1. Copper-mediated synthesis of drug-like bicyclopentanes
- Author
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Zhang, Xiaheng, Smith, Russell T., Le, Chip, McCarver, Stefan J., Shireman, Brock T., Carruthers, Nicholas I., and MacMillan, David W. C.
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Production processes ,Influence ,Analysis ,Usage ,Methods ,Copper (Metal) -- Usage ,Metal catalysts -- Influence -- Usage -- Production processes ,Chemical synthesis -- Methods -- Usage -- Analysis ,Polycyclic compounds -- Analysis -- Production processes -- Usage ,Copper -- Usage - Abstract
Author(s): Xiaheng Zhang [sup.1] , Russell T. Smith [sup.1] , Chip Le [sup.1] , Stefan J. McCarver [sup.2] , Brock T. Shireman [sup.2] , Nicholas I. Carruthers [sup.2] , David [...], Multicomponent reactions are relied on in both academic and industrial synthetic organic chemistry owing to their step- and atom-economy advantages over traditional synthetic sequences.sup.1. Recently, bicyclo[1.1.1]pentane (BCP) motifs have become valuable as pharmaceutical bioisosteres of benzene rings, and in particular 1,3-disubstituted BCP moieties have become widely adopted in medicinal chemistry as para-phenyl ring replacements.sup.2. These structures are often generated from [1.1.1]propellane via opening of the internal C-C bond through the addition of either radicals or metal-based nucleophiles.sup.3-13. The resulting propellane-addition adducts are then transformed to the requisite polysubstituted BCP compounds via a range of synthetic sequences that traditionally involve multiple chemical steps. Although this approach has been effective so far, a multicomponent reaction that enables single-step access to complex and diverse polysubstituted drug-like BCP products would be more time efficient compared to current stepwise approaches. Here we report a one-step three-component radical coupling of [1.1.1]propellane to afford diverse functionalized bicyclopentanes using various radical precursors and heteroatom nucleophiles via a metallaphotoredox catalysis protocol. This copper-mediated reaction operates on short timescales (five minutes to one hour) across multiple (more than ten) nucleophile classes and can accommodate a diverse array of radical precursors, including those that generate alkyl, [alpha]-acyl, trifluoromethyl and sulfonyl radicals. This method has been used to rapidly prepare BCP analogues of known pharmaceuticals, one of which is substantially more metabolically stable than its commercial progenitor. A one-step, three-component radical coupling of [1.1.1]propellane by a photoredox reaction mediated by a copper catalyst produces drug-like bicyclopentanes.
- Published
- 2020
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