29943-11-1Relevant articles and documents
One-Pot Synthesis of 1,4-Diketones from Nitroalkenes and Ketones
Miyashita, Masaaki,Awen, Bahlul Z. E.,Yoshikoshi, Akira
, p. 563 - 564 (1990)
A convenient one-pot synthesis of 1,4-diketones was achieved by the conjugate addition of lithium enolates of ketones to nitroalkenes, followed by in situ hydrolysis of the resulting lithium salts of aci-nitro compounds with aqueous hydrochloric acid in tetrahydrofuran.
REGIOSELECTIVE HYDRATION OF ALKYNONES BY PALLADIUM CATALYSIS
Imi, Katsuharu,Imai, Kumiko,Utimoto, Kiitiro
, p. 3127 - 3130 (2007/10/02)
Diketones are regioselectively prepared from alkynyl ketones under mild conditions by palladium catalysis; 5-heptyn-2-one and 2-(2-nonynyl)cyclohexanone give 1,4-diketones whereas 2-(2-heptynyl)cyclopentanone and 5,6-didehydroprostaglandin E2 methyl ester afford 1,5-diketones.