Literature DB >> 28841323

Organocatalytic, Dioxirane-Mediated C-H Hydroxylation under Mild Conditions Using Oxone.

William G Shuler1, Shea L Johnson1, Michael K Hilinski1.   

Abstract

Dioxiranes are among the most selective and useful reagents for C(sp3)-H hydroxylation, but the development of a general dioxirane-mediated catalytic method has been an elusive goal. A trifluoromethyl ketone catalyst in combination with Oxone is shown to enable the first dioxirane-mediated catalytic hydroxylations that approximate the reactivity and selectivity of isolated dioxiranes. The mild reaction conditions allow for selective 3° hydroxylation and 2° oxidation and are tolerant of acid-sensitive functionality and electron-neutral arenes.

Entities:  

Year:  2017        PMID: 28841323     DOI: 10.1021/acs.orglett.7b02178

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


  3 in total

1.  Organocatalytic Olefin Aziridination via Iminium-Catalyzed Nitrene Transfer: Scope, Limitations, and Mechanistic Insight.

Authors:  Shea L Johnson; Michael K Hilinski
Journal:  J Org Chem       Date:  2019-06-19       Impact factor: 4.354

2.  Amine Organocatalysis of Remote, Chemoselective C(sp3)-H Hydroxylation.

Authors:  Philip L Hahn; Jared M Lowe; Yubo Xu; Kevin L Burns; Michael K Hilinski
Journal:  ACS Catal       Date:  2022-03-28       Impact factor: 13.700

3.  Organocatalytic nitrenoid transfer: metal-free selective intermolecular C(sp3)-H amination catalyzed by an iminium salt.

Authors:  Logan A Combee; Balaram Raya; Daoyong Wang; Michael K Hilinski
Journal:  Chem Sci       Date:  2017-11-27       Impact factor: 9.825

  3 in total

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