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240 6 Polyfunctional T<strong>in</strong> <strong>Organometallics</strong> for Organic Synthesis 87 D. A. Longbottom, A. J. Morrison, D. J. Dixon, S. V. Ley, Angew. Chem. Int. Ed., 2002, 41, 2786±2789 88 O. P. Anderson, A. G. M. Barrett, J. J. Edmunds, S.-I. Hachiya, J. A. Hendrix, K. Horita, J. W. Malecha, C. J. Park<strong>in</strong>son, A. VanSicke, Can. J. Chem., 2001, 79, 1562±1592 89 H. F. Olivo, F. Velµzquez, H. C. Trevisan, Org. Lett., 2000, 2, 4055±4058; B. M. Trost, O. Dirat, J. L. Gunzer, Angew. Chem. Int. Ed., 2002, 41, 841±843 90 C. M. Beaudry, D. Trauner, Org. Lett., 2002, 4, 2221±2224 91 D. Nozawa, H. Takikawa, K. Mori, J. Chem. Soc., Perk<strong>in</strong> Trans. 1, 2000, 2043±2043 92 J. Suffert, B. Salem, P. Klotz, J. Am. Chem. Soc., 2001, 123, 12107±12108 93 M. Janka, G. K. Anderson, N. P. Rath, Inorg. Chim. Acta., 2004, 357, 2339±2344; P. D. Jones, T. E. Glass, Tetrahedron Lett., 2001, 42, 2265±2267 94 U. S. Schubert, C. Eschbaumer, M. Heller, Org. Lett., 2000, 2, 3373±3376 95 For nonexhaustive recent examples <strong>of</strong> oligopyrid<strong>in</strong>es syntheses via Stille coupl<strong>in</strong>g see: M. M. M. Raposo, A. M. C. Fonseca, G. Kirsch, Tetrahedron, 2004, 60, 4071±4078; A. Puglisi, M. Benaglia, G. Roncan, Eur. J. Org. Chem., 2003, 1552±1558;P. F. H. Schwab, F. Fleischer, J. Milch, J. Org. Chem., 2002, 67, 443±449; M. Heller, U. S. Shubert, J. Org. Chem., 2002, 67, 8269±8272; C. R. Woods, M. Benaglia, S. Toyota, K., Hardcastle, J. S. Siegel, Angew. Chem. Int. Ed., 2001, 40, 749±751; G. Ulrich, S. Bedel, C. Picard, P. Tisnes, Tetrahedron Lett., 2001, 42, 6113±6115; A. Elghayuory, R. Ziessel, J. Org. Chem., 2000, 65, 7753±7763 96 For nonexhaustive recent examples <strong>of</strong> oligothiophenes synthesis via Stille coupl<strong>in</strong>g see: H. Yu, B. Xu, T. M. Swager, J. Am. Soc., 2003, 125, 1142±1143; B. Jousselme, P. Blanchard, E. Levilla<strong>in</strong>, J. Delaunay, M. Alla<strong>in</strong>, P. Richomme, D. Rondeau, N. Gallego-Planas, J. Roncali, J. Am. Chem. Soc., 2003, 125, 1363±1370; G. Sotgiu, M. Zambianchi, G. Barbarella, F. Aruffo, F. Cipriani, A. Ventola, J. Org. Chem., 2003, 68, 1512±1520; P. A. van Hal, E. H. A. Beckers, S. C. J. Meskers, R. A. J. Janssen, B. Jousselme, P. Blanchard, J. Roncali, Chem. Eur. J., 2002, 8, 5415±5429; C. Xia, X. Fan, J. Lockl<strong>in</strong>, R. C. Adv<strong>in</strong>cula, Org. Lett., 2002, 4, 2067±2070; J. Frey, A. D. Bond, .A. B. Holmes, Chem. Commun., 2002, 20, 2424 ± 2425. 97 C. R. Woods, M. Benaglia, S. Toyota, K. Hardcastel, J. S. Siegel, Angew. Chem. Int. Ed., 2001, 40, 749±751 98 T. Bach, S. Heuser, J. Org. Chem., 2002, 67, 5789±5795; T. C. Govaerts, I. Vogels, F. Campernolle, G. Hoornaert, Tetrahedron Lett., 2002, 43, 799±802; W.-S. Kim, H.-J. Kim, C.-G. Cho, Tetrahedron Lett., 2002, 43, 9015±9017; C. Wu, H. Nakumura, A. Murai, O. Shimomura, Tetrahedron Lett., 2001, 42, 2997±3000; W. M. De Borggraeve, F. J. R. Rombouts, E. V. Van der Eycken, S. M. Toppet, G. J. Hoornaert, Tetrahedron Lett., 2001, 42, 5693±5695 99 R. Shimizu, T. Fuchikami, Tetrahedron Lett., 2001, 42, 6891±6894. 100 S.-K. Kang, H.-C. Ryu, S.-W. Lee, J. Organomet. Chem., 2000, 610, 38±41. 101 K. Kikukawa, T. Idemoto, A. Katayama, K. Kono, F. Wada, T. Matsuda, J. Chem. Soc. Perk<strong>in</strong> Trans. 1, 1987, 1511±1514 102 S.-K. Kang, T. Yamaaguchi, T.-H. Kim, P.-S. Ho, J. Org. Chem., 1996, 61, 9082±9083 103 F. Garrido, S. Raeppel, A. Mann, M. Lautens, Tetrahedron Lett., 2001, 42, 265±266 R. Shimizu, T. Fuchikami, Tetrahedron Lett., 2001, 42, 6891±6894 104 S. Ceccarelli, U. Piarulli, C. Gennari, J. Org. Chem., 2000, 65, 6254±6256 105 R. J. Franks, K. M. Nicholas, Orgnometallics, 2000, 19, 1458±1460. 106 R. D. Mazzola, Jr., S. Giese, C. L. Benson, F. G. West, J. Org. Chem., 2004, 69, 220±223 107 E. Morera, G. Ortar, Bioorg. Med. Chem. Lett., 2000, 10, 1815±1818 108 M. H. Al-Qaahtani, V. W. Pike, J. Chem. Soc., Perk<strong>in</strong> Trans. 1, 2000, 1033±1036; M. W. Nader, F. Oberdorfer, Appl. Rad. Isotopes, 2002, 57, 681±685 109 M. R. Garayt, J. M. Percy, Tetrahedron Lett., 2001, 42, 6377±6380
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Organometallics. Paul Knochel Copyr
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Handbook of Functionalized Organome
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Contents Preface XV List of Authors
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Contents 3.3.9 Oxidation of Functio
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6.3.1 Nucleophilic Addition onto Ca
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9.2.3 Preparation of Functionalized
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13.6.4 Nickel-Catalyzed Cross-coupl
