615580-19-3

Upstream product

• 824-54-4 2-bromo-4-methylbenzaldehyde 
• 66192-28-7 methyl (E)-3-(2-bromo-4-methylphenyl)acrylate 
• 615580-15-9 ((2S,4S)-7-Methyl-2-oxo-2-phenyl-3,4-dihydro-2λ⁶-benzo[c][1,2]thiazin-4-yl)-acetic acid methyl ester 
• 853685-29-7 C₁₈H₁₉NO₃S 
• 615580-17-1 2-((2S,4S)-7-Methyl-2-oxo-2-phenyl-3,4-dihydro-2λ⁶-benzo[c][1,2]thiazin-4-yl)-ethanol 

Downstream Products

• 70878-71-6 (S)-curcuphenol 
• 217301-15-0 (3S)-3-(2-Methoxy-4-methylphenyl)butan-2-ol 
• 4179-22-0 (1S)-1-(4-methylphenyl)-3-bromobutane 
• 3649-81-8 (S)-curcumene 
• 853685-27-5 (S)-trimethyl((5-methyl-2-(pent-4-en-2-yl)phenyl)ethynyl)silane 
• 853685-31-1 (S)-3-(4-methyl-2-((trimethylsilyl)ethynyl)phenyl)butan-1-ol 
• 853685-32-2 (S)-3-(4-methyl-2-((trimethylsilyl)ethynyl)phenyl)butanal 
• 615580-35-3 2-((S)-4-hydroxybutan-2-yl)-5-methylphenol 
• 1461-10-5 (S)-3-(4-methylphenyl)-1-butanol 

Relevant academic research and scientific papers

Benzothiazines in synthesis. Formal synthesis of erogorgiaene

A benzothiazine, readily available in enantiomerically pure form via a completely selective, intramolecular addition of a sulfoximine-stabilized carbanion to an α,β-unsaturated ester, could be converted to a precursor to erogorgiaene in good overall yield

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.