NHC-catalysed enantioselective intramolecular formal [4+2] cycloadditions using carboxylic acids as azolium enolate precursors-Reference-Cited by-同舟云学术

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NHC-catalysed enantioselective intramolecular formal [4+2] cycloadditions using carboxylic acids as azolium enolate precursors

Published:2020-01 Issue:4 Volume:76 Page:130835
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Attaba Nassilia,Smith Andrew D.

Funder

European Research Council

European Union’s Seventh Framework Programme

ERC

Royal Society

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference43 articles.

1. (Selection of reviews on the use of azolium enolates and references therein: )

2. Acyl anion free N-heterocyclic carbene organocatalysis

3. NHCs in Asymmetric Organocatalysis: Recent Advances in Azolium Enolate Generation and Reactivity

4. Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes

5. Carbene Catalysts

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1. Recent Advances in the Synthesis of 3,4-Dihydropyran-2-Ones Organocatalyzed by N-Heterocyclic Carbenes;Molecules;2023-04-26

2. Enantioselective N-heterocyclic carbene-catalyzed rearrangement of enol ε-lactones;Organic Chemistry Frontiers;2023

3. [4 + 2] Cycloadditions Catalyzed by Nucleophilic Catalysts;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2022

4. Oxyselenocyclization of 2‐Allylphenols for the Synthesis of 2,3‐Dihydrobenzofuran Selenides;ChemistrySelect;2021-12-22

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