Literature DB >> 15176798

Palladium-catalyzed ring expansion reaction of (Z)-1-(1,3-butadienyl)cyclobutanols with aryl iodides. stereospecific synthesis of (Z)-2-(3-aryl-1-propenyl)cyclopentanones.

Masahiro Yoshida1, Kenji Sugimoto, Masataka Ihara.   

Abstract

[reaction: see text] A novel type of cascade ring expansion process has been developed by the palladium-catalyzed reaction of (Z)-1-(1,3-butadienyl)cyclobutanols with aryl iodides. The reaction proceeds in a stereospecific manner to produce (Z)-2-(3-aryl-1-propenyl)cyclopentanones. It has also been found that regioselective alpha-arylation of alkenyl cyclopentanones proceeds to afford the alpha-arylated cyclopentanones.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15176798     DOI: 10.1021/ol049438k

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


  2 in total

1.  Stereoselective, dual-mode ruthenium-catalyzed ring expansion of alkynylcyclopropanols.

Authors:  Barry M Trost; Jia Xie; Nuno Maulide
Journal:  J Am Chem Soc       Date:  2008-12-24       Impact factor: 15.419

2.  Stereoselective total synthesis and structural revision of the diacetylenic diol natural products strongylodiols H and I.

Authors:  Pamarthi Gangadhar; Sayini Ramakrishna; Ponneri Venkateswarlu; Pabbaraja Srihari
Journal:  Beilstein J Org Chem       Date:  2018-09-04       Impact factor: 2.883

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.