Abstract

Spiroheterocycles are regarded as a privileged framework because of their wide distribution in various natural products and synthetic molecules and promising bioactivities. This review focuses on the recent advances in the synthesis of spiroheterocycles by using the strategy of N-heterocyclic carbene (NHC) organocatalysis, and is organized based on the stereoselectivity and the reactive intermediates. According to the stereochemistry, this review was divided into two main parts, covering racemic and enantioselective versions. In each part, we firstly describe the synthetic transformations using nucleophilic Breslow intermediates, and then discuss the reactions that employ electrophilic acylazolium or radical cation intermediates. With those distinct catalytic activation modes of NHC organocatlysis, we expect this synthetic protocol will possibly produce new molecules with structural novelty and complexity, which may warrant further research in the field of drug discovery.

Highlights

  • Spiroheterocycles are a class of privileged scaffolds widely occurring in many natural products and pharmaceutical compounds [1,2,3]

  • Spirotryprostatin B, which is a diketopiperazine alkaloid isolated from Aspergillus fumigatus, displays cell cycle inhibitory activity [10]

  • Many complicated complicated biochemical transformations are are catalyzed by enzymes; systems, many biochemical transformations transformations are catalyzed catalyzed by enzymes; In biological complicated example, nucleophilic acylation reaction is catalyzed transketolase enzymes

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Summary

Introduction

Spiroheterocycles are a class of privileged scaffolds widely occurring in many natural products and pharmaceutical compounds [1,2,3]. Spiroheterocycles have received special attention in medicinal chemistry because of their promising bioactivities, such as antitubercular, antiparasitic, and antitumor properties [2,4,5]. Citrinadins A and B isolated from Penicillium citrinum. A, a bioactive secondary metabolite of Penicillium species, exhibits antimycobacterial, cytotoxic and antifungal activities [7]. Trigolutes A–C isolated from Trigonostemon lutescens twigs, are used in Thai folk medicine to cure food poisoning, asthma, and poisonous snake bites [9]. Spirotryprostatin B, which is a diketopiperazine alkaloid isolated from Aspergillus fumigatus, displays cell cycle inhibitory activity [10]. Due to their important physiological functions, the corresponding skeletons have attracted great interest from synthetic chemists.

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Transformation
Catalysis Involving Nucleophilic Breslow Intermediates
16. Tautomerization of deliver
Synthesis
Catalysis Involving Acylazolium Intermediates
15. Enantioselective
Catalysis Involving Chiral Acylazolium Intermediates
80. The products
Catalysis Involving Radical Cation Intermediates
Findings
Conclusions
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