1229922-77-3

Upstream product

• 1229922-74-0 3-acetyl-1-cyclohexyl-5,6-O-isopropylidene-2-oxa-3-azabicyclo[2.2.2]oct-7-ene-5,6-diol 

Downstream Products

• 1229922-79-5 (3aR,5aR,8aR,8bS)-2,2,7-trimethyl-4-cyclohexyl-3a,5a,8a,8b-tetrahydro[1,3]dioxolo[4,5-e][1,3]benzoxazole 
• 1229922-80-8 (1S,2R,5R,6S)-6-acetylamino-1,2-O-isopropylidene-5-chloro-3-cyclohexylcyclohex-3-ene-1,2-diol 
• 1229922-81-9 N-((3aS,4R,5R,7aR)-7-cyclohexyl-5-hydroxy-2,2-dimethyl-3a,4,5,7a-tetrahydrobenzo[d][1,3]dioxol-4-yl)acetamide 
• 1229922-83-1 C₁₈H₂₉NO₆S 

Relevant academic research and scientific papers

Synthesis of 1,2- and 1,4-amino alcohols from 1,3-dienes via oxazines. Rearrangements of 1,4-amino alcohol derivatives to oxazolines

Conjugated dienes were converted to 1,2-oxazines by reaction with an acyl nitroso dienophile. The oxazines were reduced to 1,4-N-acetylamino alcohols, which were rearranged to the corresponding oxazolines upon treatment with methanesulfonyl chloride or an