127208-61-1Relevant articles and documents
Anodic benzylic C(sp3)-H amination: Unified access to pyrrolidines and piperidines
Herold, Sebastian,Bafaluy, Daniel,Mu?iz, Kilian
supporting information, p. 3191 - 3196 (2018/07/29)
An electrochemical aliphatic C-H amination strategy was developed to access the important heterocyclic motifs of pyrrolidines and piperidines within a uniform reaction protocol. The mechanism of this unprecedented C-H amination strategy involves anodic C-H activation to generate a benzylic cation, which is efficiently trapped by a nitrogen nucleophile. The applicability of the process is demonstrated for 40 examples comprising both 5- and 6-membered ring formations.
Competitive Intramolecular Cyclizations of Epoxides to Aromatic and Double Bond Positions
Taylor, Stephen K.,Bischoff, David S.,Blankespoor, Curtis L.,Deck, Paul A.,Harvey, Suzanne M.,et al.
, p. 4202 - 4207 (2007/10/02)
-