106657-30-1Relevant articles and documents
Palladium-catalyzed olefin dioxygenation
Li, Yang,Song, Datong,Dong, Vy M.
, p. 2962 - 2964 (2008/09/20)
A general method for the vicinal dioxygenation of olefins was developed using cationic Pd diphosphine complexes as the catalysts and PhI(OAc)2 as the terminal oxidant. In comparison to known Pd-catalyzed vicinal oxidations, this method is suitable for a broad range of olefins in both inter- and intramolecular reactions. An 18O-labeling experiment provides insight into the mechanism of this transformation which presumably involves Pd(II)/Pd(IV) intermediates. Copyright
DIASTEREOSELECTIVITE DANS LA REACTION DES ORGANOMAGNESIENS SUR LE TETRAHYDROFURFURAL ET SON GEM-DIACETATE EN PRESENCE DE HMPT. ACCES AUX DIOLS-1,2 ERYTHRO.
Amouroux, R.,Ejjiyar, S.,Chastrette, M.
, p. 1035 - 1038 (2007/10/02)
Grignard Reagents - HMPT complexes have been found to be highly stereoselective reagents for the addition to tetrahydrofurfural and for the substitution of an acetoxy group in tetrahydrofurfural gem-diacetate.In both cases, a high erythro/threo ratio was obtained.