615580-24-0

Upstream product

• 66192-28-7 methyl (E)-3-(2-bromo-4-methylphenyl)acrylate 
• 824-54-4 2-bromo-4-methylbenzaldehyde 
• 615580-22-8 C₂₄H₂₅NO₂S 
• 100-39-0 benzyl bromide 

Downstream Products

• 1010419-45-0 ethyl (S,E)-3-(2-(4-(benzyloxy)butan-2-yl)-5-methylphenyl)acrylate 
• 4179-22-0 (1S)-1-(4-methylphenyl)-3-bromobutane 
• 3649-81-8 (S)-curcumene 
• 1461-10-5 (S)-3-(4-methylphenyl)-1-butanol 
• 615580-26-2 1-((S)-3-Benzyloxy-1-methyl-propyl)-4-methyl-benzene 

Relevant academic research and scientific papers

Benzothiazines in synthesis: Studies directed toward the synthesis of erogorgiaene

(Chemical Equation Presented) The use of benzothiazenes for the formal total synthesis of erogorgiaene and stereoselective total syntheses of two diastereomers of this natural product is described. In particular, the stereochemical course of a radical cyc

Benzothiazines in synthesis. Formal syntheses of (+)-curcumene and (+)-curcuphenol

A benzothiazine readily available in enantiomerically pure form via a stereoselective, intramolecular Michael addition reaction could be converted to a precursor to (+)-curcuphenol and to (+)-curcumene.