The azomethine ylide route to amine C-H functionalization: redox-versions of classic reactions and a pathway to new transformations.
about
Asymmetric Redox-Annulation of Cyclic Amines.Redox-Annulation of Cyclic Amines and β-Ketoaldehydes.Intramolecular Redox-Mannich Reactions: Facile Access to the Tetrahydroprotoberberine Core.Decarboxylative Annulation of α-Amino Acids with γ-Nitroaldehydes.Stereoselective synthesis of fused tetrahydroquinazolines through one-pot double [3 + 2] dipolar cycloadditions followed by [5 + 1] annulation.C-H functionalization of cyclic amines: redox-annulations with α,β-unsaturated carbonyl compounds.An Ugi Reaction Incorporating a Redox-Neutral Amine C-H Functionalization StepAcetic Acid Promoted Redox Annulations with Dual C-H Functionalization.Redox-Neutral Aromatization of Cyclic Amines: Mechanistic Insights and Harnessing of Reactive Intermediates for Amine α- and β-C-H Functionalization.A tandem annulation with a [1,3]-hydride transfer as the key step leading to isochromans.Direct α-C-H bond functionalization of unprotected cyclic amines.Intermolecular Redox-Neutral Amine C-H Functionalization Induced by the Strong Boron Lewis Acid B(C6 F5 )3 in the Frustrated Lewis Pair Regime.Iterative direct C(sp3)-H functionalization of amines: diastereoselective divergent syntheses of α,α'-disubstituted alicyclic amines.Synthesis of α-sulfenyl monoketones via a metal-free oxidative cross dehydrogenative coupling (CDC) reaction.Classical-Reaction-Driven Stereo- and Regioselective C(sp(3) )-H Functionalization of Aliphatic Amines.A General, Concise Strategy that Enables Collective Total Syntheses of over 50 Protoberberine and Five Aporhoeadane Alkaloids within Four to Eight Steps.Chiral Phosphoric Acid Catalyzed Kinetic Resolution of Indolines Based on a Self-Redox Reaction.Metal-Free Decarboxylative Cyclization/Ring Expansion: Construction of Five-, Six-, and Seven-Membered Heterocycles from 2-Alkynyl Benzaldehydes and Cyclic Amino Acids.Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes.Synthesis of Polycyclic Imidazolidinones via Amine Redox-Annulation.Asymmetric Michael Addition of Aldimino Esters with Chalcones Catalyzed by Silver/Xing-Phos: Mechanism-Oriented Divergent Synthesis of Chiral Pyrrolines.Regio- and Diastereoselective and Enantiospecific Metal-Free C(sp(3) )-H Arylation: Facile Access to Optically Active 5-Aryl 2,5-Disubstituted Pyrrolidines.Expedient synthesis of tetrahydroquinoline-3-spirohydantoin derivatives via the Lewis acid-catalyzed tert-amino effect reaction.
P2860
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P2860
The azomethine ylide route to amine C-H functionalization: redox-versions of classic reactions and a pathway to new transformations.
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
@zh-hk
2015年論文
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2015年論文
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name
The azomethine ylide route to ...... athway to new transformations.
@en
type
label
The azomethine ylide route to ...... athway to new transformations.
@en
prefLabel
The azomethine ylide route to ...... athway to new transformations.
@en
P2860
P921
P356
P1476
The azomethine ylide route to ...... athway to new transformations.
@en
P2093
Daniel Seidel
P2860
P304
P356
10.1021/AR5003768
P407
P577
2015-01-06T00:00:00Z
2015-02-17T00:00:00Z