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  4. Enantioselective Synthesis of 1,2-disubstituted Thiocyclobutanes <i>via</i> Michael Addition
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editorial

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

Robert, Emma G. L.  
•
Waser, Jerome  
May 23, 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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Type
editorial
DOI
10.1039/d5sc01727k
Web of Science ID

WOS:001503990900001

PubMed ID

40486741

Author(s)
Robert, Emma G. L.  

École Polytechnique Fédérale de Lausanne

Waser, Jerome  

École Polytechnique Fédérale de Lausanne

Date Issued

2025-05-23

Publisher

ROYAL SOC CHEMISTRY

Published in
Chemical Science
Subjects

ASYMMETRIC CONJUGATE ADDITION

•

N-ACYLATED OXAZOLIDIN-2-ONES

•

CYCLOBUTANE DERIVATIVES

•

ENOLATE PROTONATION

•

THIOLS

•

DISCOVERY

•

CONSTRUCTION

•

SCAFFOLDS

•

COMPLEX

•

POTENT

•

Science & Technology

•

Physical Sciences

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSO  
FunderFunding(s)Grant NumberGrant URL

cole Polytechnique Fdrale de Lausanne

EPFL

200020_212129

Swiss National Science Foundation (SNSF)

Available on Infoscience
June 16, 2025
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/251363
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