Literature DB >> 19521597

Formation and [3,3]-sigmatropic rearrangement of O-allyl nitronic esters: a new route to gamma,delta-unsaturated nitro compounds.

Peter A Wade1, Alma Pipic, Manikandan Santhanaraman, Hung T Le.   

Abstract

O-Allyl nitronic esters that are obtained from tin(IV) catalyzed Diels-Alder reactions undergo thermal rearrangement to gamma,delta-unsaturated nitro compounds.

Entities:  

Year:  2009        PMID： 19521597     DOI： 10.1039/b902870f

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


  2 in total

1.  Sequential Diels-Alder/[3,3]-sigmatropic rearrangement reactions of β-nitrostyrene with 3-methyl-1,3-pentadiene.

Authors:  Peter A Wade; Alma Pipic; Matthias Zeller; Panagiota Tsetsakos
Journal:  Beilstein J Org Chem       Date:  2013-10-17       Impact factor: 2.883

2.  Understanding the Molecular Mechanism of the Rearrangement of Internal Nitronic Ester into Nitronorbornene in Light of the MEDT Study.

Authors:  Agnieszka Kącka-Zych
Journal:  Molecules       Date:  2019-01-28       Impact factor: 4.411
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.