1040274-54-1Relevant articles and documents
Copper-Catalyzed Enantioselective Construction of Tertiary Propargylic Sulfones
Gómez, José Enrique,Cristòfol, àlex,Kleij, Arjan W.
, p. 3903 - 3907 (2019)
Tertiary propargylic sulfones are of significant importance in organic synthesis and medicinal chemistry, but to date no general asymmetric synthesis approach has been developed. We disclose a versatile copper-catalyzed sulfonylation of propargylic cyclic carbonates using sodium sulfinates that allows the construction of propargylic sulfones featuring elusive quaternary stereocenters. This method provides the first successful example of such an enantioselective propargylic sulfonylation, features high asymmetric induction, wide functional group tolerance, and scalability, and enables attractive product diversification.
Poly(ethylene glycol) as a reaction matrix in platinum- or gold-catalyzed cycloisomerization: A mechanistic investigation
Spina, Rosella,Colacino, Evelina,Martinez, Jean,Lamaty, Frédéric
supporting information, p. 3817 - 3821 (2013/04/24)
Design for diversity: A new catalytic system based on PEG-3400 and a metal salt (Pt or Au) was designed to efficiently perform a cycloisomerization reaction under microwave irradiation, which gave diverse heterocycles in good to excellent yields, after a