REACTION OF CYCLIC PARTIAL PHOSPHITE ESTERS WITH ENAMINES - AN ELECTROPHILIC FORM OF THE PUDOVIK REACTION
It was established that the ease of noncatalytic addition of cyclic and acyclic partial phosphites to enamines is due to the H-donor capacity of the acids and to the degree of localization of the electron density at the C=C bond in the unsaturated partner.It was shown that cyclic phosphites add initially at the carbon-carbon multiple bond of the conjugated N-C=C-C=O system of enamino ketones with the final formation of bisphosphorylated derivatives.
Safina, Yu. G.,Malkova, G. Sh.,Cherkasov, R. A.
p. 562 - 574
(2007/10/02)
REACTIONS OF CYCLIC PARTIAL ESTERS OF PHOSPHOROUS ACID WITH ENAMINES
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Safina, Yu. G.,Malkova, G. Sh.,Cherkasov, R. A.,Ovchinnikov, V. V.
p. 193 - 194
(2007/10/02)
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