1005465-69-9

Upstream product

• 1005465-67-7 (E,1R,2R,1'R,2'R,4''S)-1-(2'-(2'',2''-dimethyl-1'',3''-dioxolan-4''-yl)cyclopropyl)dodec-3-en-6-yne-1,2-diol 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 

Downstream Products

• 1005465-73-5 (E,1R,2R,1'R,2'R,4''S)-2-(4'''-methoxybenzyloxy)-1-(2'-(2'',2''-dimethyl-1'',3''-dioxolan-4''-yl)cyclopropyl)dodec-3-en-6-yn-2-ol 
• 1005465-71-3 (E,1R,2R,1'R,2'R,4''S)-1-(4'''-methoxybenzyloxy)-1-(2'-(2'',2''-dimethyl-1'',3''-dioxolan-4''-yl)cyclopropyl)dodec-3-en-6-yn-2-ol 
• 1005465-75-7 (E,1S,4S,1'R,2'R,4''S)-1-(4'''-methoxybenzyloxy)-1-(2'-(2'',2''-dimethyl-1'',3''-dioxolan-4''-yl)cyclopropyl)dodec-2-en-6-yn-4-ol 

Relevant academic research and scientific papers

Studies toward the enantioselective syntheses of oxylipins: Total synthesis and structure revision of solandelactone E

(Chemical Equation Presented) An efficient and general entry to unsaturated cyclopropane- and lactone-containing oxylipins of marine origin has been designed and applied to the first enantioselective total synthesis of solandelactone E. The synthesis, whi