119582-40-0Relevant academic research and scientific papers
REGIO-AND STEREOSELECTIVE ADDITION OF ORGANOLITHIUMS TO NAPHTHALENES. AN EFFICIENT SYNTHESIS OF 1,1,2-TRISUBSTITUTED AND TRANS-2-DISUBSTITUTED DIHYDRONAPHTHALENES
Meyers, A.I.,Lutomski, Kathryn A.,Laucher, Dominique
, p. 3107 - 3118 (1988)
The addition of a variety of organolithium reagents to 1-naphthyloxazolines and 2-naphthyloxazolines followed by trapping with electrophiles leads to high yields of the title compounds.Very high stereoselectivity characterizes the present process in that
STEREOSPECIFIC CONJUGATE ADDITION OF ORGANOLITHIUM REAGENTS TO NAPHTHYLIMINES. A FACILE ROUTE TO 1,1,2- AND 1,2-SUBSTITUTED DIHYDRONAPHTHALENES
Meyers, A. I.,Brown, Jack D.,Laucher, Dominique
, p. 5279 - 5282 (2007/10/02)
Addition of organolithium reagents at low temperature to the cyclohexylimine of 1-naphthaldehyde followed by electrophilic trapping of the intermediate gives rise to high yields of the title compounds.
