Literature DB >> 24728307

The versatility of furfuryl alcohols and furanoxonium ions in synthesis.

Matthew J Palframan1, Gerald Pattenden.   

Abstract

Substituted furfuryl alcohols are extraordinarily versatile starting materials in synthesis. They are precursors to furanoxonium ion intermediates which are implicated in the Piancatelli reaction (leading to 2-cyclopentenones) and in the synthesis of novel dihydrofuran-based exo enol ether/cyclic ketal natural products. They are also intermediates in a recently discovered (4+3) cycloaddition reaction with 1,3-dienes leading to furan ring-fused cycloheptenes. Here we provide a perspective on recent developments in these areas of synthesis, alongside recent applications of the Achmatowicz reaction and [5+2] cycloaddition reactions of the resulting oxidopyrylium ions.

Entities:  

Year:  2014        PMID: 24728307     DOI: 10.1039/c4cc01196a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Achmatowicz Reaction and its Application in the Syntheses of Bioactive Molecules.

Authors:  Arun K Ghosh; Margherita Brindisi
Journal:  RSC Adv       Date:  2016-11-24       Impact factor: 3.361

2.  Oxidopyrylium [5+2] Cycloaddition Chemistry: Historical Perspective and Recent Advances (2008-2018).

Authors:  Lauren P Bejcek; Ryan P Murelli
Journal:  Tetrahedron       Date:  2018-04-05       Impact factor: 2.457

3.  Tandem Thio-Michael Addition/Remote Lactone Activation of 5-Hydroxymethylfurfural-Derived δ-Lactone-Fused Cyclopentenones.

Authors:  Rafael F A Gomes; Joao M J M Ravasco; Késsia H S Andrade; Jaime A S Coelho; Rui Moreira; Rafael Oliveira; Fátima Nogueira; Carlos A M Afonso
Journal:  ChemSusChem       Date:  2022-01-18       Impact factor: 9.140

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.