163277-65-4

Upstream product

• 5927-18-4 trimethyl phosphonoacetate 

Downstream Products

• 401917-10-0 toluene-4-sulfonic acid 3-(2-vinylphenyl)heptyl ester 
• 401916-96-9 toluene-4-sulfonic acid 1-[2-(2-vinylphenyl)ethyl]pentyl ester 
• 401917-19-9 toluene-4-sulfonic acid 3-phenyl-3-(2-vinylphenyl)propyl ester 
• 401917-16-6 toluene-4-sulfonic acid 4-methyl-3-(2-vinylphenyl)pentyl ester 
• 401917-03-1 toluene-4-sulfonic acid 2-methyl-1-[2-(2-vinylphenyl)ethyl]propyl ester 
• 339177-04-7 3-(2-ethenylphenyl)propionaldehyde 
• 1021-88-1 (1S,4R)-1-Methyl-4-phenyl-1,2,3,4-tetrahydro-naphthalene 
• 1021-88-1 syn-1-methyl-4-phenyl-1,2,3,4-tetrahydronaphthalene 
• 401917-48-4 1-(2-vinylphenyl)heptan-3-ol 
• 401917-52-0 4-methyl-1-(2-vinylphenyl)pentan-3-ol 
• 401917-55-3 3-(2-vinylphenyl)heptan-1-ol 
• 401917-59-7 4-methyl-3(2-vinylphenyl)pentan-1-ol 
• 401917-63-3 3-phenyl-3-(2-vinylphenyl)propan-1-ol 
• 339177-03-6 3-(2-ethenylphenyl)propan-1-ol 

Relevant academic research and scientific papers

Olefins turned alkylating agents: Diastereoselective intramolecular Zr-catalyzed olefin alkylations

(Equation Presented) 62% yield; 12 : 1 syn : anti The first examples of intramolecular Zr-catalyzed electrophilic alkylation of aryl olefins are disclosed. Substituted carbo-and heterocycles are prepared efficiently and diastereoselectively.