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Literature DB >> 12932007

Regio and diastereoselective lactonisation of enolisable 1,3-dicarbonyls by reaction with mesoionic 1,3-oxazolium-5-olates.

Giovanni Grassi¹, Francesco Risitano, Francesco Foti, Massimiliano Cordaro, Giuseppe Bruno, Francesco Nicolò.

Abstract

The one-pot reaction of enolisable 1,3-dicarbonyls and N-methyl-1,3-oxazolium-5-olate derivatives provided enol lactones directly in good yield and with excellent regio- and diastereocontrol.

Entities: Chemical

Year: 2003 PMID： 12932007 DOI： 10.1039/b304560a

Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222

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Cited

1 in total

1. A functionalized enol lactone containing a protected α-amino acid.

Authors: Giuseppe Bruno; Francesco Nicoló; Massimiliano Cordaro; Giovanni Grassi; Francesco Risitano
Journal: Acta Crystallogr Sect E Struct Rep Online Date: 2010-11-30

1 in total