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Preface Since the pioneering work o
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XVIII List of Authors Corinne Gosmi
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1 Introduction Paul Knochel and Fel
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umorganic is directly generated in
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Et H 21 Et AlBu 2 + CO 2Et Cu(CN)Mg
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8 2 Polyfunctional Lithium Organome
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10 2 Polyfunctional Lithium Organom
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R R 12 2 Polyfunctional Lithium Org
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MeO MeO R 14 2 Polyfunctional Lithi
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N 16 2 Polyfunctional Lithium Organ
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18 2 Polyfunctional Lithium Organom
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Li LiO 20 2 Polyfunctional Lithium
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Li 22 2 Polyfunctional Lithium Orga
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24 2 Polyfunctional Lithium Organom
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26 Ph O Ni-Pr 2 2 Polyfunctional Li
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28 Li 2 Polyfunctional Lithium Orga
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30 2 Polyfunctional Lithium Organom
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Li 32 203 2 Polyfunctional Lithium
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34 2 Polyfunctional Lithium Organom
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36 Br 2 Polyfunctional Lithium Orga
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38 2 Polyfunctional Lithium Organom
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40 2 Polyfunctional Lithium Organom
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42 2 Polyfunctional Lithium Organom
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3 Functionalized Organoborane Deriv
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Br SSiMe 2tBu 4 3.2 Preparation and
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B O O 3.2 Preparation and Reaction
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3.2 Preparation and Reaction of Fun
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3.2 Preparation and Reaction of Fun
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Ar H Ar = O HB O CF 3 CF 3 3.2 Prep
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3.2 Preparation and Reaction of Fun
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X X Cl Cl TfO Cl 3.2 Preparation an
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HO HO Br OH O X N N O N 3.2 Prepara
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MOMO MOMO I CbzN O 3.2 Preparation
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3.2 Preparation and Reaction of Fun
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(HO) 3B O NMe 3 N N O Br 3.2 Prepar
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H H O O N H N H O OEt O O OEt O 3.2
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t BuO2C O N H 3.2 Preparation and R
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3.2 Preparation and Reaction of Fun
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3.2 Preparation and Reaction of Fun
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3.2 Preparation and Reaction of Fun
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R H2O R R B(OH) 2 B(OH) 2 3.3 Prepa
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3.3 Preparation and Reactions of Fu
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R 124 BF 3K Br 3.3 Preparation and
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B O O I OR O OR O O O O O OR 3.3 Pr
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S N O B O I O 133 3.4 Preparation a
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3.5 Synthesis and Reactions of Func
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3.7 Synthesis and Reactions of Func
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3.7 Synthesis and Reactions of Func
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3.7 Synthesis and Reactions of Func
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3.7 Synthesis and Reactions of Func
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R TrocO S N R 1 O S N 13 12 O 1 160
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3.7 Synthesis and Reactions of Func
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3.7 Synthesis and Reactions of Func
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22 H. Nakamura, M. Fujiwara, Y. Yam
