Literature DB >> 12357781

A formal total synthesis of leucascandrolide A.

Peter Wipf1, Jonathan T Reeves.   

Abstract

A convergent synthesis of the macrocyclic core of the marine macrolide leucascandrolide A has been accomplished.

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Year:  2002        PMID： 12357781     DOI： 10.1039/b207383h

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  6 in total

1.  Nitrenium ion azaspirocyclization-spirodienone cleavage: a new synthetic strategy for the stereocontrolled preparation of highly substituted lactams and N-hydroxy lactams.

Authors:  Duncan J Wardrop; Matthew S Burge
Journal:  J Org Chem       Date:  2005-12-09       Impact factor: 4.354

2.  Studies for the enantiocontrolled preparation of substituted tetrahydropyrans: Applications for the synthesis of leucascandrolide A macrolactone.

Authors:  David R Williams; Scott V Plummer; Samarjit Patnaik
Journal:  Tetrahedron       Date:  2011-07-08       Impact factor: 2.457

3.  Total synthesis of neopeltolide and analogs.

Authors:  Yubo Cui; Wangyang Tu; Paul E Floreancig
Journal:  Tetrahedron       Date:  2010-06-26       Impact factor: 2.457

4.  Total synthesis of leucascandrolide a: a new application of the Mukaiyama aldol-Prins reaction.

Authors:  Lori J Van Orden; Brian D Patterson; Scott D Rychnovsky
Journal:  J Org Chem       Date:  2007-06-27       Impact factor: 4.354

5.  Synthesis enables identification of the cellular target of leucascandrolide A and neopeltolide.

Authors:  Olesya A Ulanovskaya; Jelena Janjic; Masato Suzuki; Simran S Sabharwal; Paul T Schumacker; Stephen J Kron; Sergey A Kozmin
Journal:  Nat Chem Biol       Date:  2008-05-30       Impact factor: 15.040

6.  Approach to the Synthesis of the C1-C11 and C14-C18 portion of Leucascandrolide A.

Authors:  T J Hunter; J Zheng; G A O'Doherty
Journal:  Org Chem Front       Date:  2016-07-12       Impact factor: 5.281
  6 in total

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