research article
Enantioselective Synthesis of 1,2-disubstituted Thiocyclobutanes via Michael Addition
May 22, 2025
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).
Loading...
Name
CS2025_D5SC01727K_goldaccess.pdf
Type
Main Document
Version
Published version
Access type
openaccess
License Condition
CC BY
Size
11.69 MB
Format
Adobe PDF
Checksum (MD5)
3d10769934aea882d5f1a5817d79a22f