67170-56-3Relevant academic research and scientific papers
SYNTHESIS OF 4,4-DISUBSTITUTED CYCLOHEXENONES. PART 1. BAEYER-VILLIGER FRAGMENTATION OF 1-METHOXYBICYCLOOCT-5-ENONES.
Holmes, Andrew B.,Madge, Nigel C.
, p. 789 - 802 (2007/10/02)
The sodium acetate-buffered peracetic acid oxidation of various 1-methoxybicyclooct-5-enones (4a-f), and (14), prepared by hydrolysis of the adducts (3) derived from dihydroanisole derivatives (2) and 2-chloroacrylonitrile leads to 4-
Synthesis of 4,4-Disubstituted Cyclohexenones by the Baeyer-Viliger Fragmentation of 1-Methoxybicyclooct-5-enones
Madge, Nigel C.,Holmes, Andrew B.
, p. 956 - 957 (2007/10/02)
The sodium acetate-buffered, peracetic acid oxidation of various 1-methoxybicyclooct-5-enones, prepared by hydrolysis of the adducts derived from dihydroanisole derivatives and α-chloroacrylonitrile, leads to 4-substituted cyclohex-2-en-1-one 4-acetic acid derivatives.
