Literature DB >> 19143488

Total synthesis of diverse carbogenic complexity within the resveratrol class from a common building block.

Scott A Snyder1, Steven P Breazzano, Audrey G Ross, Yunqing Lin, Alexandros L Zografos.   

Abstract

Although biomimetic approaches have proven capable of converting resveratrol (1) concurrently into many of the more complex oligomers produced by plants throughout the world (such as 2-10), methods to access single members of the family have proven far more difficult to identify. Herein is described a strategy-level solution based on the use of a common building block, one distinct from Nature's starting material, that can participate in a variety of highly selective, reagent-controlled reaction cascades. These endeavors have led to the controlled synthesis of 25 natural products and analogues, molecules whose architectures encompass nearly all the carbogenic diversity of the resveratrol family.

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Year:  2009        PMID: 19143488     DOI: 10.1021/ja806183r

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


  41 in total

1.  Lessons and revelations from biomimetic syntheses.

Authors:  Mina Razzak; Jef K De Brabander
Journal:  Nat Chem Biol       Date:  2011-11-15       Impact factor: 15.040

Review 2.  Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.

Authors:  K C Nicolaou; Christopher R H Hale; Christian Nilewski; Heraklidia A Ioannidou
Journal:  Chem Soc Rev       Date:  2012-06-28       Impact factor: 54.564

3.  Four-component domino reaction providing an easy access to multifunctionalized tricyclo[6.2.2.0(1,6)]dodecane derivatives.

Authors:  Bo Jiang; Chao Li; Feng Shi; Shu-Jiang Tu; Parminder Kaur; Walter Wever; Guigen Li
Journal:  J Org Chem       Date:  2010-05-07       Impact factor: 4.354

4.  Organic chemistry: Triumph for unnatural synthesis.

Authors:  Stéphane Quideau
Journal:  Nature       Date:  2011-06-22       Impact factor: 49.962

Review 5.  Chemistry and Biology of Resveratrol-Derived Natural Products.

Authors:  Mitchell H Keylor; Bryan S Matsuura; Corey R J Stephenson
Journal:  Chem Rev       Date:  2015-04-02       Impact factor: 60.622

6.  Structural revision and total synthesis of caraphenol B and C.

Authors:  Scott A Snyder; Zachary G Brill
Journal:  Org Lett       Date:  2011-09-26       Impact factor: 6.005

7.  Efficient domino approaches to multifunctionalized fused pyrroles and dibenzo[b,e][1,4]diazepin-1-ones.

Authors:  Bo Jiang; Qiu-Yun Li; Hao Zhang; Shu-Jiang Tu; Suresh Pindi; Guigen Li
Journal:  Org Lett       Date:  2012-01-19       Impact factor: 6.005

8.  Harnessing quinone methides: total synthesis of (±)-vaticanol A.

Authors:  Tue H Jepsen; Stephen B Thomas; Yunqing Lin; Christos I Stathakis; Irene de Miguel; Scott A Snyder
Journal:  Angew Chem Int Ed Engl       Date:  2014-05-19       Impact factor: 15.336

9.  Total syntheses of dalesconol A and B.

Authors:  Scott A Snyder; Trevor C Sherwood; Audrey G Ross
Journal:  Angew Chem Int Ed Engl       Date:  2010-07-12       Impact factor: 15.336

10.  Concise synthesis of pauciflorol F using a Larock annulation.

Authors:  Jenna L Jeffrey; Richmond Sarpong
Journal:  Org Lett       Date:  2009-12-03       Impact factor: 6.005

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