15905-30-3Relevant academic research and scientific papers
Organylzinc chalcogenolate promoted michael-type addition of α,β-unsaturated carbonyl compounds
Loren Nunes, Vanessa,De Oliveira, Ingryd Cristina,Soares Do Rego Barros, Olga
supporting information, p. 1525 - 1530 (2014/03/21)
We present the chemo-, regio-, and stereoselective synthesis of vinyl chalcogenide compounds promoted by organylzinc chalcogenolates. In this protocol, reductive cleavage of diorganyl dichalcogenide bonds by the Zn/NH 4OH system led to organylz
Organylzinc Chalcogenolate Promoted Michael-Type Addition of α,β-Unsaturated Carbonyl Compounds
L?ren Nunes, Vanessa,De Oliveira, Ingryd Cristina,Soares Do Rêgo Barros, Olga
supporting information, p. 1525 - 1530 (2015/10/05)
We present the chemo-, regio-, and stereoselective synthesis of vinyl chalcogenide compounds promoted by organylzinc chalcogenolates. In this protocol, reductive cleavage of diorganyl dichalcogenide bonds by the Zn/NH4OH system led to organylzi
Platinum-catalyzed intramolecular vinylchalcogenation of alkynes with β-phenylchalcogeno conjugated amides
Toyofuku, Masashi,Fujiwara, Shin-Ichi,Shin-ike, Tsutomu,Kuniyasu, Hitoshi,Kambe, Nobuaki
supporting information; experimental part, p. 10504 - 10505 (2009/02/05)
Platinum-catalyzed intramolecular vinylthiolation and -selenation of internal alkynes with vinylchalcogenides 1 having a carbamoyl group on cis-β-position of vinyl moiety was developed. The conjugated six-membered lactam framework 2 was constructed in high yields. Density functional theory calculations for alkyne insertion processes suggest seven-membered platinacycle 3 is a kinetically favored intermediate of this catalytic system. Copyright
STEREOCHEMISTRY OF THE NUCLEOPHILIC ADDITION OF SELENOLS TO CARBONYL-CONTAINING ACETYLENE DERIVATIVES
Tsoi, L. A.,Patsaev, A. K.,Ushanov, V. Zh.,Vyaznikovtsev, L. V.
, p. 1897 - 1902 (2007/10/02)
It was shown that the nucleophilic addition of selenols to carbonyl-containing acetylene compounds is highly stereospecific.Acetylenic ketones, propiolic acid, and propiolamide add selenols with the formation of vinyl selenides having only the Z structure
