Literature DB >> 18517210

Oxidative rearrangements of isobenzofurans: studies toward the synthesis of the ajudazols.

Stephen J Hobson1, Andrew Parkin, Rodolfo Marquez.   

Abstract

We present a new facet of isobenzofuran chemistry which allows for its efficient manipulation to generate biologically relevant entities. This methodology has been successfully applied toward the synthesis of ajudazol A.

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Year:  2008        PMID： 18517210     DOI： 10.1021/ol8009336

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


  3 in total

1.  Synthesis of isocoumarins with different substituted patterns via Passerini-aldol sequence.

Authors:  Guan-Hua Ma; Bo Jiang; Xing-Jun Tu; Yi Ning; Shu-Jiang Tu; Guigen Li
Journal:  Org Lett       Date:  2014-08-20       Impact factor: 6.005

2.  An Entry to Enantioenriched 3,3-Disubstituted Phthalides through Asymmetric Phase-Transfer-Catalyzed γ-Alkylation.

Authors:  Marina Sicignano; Rosaria Schettini; Giovanni Pierri; Maria Leda Marino; Irene Izzo; Francesco De Riccardis; Luca Bernardi; Giorgio Della Sala
Journal:  J Org Chem       Date:  2020-05-27       Impact factor: 4.354

3.  Catalyst-Free Synthesis of Borylated Lactones from Esters via Electrophilic Oxyboration.

Authors:  Darius J Faizi; Adena Issaian; Ashlee J Davis; Suzanne A Blum
Journal:  J Am Chem Soc       Date:  2016-02-16       Impact factor: 15.419
  3 in total

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