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- W3136235535 abstract "Abstract Due to their intrinsic rigidity, three‐dimensionality and structural novelty, spirocyclic molecules have become increasingly sought‐after moieties in drug discovery. Herein, we report a strain‐release driven synthesis of azetidine‐containing spirocycles by harnessing the inherent ring strain of the azabicyclo[1.1.0]butane (ABB) fragment. Novel ABB‐ketone precursors bearing silyl‐protected alcohols were synthesized in a single step and shown to engage in electrophile‐induced spirocyclization‐desilylation reactions. Primary, secondary and tertiary silyl ethers were effectively transformed into a library of new spiro‐azetidines, with a range of substituents and ring sizes. In addition, the products are generated with synthetically useful ketone and protected‐amine functional groups, which provides the potential for further elaboration and for this chemistry to be utilized in the rapid assembly of medicinally relevant compounds." @default.
- W3136235535 created "2021-03-29" @default.
- W3136235535 creator A5052381570 @default.
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- W3136235535 creator A5078544922 @default.
- W3136235535 date "2021-04-16" @default.
- W3136235535 modified "2023-10-09" @default.
- W3136235535 title "Strain‐Release Driven Spirocyclization of Azabicyclo[1.1.0]butyl Ketones" @default.
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- W3136235535 doi "https://doi.org/10.1002/anie.202102754" @default.
- W3136235535 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8251566" @default.
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