202190103
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Synthesis, α-Glucosidase inhibition and molecular docking studies of tyrosol derivatives.
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- Natural Product Research, 2021, v. 35, n. 10, p. 1596, doi. 10.1080/14786419.2019.1628750
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Synthesis and Absorption Properties of Trisubstituted Hetarylazo Indole Dyes.
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- Suleyman Demirel University Faculty of Arts & Science Journal of Science / Süleyman Demirel Üniversitesi Fen Edebiyat Fakültesi Fen Dergisi, 2020, v. 15, n. 1, p. 63, doi. 10.29233/sdufeffd.649535
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Phenolic 3° Phosphine Oxides as a Class of Metal-Free Catalysts for the Activation of C–O Bonds in Aliphatic Alcohols: Direct Synthesis of Catalyst Candidates, and Kinetic Studies.
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- Inorganics, 2022, v. 10, n. 3, p. 35, doi. 10.3390/inorganics10030035
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Progress of Catalytic Mitsunobu Reaction in the Two Decades.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 2, p. 1, doi. 10.1002/ajoc.202200707
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Progress of Dialkyl Azodicarboxylates in Organic Transformations.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 5, p. 964, doi. 10.1002/ajoc.202100104
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A General and Practical Synthesis of Chiral 1,2‐Oxazetidines.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 2, p. 197, doi. 10.1002/ajoc.201900754
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Reactivity of the Sultam and Strained Alkyne Groups in 2‐Aminobenzenesulfonamide‐Containing Cyclononyne (ABSACN).
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 4, p. 793, doi. 10.1002/ajoc.201700687
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1, 2‐trans‐Stereoselective 7‐O‐Glycosylation of Flavonoids with Unprotected Pyranoses by Mitsunobu Reaction.
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- Chemistry - An Asian Journal, 2022, v. 17, n. 9, p. 1, doi. 10.1002/asia.202200120
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Facile Synthesis of Hydroquinone Linked 3,3'‐Steroid Dimers via a Modified Mitsunobu Protocol.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 25, p. 1, doi. 10.1002/ejoc.202400309
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DMAPO/Boc<sub>2</sub>O‐Mediated One‐Pot Direct N1‐Acylation of Indazole with Carboxylic Acids: A Practical Synthesis of N1‐Functionalized Alkyl Indazoles.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 18, p. 1, doi. 10.1002/ejoc.202400123
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2‐Nitroimidazole Based PET Tracers: Development of a General Synthetic Approach and Fluorination Methodology.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 26, p. 1, doi. 10.1002/ejoc.202300307
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Synthesis of optically active vicinal fluorocyclopentanols and fluorocyclopentanamines by enzymatic deracemization.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 14, doi. 10.24820/ark.5550190.p011.634
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Professor György Keglevich.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 1, doi. 10.24820/ark.5550190.p001.487
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Enantioselective synthesis of C1-C4 and C5-C14 fragments of cytospolide D.
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- ARKIVOC: Online Journal of Organic Chemistry, 2021, v. 2021, p. 1, doi. 10.24820/ark.5550190.p011.648
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Nucleobase coupling by Mitsunobu reaction towards nucleoside analogs.
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- ARKIVOC: Online Journal of Organic Chemistry, 2021, v. 2021, p. 241, doi. 10.24820/ark.5550190.p011.377
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Mitsonobu reaction of cannabidiol. Synthesis of water-soluble cannabidiol derivatives.
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- ARKIVOC: Online Journal of Organic Chemistry, 2021, v. 2021, p. 198, doi. 10.24820/ark.5550190.p011.347
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Stereoselective total synthesis of antiplasmodial resorcylic acid lactone paecilomycin F.
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- ARKIVOC: Online Journal of Organic Chemistry, 2016, p. 123, doi. 10.3998/ark.5550190.p009.183
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Practical access to (S)-heterocyclic aromatic acetates via CAL-B/Na<sub>2</sub>CO<sub>3</sub>-deacylation and Mitsunobu reaction protocol.
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- Biocatalysis & Biotransformation, 2023, v. 41, n. 4, p. 261, doi. 10.1080/10242422.2022.2030726
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Synthetic 2-Nitrocinnamates: Investigation of the Antifungal Action against Candida Species.
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- Journal of Chemistry, 2023, p. 1, doi. 10.1155/2023/8525145
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Synthesis, Evaluation of Anticancer Activity and QSAR Study of Heterocyclic Esters of Caffeic Acid.
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- Iranian Journal of Pharmaceutical Research, 2013, v. 12, n. 4, p. 705
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Photomechanical effect in “side-chain” polyimides with low content of azopyridine chromophore.
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- Express Polymer Letters, 2024, v. 18, n. 6, p. 607, doi. 10.3144/expresspolymlett.2024.45
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Applications of Mitsunobu Reaction in total synthesis of natural products.
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- Applied Organometallic Chemistry, 2018, v. 32, n. 9, p. 1, doi. 10.1002/aoc.4464
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Atom-Economical Synthesis of Complex Heterocycles with NO Moiety.
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- Helvetica Chimica Acta, 2015, v. 98, n. 9, p. 1315, doi. 10.1002/hlca.201500076
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( R)-2,3-Cyclohexylideneglyceraldehyde, a Chiral Pool Synthon for the Synthesis of 2-Azido-1,3-diols.
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- Helvetica Chimica Acta, 2015, v. 98, n. 6, p. 823, doi. 10.1002/hlca.201400344
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Boyd Group Electronegativity Influence on the Parr Global Electrophilicity of Vilsmeier Reagent-Derived Imidates: New Insights toward Improving Mitsunobu Chemistry.
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- Helvetica Chimica Acta, 2015, v. 98, n. 4, p. 582, doi. 10.1002/hlca.201400340
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Synthesis and enzymatic inhibition effects of thiazolidinedione 3C-like protease inhibitors.
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- Journal of Chemical Research, 2023, v. 47, n. 1, p. 1, doi. 10.1177/17475198231152556
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An enantiodivergent synthesis of N -Boc-protected (R)- and (S)-4-amino cyclopent-2-en-1-one.
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- Journal of Chemical Research, 2022, v. 46, n. 1, p. 1, doi. 10.1177/17475198211047780
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Regioselective alkylation of saccharin with alcohols under Mitsunobu conditions.
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- Journal of Chemical Research, 2013, v. 37, n. 7, p. 417, doi. 10.3184/174751913X13716447161975
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An efficient synthesis of enantiomerically pure trans-N<sup>1</sup>,N<sup>2</sup>-dimethylcyclohexane-1,2-diamine.
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- Journal of Chemical Research, 2013, v. 37, n. 4, p. 191, doi. 10.3184/174751913X13626731204890
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Highly regioselective synthesis of C-4 (ring A) sinomenine ether derivatives.
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- Journal of Chemical Research, 2012, v. 36, n. 6, p. 315, doi. 10.3184/174751912X13344045135875
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Synthesis and photophysical properties of 2-azolyl-6-piperidinylpurines.
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 5, p. 560, doi. 10.1007/s10593-021-02943-1
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[InlineMediaObject not available: see fulltext.]NH-1,2,3-triazoles: synthesis and reactions with electrophilic agents.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 1, p. 4, doi. 10.1007/s10593-016-1821-y
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New strategies for the synthesis of N-alkylated indoles (Review).
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- Chemistry of Heterocyclic Compounds, 2012, v. 48, n. 3, p. 391, doi. 10.1007/s10593-012-1006-2
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Unsymmetrical Tripodal Phosphine Oxide with Triazole Groups: Synthesis and Molecular Structure.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 8, p. 1420, doi. 10.1134/S1070363222080084
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