Literature DB >> 19231835

Formal total synthesis of haouamine A.

Tsuyoshi Taniguchi1, Hisaaki Zaimoku, Hiroyuki Ishibashi.   

Abstract

A synthesis of the indenotetrahydropyridine unit of haouamine A is described. The construction of a diaryl quaternary center and tricyclic framework of this compound was achieved by an intramolecular cascade Mizoroki-Heck reaction.

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Year:  2009        PMID： 19231835     DOI： 10.1021/jo802787j

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  4 in total

1.  Use of a tandem Prins/Friedel-Crafts reaction in the construction of the indeno-tetrahydropyridine core of the haouamine alkaloids: formal synthesis of (-)-haouamine A.

Authors:  Erik Fenster; Charlie Fehl; Jeffrey Aubé
Journal:  Org Lett       Date:  2011-04-25       Impact factor: 6.005

2.  Total synthesis of haouamine A: the indeno-tetrahydropyridine core.

Authors:  Noah Z Burns; Mikkel Jessing; Phil S Baran
Journal:  Tetrahedron       Date:  2009-08-15       Impact factor: 2.457

3.  Scalable total synthesis and biological evaluation of haouamine A and its atropisomer.

Authors:  Noah Z Burns; Irina N Krylova; Rami N Hannoush; Phil S Baran
Journal:  J Am Chem Soc       Date:  2009-07-08       Impact factor: 15.419

4.  Intramolecular carbonickelation of alkenes.

Authors:  Rudy Lhermet; Muriel Durandetti; Jacques Maddaluno
Journal:  Beilstein J Org Chem       Date:  2013-04-12       Impact factor: 2.883
  4 in total

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