Literature DB >> 35558228

Applications of Friedel-Crafts reactions in total synthesis of natural products.

Majid M Heravi1, Vahideh Zadsirjan1, Pegah Saedi1, Tayebeh Momeni1.   

Abstract

Over the years, Friedel-Crafts (FC) reactions have been acknowledged as the most useful and powerful synthetic tools for the construction of a special kind of carbon-carbon bond involving an aromatic moiety. Its stoichiometric and, more recently, its catalytic procedures have extensively been studied. This reaction in recent years has frequently been used as a key step (steps) in the total synthesis of natural products and targeted complex bioactive molecules. In this review, we try to underscore the applications of intermolecular and intramolecular FC reactions in the total syntheses of natural products and complex molecules, exhibiting diverse biological properties. This journal is © The Royal Society of Chemistry.

Entities:  

Year:  2018        PMID: 35558228      PMCID: PMC9091380          DOI: 10.1039/c8ra07325b

Source DB:  PubMed          Journal:  RSC Adv        ISSN: 2046-2069            Impact factor:   4.036


  325 in total

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Journal:  J Biol Chem       Date:  2011-06-10       Impact factor: 5.157

7.  Catalytic enantioselective Friedel-Crafts/Michael addition reactions of indoles to ethenetricarboxylates.

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9.  A convenient protocol for the synthesis of ligands from a 4-methyl-3,5-diacylaminophenyl platform.

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  5 in total

1.  Deacylation-Aided C─H Alkylative Annulation through C─C Cleavage of Unstrained Ketones.

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2.  Carbene and photocatalyst-catalyzed decarboxylative radical coupling of carboxylic acids and acyl imidazoles to form ketones.

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3.  Development of highly efficient Friedel-Crafts alkylations with alcohols using heterogeneous catalysts under continuous-flow conditions.

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Journal:  RSC Adv       Date:  2021-07-13       Impact factor: 4.036

Review 4.  Synthetically important ring opening reactions by alkoxybenzenes and alkoxynaphthalenes.

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  5 in total

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