434342-82-2

Upstream product

• 4873-09-0 allyl tosylate 
• 434342-77-5 (1S,2R,3R,4R,6S)-6-Benzyloxy-3-benzyloxymethyl-4-methoxymethoxy-3-methyl-bicyclo[2.2.1]heptane-2-carbaldehyde 
• 434342-76-4 (S)-5-((1S,2R,3R,4R,6S)-6-Benzyloxy-3-benzyloxymethyl-4-methoxymethoxy-3-methyl-bicyclo[2.2.1]hept-2-yl)-2,2,4,4-tetramethyl-[1,3]dioxolane 
• 434343-00-7 (S)-4-((1S,2R,3R,4R,6S)-6-Benzyloxy-3-benzyloxymethyl-4-methoxymethoxy-3-methyl-bicyclo[2.2.1]hept-2-yl)-2,2-dimethyl-[1,3]dioxolane 
• 434342-90-2 (S)-1-((1S,2R,3R,4R,6S)-6-Benzyloxy-3-benzyloxymethyl-4-hydroxy-3-methyl-bicyclo[2.2.1]hept-2-yl)-2-methyl-propane-1,2-diol 
• 434342-91-3 (1S,2R,3R,4R,6S)-6-Benzyloxy-3-benzyloxymethyl-4-hydroxy-3-methyl-bicyclo[2.2.1]heptane-2-carbaldehyde 
• 434342-75-3 (1R,2S,3R,4S)-1-Methoxymethoxy-2-methyl-5-oxo-3-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-bicyclo[2.2.1]heptane-2-carboxylic acid ethyl ester 
• 434342-89-9 (1S,2S,4R,5R,6R)-5-Hydroxymethyl-4-methoxymethoxy-5-methyl-6-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-bicyclo[2.2.1]heptan-2-ol 
• 434342-74-2 (E)-2-Methyl-3-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-acrylic acid ethyl ester 
• 213816-61-6 ethyl (1R,2S,3R,4S)-3-((S)-2,2-dimethyl[1,3]dioxolan-4-yl)-1-methoxymethoxy-2-methyl-5-oxobicyclo[2.2.1]heptane-2-carboxylate 
• 100-39-0 benzyl bromide 

Downstream Products

• 434342-94-6 (1S,2R,3R,4R,6S)-6-Benzyloxy-3-benzyloxymethyl-4-methoxymethoxy-2,3-dimethyl-bicyclo[2.2.1]heptane-2-carbaldehyde 
• 434342-93-5 (1R,2R,3R,4S,5S)-5-Benzyloxy-2-benzyloxymethyl-1-methoxymethoxy-2,3-dimethyl-3-((E)-propenyl)-bicyclo[2.2.1]heptane 
• 434342-85-5 ((1S,2R,3R,4R,6S)-6-Benzyloxy-3-benzyloxymethyl-4-methoxymethoxy-2,3-dimethyl-bicyclo[2.2.1]hept-2-yl)-methanol 
• 434342-95-7 (1R,2R,3R,4S,5S)-5-Benzyloxy-2-benzyloxymethyl-1-methoxymethoxy-2,3-dimethyl-3-phenylsulfanylmethyl-bicyclo[2.2.1]heptane 
• 434342-83-3 (1S,2S,3R,4R,6S)-2-Allyl-6-benzyloxy-3-benzyloxymethyl-4-methoxymethoxy-3-methyl-bicyclo[2.2.1]heptane-2-carbaldehyde 

Relevant academic research and scientific papers

Synthesis of the optically active bicyclo[4.2.1]nonane Segment of mediterraneols

An efficient method was established for the synthesis of the optically active bicyclo[4.2.1]nonane segment of mediterraneols using diastereoselective sequential Michael reaction and then retro-aldol reaction.