Reactivity of α-trifluoromethanesulfonyl esters, amides and ketones: Decarboxylative allylation, methylation, and enol formation-Reference-Cited by-同舟云学术

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Reactivity of α-trifluoromethanesulfonyl esters, amides and ketones: Decarboxylative allylation, methylation, and enol formation

Published:2013-09 Issue: Volume:153 Page:151-161
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Kong Han Il,Gill Monica A.,Hrdina Amy H.,Crichton Jennifer E.,Manthorpe Jeffrey M.

Funder

Carleton University

Ontario Research Foundation

Natural Sciences and Engineering Research Council of Canada

Government of Ontario

Canada Foundation for Innovation

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry

Reference50 articles.

1. Trifyl activation in organic synthesis

2. USES OF THE TRIFYL GROUP IN ORGANIC SYNTHESIS. A REVIEW

3. Improved synthesis of trifluoromethyl sulfones used as intermediates for the preparation of di- or tri-substituted olefins

4. Reactions of bromotrifluoromethane and related halides. 8. Condensations with dithionite and hydroxymethanesulfinate salts

5. A new simple access to trifluoromethyl thioethers or selenoethers from trifluoromethyl trimethylsilane and disulfides or diselenides

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2. Synthetic Strategies Towards and Around the CF3S(O) Structural Motif;Current Organic Chemistry;2023-03

3. Development of Palladium-Catalyzed Decarboxylative Allylation of Electron-Deficient Sulfones and Identification of Unusual Side Products;The Journal of Organic Chemistry;2019-04-09

4. A convenient access to allylic triflones with allenes and triflyl chloride in the presence of (EtO)2P(O)H;Chemical Communications;2019

5. Rapid Interception of CnF2n+1(O)SO• Radical with Copper‐Based Carbene: A Novel Access to Perfluoroalkanesulfinate Ester;Chemistry – A European Journal;2018-12-12

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