Literature DB >> 20520878

Organic synthesis using a hypervalent iodine reagent: unexpected and novel domino reaction leading to spiro cyclohexadienone lactones.

Hiromichi Fujioka1, Hideyuki Komatsu, Taeko Nakamura, Akihito Miyoshi, Kayoko Hata, Jnashuara Ganesh, Kenichi Murai, Yasuyuki Kita.   

Abstract

The reaction of 1-(p-hydroxyaryl)cyclobutanols and phenyl iodide(III) diacetate in hexafluoroisopropanol and water produced spiro cyclohexadienone lactones via a domino reaction.

Entities:  

Mesh：

Substances：

Year:  2010        PMID： 20520878     DOI： 10.1039/b925687c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  3 in total

Review 1.  Synthesis of spirocyclic scaffolds using hypervalent iodine reagents.

Authors:  Fateh V Singh; Priyanka B Kole; Saeesh R Mangaonkar; Samata E Shetgaonkar
Journal:  Beilstein J Org Chem       Date:  2018-07-17       Impact factor: 2.883

2.  Molecular Iodine-Catalyzed Synthesis of Imidazo[1,2-a]Pyridines: Screening of Their In Silico Selectivity, Binding Affinity to Biological Targets, and Density Functional Theory Studies Insight.

Authors:  Deepika Geedkar; Ashok Kumar; Pratibha Sharma
Journal:  ACS Omega       Date:  2022-06-22

3.  Diastereoselective synthesis of 5-hydroxy-8-methoxy-1-oxaspiro[5,5]undeca-7,10-diene-9-one.

Authors:  Guy L Plourde; Thomas W Scully
Journal:  Molecules       Date:  2013-01-17       Impact factor: 4.411
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.