1274891-86-9

Upstream product

• 1225205-29-7 (1S,3S,4S,6S,8S)-6-methoxy-3,4-diphenyl-2,5-dioxabicyclo[6.4.0]dodec-11-en-10-one 
• 122876-21-5 3-chloro-1-trifluoromethanesulfonyloxy-propane 

Downstream Products

• 1274891-89-2 2-{(1S,2S,5S,6R)-2-(3-azidopropyl)-6-[(1S,2S)-2-hydroxy-1,2-diphenylethoxy]-5-methyl-3-oxocyclohexyl}acetaldehyde 
• 1274891-90-5 (2S,5S,4R,5S)-2-(3-azidopropyl)-4-[(1S,2S)-2-hydroxy-1,2-diphenylethoxy]-3-(2-hydroxy-6-methoxyhexyl)-5-methylcyclohexanone 
• 1274891-87-0 (1S,3S,4S,6S,8S,9S,12S)-9-[3-azidopropyl]-6-methoxy-12-methyl-3,4-diphenyl-2,5-dioxabicyclo[6.4.0]dodec-11-en-10-one 

Relevant academic research and scientific papers

Asymmetric total synthesis of clavolonine

The asymmetric total synthesis of clavolonine (1) has been achieved based on chiral auxiliary multiple-use methodology. Our synthetic route features stereoselective transformations on the cyclohexane ring utilizing the steric environment of the chiral aux