An efficient organocatalytic route to tertiary thiols is reported based on conjugate additions to nitro olefins of 5H-thiazol-4-ones as new sulfur based carbon pronucleophiles. Key for that realization is the development of ureidopeptide-based Brønsted bases, a new subclass of Brønsted base catalysts. Success in this transformation is presumably due to the reaction model outlined above. This model nicely accounts for the best behavior of quinolyl thiazolone substrates for this reaction, in comparison to that of naphthyl based thiazolones which provided adducts with significantly lower levels of stereoselectivity, both diastereo- and enantioselectivity.
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Catalytic Enantioselective Synthesis of Tertiary Thiols from 5H-Thiazol-4-ones: Bifunctional Ureidopeptide-Based Brønsted Base Catalyst
Published: 12 October 2016 by MDPI in MOL2NET'16, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 2nd ed. congress CHEMBIOMOL-02: Chem. Biol. & Med. Chem. Workshop, Rostock, Germany-Bilbao, Spain-Galveston, Texas, USA, 2016
Keywords: Enantioselectivity; Organocatalytic route; Pronucleophiles; Brønsted base catalysts