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102 K. A. Scheidt, A. Tasaka, T. D.
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4 Polyfunctional Magnesium Organome
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crystallize with four-coordinated M
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4.2Methods of Preparation of Grigna
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4.2Methods of Preparation of Grigna
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4.2Methods of Preparation of Grigna
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NC Br Br 4.2Methods of Preparation
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N N Ph I 4.2Methods of Preparation
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4.2Methods of Preparation of Grigna
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4.2Methods of Preparation of Grigna
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Cl MgBr 4.2Methods of Preparation o
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4.2Methods of Preparation of Grigna
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4.2Methods of Preparation of Grigna
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4.2Methods of Preparation of Grigna
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4.2Methods of Preparation of Grigna
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4.2Methods of Preparation of Grigna
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4.2Methods of Preparation of Grigna
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O O O O 4.2Methods of Preparation o
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O Me Me O Pent I 4.2Methods of Prep
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4.2Methods of Preparation of Grigna
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4.3 Further Applications of Functio
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4.3 Further Applications of Functio
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4.3 Further Applications of Functio
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OTIPS I iPrMgCl OTIPS 4.3 Further A
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4.4 Application of Functionalized M
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I O O OBn Pd(t-Bu 3P) 2 (10 mol%) 4
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4.4 Application of Functionalized M
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Me OTf CO2Et + Me 4.4 Application o
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4.4 Application of Functionalized M
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12 a) F. Bickelhaupt in H. G. Riche
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56 G. Varchi, C. Kofink, D. M. Lind
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kin Trans. 1 1992, 1393; b) M. Sato
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31, 805; J. F. Hartwig, Angew. Chem
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5 Polyfunctional Silicon Organometa
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stereocontrol [5]. Similar chiral c
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5.2 Allylic Silanes seven-membered
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SiMe 3 33 Pr OH OSiMe 3 SiMe 3 34 O
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5.2 Allylic Silanes Although alkyl
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R O Si H 60a (R = H) 60b (R = Me) R
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Bpin SiMe 2Ph (CH 2) 2Ph 73 EtCH(OE
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BnO HO SiMe2Ph 2 BnO CHO BnO O BF3
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- Page 214 and 215: 5.5 Miscellaneous Preparations and
- Page 216 and 217: 5.5 Miscellaneous Preparations and
- Page 218 and 219: 716. (c)I. E. Markó, J.-M. Planche
- Page 220 and 221: 6 Polyfunctional Tin Organometallic
- Page 222 and 223: phine ligand or Pd II (PPh 3) 2Cl 2
- Page 224 and 225: Bu 3 Sn Scheme 6.4 n-Pent + Me I O
- Page 226 and 227: N N N H 2 I Scheme 6.8 N + Me Sn 3
- Page 228 and 229: O O O NaO HO Me P O OH O OH (+)-Fos
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- Page 242 and 243: 6.3 Nucleophilic Additions ethylami
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- Page 246 and 247: 6.4 Radical Reactions of Organotins
- Page 248 and 249: TsN Scheme 6.37 + Bu 3Sn O Ph AIBN
- Page 250 and 251: 6.5.2 Tin-to-lithium Exchange 6.5.2
- Page 252 and 253: Ar OR Scheme 6.42 N H SnBu 3 n-BuLi
- Page 254 and 255: References 1 D. Azarian, S. S. Dua,
- Page 258 and 259: 110 Y. Obora, M. Nakanishi, M. Toku
- Page 260 and 261: 178 Y. Yamamoto, H. Yatagai, Y. Nar
- Page 262 and 263: J. Chem. Soc., Chem. Commun., 1995,
- Page 264 and 265: 301 D. P. G. Hamon, R. A. Massy-Wes
- Page 266 and 267: 371 I. D. Gridnev, O. L. Tok, N. A.
