Literature DB >> 19591469

Total synthesis of (+)-lyconadin A and related compounds via oxidative C-N bond formation.

Scott P West1, Alakesh Bisai, Andrew D Lim, Raja R Narayan, Richmond Sarpong.   

Abstract

The formation of carbon-nitrogen (C-N) bonds is a fundamental bond construction in organic synthesis and is indispensable for the synthesis of alkaloid natural products. In the context of the synthesis of the architecturally complex n class="Chemical">Lycopodium alkaloid lyconadin A, we have discovered a highly efficient oxidative C-N bond forming reaction that relies on the union of a nitrogen anion and a carbon anion. Empirical evidence amassed during our synthetic studies suggests that the mechanism of the C-N bond forming process encompasses polar as well as radical processes. Herein, we present our study of this novel C-N bond forming reaction and its application to the enantioselective total synthesis of lyconadin A and related derivatives.

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Year:  2009        PMID: 19591469     DOI: 10.1021/ja903868n

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  20 in total

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7.  Development of an enantioselective route toward the Lycopodium alkaloids: total synthesis of lycopodine.

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8.  Pyridone annulation via tandem Curtius rearrangement/6π-electrocyclization: total synthesis of (-)-lyconadin C.

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9.  Toward a unified approach for the lycopodines: synthesis of 10-hydroxylycopodine, deacetylpaniculine, and paniculine.

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10.  Intramolecular C(sp3)-N coupling by oxidation of benzylic C,N-dianions.

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