Literature DB >> 12688711

The first example of Nazarov reactions of vinyl cumulenyl ketones.

Eric Leclerc1, Marcus A Tius.   

Abstract

[reaction: see text] alpha-Lithio cumulenyl ethers can be prepared in situ and converted to alpha-allenyl cyclopentenones. Isomerization of the product of one such reaction has led to a furanyl cyclopentenone, the core structure of nakadomarin A.

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Year:  2003        PMID： 12688711     DOI： 10.1021/ol034110x

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


  5 in total

1.  SYNTHESIS OF TERMINAL 1,3-DIYNES VIA SONOGASHIRA COUPLING OF VINYLIDENE CHLORIDE FOLLOWED BY ELIMINATION. PREPARATION OF 1,3-DECADIYNE.

Authors:  Amanda L Kohnen; Rick L Danheiser; Scott E Denmark; Xiaorong Liu
Journal:  Organic Synth       Date:  2007

Review 2.  Transition metal-mediated synthesis of monocyclic aromatic heterocycles.

Authors:  Anton V Gulevich; Alexander S Dudnik; Natalia Chernyak; Vladimir Gevorgyan
Journal:  Chem Rev       Date:  2013-01-10       Impact factor: 60.622

3.  Total synthesis of (-)-nakadomarin A.

Authors:  Mark G Nilson; Raymond L Funk
Journal:  Org Lett       Date:  2010-11-05       Impact factor: 6.005

4.  Synthetic Studies Towards the Core Structure of Nakadomarin A by a Thioamide-Based Strategy.

Authors:  Jai K Chavda; Panayiotis A Procopiou; Peter N Horton; Simon J Coles; Michael J Porter
Journal:  European J Org Chem       Date:  2013-11-14

5.  The first intermolecular interrupted imino-Nazarov reaction: expeditious access to carbocyclic nucleoside analogues.

Authors:  Ronny William; Wei Lin Leng; Siming Wang; Xue-Wei Liu
Journal:  Chem Sci       Date:  2015-10-27       Impact factor: 9.825
  5 in total

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