(Q37181853)

18 August 2017

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title

One-pot oxidative esterification and amidation of aldehydes (English)

1 reference

18 August 2017

Kekeli Ekoue-Kovi

1

1 reference

PubMed ID

18523938

18 August 2017

Christian Wolf

series ordinal

2

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PubMed ID

18523938

18 August 2017

language of work or name

English

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publication date

1 January 2008

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Chemistry—A European Journal

18 August 2017

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18 August 2017

14

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18 August 2017

21

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18 August 2017

6302-6315

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Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides

18 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Facile oxidation of aldehydes to acids and esters with Oxone

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

New methods for the oxidation of aldehydes to carboxylic acids and esters

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Efficient heterogeneous catalytic intramolecular Tishchenko reaction of o-phthalaldehyde to phthalide with alkaline earth oxides

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Lithium bromide as a flexible, mild, and recyclable reagent for solvent-free Cannizzaro, Tishchenko, and Meerwein-Ponndorf-Verley reactions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Samarium-catalyzed intramolecular Tishchenko reduction of .beta.-hydroxy ketones. A stereoselective approach to the synthesis of differentiated anti 1,3-diol monoesters

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Facile Conversion of Alcohols into Esters and Dihydrogen Catalyzed by New Ruthenium Complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

A novel rhodium-catalyzed reduction-oxidation process: reaction of 4-alkynals with phenol to provide cis-4-alkenoates

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Peroxovanadium-catalyzed oxidative esterification of aldehydes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Enantioselective protonation of catalytically generated chiral enolates as an approach to the synthesis of alpha-chloroesters

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Chiral N-heterocyclic carbene catalyzed, enantioselective oxodiene Diels-Alder reactions with low catalyst loadings

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Organocatalyzed conjugate umpolung of alpha,beta-unsaturated aldehydes for the synthesis of gamma-butyrolactones

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Catalytic generation of activated carboxylates: direct, stereoselective synthesis of beta-hydroxyesters from epoxyaldehydes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

N-heterocyclic carbene catalyzed C--C bond cleavage in redox esterifications of chiral formylcyclopropanes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Room-temperature Cannizzaro reaction under mild conditions facilitated by magnesium bromide ethyl etherate and triethylamine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Synthesis of carboxamides by LDA-catalyzed Haller-Bauer and Cannizzaro reactions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Rh(II)-catalyzed intermolecular oxidative sulfamidation of aldehydes: a mild efficient synthesis of N-sulfonylcarboxamides

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Nucleophilic carbene and HOAt relay catalysis in an amide bond coupling: an orthogonal peptide bond forming reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

N-heterocyclic carbene-catalyzed redox amidations of alpha-functionalized aldehydes with amines

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Mild oxidative one-carbon homologation of aldehyde to amide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Samarium Ion-Promoted Cross-Aldol Reactions and Tandem Aldol/Evans−Tishchenko Reactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

Direct Conversion of Aldehydes to Amides, Tetrazoles, and Triazines in Aqueous Media by One-Pot Tandem Reactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200800353

21 January 2018

Identifiers

DOI

10.1002/CHEM.200800353

1 reference

18 August 2017

1 reference

PubMed ID

18523938