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176 References [43] Eaborn, C.; Varma, I. D., J. Organomet. Chem., (1967) 9, 377. [44] Lukevics, E.; Ignatovich, L.; Goldberg, Y.; Polyak, F.; Gaukhman, A.; Rozite, S.; Popelis, J., J. Organomet. Chem., (1988) 348, 11. [45] Laurent, R.; Laporterie, A.; Dubac, J.; Berlan, J., Organometallics, (1994) 13, 2493. [46] Shostakovskii, M. F.; Sokolov, B. A.; Ermakova, L. T., J. Gen. Chem. USSR (Engl. Transl.), (1961) 32, 1698. [47] Bardin, V. V.; Pressman, L. S.; Furin, G. G., J. Organomet. Chem., (1993) 448, 55. [48] Terunuma, D.; Masuo, K.; Kizaki, H.; Nohira, H., Bull. Chem. Soc. Jpn., (1994) 67, 160. [49] Spivey, A. C.; Diaper, C. M.; Adams, H.; Rudge, A. J., J. Org. Chem., (2000) 65, 5253. [50] Denat, F.; Gaspard-Iloughmane, H.; Dubac, J., Synthesis, (1992), 954. [51] Denat, F.; Gaspard-Iloughmane, H.; Dubac, J., J. Organomet. Chem., (1992) 423, 173. [52] Terunuma, D.; Kizaki, H.; Sato, T.; Masuo, K.; Nohira, H., Bull. Chem. Soc. Jpn., (1993) 66, 664. [53] Mironov, V. F.; Fedotov, N. S., J. Gen. Chem. USSR (Engl. Transl.), (1964) 34, 4186. [54] Cerveau, G.; Chuit, C.; Corriu, R. J. P.; Reye, C., Organometallics, (1991) 10, 1510. [55] Eaborn, C.; Pande, C., J. Chem. Soc., (1960), 3200. [56] Fomina, N. V.; Sheverdina, N. I.; Dobrova, E. I.; Sosnina, I. V.; Kocheshkov, K. A., Dokl. Chem. (Engl. Transl.), (1973) 201, 439. [57] David-Quillot, F.; Lunot, S.; Marsacq, D.; Duchene, A., Tetrahedron Lett., (2000) 41, 4905. [58] Azizian, H.; Eaborn, C.; Pidock, A., J. Organomet. Chem., (1981) 215, 49. [59] Azizian, D.; Dua, S. S.; Eaborn, C.; Walton, D. N. R., J. Organomet. Chem., (1976) 117, C55. [60] Yamashita, H.; Kobayashi, T.-a.; Tanaka, M.; Samuels, J. A.; Streib, W. E., Organometallics, (1992) 11, 2330. [61] Reddy, N. P.; Hayashi, T.; Tanaka, M., Chem. Lett., (1991), 677. [62] Barrau, J.; Rima, G.; Akkari, A.; Satge, J., Inorg. Chim. Acta, (1997) 260, 11. [63] Barrau, J.; Rima, G.; Amine, M.; Satge, J., Synth. React. Inorg. Met.-Org. Chem., (1988), 21. [64] Poskozim, P. S., J. Organomet. Chem., (1968) 12, 115-21. [65] Satge, J.; Massol, M.; Riviere, P., J. Organomet. Chem., (1973) 56,1. [66] Shcherbinin, V. V.; Shvedov, I. P.; Pavlov, K. V.; Komalenkova, N. G.; Chernyshev, E. A., Russ. J. Gen. Chem., (1998) 68, 1013. [67] Jurayev, A. D.; Makhsumov, A. G.; Yuldasheva, K.; Tolipova, M. A., J. Organomet. Chem., (1992) 431, 129. [68] Piterskaya, Y. L.; Khramchikhin, A. V.; Stadnichuk, M. D., Russ. J. Gen. Chem., (1996) 66, 1158. [69] Sauer, J.; Heldmann, D. K., Tetrahedron, (1998) 54, 4297. [70] Sauer, J.; Heldmann, D. K.; Hetzenegger, J.; Krauthan, J.; Sichert, H.; Schuster, J., Eur. J. Org. Chem., (1998), 2885. [71] Guillier, F.; Orain, D.; Bradley, M., Chem. Rev., (2000) 100, 2091. [72] Showalter, H. D., Chemtracts -Org. Chem., (1996) 9, 231. [73] Han, Y.; Walker, S. D.; Young, R. N., Tetrahedron Lett., (1996) 37, 2703. [74] Plunkett, M. J.; Ellman, J. A., J. Org. Chem., (1997) 62, 2885. [75] Dallaire, C.; Brook, M. A., Organometallics, (1993) 12, 2332. [76] Pitt, C. G., J. Organomet. Chem., (1973) 61, 49. [77] Egorochkin, A. N.; Razuvaev, G. A.; Lopatin, M. A., J. Organomet. Chem., (1988) 344, 49. [78] Spivey, A. C.; Diaper, C. M.; Rudge, A. J., Chem. Commun. (Cambridge), (1999), 835. [79] Nakamura, T.; Kinoshita, M.; Shinokubo, M.; Oshima, K., Org. Lett., (2002) 4, 3165.
