Literature DB >> 17929230

O-alkyl S-3,3-dimethyl-2-oxobutyl dithiocarbonates as versatile sulfur-transfer agents in radical C(sp3)-H functionalization.

Akinori Sato1, Hideki Yorimitsu, Koichiro Oshima.   

Abstract

Boiling of the title compounds in ethereal solvents or cycloalkanes in the presence of a radical initiator leads to radical C(sp3)-H functionalization, by which a sulfur atom is introduced into the ethereal solvents at the oxygenated carbon atom or into the cycloalkanes. Both acyclic and cyclic ethers, such as [18]crown-6 and [D8]THF, undergo the sulfur transfer. The reaction is useful for the synthesis of monothioacetals, thiols, and sulfides from simple starting materials.

Entities:  

Year:  2007        PMID: 17929230     DOI: 10.1002/asia.200700251

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  4 in total

1.  Modifying Positional Selectivity in C-H Functionalization Reactions with Nitrogen-Centered Radicals: Generalizable Approaches to 1,6-Hydrogen-Atom Transfer Processes.

Authors:  Melanie A Short; J Miles Blackburn; Jennifer L Roizen
Journal:  Synlett       Date:  2019-11-27       Impact factor: 2.454

2.  C-H Xanthylation: A Synthetic Platform for Alkane Functionalization.

Authors:  William L Czaplyski; Christina G Na; Erik J Alexanian
Journal:  J Am Chem Soc       Date:  2016-10-14       Impact factor: 15.419

3.  Sulfamate Esters Guide C(3)-Selective Xanthylation of Alkanes.

Authors:  Suraj K Ayer; J L Roizen
Journal:  J Org Chem       Date:  2019-02-26       Impact factor: 4.354

Review 4.  Strategies to Generate Nitrogen-centered Radicals That May Rely on Photoredox Catalysis: Development in Reaction Methodology and Applications in Organic Synthesis.

Authors:  Kitae Kwon; R Thomas Simons; Meganathan Nandakumar; Jennifer L Roizen
Journal:  Chem Rev       Date:  2021-10-08       Impact factor: 60.622

  4 in total

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