24785-45-3Relevant academic research and scientific papers
Synthesis and investigation of antioxidant properties of alkylated hydroxybenzyl dodecyl sulfides
Prosenko,Dyubchenko,Terakh,Markov,Gorokh,Boiko
, p. 283 - 288 (2006)
Various alkyl-substituted hydroxybenzyl dodecyl sulfides were synthesized, and a comparative study of their antiradical activity in the model reaction of initiated styrene oxidation and the overall inhibiting activity in the thermal autooxidation of white
Iodine-Mediated Direct Generation of o-Quinone Methides at Room Temperature: A Facile Protocol for the Synthesis of ortho-Hydroxybenzyl Thioethers
Basha, R. Sidick,Chen, Chia-Wei,Reddy, Daggula Mallikarjuna,Lee, Chin-Fa
, p. 2475 - 2483 (2018/05/29)
An iodine-mediated preparation of ortho-quinone methides (o-QMs) from ortho-hydroxybenzyl alcohols by a C?O bond scission strategy is described. The in situ generated o-QMs were then employed for C?S bond formation by thio-Michael addition of thiols to provide the ortho-hydroxybenzyl thioethers (o-HBT) in moderate to excellent yields.
Catalytic thioalkylation of phenols based on mannich-type phenol
Liu, Peng,Zhu, Lunyu,Fang, Yan,Zhang, Huaiping,Chen, Dehong,He, Tao,Chen, Mingcai,Xu, Kai
, p. 2609 - 2613 (2008/02/10)
A thioalkylation of phenols involving reactive phenols, aldehydes, and thiols is described under Mannich-type phenol catalysis to afford thiomethyl phenols in good yields. Copyright Taylor & Francis Group, LLC.
