Literature DB >> 11820903

Facile palladium(0)-catalyzed ring expansion reactions of hydroxy methoxyallenyl cyclic compounds via hydropalladation.

Yoshimitsu Nagao1, Akiharu Ueki, Kazunori Asano, Satoru Tanaka, Shigeki Sano, Motoo Shiro.   

Abstract

Palladium(0)-catalyzed one-atom ring expansion of various hydroxy methoxyallenyl compounds has been achieved in excellent yields without the use of aryl halides. Hydroxy methoxyallenylisoindolinones, -indanones, and -phthalans have been readily converted to the corresponding isoquinolones, naphthoquinones, and isochromanones in the presence of P(o-tolyl)(3).

Entities:  

Year:  2002        PMID: 11820903     DOI: 10.1021/ol010287k

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


  1 in total

1.  Stereoselective, dual-mode ruthenium-catalyzed ring expansion of alkynylcyclopropanols.

Authors:  Barry M Trost; Jia Xie; Nuno Maulide
Journal:  J Am Chem Soc       Date:  2008-12-24       Impact factor: 15.419

  1 in total

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