- Page 268 and 269: 252 7 Polyfunctional Zinc Organomet
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- Page 272 and 273: 256 7 Polyfunctional Zinc Organomet
- Page 274 and 275: 258 7 Polyfunctional Zinc Organomet
- Page 276 and 277: BnO H Me 37 :1:1mixtureof diastereo
- Page 278 and 279: 262 Me 3Si 7 Polyfunctional Zinc Or
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- Page 282 and 283: 266 7 Polyfunctional Zinc Organomet
- Page 284 and 285: Bu S O IZn(CH 2) 4ZnI 94 268 7 Poly
- Page 286 and 287: 270 7 Polyfunctional Zinc Organomet
- Page 288 and 289: OAc MeO I EtO 2C 272 CHO S C N 7 Po
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- Page 296 and 297: 280 E 7 Polyfunctional Zinc Organom
- Page 298 and 299: 282 MeO 2C O I 7 Polyfunctional Zin
- Page 300 and 301: H Ph 284 7 Polyfunctional Zinc Orga
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290 7 Polyfunctional Zinc Organomet
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292 7 Polyfunctional Zinc Organomet
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294 IZn AcO 7 Polyfunctional Zinc O
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296 7 Polyfunctional Zinc Organomet
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298 7 Polyfunctional Zinc Organomet
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300 7 Polyfunctional Zinc Organomet
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302 7 Polyfunctional Zinc Organomet
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304 7 Polyfunctional Zinc Organomet
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306 7 Polyfunctional Zinc Organomet
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308 7 Polyfunctional Zinc Organomet
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O 310 7 Polyfunctional Zinc Organom
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312 7 Polyfunctional Zinc Organomet
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314 7 Polyfunctional Zinc Organomet
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316 7 Polyfunctional Zinc Organomet
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318 AcO 7 Polyfunctional Zinc Organ
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EtO 2C 320 MeO 7 Polyfunctional Zin
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MeO O 322 n-Hept O O I Me 7 Polyfun
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MeO 462 324 460 Br I 463 7 Polyfunc
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326 7 Polyfunctional Zinc Organomet
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328 7 Polyfunctional Zinc Organomet
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330 7 Polyfunctional Zinc Organomet
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332 7 Polyfunctional Zinc Organomet
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334 7 Polyfunctional Zinc Organomet
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336 7 Polyfunctional Zinc Organomet
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338 7 Polyfunctional Zinc Organomet
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340 7 Polyfunctional Zinc Organomet
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342 7 Polyfunctional Zinc Organomet
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344 7 Polyfunctional Zinc Organomet
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346 7 Polyfunctional Zinc Organomet
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348 8 Polyfunctional 1,1-Organodime
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350 O 8 Polyfunctional 1,1-Organodi
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352 8 Polyfunctional 1,1-Organodime
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354 8 Polyfunctional 1,1-Organodime
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356 8 Polyfunctional 1,1-Organodime
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358 8 Polyfunctional 1,1-Organodime
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360 8 Polyfunctional 1,1-Organodime
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CH 2(ZnI) 2 4 362 8 Polyfunctional
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364 8 Polyfunctional 1,1-Organodime
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366 8 Polyfunctional 1,1-Organodime
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368 8 Polyfunctional 1,1-Organodime
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370 8 Polyfunctional 1,1-Organodime
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372 8 Polyfunctional 1,1-Organodime
