Hypervalent iodine-catalyzed oxidative functionalizations including stereoselective reactions.
about
Thioamination of Alkenes with Hypervalent Iodine ReagentsEnantioselective diamination with novel chiral hypervalent iodine catalysts.Selective CH functionalization of methane, ethane, and propane by a perfluoroarene iodine(III) complex.Hypervalent-Iodine(III)-Mediated Oxidative Methodology for the Synthesis of Fused Triazoles.Synthetic applications of pseudocyclic hypervalent iodine compounds.Hypervalent iodine(iii) fluorinations of alkenes and diazo compounds: new opportunities in fluorination chemistry.Structurally Defined Molecular Hypervalent Iodine Catalysts for Intermolecular Enantioselective Reactions.Iodine(III)-Mediated para-Selective Direct Imidation of Anilides.Iodoarene-catalyzed cyclizations of N-propargylamides and β-amidoketones: synthesis of 2-oxazolines.PIFA-mediated ethoxyiodination of enamides with potassium iodide.Iodine(III)-catalyzed rearrangements of imides: a versatile route to α,α-dialkylated α-hydroxy carboxylamides.Design, Synthesis, and Screening of Triazolopyrimidine-Pyrazole Hybrids as Potent Apoptotic Inducers.Organocatalytic Chemoselective Primary Alcohol Oxidation and Subsequent Cleavage of Lignin Model Compounds and Lignin.Electrophilic Activation of Iodonium Ylides by Halogen-Bond-Donor Catalysis for Cross-Enolate Coupling.Benzimidazopurine nucleosides from N6-aryl adenosine derivatives by PhI(OAc)2-mediated C-N bond formation, no metal needed.Photoactivated N-Acyliminoiodinanes Applied to Amination: an ortho-Methoxymethyl Group Stabilizes Reactive Precursors.Preparation, Structure, and Reactivity of Pseudocyclic Benziodoxole Tosylates: New Hypervalent Iodine Oxidants and Electrophiles.From Anilines to Quinolines: Iodide- and Silver-Mediated Aerobic Double C-H Oxidative Annulation-Aromatization.The Multiple Facets of Iodine(III) Compounds in an Unprecedented Catalytic Auto-amination for Chiral Amine Synthesis.Synthesis of the Strychnos Alkaloid (-)-Strychnopivotine and Confirmation of its Absolute Configuration.One-step formation of dihydrofuranoindoline cores promoted by a hypervalent iodine reagent.Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents.Formation of the Main Cores Present in Natural Products by Tandem Additions.Stereoselective Formation of Substituted 1,3-Dioxolanes through a Three-Component Assembly during the Oxidation of Alkenes with Hypervalent Iodine(III).Enantioselective dioxytosylation of styrenes using lactate-based chiral hypervalent iodine(III).2-Iodo-N-isopropyl-5-methoxybenzamide as a highly reactive and environmentally benign catalyst for alcohol oxidation.Iodine(III)-mediated halogenations of acyclic monoterpenoids.Fluorocyclisation via I(I)/I(III) catalysis: a concise route to fluorinated oxazolines.Recyclable hypervalent-iodine-mediated solid-phase peptide synthesis and cyclic peptide synthesis.Synthesis of Sulfoximidoyl-Containing Hypervalent Iodine(III) Reagents and Their Use in Transition-Metal-Free Sulfoximidations of AlkynesDFT Rationalization of the Diverse Outcomes of the Iodine(III)-Mediated Oxidative Amination of Alkenes
P2860
Q36497315-D23369CB-CA5A-4CF8-8FA7-42E47EF04C7DQ36530486-ABDDB644-2ABE-41A9-A9A9-C624E9DDF65FQ38448077-67B98A7D-51C9-47B7-8D2E-BA0F562DD629Q38819718-1E0C195F-37C1-43E7-BC57-D57DE33CC154Q38824952-AB10B3FA-03C3-496F-AFB1-B8F0C09B57FDQ38896999-822D3203-AAD4-49F8-892B-4CF156BB6488Q40213939-D8635531-8D46-47E3-ACED-A74F03BF9266Q40815622-C35AC375-3827-4635-A66B-6603AAE2FAEBQ41596817-69A8738A-7C55-4A46-9CF8-E547C769A04CQ46479909-7C1CA6DE-A51B-4816-9210-80A3FC591764Q46803535-26CDDD78-5863-4489-AB47-03D1940AE8EAQ47442477-251B80E3-3AF6-44EB-801F-8FBF6F19D537Q48122739-BD719A93-CAD3-4398-B7E1-6BA95F3DB98DQ48148825-CA7025DD-16E7-4688-B04C-C51F43D3AEE5Q48152386-ADCB3BE2-4E5E-4038-A00D-CAF8C9E1923AQ48201142-08F77EA1-2CF7-4084-ACA0-EFFABD5E4851Q48266771-93631B58-0058-4BC3-9196-F7AF941868A3Q48347913-A5BC7853-3A70-4D8A-B323-42910F97A216Q50855049-C8A97657-C99B-4241-9BC6-657E3247956CQ50867635-0BBC9F78-2B36-437C-A804-64E6CFC82FA2Q52682187-D911D148-0F99-438E-A97D-DBFE4F886ABAQ53136152-42DE8DF6-6284-4E2C-A603-5B5760AE916AQ53664674-76BF01E1-202D-45AD-913A-9D3B0A9BBEEAQ53669539-786AEE40-FE5F-4616-9F4E-BA4E97433D30Q55222304-46A4B113-2203-4C60-9792-3832FFC988CEQ55413399-08030491-FBE7-4EDF-95CC-AD5821767B87Q55425627-E00BBC04-53E1-4B41-A388-041C24E3761DQ55438946-46348F82-E5CA-410A-A575-E5C1B0AB13B6Q55453485-BC6F5076-B1E5-40F2-BD82-4D25C0023F17Q57404715-014F49D7-D363-4F07-AB3B-65BC0728F1BAQ58830878-E0330DE5-70FC-4802-BACB-9E8C50898C99
P2860
Hypervalent iodine-catalyzed oxidative functionalizations including stereoselective reactions.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Hypervalent iodine-catalyzed o ...... ing stereoselective reactions.
@en
type
label
Hypervalent iodine-catalyzed o ...... ing stereoselective reactions.
@en
prefLabel
Hypervalent iodine-catalyzed o ...... ing stereoselective reactions.
@en
P2860
P356
P1476
Hypervalent iodine-catalyzed o ...... ding stereoselective reactions
@en
P2093
Fateh V Singh
P2860
P304
P356
10.1002/ASIA.201301582
P577
2014-02-12T00:00:00Z