Literature DB >> 11843617

Unprecedented microwave effects on the cycloaddition of fulvenes. A new approach to the construction of polycyclic ring systems.

Bor-Cherng Hong1, Yeong-Jou Shr, Ju-Hsiou Liao.   

Abstract

[reaction: see text] Novel cycloaddition reactions between fulvenes and various alkenes and alkynes are promoted by the use of microwave irradiation. These processes result in the formation of intriguing polycyclic ring systems such as those found in isobarbatene, alcyopterosin, and enokipodin A. Importantly, these reactions do not occur under conventional thermolytic conditions.

Entities:  

Year:  2002        PMID: 11843617     DOI: 10.1021/ol017304q

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


  3 in total

1.  A cope rearrangement-based route to hexahydroazulenes.

Authors:  Curtis A Seizert; Valentina D Bumbu; Vladimir B Birman
Journal:  Org Lett       Date:  2010-08-06       Impact factor: 6.005

2.  Microwave enhanced Akabori reaction for peptide analysis.

Authors:  Ajay K Bose; Yao Hain Ing; Nina Lavlinskaia; Chaitanya Sareen; Birendra N Pramanik; Peter L Bartner; Yan-Hui Liu; Larry Heimark
Journal:  J Am Soc Mass Spectrom       Date:  2002-07       Impact factor: 3.109

Review 3.  An overview of the cycloaddition chemistry of fulvenes and emerging applications.

Authors:  Ellen Swan; Kirsten Platts; Anton Blencowe
Journal:  Beilstein J Org Chem       Date:  2019-09-06       Impact factor: 2.883

  3 in total

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