Literature DB >> 32702201

Advances in Total Synthesis of Some 2,3,5-Trisubstituted Tetrahydrofuran Natural Products.

Rodney A Fernandes1, Ramdas S Pathare1, Dnyaneshwar A Gorve1.   

Abstract

2,3,5-Trisubstituted tetrahydrofuran moiety is ubiquitous in natural products. These have served as appealing candidates for total synthesis due to their varied bio- and pharmaceutical activities. This tutorial review delineates the ingenious efforts by many researchers in the total synthesis of selected natural products based on a common 2,3,5-trisubstituted tetrahydrofuran core structure. Many of the syntheses display nuanced interplay between new methods and the ingenuity of planned strategies achieved through catalysis or cascade chemistry. In some cases, the chiron approach has come quite handy, wherein the structural features and the stereochemistry in select molecules could map well with naturally available starting materials. This compilation also aims to enhance the diversity space based on these natural products and further interest in sustainable total synthesis.
© 2020 Wiley-VCH GmbH.

Entities:  

Keywords:  Natural products; Total synthesis; Trisubstituted tetrahydrofuran; allenes; lactones; oxylipids

Mesh:

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Year:  2020        PMID: 32702201     DOI: 10.1002/asia.202000753

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  3 in total

Review 1.  The Tetrahydrofuran Motif in Polyketide Marine Drugs.

Authors:  Laura Fernández-Peña; Carlos Díez-Poza; Paula González-Andrés; Asunción Barbero
Journal:  Mar Drugs       Date:  2022-02-03       Impact factor: 5.118

Review 2.  The Complexity of Sesquiterpene Chemistry Dictates Its Pleiotropic Biologic Effects on Inflammation.

Authors:  Narcy Arizmendi; Syed Benazir Alam; Khalid Azyat; Darren Makeiff; A Dean Befus; Marianna Kulka
Journal:  Molecules       Date:  2022-04-11       Impact factor: 4.927

3.  Oxo-Rhenium-Mediated Allylation of Furanoside Derivatives: A Computational Study on the Mechanism and the Stereoselectivity.

Authors:  Emanuele Casali; Alessio Porta; Lucio Toma; Giuseppe Zanoni
Journal:  J Org Chem       Date:  2022-07-12       Impact factor: 4.198

  3 in total

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