piperidines and fluoroform

piperidines has been researched along with fluoroform* in 2 studies

Other Studies

2 other study(ies) available for piperidines and fluoroform

Article	Year
Diastereoselective synthesis of CF3-substituted, epoxide-fused heterocycles with β-(trifluoromethyl)vinylsulfonium salts. Organic letters, 2012, Dec-21, Volume: 14, Issue:24 CF(3)-substituted vinyl diphenylsulfonium triflate is an effective annulation reagent for the formation of α-CF(3) substituted, epoxide-fused heterocycles (pyrrolidines, piperidines, and tetrahydrofurans). This simple method affords a variety of valuable heterocyclic building blocks in a highly diastereoselective manner (dr >20:1). Topics: Catalysis; Chlorofluorocarbons, Methane; Combinatorial Chemistry Techniques; Epoxy Compounds; Furans; Molecular Structure; Piperidines; Pyrrolidines; Salts; Stereoisomerism	2012
RCM-mediated synthesis of trifluoromethyl-containing nitrogen heterocycles. The Journal of organic chemistry, 2006, Sep-29, Volume: 71, Issue:20 A ring-closing metathesis mediated pathway to trifluoromethyl-containing piperidines is detailed. This involves the development of a synthetic route to a new (trifluoromethyl)allylating reagent via a Diels-Alder/retro-Diels-Alder strategy, its application in the synthesis of a series of trifluormethyl-substituted diolefin precursors for ring-closing metathesis, and eventually the successful cyclization of these precursor molecules into the corresponding functionalized piperidines. Topics: Chlorofluorocarbons, Methane; Cyclization; Heterocyclic Compounds; Nitrogen; Piperidines	2006

Article

Year

Diastereoselective synthesis of CF3-substituted, epoxide-fused heterocycles with β-(trifluoromethyl)vinylsulfonium salts.

Organic letters, 2012, Dec-21, Volume: 14, Issue:24

CF(3)-substituted vinyl diphenylsulfonium triflate is an effective annulation reagent for the formation of α-CF(3) substituted, epoxide-fused heterocycles (pyrrolidines, piperidines, and tetrahydrofurans). This simple method affords a variety of valuable heterocyclic building blocks in a highly diastereoselective manner (dr >20:1).

Topics: Catalysis; Chlorofluorocarbons, Methane; Combinatorial Chemistry Techniques; Epoxy Compounds; Furans; Molecular Structure; Piperidines; Pyrrolidines; Salts; Stereoisomerism

2012

RCM-mediated synthesis of trifluoromethyl-containing nitrogen heterocycles.

The Journal of organic chemistry, 2006, Sep-29, Volume: 71, Issue:20

A ring-closing metathesis mediated pathway to trifluoromethyl-containing piperidines is detailed. This involves the development of a synthetic route to a new (trifluoromethyl)allylating reagent via a Diels-Alder/retro-Diels-Alder strategy, its application in the synthesis of a series of trifluormethyl-substituted diolefin precursors for ring-closing metathesis, and eventually the successful cyclization of these precursor molecules into the corresponding functionalized piperidines.

Topics: Chlorofluorocarbons, Methane; Cyclization; Heterocyclic Compounds; Nitrogen; Piperidines

2006