Literature DB >> 22991946

Nitroxyl radical/PhI(OAc)2: one-pot oxidative cleavage of vicinal diols to (di)carboxylic acids.

Masatoshi Shibuya1, Takuro Shibuta, Hayato Fukuda, Yoshiharu Iwabuchi.   

Abstract

A mild and user-friendly one-pot oxidative cleavage of vicinal diols to their corresponding (di)carboxylic acids using AZADOs and PhI(OAc)(2) is described. 1,2-Diols and 2,3-diols as well as 1,2,3-triol gave one- or two-carbon-unit-shorter carboxylic acids. Internal vicinal diols also smoothly underwent one-pot oxidative cleavage to afford the corresponding dicarboxylic acids. Cyclic vicinal diols are converted to their corresponding open-form dicarboxylic acids.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22991946     DOI: 10.1021/ol3021435

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


  1 in total

1.  Ring expansion of cyclic 1,2-diols to form medium sized rings via ruthenium catalyzed transfer hydrogenative [4+2] cycloaddition.

Authors:  Zachary A Kasun; Laina M Geary; Michael J Krische
Journal:  Chem Commun (Camb)       Date:  2014-07-18       Impact factor: 6.222

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.