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research article

Enantioselective Synthesis of 1,2-disubstituted Thiocyclobutanes via Michael Addition

Robert, Emma Gabrielle Louise  
•
Waser, Jérôme  
May 22, 2025
Chemical Science

We report the diastereoselective and enantioselective synthesis of thio-substituted cyclobutanes via a sulfa-Michael addition using cyclobutenes. In the presence of DBU, various thio-cyclobutane esters and amides were obtained in up to quantitative yield and >95 : 5 dr. Using a chiral chinchona-based squaramide bifunctional acid-base catalyst and an N-acyl-oxazolidinone-substituted cyclobutene, thio-cyclobutanes were obtained with high yield and enantioselectivity (er up to 99.7 : 0.3).

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CS2025_D5SC01727K_goldaccess.pdf

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Main Document

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Published version

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openaccess

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CC BY

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11.69 MB

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Checksum (MD5)

3d10769934aea882d5f1a5817d79a22f

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