Literature DB >> 26452462

Palladium-Catalyzed Carbonylative Annulation Reactions Using Aryl Formate as a CO Source: Synthesis of 2-Substituted Indene-1,3(2H)-dione Derivatives.

Ying Zhang1, Jing-Lei Chen1, Zhen-Bang Chen1, Yong-Ming Zhu1, Shun-Jun Ji2.   

Abstract

An efficient synthesis of 2-substituted indene-1,3(2H)-diones from stable and readily available 1-(2-halophenyl)-1,3-diones by employing phenyl formate as a CO source has been developed. The reaction occurred via palladium-catalyzed intramolecular carbonylative annulation using K3PO4 as a base and DMSO as a solvent at 95 °C. In this protocol, the reaction showed a broad substrate scope with good to excellent yields.

Entities:  

Year:  2015        PMID: 26452462     DOI: 10.1021/acs.joc.5b01758

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Achieving Moderate Pressures in Sealed Vessels Using Dry Ice As a Solid CO2 Source.

Authors:  Mohit Kapoor; Pratibha Chand-Thakuri; Justin M Maxwell; Michael C Young
Journal:  J Vis Exp       Date:  2018-08-17       Impact factor: 1.355

2.  A Method for C2 Acylation of 1,3-Indandiones.

Authors:  Brian J Larsen; Robert J Rosano; Thomas A Ford-Hutchinson; Allen B Reitz; Jay E Wrobel
Journal:  Tetrahedron       Date:  2018-04-17       Impact factor: 2.457

  2 in total

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