Literature DB >> 15602601

Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (+/-)-hippodamine and (+/-)-epi-hippodamine.

Martin Rejzek1, Robert A Stockman, David L Hughes.   

Abstract

Two-directional total stereoselective syntheses of (+/-)-hippodamine and (+/-)-epi-hippodamine, utilising a tandem deprotection/intramolecular double Michael addition sequence as the key step, are presented.

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Year:  2004        PMID： 15602601     DOI： 10.1039/b413052a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN： 1477-0520            Impact factor:   3.876


  3 in total

1.  Aza-[3 + 3] Annulations: A New Unified Strategy in Alkaloid Synthesis.

Authors:  Grant S Buchanan; John B Feltenberger; Richard P Hsung
Journal:  Curr Org Synth       Date:  2010-08-01       Impact factor: 1.975

2.  Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds.

Authors:  Kieron M G O'Connell; Monica Díaz-Gavilán; Warren R J D Galloway; David R Spring
Journal:  Beilstein J Org Chem       Date:  2012-06-06       Impact factor: 2.883

3.  Combining two-directional synthesis and tandem reactions, part 11: second generation syntheses of (+/-)-hippodamine and (+/-)-epi-hippodamine.

Authors:  Annabella F Newton; Martin Rejzek; Marie-Lyne Alcaraz; Robert A Stockman
Journal:  Beilstein J Org Chem       Date:  2008-01-17       Impact factor: 2.883
  3 in total

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