28053-13-6Relevant articles and documents
Type 2 intramolecular N-acylazo Diels-Alder reaction: Regio- and stereoselective synthesis of bridgehead bicyclic 1,2-diazines
Molina, Claudia L.,Chow, Chun P.,Shea, Kenneth J.
, p. 6816 - 6823 (2007)
(Chemical Equation Presented) The type 2 intramolecular N-acylazo Diels-Alder reaction provides a regio- and stereoselective synthesis of bicyclic 1,2-diazine systems. A new method for the generation of N-acylazo dienophiles with tetra-n-butylammonium periodate is reported. X-ray crystallographic analysis allowed the quantification of structural distortions of the nonplanar bridgehead olefin and lactam functionalities in 1,2-diazine cycloadducts 11 and 15. Caprolactams and enantholactams were formed by stereoselective bridgehead alkene reduction, a process that transfers stereochemistry from the bridgehead lactam nitrogen to the bridgehead carbon. The sequence of transformations offers a convenient route for the diastereoselective synthesis of medium-ring nitrogen heterocycles and 1,4-diamines.
