Literature DB >> 19750686

The Diels--Alder reaction in total synthesis.

K C Nicolaou1, Scott A Snyder, Tamsyn Montagnon, Georgios Vassilikogiannakis.   

Abstract

The Diels-Alder reaction has both enabled and shaped the art and science of total synthesis over the last few decades to an extent which, arguably, has yet to be eclipsed by any other transformation in the current synthetic repertoire. With myriad applications of this magnificent pericyclic reaction, often as a crucial element in elegant and programmed cascade sequences facilitating complex molecule construction, the Diels-Alder cycloaddition has afforded numerous and unparalleled solutions to a diverse range of synthetic puzzles provided by nature in the form of natural products. In celebration of the 100th anniversary of Alder's birth, selected examples of the awesome power of the reaction he helped to discover are discussed in this review in the context of total synthesis to illustrate its overall versatility and underscore its vast potential which has yet to be fully realized.

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Year:  2002        PMID: 19750686     DOI: 10.1002/1521-3773(20020517)41:10<1668::aid-anie1668>3.0.co;2-z

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


  184 in total

1.  Enantioselective Crossed Photocycloadditions of Styrenic Olefins by Lewis Acid Catalyzed Triplet Sensitization.

Authors:  Zachary D Miller; Byung Joo Lee; Tehshik P Yoon
Journal:  Angew Chem Int Ed Engl       Date:  2017-08-30       Impact factor: 15.336

Review 2.  The essence of total synthesis.

Authors:  K C Nicolaou; Scott A Snyder
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-09       Impact factor: 11.205

3.  Dynamics, transition states, and timing of bond formation in Diels-Alder reactions.

Authors:  Kersey Black; Peng Liu; Lai Xu; Charles Doubleday; Kendall N Houk
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-02       Impact factor: 11.205

4.  Biochemistry. Reengineering enzymes.

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

5.  Allenoates in Enantioselective [2+2] Cycloadditions: From a Mechanistic Curiosity to a Stereospecific Transformation.

Authors:  Johannes M Wiest; Michael L Conner; M Kevin Brown
Journal:  J Am Chem Soc       Date:  2018-11-05       Impact factor: 15.419

6.  Synthetic Studies towards Maoecrystal V.

Authors:  Feng Peng; Maolin Yu; Samuel J Danishefsky
Journal:  Tetrahedron Lett       Date:  2009-11-25       Impact factor: 2.415

7.  Total synthesis and absolute configuration of the bisanthraquinone antibiotic BE-43472B.

Authors:  K C Nicolaou; Yee Hwee Lim; Jochen Becker
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

8.  An unexpected Lewis acid catalyzed Diels-Alder cycloaddition of aryl allenes and acrylates.

Authors:  Michael L Conner; M Kevin Brown
Journal:  Tetrahedron       Date:  2016-02-18       Impact factor: 2.457

9.  Fusarisetin A: Scalable Total Synthesis and Related Studies.

Authors:  Jing Xu; Eduardo J E Caro-Diaz; Michelle H Lacoske; Chao-I Hung; Colin Jamora; Emmanuel A Theodorakis
Journal:  Chem Sci       Date:  2012-08-23       Impact factor: 9.825

10.  Cationic-oxazaborolidine-catalyzed enantioselective Diels-Alder reaction of alpha,beta-unsaturated acetylenic ketones.

Authors:  Joshua N Payette; Hisashi Yamamoto
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

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