Literature DB >> 27730740

Iridium-Catalyzed Carbonylative Synthesis of Chromenones from Simple Phenols and Internal Alkynes at Atmospheric Pressure.

Fengxiang Zhu1, Yahui Li1, Zechao Wang1, Xiao-Feng Wu2,3.   

Abstract

A novel procedure on the carbonylative synthesis of chromenones has been developed. With simple phenols and internal alkynes as the substrates, various chromenones were isolated in moderate to good yields with excellent regioselectivity and functional-group tolerance by using iridium as the catalyst and copper as the promotor at atmospheric pressure. Notably, this is the first example on carbonylative annulation of simple phenols and alkynes.
© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  annulations; carbonylation; heterocycles; iridium; reaction mechanisms

Year:  2016        PMID: 27730740     DOI: 10.1002/anie.201608715

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Transition-metal-free synthesis of 3-sulfenylated chromones via KIO3-catalyzed radical C(sp2)-H sulfenylation.

Authors:  Yanhui Guo; Shanshan Zhong; Li Wei; Jie-Ping Wan
Journal:  Beilstein J Org Chem       Date:  2017-09-27       Impact factor: 2.883

Review 2.  3-Phenylcoumarins as a Privileged Scaffold in Medicinal Chemistry: The Landmarks of the Past Decade.

Authors:  Maria J Matos; Eugenio Uriarte; Lourdes Santana
Journal:  Molecules       Date:  2021-11-08       Impact factor: 4.411

  2 in total

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