106472-39-3Relevant academic research and scientific papers
The evaluation of dicyclopentadienylsamarium as a reagent in organic synthesis
Namy,Collin,Zhang,Kagan
, p. 81 - 86 (1987)
SmCp2, which is easily prepared from SmI2, has been screened as a reducing agent for organic chemistry. In particular, SmCp2 promotes the pseudo-Barbier reaction between carbonyl compounds (aldehydes and ketones) and aliphatic or allylic halides more efficiently than does SmI2.
Iron-Catalyzed Nucleophilic Addition Reaction of Organic Carbanion Equivalents via Hydrazones
Li, Chen-Chen,Dai, Xi-Jie,Wang, Haining,Zhu, Dianhu,Gao, Jian,Li, Chao-Jun
, p. 3801 - 3805 (2018/07/25)
Earth-abundant and well-defined iron complexes are found to be cheap and effective catalysts for a series of "umpolung" nucleophilic additions of hydrazones. The new catalytic system not only maintains the broad substrate scope of an earlier expensive ruthenium system but also attains chemoselectivity of different kinds of carbonyl groups. Furthermore, the iron catalyst enables this reaction at ambient temperature.
Preparation of alcohols from sulfones and trialkylboranes
Billaud, Célia,Goddard, Jean-Philippe,Le Gall, Thierry,Mioskowski, Charles
, p. 4451 - 4454 (2007/10/03)
The reaction of sulfone anions with trialkylboranes followed by thermal isomerization of the obtained boron compounds in the presence of excess borane-methyl sulfide complex and by alkaline hydroperoxide oxidation yields primary alcohols.
Methyl Group Migration in the Reactions of Alkynyltrialkylborates
Pelter, Andrew,Drake, Robert A.
, p. 4181 - 4184 (2007/10/02)
It is shown that the methyl group cannot be used as a cheap, non-migrating group in the reactions of alkynyltrialkylborates with electrophiles.However, trimethylborane can be used as a methylboronating agent for alkynes, given the right choice of solvent, and this may be of use in terpene synthesis.
