125475-26-5

Upstream product

• 2466-76-4 N-Acetylimidazole 
• 125475-15-2 2-Hydroxy-1-(1-methyl-cyclopenta-2,4-dienyl)-4-methylene-cyclohexanecarbaldehyde 
• 125475-50-5 2-(1-Methyl-cyclopenta-2,4-dienyl)-2-[3-methyl-4-(2-nitro-phenylselanyl)-butyl]-malonic acid dimethyl ester 
• 125475-24-3 dimethyl 2-<4-<(tert-butyldimethylsilyl)oxy>-3-methylbutyl>-2-<5-(5-methyl-1,3-cyclopentadienyl)>malonate 
• 125475-25-4 2-(3-methyl-3-butenyl)-2-<5-(5-methyl-1,3-cyclopentadienyl)>-1,3-propanediol 
• 125475-16-3 2-(3-methyl-3-butenyl)-2-<5-(5-methyl-1,3-cyclopentadienyl)>malondialdehyde 
• 90511-20-9 (1-Methylcyclopent-2-enyl)essigsaeure-methylester 
• 125494-78-2 dimethyl 2-(4-hydroxy-3-methylbutyl)-2-<5-(5-methyl-1,3-cyclopentadienyl)>malonate 
• 125475-21-0 dimethyl 2-(3-methyl-3-butenyl)-2-<5-(5-methyl-1,3-cyclopentadienyl)>malonate 
• 125475-45-8 2-(4-Bromo-1-methyl-cyclopent-2-enyl)-malonic acid dimethyl ester 
• 125475-18-5 dimethyl 2-<3-(3-methyl-1-cyclopentenyl)>malonate 
• 125475-19-6 dimethyl 2-<5-(5-methyl-1,3-cyclopentadienyl)>malonate 

Downstream Products

• 125475-55-0 4(R^*)-<<(tert-butyldimethylsilyl)oxy>methyl>-4(R^*)-<4-<3(R^*),5(S^*)-dihydroxy-4(r)-methyl-1-cyclopentenyl>>-3(R^*)-<(methoxymethyl)oxy>methylenecyclohexane 
• 125475-53-8 4(R^*)-<<(tert-butyldimethylsilyl)oxy>methyl>-4(R^*)-<4-<3(R^*),5(S^*)-dihydroxy-4(r)-methyl-1-cyclopentenyl>>-3(R^*)-hydroxymethylenecyclohexane 
• 125475-56-1 3(R^*)-<(methoxymethyl)oxy>-4(R^*)-<5-(5-methyl-1,3-cyclopentadienyl)>-4(R^*)-<<(tert-butyldimethylsilyl)oxy>methyl>methylenecyclohexane 
• 125475-54-9 3(R^*)-acetoxy-4(R^*)-<5-(5-methyl-1,3-cyclopentadienyl)>-4(R^*)-<<(tert-butyldimethylsilyl)oxy>methyl>methylenecyclohexane 
• 125475-52-7 2(R^*)-<<(tert-butyldimethylsilyl)oxy>methyl>-2(R^*)-<5-(5-methyl-1,3-cyclopentadienyl)>-5-methylenecyclohexan-1(R^*)-ol 
• 125475-57-2 Acetic acid (1S,2S)-2-hydroxymethyl-2-(1-methyl-cyclopenta-2,4-dienyl)-5-methylene-cyclohexyl ester 

Relevant academic research and scientific papers

Synthesis of a highly functionalized carbon ring skeleton for the trichothecene anguidine

A strategy directed toward the synthesis of the highly functionalized trichothecene anguidine (1) is detailed. The route entails several challenges. The first of these is the synthesis of the congested, achiral cyclopentadienyl malondialdehyde 8, which is