Abbreviations Chemical Name Used in Text Abbreviation Used in Tables and on Arrow in Schemes Abbreviation Used in Experimental Procedures (R)-1-amino-2-(methoxymethyl)pyrrolidine RAMP RAMP (S)-1-amino-2-(methoxymethyl)pyrrolidine SAMP SAMP ammonium cerium(IV) nitrate CAN CAN 2,2¢-azobisisobutyronitrile AIBN AIBN barbituric acid BBA BBA benzyltriethylammonium bromide TEBAB benzyltriethylammonium bromide benzyltriethylammonium chloride TEBAC benzyltriethylammonium chloride N,O-bis(trimethylsilyl)acetamide BSA BSA 9-borabicyclo[3.3.1]nonane 9-BBNH 9-BBNH borane–methyl sulfide complex BMS BMS N-bromosuccinimide NBS NBS tert-butyldimethylsilyl chloride TBDMSCl TBDMSCl tert-butyl peroxybenzoate TBPB tert-butyl peroxybenzoate 10-camphorsulfonic acid CSA CSA chlorosulfonyl isocyanate CSI chlorosulfonyl isocyanate 3-chloroperoxybenzoic acid MCPBA MCPBA N-chlorosuccinimide NCS NCS chlorotrimethylsilane TMSCl TMSCl 1,4-diazabicyclo[2.2.2]octane DABCO DABCO 1,5-diazabicyclo[4.3.0]non-5-ene DBN DBN 1,8-diazabicyclo[5.4.0]undec-7-ene DBU DBU dibenzoyl peroxide DBPO dibenzoyl peroxide dibenzylideneacetone dba dba di-tert-butyl azodicarboxylate DBAD di-tert-butyl azodicarboxylate 2,3-dichloro-5,6-dicyanobenzo- 1,4-quinone DDQ DDQ dichloromethyl methyl ether DCME DCME dicyclohexylcarbodiimide DCC DCC N,N-diethylaminosulfur trifluoride DAST DAST diethyl azodicarboxylate DEAD DEAD diethyl tartrate DET DET 2,2¢-dihydroxy-1,1¢-binaphthyllithium aluminum hydride BINAL-H BINAL-H diisobutylaluminum hydride DIBAL-H DIBAL-H 177
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Science of Synthesis Houben-Weyl Me
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8 Science of Synthesis Category 1:
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Volume 1: Compounds withTransition
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Table of Contents Volume 2 13 Volum
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Table of Contents 15 Volume 4: Comp
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Table of Contents 17 4.4.27 Product
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2001 Georg Thieme Verlag Rüdigerst
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1.1 Product Class 1: Organometallic
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1.1 Product Class 1: Organometallic
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1.1.1 Nickel Complexes of 1,3-Diene
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1.1.1 Nickel Complexes of 1,3-Diene
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1.1.2 Nickel-Allyl Complexes 37 tra
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1.1.2 Nickel-Allyl Complexes 39 Bis
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1.1.2 Nickel-Allyl Complexes 41 App
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1.1.2 Nickel-Allyl Complexes 43 NiC
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1.1.2 Nickel-Allyl Complexes 45 Sch
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1.1.2 Nickel-Allyl Complexes 47 Sch
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1.1.3 Nickel-Alkyne Complexes 49 Ca
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1.1.3 Nickel-Alkyne Complexes 51 (2
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1.1.3 Nickel-Alkyne Complexes 53 Sc
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1.1.3 Nickel-Alkyne Complexes 55 at
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1.1.3 Nickel-Alkyne Complexes 57 Sc
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1.1.3 Nickel-Alkyne Complexes 59 en
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1.1.3 Nickel-Alkyne Complexes 61 of
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1.1.4 Nickel-Alkene Complexes 63 Bi
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1.1.4 Nickel-Alkene Complexes 65 Sc
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1.1.4 Nickel-Alkene Complexes 67 1.
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1.1.4 Nickel-Alkene Complexes 69 Sc
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1.1.4 Nickel-Alkene Complexes 71 [5
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1.1.4 Nickel-Alkene Complexes 75 4-
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References 79 References [1] Chetcu
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References 81 [98] Tsuda, T.; Mizun
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86 Biographical Sketches Rinaldo Po
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88 2.6.4.2.2 Variation 2: Two-Elect
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90 2.6 Product Class 6: Organometal
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92 Science of Synthesis 2.6 Complex
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100 Science of Synthesis 2.6 Comple
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Page 166 and 167: 166 Biographical Sketches Alan Spiv
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Page 178 and 179: 178 Abbreviations Chemical (cont.)
Page 180 and 181: 180 Abbreviations Ligands (cont.) 2
Page 182: 182 Abbreviations General (cont.) q
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