1007401-47-9

Upstream product

• 1007401-46-8 (S)-7-(tert-butyldiphenylsilyloxy)-3-hydroxyheptyl pivalate 
• 107-30-2 chloromethyl methyl ether 
• 1007401-44-6 ((2S,3S)-2-(4-(tert-butyldiphenylsilyloxy)butyl)oxiran-2-yl)methanol 
• 1007401-45-7 (S)-7-(tert-butyldiphenylsilyloxy)heptane-1,3-diol 

Downstream Products

• 1007401-49-1 (7S)-1-benzyloxy-11-(tert-butyldiphenylsilyloxy)-7-(methoxymethoxy)undec-3-yn-5-ol 
• 1007401-54-8 (2R,4aS,5S,8aR)-1-benzyl-2-(2-benzyloxy)ethyl-4-(tert-butyldimethylsilyloxy)-5-methoxymethoxy-1,2,4a,5,6,7,8,8a-octahydroquinoline 
• 1007401-50-4 (7S,E)-1-benzyloxy-11-(tert-butyldiphenylsilyloxy)-7-(methoxymethoxy)undec-3-en-5-ol 
• 1007401-52-6 (S,6Z,8E)-11-benzyloxy-7-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)undeca-6,8-dienyl acetate 
• 1007401-59-3 (S,6Z,8E)-11-benzyloxy-7-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)undeca-6,8-dien-1-ol 
• 1007401-53-7 (S,6Z,8E)-11-benzyloxy-7-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)undeca-6,8-dienal 
• 1007401-58-2 (S,E)-11-benzyloxy-5-methoxymethoxy-7-oxoundec-8-enyl acetate 
• 1007401-57-1 11-benzyloxy-5-methoxymethoxy-undec-8-ene-1,7-diol 
• 1007401-51-5 (S,E)-1-benzyloxy-11-hydroxy-7-(methoxymethoxy)undec-3-en-5-one 
• 1007401-48-0 (S)-7-(tert-butyldiphenylsilyloxy)-3-(methoxymethoxy)heptan-1-ol 

Relevant academic research and scientific papers

Synthesis of 2,5-disubstituted octahydroquinolin-4-ones via an intramolecular hetero Diels-Alder reaction

A route for the preparation of 2,5-disubstituted octahydroquinolin-4-ones, synthetic precursors of the decahydroquinoline-type toxins, is presented. The key steps are an asymmetric epoxidation and an intramolecular hetero Diels-Alder reaction between an a