109066-06-0

Upstream product

• 109066-05-9 3-(methoxymethoxy)propionaldehyde 
• 52406-33-4 3-(methoxymethoxy)propanenitrile 
• 100-39-0 benzyl bromide 
• 501665-81-2 5-(methoxymethoxy)pent-1-en-3-ol 

Downstream Products

• 813433-32-8 but-3-enoic acid 3-(benzyloxy)pent-4-enyl ester 
• 813433-35-1 acetic acid 6-(benzyloxy)oxocan-2-yl ester 
• 813433-33-9 acetic acid 1-(3-benzyloxypent-4-enyloxy)but-3-enyl ester 
• 109066-03-7 (2R,3S)-3-Benzyloxy-2-phenylselanylmethyl-tetrahydro-furan 
• 109066-02-6 (2S,3S)-3-Benzyloxy-2-phenylselanylmethyl-tetrahydro-furan 
• 109065-92-1 (2R,3S)-3-Benzyloxy-2-iodomethyl-tetrahydro-furan 
• 109065-85-2 3-(benzyloxy)-4-penten-1-ol 

Relevant academic research and scientific papers

Using nucleophilic substitution reactions to understand how a remote alkyl or alkoxy substituent influences the conformation of eight-membered ring oxocarbenium ions

(Chemical Equation Presented) A remote alkoxy substituent strongly stabilizes one particular conformer of an eight-membered ring oxocarbenium ion by a through-space electrostatic effect. X-ray crystallographic analysis of a crystalline derivative proves t

Stereoselectivity of Electrophile-Promoted Cyclizations of γ-Hydroxyalkenes. An Investigation of Carbohydrate-Derived and Model Substrates

We have investigated cyclization reactions of γ-hydroxyalkenes bearing an alkoxy or alkyl substituent on the allylic carbon.A variety of electrophiles N-bromosuccinimide, N-iodosuccinimide, iodine, mercury(II) acetate, mercury(II) trifluoroacetate, mercu