1542147-91-0

Upstream product

• 50870-61-6 2-bromocyclohex-2-en-1-one 
• 98-98-6 2-Picolinic acid 
• 61426-49-1 (1R)-2-bromocyclohex-2-en-1-ol 
• 930-68-7 cyclohexenone 

Downstream Products

• 1542147-96-5 C₁₄H₁₈O 
• 1542147-98-7 (S)-1-(1,4,5,6-tetrahydro-[1,1'-biphenyl]-2-yl)ethanone 
• 1542148-01-5 (R)-1-((S)-1,4,5,6-tetrahydro-[1,1'-biphenyl]-2-yl)ethyl picolinate 
• 1542147-99-8 C₁₄H₁₈O 
• 1542149-17-6 [(1R,3R,Z)-2-ethylidene-3-methylcyclohexyl]benzene 
• 1542149-18-7 (2R,6S)-2-methyl-6-phenylcyclohexanone 
• 1542149-19-8 [(1R,3R,Z)-3-butyl-2-ethylidenecyclohexyl]benzene 
• 1542149-21-2 [(1S,3S)-2-ethylidenecyclohexane-1,3-diyl]dibenzene 
• 915137-58-5 C₁₃H₁₆ 
• 17540-19-1 (+)-(R)-3-phenylcyclohexene 
• 129527-97-5 1,4,5,6-tetrahydro-[1,1'-biphenyl]-2-carbonitrile 
• 1632352-41-0 6-(phenylethynyl)-1,2,3,4-tetrahydro-1,1'-biphenyl 
• 1542147-92-1 (S)-6-bromo-1,2,3,4-tetrahydro-1,1'-biphenyl 

Relevant academic research and scientific papers

Synthesis of trans -2,6-disubstituted cyclohexanones through allylic substitution

trans-2,6-Disubstituted cyclohexanones were synthesized with high regio- and stereoselectivity by allylic substitution followed by ozonolysis. Both alkyl and aryl groups were successfully installed to the cyclohexane ring. The stereochemistry of the Ssub

Allylic substitution of esters derived from 2-bromocyclohex-2-enol with aryl copper reagents and synthetic utilization of the derived anti s N2′ products

Allylic substitution of esters derived from 2-bromocyclohex-2-enol with PhMgBr-based copper reagent was investigated to find high anti S N2′ selectivity with the diethyl phosphate, whereas other esters such as picolinate, acetate, and mesylate resulted in partial racemization or recovery of the starting esters. This protocol was applied to the copper reagent derived from 2-Me-4-MeOC6H3MgBr and CuBr·SMe2 and the olefin part of the anti S N2′ product was cleaved for a synthesis of patchouli alcohol. Georg Thieme Verlag Stuttgart New York.