858005-68-2Relevant articles and documents
Synthesis of 1-(arenesulfonyl)-2-arylpyrrolidines by reaction of N-(4,4-diethoxybutyl)-4-methylbenzene-sulfonamide with phenols
Smolobochkin,Anikina,Gazizov,Burilov,Pudovik
, (2016)
New 1-(arenesulfonyl)-2-arylpyrrolidines were synthesized by reactions of several phenols with N-(4,4-diethoxybutyl)-4-methylbenzenesulfonamide in the presence of trifluoroacetic acid.
Acid-catalyzed reaction of phenols with N-(4,4-diethoxybutyl)sulfonamides – a new method for the synthesis of 2-aryl-1-sulfonylpyrrolidines
Smolobochkin, Andrey V.,Gazizov, Almir S.,Anikina, Ekaterina A.,Burilov, Alexander R.,Pudovik, Michael A.
, p. 161 - 166 (2017)
[Figure not available: see fulltext.]We have developed a new method for the synthesis of 2-aryl-1-sulfonylpyrrolidines on the basis of reactions between various phenols and N-(4,4-diethoxybutyl)sulfonamides in the presence of trifluoroacetic acid. The str
Enantioselective intramolecular aldehyde α-alkylation with simple olefins: Direct access to homo-ene products
Comito, Robert J.,Finelli, Fernanda G.,Macmillan, David W. C.
supporting information, p. 9358 - 9361 (2013/07/26)
A highly selective method for the synthesis of asymmetrically substituted carbocycles and heterocycles from unactivated aldehyde-olefin precursors has been achieved via enantioselective SOMO-catalysis. Addition of a catalytically generated enamine radical cation across a pendent olefin serves to establish a general asymmetric strategy toward the production of a wide range of formyl-substituted rings with alkene transposition. Conceptually, this novel mechanism allows direct access to "homo-ene"-type products.
