113308-77-3

Upstream product

• 674-82-8 4-methyleneoxetan-2-one 
• 14398-34-6 4-(3-hydroxy-2,6,6-trimethylcyclohex-1-enyl)but-3-en-2-one 

Downstream Products

• 14398-34-6 4-(3-hydroxy-2,6,6-trimethylcyclohex-1-enyl)but-3-en-2-one 
• 113308-76-2 (2aR*,8aS*,8bR*) 3,6,6,8b-Tetramethyl-2a,6,7,8,8a,8b-hexahydro-2H-naphtho<1,8-bc>furan-2-one 
• 71629-13-5 (-)-(R)-4-hydroxy-β-ionone 
• 71629-15-7 4-(3-Hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one 
• 151726-13-5 4-Nitro-benzoic acid (S)-2,4,4-trimethyl-3-((E)-3-oxo-but-1-enyl)-cyclohex-2-enyl ester 
• 113308-78-4 3-Oxo-pentanoic acid 2,4,4-trimethyl-3-((E)-3-oxo-but-1-enyl)-cyclohex-2-enyl ester 

Relevant academic research and scientific papers

Expedient construction of the ziegler intermediate useful for the synthesis of forskolin via consecutive rearrangements

"Chemical Equation Presented" The Ziegler Intermediate, useful for the total synthesis of forskolin, was synthesized in 10 reaction steps starting from commercially available a-lonone. This highly efficient synthesis relies on the success of two consecuti