1463-03-2Relevant academic research and scientific papers
Double decarboxylative Claisen rearrangement reactions: Microwave-assisted de novo synthesis of pyridines
Craig, Donald,Paina, Federica,Smith, Stephen C.
supporting information; experimental part, p. 3408 - 3410 (2009/02/05)
Microwave-assisted double decarboxylative Claisen rearrangement of bis(allyl) 2-tosylmalonates provides substituted 1,6-heptadienes, which may be alkylated, and then converted into pyridines by ozonolysis followed by reaction with ammonia generated in sit
A Suzuki-Miyaura approach to a series of forensically relevant pyridines
Blachut, Dariusz,Czarnocki, Zbigniew,Wojtasiewicz, Krystyna
, p. 2855 - 2864 (2008/02/07)
A convenient and general method for the preparation of sixteen 3,5-diarylsubstituted 2,4- and 2,6-dimethylpyridines of high forensic importance is described. The Suzuki cross-coupling reaction between a range of ring-substituted phenylboronic acids and 3,
