Literature DB >> 19053734

Carboxylate directed cross-coupling reactions in the synthesis of trisubstituted benzoic acids.

Ioannis N Houpis1, Changkang Huang, Ulrike Nettekoven, Jason G Chen, Renmao Liu, Martine Canters.   

Abstract

The carboxylate anion has been used as a directing group to effect selective ortho-substituted derivatives 3 (>99:1 selectivity 50-80% yield). The solvent, base, and equivalents of base are the determining factors for the success of this reaction. The directing effect can be reversed by the appropriate use of phosphine ligands to prepare the para-substituted 4 selectively (ca. 12:1 selectivity).

Entities:  

Year:  2008        PMID: 19053734     DOI: 10.1021/ol802349u

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


  3 in total

1.  Application of High-Throughput Competition Experiments in the Development of Aspartate-Directed Site-Selective Modification of Tyrosine Residues in Peptides.

Authors:  Alex J Chinn; Jaeyeon Hwang; Byoungmoo Kim; Craig A Parish; Shane W Krska; Scott J Miller
Journal:  J Org Chem       Date:  2020-07-02       Impact factor: 4.354

2.  Intermolecular Heck Coupling with Hindered Alkenes Directed by Potassium Carboxylates.

Authors:  Tucker R Huffman; Yebin Wu; Alexis Emmerich; Ryan A Shenvi
Journal:  Angew Chem Int Ed Engl       Date:  2019-01-25       Impact factor: 15.336

3.  Dynamic Strategic Bond Analysis Yields a Ten-Step Synthesis of 20-nor-Salvinorin A, a Potent κ-OR Agonist.

Authors:  Jeremy J Roach; Yusuke Sasano; Cullen L Schmid; Saheem Zaidi; Vsevolod Katritch; Raymond C Stevens; Laura M Bohn; Ryan A Shenvi
Journal:  ACS Cent Sci       Date:  2017-12-13       Impact factor: 14.553

  3 in total

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