Literature DB >> 16178520

Facile synthesis of the indeno-tetrahydropyridine core of haouamine A.

Nicole D Smith1, Joji Hayashida, Viresh H Rawal.   

Abstract

[reaction: see text] The tricyclic indeno-tetrahydropyridine core of haouamine A, containing five of the seven rings of the natural product, was constructed by a simple, concise route that features an acid-catalyzed Friedel-Crafts ring closure.

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Year:  2005        PMID： 16178520     DOI： 10.1021/ol0512740

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


  5 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.  Formal total synthesis of the cytotoxic marine ascidian alkaloid haouamine A.

Authors:  Jeannie H Jeong; Steven M Weinreb
Journal:  Org Lett       Date:  2006-05-25       Impact factor: 6.005

3.  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

4.  Chemoselectivity: the mother of invention in total synthesis.

Authors:  Ryan A Shenvi; Daniel P O'Malley; Phil S Baran
Journal:  Acc Chem Res       Date:  2009-04-21       Impact factor: 22.384

5.  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
  5 in total

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