Literature DB >> 29333548

Efficient generation of an oxidopyrylium ylide using a Pd catalyst and its [5+2] cycloadditions with several dipolarophiles.

Hiroyuki Suga1, Taichi Iwai, Masahiro Shimizu, Kie Takahashi, Yasunori Toda.   

Abstract

An efficient method for the generation of an oxidopyrylium ylide from 6-acetoxy-6-acetoxymethyl-2H-pyran-3(6H)-one using a Pd catalyst and [5+2] cycloadditions of the resulting ylide are described. Among substituted styrene derivatives as dipolarophiles, electron-rich styrenes showed higher yield (up to 80%). The [5+2] cycloaddition reactions can also be applied to exo-methylene cyclic compounds, and an improved method for the synthesis of polygalolide intermediate has been demonstrated.

Entities:  

Year:  2018        PMID: 29333548     DOI: 10.1039/c7cc09552j

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


  3 in total

1.  Maltol- and Allomaltol-Derived Oxidopyrylium Ylides: Methyl Substitution Pattern Kinetically Influences [5 + 3] Dimerization versus [5 + 2] Cycloaddition Reactions.

Authors:  Lauren P Bejcek; Aswin K Garimallaprabhakaran; Duygu M Suyabatmaz; Alexander Greer; William H Hersh; Edyta M Greer; Ryan P Murelli
Journal:  J Org Chem       Date:  2019-10-25       Impact factor: 4.354

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.  Investigations into a Stoichiometrically Equivalent Intermolecular Oxidopyrylium [5 + 2] Cycloaddition Reaction Leveraging 3-Hydroxy-4-pyrone-Based Oxidopyrylium Dimers.

Authors:  Daniel V Schiavone; Diana M Kapkayeva; Ryan P Murelli
Journal:  J Org Chem       Date:  2021-02-15       Impact factor: 4.354

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.