204381-89-5Relevant academic research and scientific papers
Samarium diiodide-promoted diiodomethylation of carbonyl compounds with iodoform. Synthetic applications of diiodoalcohols
Concellon, Jose M.,Bernad, Pablo L.,Perez-Andres, Juan A.
, p. 1409 - 1412 (1998)
A rapid and effective diiodomethylation of carbonyl compounds using SmI2 and iodoform is described. Transformations of the obtained diiodoalcohols 2 into α-iodoaldehydes 5 and α-hydroxyacids 6 is also reported.
Synthesis of (E)-α,β-unsaturated esters and (Z)-vinyl halides with total or high diastereoselectivity by using samarium metal
Concellon, Jose M.,Rodriguez-Solla, Humberto,Huerta, Monica,Perez-Andres, Juan A.
, p. 1839 - 1847 (2007/10/03)
A highly diastereoselective β-elimination of 2-halo-3-hydroxy esters 1 or O-acetylated 1,1-dihaloalkan-2-ols 4 is achieved with samarium in the presence of diiodomethane, yielding α,β-unsaturated esters 2 or vinyl halides 5, respectively. The β-elimination reaction was promoted by samarium diiodide, which was generated in situ. The starting halohydrins 1 or 4 are easily prepared by reaction of the corresponding lithium enolates of α-halo esters or dihalomethyllithium with aldehydes at -78°C. The influence of the reaction conditions and the structure of the starting compounds on the diastereoselectivity of the β-elimination reactions is discussed, A comparative study of the β-elimination reaction with preformed SmI2 and metallic samarium is also performed. These elimination reactions can be explained by the proposed mechanism. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002).
