23904-33-8Relevant articles and documents
A STEREOSELECTIVE SYNTHESIS OF (Z)-1-IODO-1-ALKENES
Stork, Gilbert,Zhao, Kang
, p. 2173 - 2174 (1989)
(Z)-1-iodo-1-alkenes can be synthesized stereoselectively via the Wittig reaction of iodomethylenetriphenylphosphorane with aldehydes.
A New Entry of Practical and Chemoselective Iodocarbenoids for Carbonyl Iodomethylenation
Yan, Tu-Hsin,Chen, Mei-Yuan
, p. 390 - 394 (2017/04/24)
Direct oxidative addition of CHI3 to the Mg-TiCl4 bimetallic species resulted in the generation of a highly chemoselective and practically convenient iodomethylenetitanium complex, which efficiently effected condensation even with enolizable or inert carbonyl compounds, such as sterically congested ketones, to provide vinyl iodide compounds.
Halodephosphorylation of α,β-unsaturated phosphonic acid monoesters
Lahrache, Hind,Robin, Sylvie,Rousseau, Gérard
, p. 1635 - 1637 (2007/10/03)
Reaction of α,β-ethylenic and acetylenic phosphonic acid monoesters with (biscollidine)iodine(I) or (biscollidine)bromine(I) hexafluorophosphate led to α,β-unsaturated halides by, without precedent, dephosphorylation reactions.