753496-82-1Relevant articles and documents
Highly efficient, base-catalysed, intramolecular hydroamination of non-activated olefins
Quinet, Coralie,Jourdain, Pierre,Hermans, Christophe,Ates, Ali,Lucas, Isabelle,Markó, István E.
, p. 1077 - 1087 (2008/09/17)
The intramolecular hydroamination of a large variety of non-activated alkenes can be efficiently catalysed by small amounts of lithium bases, providing smoothly and in high yields the corresponding five- and six-membered ring heterocycles. Fused and bridged bicyclic amines, of varying ring sizes, can be readily prepared either by a sequential hydroamination process or by a tandem, double addition reaction.
Reverse Cope Elimination Reactions. 2. Application to Synthesis
Ciganek, Engelbert
, p. 5803 - 5807 (2007/10/03)
Intramolecular addition of N,N-disubstituted hydroxylamines to unactivated olefins was used to prepare an indolizine, a pyrroloisoquinoline, a 1,8-diazaspirodecane, a cyclopentapyrrole, and an isoindoline.A pyrrolizine and a 1-azabicyclo2.
Syntheses in the Group of Nuphar Alkaloids. VI. Some Transformations of 3-Bromomethyl-2,3-dihydro-1H-indolizinium Salts
Szychowski, Jerzy,Wrobel, Jerzy T.,Leniewski, Andrzej
, p. 9 - 17 (2007/10/02)
Structure, spectral characteristics and chemical transformations of the title compounds are described.