Literature DB >> 20669958

Diels-Alder chemistry of siloles and their transformation into cyclohex-2-ene-1,4-cis-diols.

Andrew C Stevens1, Brian L Pagenkopf.   

Abstract

The synthesis of siloles with substitution patterns that are continuative toward natural product synthesis are described. Their reactivity in Diels-Alder chemistry was explored through thermal, Lewis acid, and high-pressure reactions. Furthermore, bicyclic adducts were oxidatively cleaved to reveal a highly functionalized cyclohexene core.

Entities:  

Year:  2010        PMID: 20669958     DOI: 10.1021/ol101453e

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Formation of Hindered Arylcarbamates using Alkyl Aryl Carbonates under Highly Reactive Conditions.

Authors:  Shahien Shahsavari; James Gooding; Travis Wigstrom; Shiyue Fang
Journal:  ChemistrySelect       Date:  2017-05-10       Impact factor: 2.109

2.  Conformationally Biased Ketones React Diastereoselectively with Allylmagnesium Halides.

Authors:  Nicole D Bartolo; Krystyna M Demkiw; Jacquelyne A Read; Elizabeth M Valentín; Yingying Yang; Alexandra M Dillon; Chunhua T Hu; Michael D Ward; K A Woerpel
Journal:  J Org Chem       Date:  2022-02-15       Impact factor: 4.198

  2 in total

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