498555-08-1

Upstream product

• 69739-34-0 t-butyldimethylsiyl triflate 
• 5503-12-8 L-perillaldehyde 
• 18031-40-8 (S)-(-)-perillaldehyde 

Downstream Products

• 1425631-48-6 ((3S,4S)-3-(diethoxymethyl)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl)methanol 
• 1425631-50-0 ((3S,4S)-3-(diethoxymethyl)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl)methyl 3-oxopentanoate 
• 1425631-46-4 (3S,4S)-3-(diethoxymethyl)-4-(prop-1-en-2-yl)cyclohex-1-enecarbaldehyde 

Relevant academic research and scientific papers

Concise total synthesis of spirocurcasone

A concise total synthesis of spirocurcasone was accomplished. Key features of the synthesis involved a vinylogous Mukaiyama aldol reaction, a Carroll rearrangement of β-keto allyl ester derivative, an intramolecular aldol condensation, and a spiro ring fo

Synthesis of both enantiomers of isorobinal, a novel cyclic monoterpene isolated from the astigmatid mite, Rhizoglyphus sp.

Both enantiomers of isorobinal, a cyclic monoterpene isolated from the astigmatid mite (Rhizoglyphus sp.), were synthesized from the enantiomers of perillaldehyde in four steps by using PCC-oxidation of a tertiary allylic alcohol intermediate as the key s