Literature DB >> 17824710

Direct alpha-oxytosylation of carbonyl compounds: one-pot synthesis of heterocycles.

Oliver R S John1, Niall M Killeen, Deborah A Knowles, Sze Chak Yau, Mark C Bagley, Nicholas C O Tomkinson.   

Abstract

N-Methyl-O-tosylhydroxylamine is an effective reagent for the direct alpha-oxytosylation of carbonyl compounds. The reactions proceed smoothly at room temperature in the presence of both moisture and air and functional group tolerance in the substrate is good. With nonsymmetrical substrates regioselectivity for primary over secondary centers is observed and complete regiospecificity for primary over tertiary centers is obtained. Addition of a bis-heteronucleophile directly to the crude reaction mixture in a one-pot process leads to the corresponding heterocyclic product.

Entities:  

Year:  2007        PMID: 17824710     DOI: 10.1021/ol701774y

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Dirhodium-catalyzed C-H arene amination using hydroxylamines.

Authors:  Mahesh P Paudyal; Adeniyi Michael Adebesin; Scott R Burt; Daniel H Ess; Zhiwei Ma; László Kürti; John R Falck
Journal:  Science       Date:  2016-09-09       Impact factor: 47.728

2.  A reagent for the convenient, solid-phase synthesis of N-terminal peptide hydroxylamines for chemoselective ligations.

Authors:  Takeo Fukuzumi; Jeffrey W Bode
Journal:  J Am Chem Soc       Date:  2009-03-25       Impact factor: 15.419

  2 in total

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