126325-69-7

Upstream product

• 67-56-1 methanol 
• 69125-55-9 4-hydroxy-1-methoxy-1-cyclohexene 

Downstream Products

• 115276-20-5 4-phenyl-3-cyclohexene-1,2-dione 1-<(2S,3S)-1,4-dimethoxy-2,3-butylene>acetal 
• 77784-05-5 (R)-(-)-3'-methoxy-4'-O-methyljoubertiamine 
• 126325-72-2 2,4-dihydroxy-4-phenylcyclohexanedione (2S,3S)-1,4-dimethoxy-2,3-butylene acetal 
• 126325-73-3 2,4-dihydroxy-4-(3,4-dimethoxyphenyl)cyclohexanone 1-(2S,3S)-1,4-dimethoxy-2,3-butylene acetal 
• 126325-68-6 4-(3,4-dimethoxyphenyl)-3-cyclohexene-1,2-dione 1-<(2S,3S)-1,4-dimethoxy-2,3-butylene>acetal 
• 59096-18-3 (S)-(-)-3'-methoxy-4'-O-methyljoubertiamine 
• 115276-23-8 2-hydroxy-4-phenyl-3-cyclohexen-1-one (2S,3S)-1,4-dimethoxy-2,3-butylene acetal 
• 126325-74-4 2R-4-(3,4-dimethoxyphenyl)-2-hydroxy-3-cyclohexene-1-one (2S,3S)-1,4-dimethoxy-2,3-butylene acetal 
• 126325-74-4 2S-4-(3,4-dimethoxyphenyl)-2-hydroxy-3-cyclohexene-1-one (2S,3S)-1,4-dimethoxy-2,3-butylene acetal 
• 126325-75-5 4S-4-(3,4-dimethoxyphenyl)-4-(2-N,N-dimethylamino-2-oxo-ethyl)-2-cyclohexene-1-one (2S,3S)-1,4-dimethoxy-2,3-butylene acetal 
• 126325-75-5 4R-4-(3,4-dimethoxyphenyl)-4-(2-N,N-dimethylamino-2-oxo-ethyl)-2-cyclohexene-1-one (2S,3S)-1,4-dimethoxy-2,3-butylene acetal 

Relevant academic research and scientific papers

Asymmetric Synthesis Using Chiral Acetals: Highly Stereoselective Reduction of Chiral α-Keto-β,γ-unsaturated Acetals and Its Application for the Synthesis of (R)-(-)- and (S)-(+)-3'-Methoxy-4'-O-methyljoubertiamine

Reduction of the chiral α-keto-β,γ-unsaturated acetals (1) derived from (-)-(2S,3S)-1,4-dimethoxy-2,3-butanediol was studied.Extremily high stereoselectivity was attained with LiAlH4 and two epimeric allyl alcohols (2aA-2cA and 2aB-2cB) were prepared selectively by a proper choice of additive.As an application of this methodology, total syntheses of (R)-(-)-3'-methoxy-4'-O-methyljoubertiamine and its enantiomer were achieved from the single chiral enone acetal (3) through a highly stereocontrolled reduction followed by the Claisen-Eschenmoser rearrangement.