124745-27-3Relevant academic research and scientific papers
THE LITHIATION AND ALKYLATION OF 4-(2'-ALKENESULPHINYL)-MORPHOLINES, A SIMPLE ROUTE TO SUBSTITUTED ALLYLIC SULPHINAMIDES
Baudin, Jean-Bernard,Julia, Sylvestre A.
, p. 1963 - 1966 (1989)
By the reaction with 4-morpholinesulphenyl chloride carried out in the presence of trimethylamine, several substituted allylic alcohols have been converted into the corresponding allylic sulphinamides 2.As a complementary method, the new lithio-derivative
Subsituted 4-(2-alkenylsulfinyl)morpholines : preparation and conversion into the corresponding sulfinic acids and esters. Stereochemistry of olefin formation by hydrolytic desulfinylation of allylic sulfinamides.
Baudin, Jean-Bernard,Julia, Sylvestre
, p. 196 - 214 (2007/10/02)
By reaction with 4-(chlorosulfenyl)morpholine in the presence of triethylamine, several substituted allylic alcohols have been converted into the title sulfinamides.As a complementary method, the new α-lithio allylic sulfinamides have been prepared and efficiently alkylated with organic halides.The boron trifluoride-etherate catalyzed treatment of the allylic sulfinamides with simple saturated alcohols provided the corresponding alkyl sulfinates while propargylic and allylic alcohols opened a route to various α,α'-bis-unsaturated sulfones.Efficient conditions for the acid-catalyzed hydrolysis of allylic sulfinamides are described and some allylic sulfinic acids bearing an electron-withdrawing group were isolated.Smooth fragmentation of the homoconjugated sulfinic acids gave the corresponding (E)-olefins stereoselectively. - Key words: sigmatropic rearrangement / allylic sulfinamide / allylic sulfinic ester / organolithium derivative / sulfone / retro-ene reaction / sulfur dioxide elimination / stereochemistry
