Literature DB >> 12866094

Chemistry and biology of biosynthetic Diels-Alder reactions.

Emily M Stocking1, Robert M Williams.   

Abstract

Nature's repertoire of biosynthetic transformations has recently been recognized to include the Diels-Alder cycloaddition reaction. Evidence now exists that there are enzymes that mediate the Diels-Alder reaction in secondary metabolic biosynthetic pathways. 2002 marked the 100th anniversary of Alder's birth and 75 years since the discovery of the Diels-Alder reaction. It would appear that living systems discovered and made use of this ubiquitously useful ring-forming reaction eons ago for the construction of complex natural products. In this Review an overview is given of all of the known classes of natural products (polyketides, isoprenoids, phenylpropanoids, alkaloids) that have been speculated to arise by a biological Diels-Alder reaction.

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Year:  2003        PMID: 12866094     DOI: 10.1002/anie.200200534

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


  66 in total

1.  Function and Structure of MalA/MalA', Iterative Halogenases for Late-Stage C-H Functionalization of Indole Alkaloids.

Authors:  Amy E Fraley; Marc Garcia-Borràs; Ashootosh Tripathi; Dheeraj Khare; Eduardo V Mercado-Marin; Hong Tran; Qingyun Dan; Gabrielle P Webb; Katharine R Watts; Phillip Crews; Richmond Sarpong; Robert M Williams; Janet L Smith; K N Houk; David H Sherman
Journal:  J Am Chem Soc       Date:  2017-08-21       Impact factor: 15.419

2.  Total synthesis of (-)-spinosyn A.

Authors:  Dustin J Mergott; Scott A Frank; William R Roush
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-01       Impact factor: 11.205

3.  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

4.  Biochemistry. Reengineering enzymes.

Authors:  Stefan Lutz
Journal:  Science       Date:  2010-07-16       Impact factor: 47.728

5.  Selection of ribozymes that catalyse multiple-turnover Diels-Alder cycloadditions by using in vitro compartmentalization.

Authors:  Jeremy J Agresti; Bernard T Kelly; Andres Jäschke; Andrew D Griffiths
Journal:  Proc Natl Acad Sci U S A       Date:  2005-10-31       Impact factor: 11.205

6.  Synthesis of many different types of organic small molecules using one automated process.

Authors:  Junqi Li; Steven G Ballmer; Eric P Gillis; Seiko Fujii; Michael J Schmidt; Andrea M E Palazzolo; Jonathan W Lehmann; Greg F Morehouse; Martin D Burke
Journal:  Science       Date:  2015-03-13       Impact factor: 47.728

7.  Total synthesis of (+)-superstolide A.

Authors:  Mariola Tortosa; Neal A Yakelis; William R Roush
Journal:  J Org Chem       Date:  2008-12-19       Impact factor: 4.354

8.  The biosynthesis of spinosyn in Saccharopolyspora spinosa: synthesis of the cross-bridging precursor and identification of the function of SpnJ.

Authors:  Hak Joong Kim; Rongson Pongdee; Qingquan Wu; Lin Hong; Hung-wen Liu
Journal:  J Am Chem Soc       Date:  2007-11-07       Impact factor: 15.419

9.  Enantioselective synthesis of (+)-chamaecypanone C: a novel microtubule inhibitor.

Authors:  Suwei Dong; Ernest Hamel; Ruoli Bai; David G Covell; John A Beutler; John A Porco
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

10.  Natural Diels-Alderases: Elusive and Irresistable.

Authors:  Kimberly Klas; Sachiko Tsukamoto; David H Sherman; Robert M Williams
Journal:  J Org Chem       Date:  2015-12-04       Impact factor: 4.354

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