Synthesis of benzyl esters using 2-benzyloxy-1-methylpyridinium triflate.

Synthesis of benzyl esters using 2-benzyloxy-1-methylpyridinium triflate. Research Abstract Details 

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Synthesis of benzyl esters using 2-benzyloxy-1-methylpyridinium triflate. Abstract Text:

Jumreang Tummatorn,Philip A Albiniak,Gregory B Dudley,Jumreang Tummatorn,Philip A Albiniak,Gregory B Dudley,

Triethylamine (Et3N) mediates esterification reactions between the title reagent (1) and carboxylic acids. Alcohols, phenols, amides, and other sensitive functionality are not affected; a dual role for Et3N as a promoter and a scavenger is postulated. Benzyl esters are obtained from substrates including amino acid and sugar derivatives.

Synthesis of benzyl esters using 2-benzyloxy-1-methylpyridinium triflate. Publishing Authors By Initials

J Tummatorn,PA Albiniak,GB Dudley,J Tummatorn,PA Albiniak,GB Dudley,

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Synthesis of benzyl esters using 2-benzyloxy-1-methylpyridinium triflate. Journal Published:

PUBLICATION TYPE: Research Support, Non-U.S. Gov

Journal: The Journal of organic chemistry

VOLUME: 72

Page Numbers: 8962-4

Journal Abbreviation: J. Org. Chem.

ISSN: 0022-3263

DAY: 13

MONTH: 10

YEAR: 2007

Synthesis of benzyl esters using 2-benzyloxy-1-methylpyridinium triflate. Information

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LANGUAGE: eng

NlmUniqueID: 2985193

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AFFILIATION: Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306-4390, USA.

Country: United States

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MEDLINETA: J Org Chem

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