124888-31-9Relevant academic research and scientific papers
Aldolisation-type reaction versus Michael-type addition. Hemiacetal vinylogs: Versatile synthons
Duhamel,Guillemont,Poirier,Chabardes
, p. 4197 - 4200 (1993)
Depending on the steric hindrance of the reaction centers, hemiacetal vinylogs 1 in the presence of BF3.OEt2 can, with enol ethers, lead to a Michael-type addition (4) or an aldolisation-type reaction (3). Hemiacetal vinylog 1b always yields the second reaction leading to β-methoxy-γ,δ-ethylenic carbonyl compounds 4 precursors of polyenic carbonyl compounds 5. Crotonaldehyde and methanol can be used instead of compound 1b.
Efficient Activation of Acetals, Aldehydes, and Imines toward Silylated Nucleophiles by the Combined Use of Catalytic Amounts of 2 and TMS-CN under Almost Neutral Conditions
Soga, Tsunehiko,Takenoshita, Haruhiro,Yamada, Masaaki,Mukaiyama, Teruaki
, p. 3122 - 3131 (2007/10/02)
In the presence of catalytic amount of a transition metal compound such as 2, Co(acac)2, or NiCl2, trimethylsilyl cyanide smoothly reacts with acetals to form α-methoxy carbonitriles in good yields.In the coexistence of catalytic amounts of Rh
Efficient Activation of Acetals toward Nucleophiles with 2 Catalyst. New Method for the Preparation of Aldols from Acetals and Silyl Enol Ethers by the Combined Use of Catalytic Amounts of 2 and Trimethylsilyl Cyanide
Mukaiyama, Teruaki,Soga, Tsunehiko,Takenoshita, Haruhiro
, p. 1273 - 1276 (2007/10/02)
In the presence of a catalytic amount of 2, di-μ-chloro-bis(1,5-cyclooctadiene)dirhodium, trimethylsilyl cyanide smoothly reacts with acetals derived from aliphatic, unsaturated and aromatic aldehydes to form the corresponding α-cyano derivativ
