Literature DB >> 33166067

Dearomatization-Rearomatization Strategy for ortho-Selective Alkylation of Phenols with Primary Alcohols.

Jianjin Yu1, Chao-Jun Li2, Huiying Zeng1.   

Abstract

Phenols are common precursors and core structures of a variety of industrial chemicals ranging from pharmaceuticals to polymers. However, the synthesis of site-specifically substituted phenols is challenging, and thus the development of new methods for this purpose would be highly desirable. Reported here is a protocol for palladium-catalyzed ortho-selective alkylation reactions of phenols with primary alcohols by a dearomatization-rearomatization strategy, with water as the sole by-product. Various substituted phenols and primary alcohols were compatible with the standard reaction conditions. The detailed mechanism of this transformation was also investigated.
© 2020 Wiley-VCH GmbH.

Entities:  

Keywords:  aromaticity; cross-coupling; palladium; reaction mechanisms; synthetic methods

Year:  2020        PMID: 33166067     DOI: 10.1002/anie.202010845

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

Review 1.  Bakuchiol - a natural meroterpenoid: structure, isolation, synthesis and functionalization approaches.

Authors:  T P Adarsh Krishna; Baldev Edachery; Sunil Athalathil
Journal:  RSC Adv       Date:  2022-03-21       Impact factor: 3.361

  1 in total

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