4.8 Article

Synthesis of Ynolates via Double Deprotonation of Nonbronninated Esters

Journal

ORGANIC LETTERS
Volume 21, Issue 17, Pages 6585-6588

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b02069

Keywords

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Funding

  1. JSPS KAKENHI [JP22390002, JP24106731, JP16H01157, JP26293004, JP17K14449, JP18H04418, JP18H04624, JP18H02557]
  2. Asahi Glass Foundation
  3. MEXT Project of Integrated Research Consortium on Chemical Sciences

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Herein, we report a double deprotonation method used for the preparation of ynolates starting from nonbrominated 2,6-di-tertbutylphenyl esters. The current method is superior to the previously described double lithium/halogen exchange approach because easily accessible starting materials are used. This method will be especially useful for preparation of ynolates bearing functional groups in organic synthesis.

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