Literature DB >> 20301158

Concise synthesis of (-)-nakadomarin A.

David B C Martin1, Christopher D Vanderwal.   

Abstract

The beautiful orchestration of new methods and synthesis design was instrumental to the very efficient synthesis of the manzamine alkaloid (-)-nakadomarin A. In only six operations, the two relatively simple compounds shown were converted into the hexacyclic natural product.
Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2010        PMID: 20301158     DOI: 10.1002/anie.201000045

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  4 in total

1.  STUDIES DIRECTED TOWARD THE SYNTHESIS OF NAKADOMARIN A.

Authors:  Thomas Haimowitz; Mark E Fitzgerald; Jeffrey D Winkler
Journal:  Tetrahedron Lett       Date:  2011-04-27       Impact factor: 2.415

2.  A versatile enantioselective synthesis of azabicyclic ring systems: a concise total synthesis of (+)-grandisine D and unnatural analogues.

Authors:  Olugbeminiyi O Fadeyi; Timothy J Senter; Kristopher N Hahn; Craig W Lindsley
Journal:  Chemistry       Date:  2012-03-30       Impact factor: 5.236

3.  A General, Enantioselective Synthesis of 1-Azabicyclo[m.n.0]alkane Ring Systems.

Authors:  Timothy J Senter; Michael L Schulte; Leah C Konkol; Tyler E Wadzinski; Craig W Lindsley
Journal:  Tetrahedron Lett       Date:  2013-03-27       Impact factor: 2.415

Review 4.  Macrocyclic drugs and synthetic methodologies toward macrocycles.

Authors:  Xufen Yu; Dianqing Sun
Journal:  Molecules       Date:  2013-05-24       Impact factor: 4.411

  4 in total

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