3891-70-1

Upstream product

• 99169-98-9 2,4-dicyano-2-methyl-valeric acid ethyl ester 
• 609-02-9 methyl-malonic acid dimethylester 
• 80-62-6 methacrylic acid methyl ester 
• 82262-31-5 4,6-dimethyl-1,3-cyclohexanedione 

Downstream Products

• 174627-70-4 (2R,4S,6S)-7-(benzyloxy)-2,4,6-trimethylheptan-1-ol 
• 1333430-90-2 (4S)-4-benzyl-3-{(4R,6R)-7-[1-(tert-butyl)-1,1-dimethylsilyl]oxy-4,6-dimethylheptanoyl}-1,3-oxazolan-2-one 
• 1333430-91-3 (4S)-4-benzyl-3-{(2S,4S,6R)-7-[1-(tert-butyl)-1,1-dimethylsilyl]oxy-2,4,6-trimethylheptanoyl}-1,3-oxazolan-2-one 
• 96481-80-0 Benzoic acid (4E,8E)-(S)-1-[(2S,4R)-1-benzenesulfonyl-2-methyl-4-(2-methyl-[1,3]dioxolan-2-yl)-pentyl]-5-ethyl-11-methoxycarbonyl-3,9-dimethyl-undeca-4,8-dienyl ester 

Relevant academic research and scientific papers

Accessing the structural diversity of pyridone alkaloids: Concise total synthesis of rac-citridone A

A unique route to the structural diversity of pyridone alkaloids is described based on the concept of a common synthetic strategy. Three different core structure analogues corresponding to akanthomycin, septoriamycin A, and citridone A have been prepared by using a highly selective and novel carbocyclization reaction.