4.8 Article

Rhodium-Catalyzed Cleavage Reaction of Aryl Methyl Ethers with Thioesters

Journal

ORGANIC LETTERS
Volume 14, Issue 3, Pages 855-857

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol2033724

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Funding

  1. GCOE
  2. WPI Initiative from JSPS
  3. Japan Science Technology Agency
  4. Asahi Glass Foundation
  5. [21229001]
  6. [22689001]
  7. Grants-in-Aid for Scientific Research [21229001, 22689001] Funding Source: KAKEN

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A rhodium complex catalyzed the reaction of aryl methyl ethers and thioesters giving the corresponding aryl esters and methyl sulfides. S-(p-Chlorophenyl) p-(dimethylamino)benzothioate was used for the reaction of methyl aryl ethers with electron-withdrawing groups, and an S-(p-tolyl) derivative was used for those with electron-donating groups. Polymethoxybenzenes were converted to the esters in a regioselective manner.

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