109458-85-7

Upstream product

• 21378-21-2 3-methylcyclohex-2-en-1-ol 
• 1193-18-6 3-methylcyclohexen-2-one 
• 23758-27-2 1-methylcyclohex-2-en-1-ol 
• 1489-57-2 2-methylcyclohexa-1,3-diene 
• 16510-84-2 (r-1,t-2)-1,2-dibromo-1-methylcyclohexane 

Downstream Products

• 110535-57-4 (1S,5R,8R)-8-Chloro-1,6-dimethyl-7-phenyl-bicyclo[3.2.1]oct-6-ene 
• 109458-97-1 8-Chloro-1,6-dimethyl-7-phenylsulfanyl-bicyclo[3.2.1]oct-6-ene 
• 110516-38-6 (1S,5R,8R)-8-Chloro-6-methoxymethyl-1-methyl-7-phenyl-bicyclo[3.2.1]oct-6-ene 
• 109458-95-9 8-Chloro-1-methyl-7-phenylsulfanyl-bicyclo[3.2.1]oct-6-ene 
• 110516-37-5 (1S,5R,8R)-8-Chloro-1-methyl-7-phenyl-bicyclo[3.2.1]oct-6-ene 
• 1193-18-6 3-methylcyclohexen-2-one 
• 349478-64-4 6-methoxymethyl-1-methyl-7-phenylsulfanyl-bicyclo[3.2.1]oct-6-en-8-ol 
• 1219117-85-7 C₁₀H₁₈ 
• 13828-31-4 m-menth-1-ene 
• 1219117-78-8 C₁₃H₁₅F 
• 938446-30-1 1-methyl-3-cyclohexenylzinc chloride 

Relevant academic research and scientific papers

New routes to ss-cycloalkylalanine derivatives using serine-derived organozinc reagents

Two distinct routes to β-cycloalkylalanine derivatives have been developed. The first route employs the reaction of the iodoalanine-derived zinc-copper reagent 2 with cycloalk-l-en-3-yl phosphates, and the second uses the palladium-catalysed coupling of t

GRACILIN A AND CONGENERS AS IMMUNOSUPPRESSIVE AND NEUROPROTECTIVE AGENTS

Gracilin A congeners and methods for their use as immunosuppressive and neuroprotective agents.

TRIAZOLYL DERIVATIVES AS SYK INHIBITORS

Provided are triazole derivatives of Formula I which are potent inhibitors of spleen tyrosine kinase and pharmaceutical composition. The triazole derivatives are useful in the treatment and prevention of diseases mediated by said enzyme, such as asthma, COPD, rheumatoid arthritis, and cancer.

Development of a catalytic platform for nucleophilic substitution: Cyclopropenone-catalyzed chlorodehydration of alcohols

Cyclopropenone makes the switch: 2,3-Bis-(p-methoxyphenyl)cyclopropenone is a highly efficient catalyst for the chlorodehydration of 20 diverse alcohol substrates (see scheme; X=Cl). With oxalyl chloride as catalytic activator, this nucleophilic substitution proceeded through cyclopropenium-activated intermediates and resulted in complete stereochemical inversion in substrates with chiral centers.

Mild two-step process for the transition-metal-free synthesis of carbon-carbon bonds from allylic alcohols/ethers and grignard reagents

Chemical Equation Represented A mild two-step process for the regioselective, transition-metal-free preparation of carbon-carbon bonds from allylic alcohols/ethers and Grignard reagents is described. This process obviates the need for the harsh deprotecti