Literature DB >> 19994906

Ring-rearrangement metathesis of cyclopropenes: synthesis of heterocycles.

Frédéric Miege1, Christophe Meyer, Janine Cossy.   

Abstract

Cyclopropenes substituted by an unsaturated side chain have been successfully involved in ring-rearrangement metatheses leading to heterocyclic compounds, thereby expanding the synthetic potential of metathesis reactions with this class of highly strained cycloalkenes.

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Year:  2010        PMID： 19994906     DOI： 10.1021/ol9025606

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


  5 in total

1.  Functionalized Cyclopropenes and Methylenecyclopropenes from Dianions of 3-Hydroxymethylcyclopropenes.

Authors:  Matthew D Hassink; Joseph M Fox
Journal:  Synthesis (Stuttg)       Date:  2012       Impact factor: 3.157

2.  Selective syntheses of Δ(α,β) and Δ(β,γ) butenolides from allylic cyclopropenecarboxylates via tandem ring expansion/[3,3]-sigmatropic rearrangements.

Authors:  Xiaocong Xie; Yi Li; Joseph M Fox
Journal:  Org Lett       Date:  2013-03-20       Impact factor: 6.005

3.  Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps.

Authors:  Sambasivarao Kotha; Ongolu Ravikumar; Jadab Majhi
Journal:  Beilstein J Org Chem       Date:  2015-08-27       Impact factor: 2.883

4.  Design and synthesis of fused polycycles via Diels-Alder reaction and ring-rearrangement metathesis as key steps.

Authors:  Sambasivarao Kotha; Ongolu Ravikumar
Journal:  Beilstein J Org Chem       Date:  2015-07-27       Impact factor: 2.883

Review 5.  Recent applications of ring-rearrangement metathesis in organic synthesis.

Authors:  Sambasivarao Kotha; Milind Meshram; Priti Khedkar; Shaibal Banerjee; Deepak Deodhar
Journal:  Beilstein J Org Chem       Date:  2015-10-07       Impact factor: 2.883
  5 in total

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