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rdf:type
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description
| - videnskabelig artikel (da)
- article científic (ca)
- articol științific (ro)
- articolo scientifico (it)
- artigo científico (gl)
- artigo científico (pt)
- artigo científico (pt-br)
- artikull shkencor (sq)
- artículo científico (es)
- bilimsel makale (tr)
- scienca artikolo (eo)
- vedecký článok (sk)
- vetenskaplig artikel (sv)
- vitenskapelig artikkel (nb)
- vitskapeleg artikkel (nn)
- vědecký článek (cs)
- wetenschappelijk artikel (nl)
- wissenschaftlicher Artikel (de)
- научная статья (ru)
- научни чланак (sr)
- מאמר מדעי (he)
- artikel ilmiah (id)
- article scientifique (fr)
- বৈজ্ঞানিক নিবন্ধ (bn)
- artículu científicu espublizáu en 2014 (ast)
- наукова стаття, опублікована у вересні 2014 (uk)
- مقالة علمية نشرت في سبتمبر 2014 (ar)
- scientific article published on September 2014 (en)
- scientific article published on September 2014 (en-ca)
- scientific article published on September 2014 (en-gb)
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publication date
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publication date
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cites work
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cites work
| - Concise total synthesis of (+/-)-salinosporamide A, (+/-)-cinnabaramide A, and derivatives via a bis-cyclization process: implications for a biosynthetic pathway?
- The advent and development of organocatalysis
- Iminium catalysis
- Asymmetric enamine catalysis
- Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts.
- Recent developments in the use of catalytic asymmetric ammonium enolates in chemical synthesis
- Lewis Base Catalysis in Organic Synthesis
- Isothiourea-mediated one-pot synthesis of functionalized pyridines.
- Asymmetric synthesis of bicyclic beta-lactones via the intramolecular, nucleophile-catalyzed aldol lactonization: improved efficiency and expanded scope
- N-heterocyclic-carbene-catalyzed asymmetric oxidative hetero-Diels-Alder reactions with simple aliphatic aldehydes
- Bioinspired total synthesis and human proteasome inhibitory activity of (-)-salinosporamide A, (-)-homosalinosporamide A, and derivatives obtained via organonucleophile promoted bis-cyclizations
- A(1,3)-strain enabled retention of chirality during bis-cyclization of beta-ketoamides: total synthesis of (-)-salinosporamide A and (-)-homosalinosporamide A.
- Double diastereoselective, nucleophile-catalyzed aldol lactonizations (NCAL) leading to beta-lactone fused carbocycles and extensions to beta-lactone fused tetrahydrofurans
- Concise synthesis of spirocyclic, bridged gamma-butyrolactones via stereospecific, dyotropic rearrangements of beta-lactones involving 1,2-acyl and delta-lactone migrations
- N-heterocyclic carbene catalyzed activation of esters: a new option for asymmetric domino reactions.
- Organocatalytic enantioselective γ-aminoalkylation of unsaturated ester: access to pipecolic acid derivatives.
- Benzotetramisole-catalyzed dynamic kinetic resolution of azlactones
- Asymmetric access to the smallest enolate intermediate via organocatalytic activation of acetic ester.
- Organocatalytic activation of alkylacetic esters as enolate precursors to react with α,β-unsaturated imines.
- Catalytic, asymmetric reactions of ketenes and ketene enolates.
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author name string
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author name string
| - Andrew D Smith
- Louis C Morrill
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rdfs:label
| - Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. (en)
- Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. (nl)
- Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. (ast)
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skos:prefLabel
| - Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. (en)
- Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. (nl)
- Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. (ast)
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name
| - Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. (en)
- Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. (nl)
- Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. (ast)
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author
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author
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title
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title
| - Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates (en)
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