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Volumn 356, Issue 6, 2014, Pages 1292-1300

Catalytic asymmetric conjugate addition of mercaptans to β-substituted-β-trifluoromethyl oxazolidinone enoates: Access to chiral trifluoromethylated tertiary thioethers and thiols

Author keywords

asymmetric organocatalysis; oxazolidinone enoates; sulfa Michael reaction; tertiary thiols; trifluoromethylation

Indexed keywords


EID: 84898878894     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201301027     Document Type: Article
Times cited : (38)

References (101)
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    • Before submission of this manuscript, an organocatalytic cascade sulfa-Michael/aldol reaction of β,β-disubstitutued enones with good enantioselectivity (up to 89% ee) was shown to construct chiral trifluoromethylated tertiary thioethers, see:, Y. Su, J.-B. Ling, S. Zhang, P.-F. Xu, J. Org. Chem. 2013, 78, 11053.
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    • CCDC 983031 (1f) and CCDC 962342 (3f) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.