106813-52-9Relevant academic research and scientific papers
STEREOSELECTIVE SYNTHESIS OF CIS OR TRANS N-PHENYL 2-PHENYL DECAHYDROQUINOLIN-4 ONES BY CATALYZED HETERO-DIELS-ALDER REACTION.
Veyrat, Christine,Wartski, Lya,Seyden-Penne, Jacqueline
, p. 2981 - 2984 (1986)
Cis or trans N-phenyl 2-phenyl decahydroquinolin-4 ones can be synthesized highly selectively.
High degree of exo selectivity in imino Diels-Alder reactions catalyzed by tert-butyldimethylsilyltriflate
Nogue,Paugam,Wartski
, p. 1265 - 1268 (2007/10/02)
Diels-Alder reactions of silyloxydiene 1 derived from 1-acetylcyclohexene with imines 2b and 2c occur with high exo selectivity depending upon experimental conditions: exo cycloadducts 3b-c are exclusively formed under kinetic control using tert-butyldime
Synthesis of 2-Phenyldecahydroquinolin-4-ones via Imino Diels-Alder Reaction: Influence of the Imine Nitrogen Substituent on the Reaction Course and on the Heterocycle Conformation
Coz, Linda Le,Veyrat-Martin, Christine,Wartski, Lya,Seyden-Penne, Jacqueline,Bois, Claudette,Philoche-Levisalles, Michele
, p. 4870 - 4879 (2007/10/02)
Reaction of acetylcyclohexene trimethylsilyl enol ether (1) with N-substituted phenyl imines 2 takes place in the presence of Lewis acids.When the N-substituent in 2 is phenyl, p-tolyl, or p-methoxyphenyl, the cycloaddition gives exo and endo enoxysilanes
