Literature DB >> 21774523

Iodonium salts are key intermediates in Pd-catalyzed acetoxylation of pyrroles.

Dmitrijs Lubriks1, Igors Sokolovs, Edgars Suna.   

Abstract

A mild, room-temperature Pd-catalyzed acetoxylation of pyrroles with phenyliodonium acetate is described. The acetoxylation was found to proceed via the initial formation of pyrrolyl(phenyl)iodonium acetates, which were converted to acetoxypyrroles in the presence of Pd(OAc)(2). The acetoxylation could also be carried out as a one-pot sequential procedure without the isolation of the intermediate iodonium salts.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID: 21774523     DOI: 10.1021/ol201665c

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


  4 in total

1.  Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III) reagents: an opportunity for rational catalyst design?

Authors:  Andrew M Harned
Journal:  Tetrahedron Lett       Date:  2014-08-20       Impact factor: 2.415

2.  Multifunctionalized 3-hydroxypyrroles in a three-step, one-pot cascade process from methyl 3-TBSO-2-diazo-3-butenoate and nitrones.

Authors:  Xinfang Xu; Maxim O Ratnikov; Peter Y Zavalij; Michael P Doyle
Journal:  Org Lett       Date:  2011-10-27       Impact factor: 6.005

3.  General and practical carboxyl-group-directed remote C-H oxygenation reactions of arenes.

Authors:  Yang Wang; Anton V Gulevich; Vladimir Gevorgyan
Journal:  Chemistry       Date:  2013-10-21       Impact factor: 5.236

4.  Pd(II)-Catalyzed Aminoacetoxylation of Alkenes Via Tether Formation.

Authors:  Thomas Rossolini; Ashis Das; Stefano Nicolai; Jérôme Waser
Journal:  Org Lett       Date:  2022-07-11       Impact factor: 6.072

  4 in total

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