The palladium-tributylammonium formate reagent in the stereoselective hydrogenation, and stereo- and regioselective hydroarylation of alkyl 4-hydroxy-2-alkynoates: a route to substituted butenolides
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S. Cacchi | A. Arcadi | F. Marinelli | A. Burini | B. Pietroni | E. Bernocchi | Antonio Arcadi | S. Cacchi*
[1] J. Carretero,et al. Methyl 3-phenylsulphonyl orthopropionate: an efficient reagent for the synthesis of γ-lactones and butenolides , 1987 .
[2] S. Cacchi,et al. The palladium-catalysed reductive addition of aryl iodides to propargyl alcohols: a route to /gg,/gg-diaryl allylic alcohols , 1985 .
[3] S. Cacchi,et al. The palladium-catalyzed reaction of aryl iodides with mono and disubstituted acetylenes: a new synthesis of trisubstituted alkenes. , 1984 .
[4] M. Figueredo,et al. Studies on structurally simple α,β-butenolides. III. , 1982 .
[5] Jean-Pierre Vigneron,et al. Preparation d'alkyl-4 γ-lactones insaturee optiquement pures. Application a la synthese de la (+) tetrahydrocerulenine. , 1980 .
[6] A. Tramontano,et al. Synthesis of alkyl 4-hydroxy-2-alkynoates , 1980 .
[7] Takashi Takahashi,et al. Facile synthesis of acetylenecarboxylates by the oxidative carbonylation of terminal acetylenes catalyzed by PdCl2 under mild conditions , 1980 .
[8] G. Pattenden. 天然4‐イリデンブテノリドと4‐イリデンテトロン酸 , 1978 .
[9] M. Wall,et al. Germination of Witchweed (Striga lutea Lour.): Isolation and Properties of a Potent Stimulant , 1966, Science.