Literature DB >> 26090926

Tandem Dehydrogenation/Oxidation/Oxidative Cyclization Approach to Wrightiadione and Its Derivatives.

Yujeong Jeong1,2, Youngtaek Moon1,2, Sungwoo Hong1,2.   

Abstract

Wrightiadione contains a unique tetracyclic isoflavone moiety and has been shown to exhibit a broad range of biological activities. An efficient and straightforward synthetic method for generating the molecular complexity of wrightiadione was developed through three-step tandem dehydrogenation/oxidation/oxidative cyclization reactions with a Pd/Cu catalytic system. This unprecedented one-pot route utilizes a broad range of substrates, providing a convenient and powerful synthetic tool for accessing naturally occurring tetracyclic isoflavone wrightiadione and its nitrogen-containing derivatives.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 26090926     DOI: 10.1021/acs.orglett.5b01618

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


  2 in total

1.  Co/NHPI-mediated aerobic oxygenation of benzylic C-H bonds in pharmaceutically relevant molecules.

Authors:  Damian P Hruszkewycz; Kelsey C Miles; Oliver R Thiel; Shannon S Stahl
Journal:  Chem Sci       Date:  2016-10-07       Impact factor: 9.825

2.  Total Synthesis of (+)-Cochlearol B by an Approach Based on a Catellani Reaction and Visible-Light-Enabled [2+2] Cycloaddition.

Authors:  Alistair D Richardson; Trenton R Vogel; Emily F Traficante; Kason J Glover; Corinna S Schindler
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-23       Impact factor: 16.823

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.