1295581-06-4

Upstream product

• 252953-35-8 (R)-N-(tert-butoxycarbonyl)-4-formyl-2,2,4-trimethyl-3-oxazolidine 
• 56691-80-6 geranyl phenyl sulfone 
• 1295581-05-3 C₁₇H₃₀BrNO₃ 
• 1295581-19-9 C₁₇H₃₁NO₄ 
• 1295581-03-1 (S,E)-tert-butyl 4-(5-ethoxy-4-methyl-5-oxopent-3-enyl)-2,2,4-trimethyloxazolidine-3-carboxylate 
• 1295581-18-8 (S)-tert-butyl 4-(3-ethoxy-3-oxopropyl)-2,2,4-trimethyloxazolidine-3-carboxylate 
• 1295581-02-0 (S,E)-tert-butyl 4-(3-ethoxy-3-oxoprop-1-enyl)-2,2,4-trimethyloxazolidine-3-carboxylate 
• 1295581-01-9 (S,E)-tert-butyl 2,2,4-trimethyl-4-(prop-1-enyl)oxazolidine-3-carboxylate 
• 1295581-17-7 C₁₁H₂₁NO₃ 
• 1295580-98-1 (S,E)-tert-butyl 1-(tert-butyldiphenylsilyloxy)-2-methylpent-3-en-2-ylcarbamate 
• 1314895-87-8 C₂₃H₂₉NO₂Si 

Downstream Products

• 1295581-16-6 C₂₉H₄₄N₂O 
• 57766-63-9 (3S)-geranyllinaloisocyanide 

Relevant academic research and scientific papers

Asymmetric synthesis of (+)-geranyllinaloisocyanide: Assignment of absolute stereochemistry

The first nonracemic synthesis of (+)-geranyllinaloisocyanide, starting with (-)-lactic acid methyl ester, has been accomplished by exploiting a [3.3] sigmatropic rearrangement of allyl cyanate. The synthesis enables assignment of the S configuration of the C(3) isocyano substituted, quaternary stereogenic center in natural geranyllinaloisocyanide.