Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones

Enantioselective sulfa-Michael additions to α,β unsaturated diazocarbonyl compounds have been developed. Quinine-derived squaramide was found to be the best catalyst to promote C–S bond formation in a highly stereoselective fashion for alkyl and aryl thiols. The easy-to-follow protocol allowed the p...

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Veröffentlicht in:Journal of organic chemistry 2022-03, Vol.87 (5), p.3482-3490
Hauptverfasser: Momo, Patricia B, Mizobuchi, Eduardo F, Echemendía, Radell, Baddeley, Isabel, Grayson, Matthew N, Burtoloso, Antonio C. B
Format: Artikel
Sprache:eng
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Zusammenfassung:Enantioselective sulfa-Michael additions to α,β unsaturated diazocarbonyl compounds have been developed. Quinine-derived squaramide was found to be the best catalyst to promote C–S bond formation in a highly stereoselective fashion for alkyl and aryl thiols. The easy-to-follow protocol allowed the preparation of 22 examples in enantiomeric ratios up to 97:3 and reaction yields up to 94%. The mechanism and origins of enantioselectivity were determined through density functional theory (DFT) calculations.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.1c03045