75456-57-4

Upstream product

• 111-71-7 heptanal 
• 13865-50-4 methoxymethyl phenyl sulfide 
• 57788-49-5 methoxy(phenylthio)methane lithium 

Downstream Products

• 121862-25-7 4-Methoxy-5-phenylsulfanyl-undecan-2-one 
• 115205-51-1 (E)-4-Phenylsulfanyl-dec-3-enoic acid ethyl ester 
• 115205-51-1 (Z)-4-Phenylsulfanyl-dec-3-enoic acid ethyl ester 
• 86254-27-5 (E)-5-Phenylsulfanyl-undec-4-en-2-one 
• 95270-02-3 (Z)-5-Phenylsulfanyl-undec-4-en-2-one 
• 7018-92-0 2,5-Undecanedione 
• 200347-28-0 tert-Butyl-{(Z)-1-tert-butyl-3-[1-(methoxy-phenylsulfanyl-methyl)-heptyloxy]-propenyloxy}-dimethyl-silane 
• 200347-24-6 1-[1-(Methoxy-phenylsulfanyl-methyl)-heptyloxy]-4,4-dimethyl-pentan-3-one 
• 81447-41-8 2-(phenylthio)octanal 

Relevant academic research and scientific papers

Heterocyclic synthesis by C-C bond formation. Tetrahydrofuran and tetrahydropyran synthesis via oxonium ion-mediated cyclisation reactions

Dimethyl(methylthio)sulfonium tetrafluoroborate triggers ionisation and cyclisation of hemithioacetals 3 to give tetrahydrofurans 8-11 in good yields and stereoselectivities. The homologous sulfone analogues 17 give tetrahydropyrans on treatment with ethy

ELONGATION OF CARBONYL COMPOUNDS BY UTILIZING ELECTROREDUCTION AS A KEY STEP

This transformation of aldehydes, ketones and esters to the next higher homologous aldehydes was accomplished by utilizing electroreductive 1,2-elimination as a key step.