Pure Appl. Chem., 1987, Vol. 59, No. 8, pp. 1021-1026
http://dx.doi.org/10.1351/pac198759081021
Lithium pentaalkyl/aryl stannate complexes as intermediates in the lithium-tin exchange reaction
CrossRef Cited-by Linking
- Reich Hans J.: Role of Organolithium Aggregates and Mixed Aggregates in Organolithium Mechanisms. Chem. Rev. 2013, 113, 7130. <http://dx.doi.org/10.1021/cr400187u>
- Reich Hans J.: What’s Going on with These Lithium Reagents?. J. Org. Chem. 2012, 77, 5471. <http://dx.doi.org/10.1021/jo3005155>
- Saito Masaichi, Imaizumi Sanae, Tajima Tomoyuki: Formation of Pentaorganostannates from Bis(2-bromo-2′-biphenyl)stannanes and tert-Butyllithium upon Substitution of Alkyl and Aryl Groups on Tin Atoms. Euro J Inorg Chem 2010, 2010, 2153. <http://dx.doi.org/10.1002/ejic.201000089>
- Monje Pablo, Graña Paula, Paleo M. Rita, Sardina F. Javier: Quantitative Data on the Effects of Alkyl Substituents and Li–O and Li–N Chelation on the Stability of Secondary α-Oxy-Organolithium Compounds. Chem Eur J 2007, 13, 2277. <http://dx.doi.org/10.1002/chem.200600864>
- Hoffmann Reinhard W., Brönstrup Mark, Müller Michael: The Second Step of the Halogen/Metal Exchange Reaction. Org Lett 2003, 5, 313. <http://dx.doi.org/10.1021/ol027307i>
- Boche Gernot, Schimeczek Michael, Cioslowski Jerzy, Piskorz Pawel: The Role of Ate Complexes in Halogen(Metalloid)–Metal Exchange Reactions: A Theoretical Study. Eur J Org Chem 1998, 1998, 1851. <http://dx.doi.org/10.1002/(SICI)1099-0690(199809)1998:9<1851::AID-EJOC1851>3.0.CO;2-N>
- Takahashi O., Furukawa N., Sato S.: Recent progress in hypervalent organochalcogenuranes bearing four carbon ligands. Coord Chem Rev - 1998, 176, 483. <http://dx.doi.org/10.1016/S0010-8545(98)00146-5>
- Masutomi Yutaka, Furukawa Naomichi, Erata Tomoki: Low-temperature1H,13C,77Se, and125Te NMR studies on the apical-apical ligand exchange via the hypervalent tellurium and selenium ate complexes [10-M-3(C3); M = Se, Te] in the reactions of diaryl tellurides and selenides with aryllithium reagents. Heteroatom Chem 1995, 6, 19. <http://dx.doi.org/10.1002/hc.520060107>
- Maercker Adalbert, Bodenstedt Heinrich, Brandsma Lambert: Steuerung der Reaktion vonn-Butyllithium mit Benzo[b]tellurol durch das Lösungsmittel – wahlweise Metallierung oder Tellur-Lithium-Austausch zu einem interessanten Lithiostyryllithium. Angew Chem 1992, 104, 1387. <http://dx.doi.org/10.1002/ange.19921041021>
- Ogawa Satoshi, Masutomi Yutaka, Furukawa Naomichi, Erata Tomoki: NMR studies on the ligand exchange reactions between diaryl tellurides and phenyllithium: Detection of hypervalent triaryl tellurium ate complexes. Heteroatom Chem 1992, 3, 423. <http://dx.doi.org/10.1002/hc.520030417>
- Ogawa Satoshi, Sato Soichi, Erata Tomoki, Furukawa Naomichi: Dynamic NMR studies on the solution-state structure and the pseudorotation of bis(2,2′-biphenylylene)selenurane and tellurane. Tetrahetron Lett 1992, 33, 1915. <http://dx.doi.org/10.1016/S0040-4039(00)74177-3>
- Ogawa Satoshi, Masutomi Yutaka, Erata Tomoki, Furukawa Naomichi: First Crucial Evidence for Apical-Apical Exchange via a Hypervalent Tellurium Ate Complex in the Reactions of Diaryl Tellurides with Aryllithium Reagents. Chem Lett 1992, 2471. <http://dx.doi.org/10.1246/cl.1992.2471>
- Shiner Christopher S., Tsunoda Tetsuto, Goodman Burton A., Ingham Stephen, Lee Shi Hung, Vorndam Paul E.: (Dialkoxymethyl)lithiums: generation, stability, and synthetic transformations. J. Am. Chem. Soc. 1989, 111, 1381. <http://dx.doi.org/10.1021/ja00186a036>
- Carola Acuña A., Zapata Antonio: Synthetic Utility of α-Stannyl α,β-Unsaturated Esters as Reagents for β-Substituted Acrylate α-Anion Synthons: Tin-Lithium Exchange and Palladium-Catalized Coupling Reactions. Synth Common 1988, 18, 1125. <http://dx.doi.org/10.1080/00397918808060899>