1620-52-6Relevant articles and documents
(E)-Specific direct Julia-olefination of aryl alcohols without extra reducing agents promoted by bases
Yao, Chuan-Zhi,Li, Qiang-Qiang,Wang, Mei-Mei,Ning, Xiao-Shan,Kang, Yan-Biao
supporting information, p. 7729 - 7732 (2015/05/12)
An unprecedented base-promoted direct olefination of aryl alcohols with sulfones via a Julia-type reaction has been described. No extra reductants are needed for Julia reaction since alcohols work as double sources of aldehydes and the hydride. Generally high yields were given for both terminal and highly (E)-selective internal olefins.
Efficient new protocol to synthesize aromatic and heteroaromatic dithioesters
Abrunhosa, Isabelle,Gulea, Mihaela,Masson, Serge
, p. 928 - 934 (2007/10/03)
A very efficient, high yielding procedure to synthesize substituted aromatic and heteroaromatic dithioesters is described. It involves the reaction between (phenylsulfonyl)methyl (hetero)aromatic derivatives and elemental sulfur in basic medium, followed by alkylation.
Vicarious nucleophilic substitution of pyridines via their dicyanomethylide derivatives
Itoh,Nagata,Okada,Ohsawa
, p. 220 - 222 (2007/10/02)
Vicarious nucleophilic substitution of pyridinium 1-dicyanomethylides with 1-chloromethyl phenyl sulfone gave corresponding 4-substituted derivatives. The dicyanomethylene group was readily eliminated via radical reaction to afford 4-phenylsulfonylmethylp