Literature DB >> 21423880

Synthesis of Oxazolidinone and Tosyl Enamines by Tertiary Amine Catalysis.

Nicholas A Eddy1, Peter D Morse, Martha D Morton, Gabriel Fenteany.   

Abstract

A procedure for the synthesis of oxazolidinone and tosyl enamines is reported. Alkynoyl oxazolidinones and tosyl imides undergo reaction to form enamines in the presence of catalytic amounts of tertiary amines. The data suggest that an amide anion is formed during the reaction, which undergoes conjugate addition to form the final product.

Entities:  

Year:  2011        PMID: 21423880      PMCID: PMC3059314          DOI: 10.1055/s-0030-1259561

Source DB:  PubMed          Journal:  Synlett        ISSN: 0936-5214            Impact factor:   2.454


  21 in total

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Authors:  J Guo; H W Wu; G Hu; X Han; W De; Y J Sun
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9.  Catalytic asymmetric intramolecular alpha-alkylation of aldehydes.

Authors:  Nicola Vignola; Benjamin List
Journal:  J Am Chem Soc       Date:  2004-01-21       Impact factor: 15.419

10.  The direct and enantioselective organocatalytic alpha-oxidation of aldehydes.

Authors:  Sean P Brown; Michael P Brochu; Christopher J Sinz; David W C MacMillan
Journal:  J Am Chem Soc       Date:  2003-09-10       Impact factor: 15.419

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