105824-59-7Relevant articles and documents
SYNTHESIS OF α-SELENOALKYLLITHIUM COMPOUNDS
Krief, A.,Dumont, W.,Clarembeau, M.,Bernard, G.,Badaoui, E.
, p. 2005 - 2022 (2007/10/02)
α-Phenylselenoalkyllithiums and α-methylselenoalkyllithiums have been prepared from the corresponding selenoacetals and alkyllithiums.Several features of this reaction are disclosed.For example, the reaction is more readily achieved on phenylselenoacetals than on methylseleno analogues.Those derived from hindered carbonyl compounds are less readily cleaved. s-BuLi/THF proved superior to n-BuLi in THF, itself better than n-BuLi in ether.
A NOVEL METHOD FOR THE GEMINAL DIALKYLATION OF THE CARBONYL GROUP OF AROMATIC ALDEHYDES AND KETONES
Clarembeau, M.,Krief, A.
, p. 1719 - 1722 (2007/10/02)
The title transformation is efficiently achieved by using the selenium methodology which involves the sequential reductive alkylation of arylselenoacetals and of benzylselenides.
METALLATION OF BENZYL SELENIDES AND OF α-ARYL SELENOACETALS. SCOPE AND LIMITATIONS.
Clarembeau, M.,Krief, A.
, p. 1723 - 1726 (2007/10/02)
α-Metallo benzylselenides and α-metallo selenoacetals derived from aromatic aldehydes have been conveniently prepared by metallation of the corresponding carbon acids.KDA in THF proved among the various basic systems tested, the most efficient.