55843-74-8Relevant academic research and scientific papers
Silylcupration of 1-alkynylphosphine oxides: Stereo- and regioselective synthesis of β-silyl substituted vinylphosphine oxides
Huang, Xian,Xu, Lubin
, p. 231 - 236 (2006)
β-Silyl substituted vinylphosphine oxides were prepared stereo- and regioselectively by the silylcupration of 1-alkynylphosphine oxides followed by hydrolysis or by reacting with other electrophiles. Georg Thieme Verlag Stuttgart.
Cis-carbocupration of acetylenic phosphine oxides and its application in the stereoselective synthesis of polysubstituted vinyl phosphine oxides
Huang, Xian,Wu, Zhimeng
, p. 2445 - 2448 (2004)
Bisubstituted or 1,2,2-trisubstituted vinyl phosphine oxides were prepared stereoselectively by the carbocupration of acetylenic phosphine oxides followed by hydrolysis or by reacting with other electrophiles.
Synthesis and X-Ray Structure of 1,8-Bis(phenyltelluro)naphthalene and Its Peri Tellurium-Tellurium Interaction
Fujihara, Hisashi,Ishitani, Hideya,Takaguchi, Yutaka,Furukawa, Naomichi
, p. 571 - 572 (1995)
New 1,8-diaryl and dialkyl substituted ditelluronaphthalenes, 1,8-bis(phenyltelluro)naphthalene (1) and 1,8-bis(butyltelluro)naphthalene, have been synthesized.The cyclic voltammogram of 1 showed the reversible electrochemical oxidation with remarkably lo
Synthesis of Isoxazolines by the Electrophilic Chalcogenation of β,γ-Unsaturated Oximes: Fishing Novel Anti-Inflammatory Agents
Lopes, Eric F.,Penteado, Filipe,Thurow, Samuel,Pinz, Mikaela,Reis, Angelica S.,Wilhelm, Ethel A.,Luchese, Cristiane,Barcellos, Thiago,Dalberto, Bianca,Alves, Diego,Da Silva, Marcio S.,Lenard?o, Eder J.
, p. 12452 - 12462 (2019/10/11)
Herein, we describe a new strategy to prepare chalcogen-functionalized isoxazolines. The strategy involves the reaction of β,γ-unsaturated oximes with electrophilic selenium and tellurium species, affording 19 new selenium- and tellurium-containing isoxaz
Peri -substituted phosphorus-tellurium systems-an experimental and theoretical investigation of the p?te through-space interaction
Nordheider, Andreas,Hupf, Emanuel,Chalmers, Brian A.,Knight, Fergus R.,Bühl, Michael,Mebs, Stefan,Checińska, Lilianna,Lork, Enno,Camacho, Paula Sanz,Ashbrook, Sharon E.,Athukorala Arachchige, Kasun S.,Cordes, David B.,Slawin, Alexandra M. Z.,Beckmann, Jens,Woollins, J. Derek
supporting information, p. 2435 - 2446 (2015/03/18)
A series of peri-substituted phosphorus-tellurium systems R′Te-Acenap-PR2 (R′ = Ph, p-An, Nap, Mes, Tip; Acenap = acenaphthene-5,6-diyl (-C12H8); R = iPr, Ph) exhibiting large "through-space" spin-spin coupling
Facile synthesis of β-organotellurobutenolides via electrophilic tellurolactonization of α-allenoic acids
Xu, Qing,Huang, Xian,Yuan, Jingqi
, p. 6948 - 6951 (2007/10/03)
We report a convenient and highly efficient method for the synthesis of β-organotellurobutenolides by the aryltellurenyl halides-induced electrophilic tellurolactonization of α-allenoic acids under mild conditions. The resulting β-organotellurobutenolides
A general method for the synthesis of Te-aryl phosphorotellurate triesters
Hayashi, Minoru,Miura, Toshiyuki,Matsuchika, Keiji,Watanabe, Yutaka
, p. 1481 - 1485 (2007/10/03)
A general and practical method for the synthesis of Te-aryl phosphorotellurates is described. A series of Te-aryl phosphorotellurates could be synthesized in good to excellent yields by the reaction of dialkyl, diaryl and trialkyl phosphites with arenetel
Alkyne-based, highly stereo- and regioselective synthesis of stereodefined functionalized vinyl tellurides
Huang,Liang,Xu,He
, p. 74 - 80 (2007/10/03)
(Z)-β-Aryltellurovinylphosphonates and (Z)-β-aryltellurovinyl sulfones were synthesized via the highly stereoselective anti-hydrotelluration of 1-alkynylphosphonates and 1-alkynyl sulfones. The configurations of these compounds were characterized via sup
