116606-91-8Relevant academic research and scientific papers
Asymmetric Synthesis XI: Stereoselective Synthesis of α-Alkyl-2-furfurylamines via d-Camphor Ketimine Intermediate
Yaozhong, Jiang,Jingen, Deng,Wenhao, Hu,Giulan, Liu,Aiqiao, Mi
, p. 3077 - 3083 (2007/10/02)
(R)-α-alkyl-2-furfurylamines (7), ranging from 5-67percentd.e., are obtained by asymmetric alkylation of d-camphor ketimine (3).Using 1,3-diiodopropane and dibromoxylene as alkylating reagents, diimine derivatives (6f) and (6g) are formed.However, 1,2-dibromoethane gives coupling product (6h).
