98349-59-8Relevant academic research and scientific papers
MODULATION DE LA REGIOSELECTIVITE LORS DE LA CYCLOADDITION DE LA DIPHENYLNITRILIMINE SUR DIVERS DIHYDRO-1,2 NAPHTALENES SUBSTITUES. STEREOSPECIFICITE DE LA REACTION
Tshiamala, Kabula,Kitane, Said,Vebrel, Joel,Laude, Bernard
, p. 1083 - 1098 (2007/10/02)
In order to control the regiochemistry of the cycloaddition of diphenylnitrilimine on 1,2-dihydronaphtalene and at-1 or -2 substituted derivatives and to obtain either regioisomer, we introduce a methoxycarbonyl group at the 4- or 3- position of the dipol
