Literature DB >> 12949873

Formal synthesis of leucascandrolide A.

David R Williams1, Scott V Plummer, Samarjit Patnaik.   

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Year:  2003        PMID: 12949873     DOI: 10.1002/anie.200351817

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


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  7 in total

1.  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

2.  Total synthesis of neopeltolide and analogs.

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

3.  Development of a general, sequential, ring-closing metathesis/intramolecular cross-coupling reaction for the synthesis of polyunsaturated macrolactones.

Authors:  Scott E Denmark; Joseck M Muhuhi
Journal:  J Am Chem Soc       Date:  2010-08-25       Impact factor: 15.419

4.  Studies for the synthesis of marine natural products.

Authors:  David R Williams; Martin J Walsh; Christopher D Claeboe; Nicolas Zorn
Journal:  Pure Appl Chem       Date:  2009       Impact factor: 2.453

5.  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

6.  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

7.  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

  7 in total

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