99789-33-0Relevant articles and documents
Tetrabutylammonium phenoxide induced reaction of silyl nucleophiles
Capperucci, Antonella,Tiberi, Caterina,Pollicino, Salvatore,Degl'Innocenti, Alessandro
experimental part, p. 2808 - 2810 (2009/09/30)
Reaction of silyl dithiolanes with electrophiles can be efficiently promoted by catalytic amounts of tetrabutylammonium phenoxide (PhONn-Bu4), leading to a convenient access to functionalized dithiolanes. PhONn-Bu4 proved effective a
Regioselective ring opening of epoxides by nucleophiles mediated by lithium bistrifluoromethanesulfonimide
Cossy, Janine,Bellosta, Véronique,Hamoir, Claire,Desmurs, Jean-Roger
, p. 7083 - 7086 (2007/10/03)
In the presence of LiNTf2, epoxides undergo ring opening with high regioselectivity and in good yield when they are treated with nucleophiles such as amines, hydrazines and thiophenol.
Intermolecular Pinacol Coupling of Sulfur-Substituted Aldehydes by 2(Zn2Cl6). The Effect of the Substitution at Sulfur on the Stereochemical Outcome of the Coupling Reaction
Kraynack, Erica A.,Pedersen, Steven, F.
, p. 6114 - 6117 (2007/10/02)
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