Literature DB >> 11433483

Programming Organic Molecules: Design and Management of Organic Syntheses through Free-Radical Cascade Processes.

Andrew J. McCarroll1, John C. Walton.   

Abstract

Cascade, domino, or tandem processes, that link together two or more transformations in one pot, are increasing in popularity because they lead to improvements in synthetic efficiency and decreases in environmental impact. Not only do these cascades contain choice mechanistic gems but they also deliver compact and elegant syntheses of complex natural products. Longer cascades require more functional groups precisely configured within carefully designed initial molecular architectures. Such "purposeful" molecules can be thought of as chemical algorithms.This article surveys the phenomenal range of unimolecular free-radical cascades. A convenient system for classifying free-radical cascades is described that is useful for evaluating and comparing cascades and aids the design of synthetic routes to polycyclic structures.Double cyclization cascades lead to cyclopentylcyclopentane or bicyclo[3.3.0]octane derivatives. Precursors that contain a ring as a template have been used to control stereochemistry in syntheses of triquinanes and many related compounds. Of the cascades containing ring-cleavage steps, the most useful are the ring expansions which have opened up new synthetic routes to medium ring polycycles.The key design features of three-stage unimolecular free-radical cascades that yielded steroid structures, are linear arrays of radical acceptor units associated with methyl groups distributed every fifth C-atom in the precursor polyenes. Ring cleavage is the reverse of cyclization. In special, symmetrical structures, therefore, this led to sequences that were reversible, thus launching endlessly repeating cascades supported by delightfully fluxional structures. The science of "programming" organic molecules to achieve particular target structures is maturing rapidly. Coordination and classification of the welter of information in this area is intended to facilitate design and hence to extend the range and complexity of attainable structures.

Entities:  

Year:  2001        PMID: 11433483     DOI: 10.1002/1521-3773(20010618)40:12<2224::aid-anie2224>3.0.co;2-f

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


  7 in total

1.  Stereoselective cascade reactions that incorporate a 7-exo acyl radical cyclization.

Authors:  Seth W Grant; Koudi Zhu; Yu Zhang; Steven L Castle
Journal:  Org Lett       Date:  2006-04-27       Impact factor: 6.005

Review 2.  Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products.

Authors:  Zachary G Brill; Matthew L Condakes; Chi P Ting; Thomas J Maimone
Journal:  Chem Rev       Date:  2017-03-15       Impact factor: 60.622

3.  Enantioselective synthesis of an ophiobolin sesterterpene via a programmed radical cascade.

Authors:  Zachary G Brill; Huck K Grover; Thomas J Maimone
Journal:  Science       Date:  2016-05-27       Impact factor: 47.728

Review 4.  Biosynthesis and chemical synthesis of presilphiperfolanol natural products.

Authors:  Allen Y Hong; Brian M Stoltz
Journal:  Angew Chem Int Ed Engl       Date:  2014-04-25       Impact factor: 15.336

Review 5.  Total synthesis of complex terpenoids employing radical cascade processes.

Authors:  Kevin Hung; Xirui Hu; Thomas J Maimone
Journal:  Nat Prod Rep       Date:  2018-02-21       Impact factor: 13.423

Review 6.  Progress in the synthesis of δ-sultones.

Authors:  Christina Gaunersdorfer; Mario Waser
Journal:  Monatsh Chem       Date:  2017-07-15       Impact factor: 1.451

Review 7.  Difunctionalization of Alkenes and Alkynes via Intermolecular Radical and Nucleophilic Additions.

Authors:  Hongjun Yao; Wenfei Hu; Wei Zhang
Journal:  Molecules       Date:  2020-12-28       Impact factor: 4.411

  7 in total

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