Literature DB >> 16671808

A new modular indole synthesis. Construction of the highly strained CDEF parent tetracycle of nodulisporic acids A and B.

Amos B Smith1, Laszló Kürti, Akin H Davulcu.   

Abstract

[reaction: see text] Construction of the highly strained CDEF parent tetracycle, a structural motif found only in the potent ectoparasiticidal agents (+)-nodulisporic acids A and B and related congeners, has been achieved via a new modular indole synthesis, exploiting a sequential Stille cross-coupling/Buchwald-Hartwig union/cyclization tactic. The new indole synthesis holds the promise of rapid assembly of diverse, highly substituted indoles possessing uncommon substitution patterns.

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Year:  2006        PMID: 16671808     DOI: 10.1021/ol0606536

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Twelve-Step Asymmetric Synthesis of (-)-Nodulisporic Acid C.

Authors:  Nicole A Godfrey; Devon J Schatz; Sergey V Pronin
Journal:  J Am Chem Soc       Date:  2018-09-28       Impact factor: 15.419

2.  Catalytic enantioselective synthesis of indanes by a cation-directed 5-endo-trig cyclization.

Authors:  Craig P Johnston; Abhishek Kothari; Tetiana Sergeieva; Sergiy I Okovytyy; Kelvin E Jackson; Robert S Paton; Martin D Smith
Journal:  Nat Chem       Date:  2015-01-12       Impact factor: 24.427

3.  Free radical-mediated aryl amination: convergent two- and three-component couplings to chiral 2,3-disubstituted indolines.

Authors:  Rajesh Viswanathan; Colin R Smith; Erode N Prabhakaran; Jeffrey N Johnston
Journal:  J Org Chem       Date:  2008-03-20       Impact factor: 4.198

  3 in total

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