Literature DB >> 31021533

Base-Mediated Transition-Metal-Free Dehydrative C-C and C-N Bond-Forming Reactions from Alcohols.

Andrea Porcheddu1, Giorgio Chelucci2.   

Abstract

In recent years, there has been an increasing interest in using alcohols as alkylating agents for C-C and C-N bond-forming processes employing mainly TM-catalysts. Although BH-catalysis looks like a green atom economy process since water is the only by-product, it often suffers from one or more drawbacks, such as the use of expensive noble metal complexes, capricious ligands, and toxic organic solvents. Therefore, straightforward, efficient, atom economy and environmentally benign alternative protocols are desirable. This review aims to summarize the current knowledge within the published literature about dehydrative processes developed without TM-catalysts. The most recent contributions to this topic have been reviewed keeping into account the new findings reported in this area. The features, strengths, and limitations of these alcohol-based C-C and C-N bond-forming processes has also been taken into account.
© 2019 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Oppenauer-type oxidation; TM-free reactions; hydrogen auto-transfer (HA) catalysis; transition metal-free C−H activation.; α-alkylation of ketones

Year:  2019        PMID: 31021533     DOI: 10.1002/tcr.201800170

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  4 in total

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Authors:  Jingxiu Xu; Qingmao Chen; Zhigao Luo; Xiaodong Tang; Jinwu Zhao
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Review 3.  Aldehyde catalysis - from simple aldehydes to artificial enzymes.

Authors:  Zeqin Yuan; Jun Liao; Hao Jiang; Peng Cao; Yang Li
Journal:  RSC Adv       Date:  2020-09-25       Impact factor: 4.036

4.  Mimicking transition metals in borrowing hydrogen from alcohols.

Authors:  Ananya Banik; Jasimuddin Ahmed; Swagata Sil; Swadhin K Mandal
Journal:  Chem Sci       Date:  2021-05-07       Impact factor: 9.825

  4 in total

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