478176-17-9Relevant academic research and scientific papers
Remarkably high 1,5-diastereoselectivity in a nickel-catalyzed conjugate addition of Me2Zn and carbonyl compounds to 1,ω-dienynes with through-space coupling
Ezoe, Akihiro,Kimura, Masanari,Inoue, Takahiro,Mori, Masahiko,Tamaru, Yoshinao
, p. 2784 - 2786 (2002)
A four-component reaction: A nickel catalyst promotes the conjugate addition of Me2Zn and a carbonyl compound to 1,ω-dienynes 1 at the terminal positions of the alkyne and the diene moieties, respectively; the through-space interactions of the
Nickel-catalyzed addition of dimethylzinc to aldehydes across alkynes and 1,3-butadiene: An efficient four-component connection reaction
Kimura, Masanari,Ezoe, Akihiro,Mori, Masahiko,Tamaru, Yoshinao
, p. 201 - 209 (2007/10/03)
In the presence of 10 mol % of Ni(acac)2, four components comprising Me2Zn, alkynes, 1,3-butadiene, and carbonyl compounds combine in this order in 1:1:1:1 ratio to furnish (3E,6Z)-octadien-1-ols 1 in good yields. Similarly, the coupling reaction of Me2Zn, 1,ω-dienynes 5, and carbonyls furnishes 1-alkylidene-2-(4′-hydroxy- (1′E)-alkenyl)cyclopentanes and -cyclohexanes 6 and their oxygen and nitrogen heterocycle derivatives in good yield and an excellent level of 1,5-diastereoselectivity with respect to the cycloalkane methine carbon and the OH-bearing carbon of the C2 side chain. The reaction is completed in most cases within 1 h at room temperature under nitrogen, tolerates an ester, a hydroxy, an allyl and propargyl ethers, an allylamino, and a pyridyl functionalities, and accommodates a variety of aromatic and aliphatic alkynes and carbonyls (aldehydes and ketones).
