Literature DB >> 16941713

Formal total synthesis of (+)-zaragozic acid C through an Ireland-Claisen rearrangement.

Jens O Bunte1, Anthony N Cuzzupe, Alica M Daly, Mark A Rizzacasa.   

Abstract

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Year:  2006        PMID： 16941713     DOI： 10.1002/anie.200602507

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


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  7 in total

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3.  Silyl glyoxylates. Conception and realization of flexible conjunctive reagents for multicomponent coupling.

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4.  Self-consistent synthesis of the squalene synthase inhibitor zaragozic acid C via controlled oligomerization.

Authors:  David A Nicewicz; Andrew D Satterfield; Daniel C Schmitt; Jeffrey S Johnson
Journal:  J Am Chem Soc       Date:  2008-12-24       Impact factor: 15.419

Review 5.  [3,3]-Sigmatropic rearrangements: recent applications in the total synthesis of natural products.

Authors:  Elizabeth A Ilardi; Craig E Stivala; Armen Zakarian
Journal:  Chem Soc Rev       Date:  2009-09-02       Impact factor: 54.564

6.  Enantiospecific total synthesis of the squalene synthase inhibitors (-)-CJ-13,982 and its enantiomer from a common intermediate.

Authors:  Dayna Sturgess; Zongjia Chen; Jonathan M White; Mark A Rizzacasa
Journal:  J Antibiot (Tokyo)       Date:  2017-10-25       Impact factor: 2.649

7.  A convenient enantioselective decarboxylative aldol reaction to access chiral α-hydroxy esters using β-keto acids.

Authors:  Zhiqiang Duan; Jianlin Han; Ping Qian; Zirui Zhang; Yi Wang; Yi Pan
Journal:  Beilstein J Org Chem       Date:  2014-04-29       Impact factor: 2.883
  7 in total

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