66164-29-2

Upstream product

• 56724-09-5 5-methoxy-2-methylbenzaldehyde 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 75-16-1 methylmagnesium bromide 
• 139469-06-0 1-bromo-5-dimethoxy-2-vinylbenzene 
• 19614-12-1 2-bromo-5-methoxybenzyl bromide 
• 100-84-5 1-methoxy-3-methyl-benzene 

Downstream Products

• 66164-30-5 4-methyl-3-vinylphenol 
• 1527523-54-1 (1R,3aS,4R,5S,7aR)-4-(5-methoxy-2-methylphenethyl)-7a-methyl-1-((R)-6-methylheptan-2-yl)-octahydro-1H-inden-5-ol 
• 328570-91-8 (1R,3aS,4S,5R,7aR)-4-(5-methoxy-2-methylphenethyl)-7a-methyl-1-((R)-6-methylheptan-2-yl)-octahydro-1H-inden-5-ol 
• 33348-61-7 2-(5-methoxy-2-methylphenyl)ethanol 
• 89691-66-7 1-(5-methoxy-2-methylphenyl)ethanol 
• 1352331-60-2 2-(2-bromoethyl)-4-methoxy-1-methylbenzene 

Relevant academic research and scientific papers

Hydrazide-Catalyzed Polyene Cyclization: Asymmetric Organocatalytic Synthesis of cis-Decalins

Polyene cyclizations offer rapid entry into terpenoid ring systems. Although enantioselective cyclizations of (E)-polyenes to form trans-decalin ring systems are well precedented, highly enantioselective cyclizations of (Z)-polyenes to form the correspond

A route to the 9,10-secosteroid astrogorgiadiol featuring a key sp 2-sp3 Suzuki type cross-coupling

The described semi-synthetic route differs from the previously published approaches by an original C-7-C-8 disconnection. The kinetic enol triflate of Grundmann ketone was chosen as the CD-ring platform on which to couple an A-ring synthon via a challengi