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374 8 Polyfunctional 1,1-Organodime
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376 8 Polyfunctional 1,1-Organodime
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9 Polyfunctional Organocopper Reage
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S 5 CuI·LiCl Cu(CN)Li Li naphthale
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Br CO 2Et I CO 2Et CO 2Et Np 2CuLi
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9.2 Preparation of Functionalized O
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Pent I O O Pent I CO 2Et O Br Pent
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Ph Ph N OMe 1) n-BuLi 2) alkynylcop
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9.3 Applications of Functionalized
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PrCu·MgBr 2·SMe 2 Pr Me H Pr H HO
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19 X. Yang, T. Rotter, C. Piazza, P
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n-C 7H 15 398 10 Functional Organon
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400 10 Functional Organonickel Reag
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402 10 Functional Organonickel Reag
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404 10 Functional Organonickel Reag
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406 10 Functional Organonickel Reag
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408 10 Functional Organonickel Reag
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410 10 Functional Organonickel Reag
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412 10 Functional Organonickel Reag
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414 10 Functional Organonickel Reag
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416 10 Functional Organonickel Reag
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418 10 Functional Organonickel Reag
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420 10 Functional Organonickel Reag
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422 10 Functional Organonickel Reag
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O 424 10 Functional Organonickel Re
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TIPSO R 1 Cp 2ClZr O H 426 O N 10 F
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428 10 Functional Organonickel Reag
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430 10 Functional Organonickel Reag
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432 10 Functional Organonickel Reag
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434 10 Functional Organonickel Reag
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436 10 Functional Organonickel Reag
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O 438 O Br 10 Functional Organonick
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440 10 Functional Organonickel Reag
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Cl 442 CN 10 Functional Organonicke
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444 10 Functional Organonickel Reag
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446 10 Functional Organonickel Reag
- Page 462 and 463:
448 10 Functional Organonickel Reag
- Page 464 and 465:
11 Polyfunctional Metal Carbenes fo
- Page 466 and 467:
11.2 Chromium-Templated Cycloadditi
- Page 468 and 469:
11.2 Chromium-Templated Cycloadditi
- Page 470 and 471:
(CO) 5Cr O Ph 15 1) t Bu t BuOMe, 5
- Page 472 and 473:
O MeO O O O O MeO O OMe Cr(CO) 5 Me
- Page 474 and 475:
11.2.3 Cyclization of Chromium Olig
- Page 476 and 477:
(CO)5Cr OR * O S + OMe 11.2 Chromiu
- Page 478 and 479:
[2+2+1] R 1 R 1 OH (CO) 5Cr R 2 (CO
- Page 480 and 481:
11.3 Reactions of Higher Nuclearity
- Page 482 and 483:
Br O X Br O R 2 R 2 O 85: X = Si-tB
- Page 484 and 485:
11.3 Reactions of Higher Nuclearity
- Page 486 and 487:
11.4 Metathesis Reactions Catalyzed
- Page 488 and 489:
R 2 R 1 O R O 3 O 11.4 Metathesis R
- Page 490 and 491:
i Pr i Pr i Pr Me Me (R)-160 Ph O O
- Page 492 and 493:
11.5 Transmetallation The dimerizat
- Page 494 and 495:
11.6 Metal Carbenes in Peptide Chem
- Page 496 and 497:
11.7 Stereoselective Syntheses with
- Page 498 and 499:
11.7 Stereoselective Syntheses with
- Page 500 and 501:
11.7 Stereoselective Syntheses with
- Page 502 and 503:
11.7 Stereoselective Syntheses with
- Page 504 and 505:
11.7 Stereoselective Syntheses with
- Page 506 and 507:
O O O O 100% H 2N O O O O O 311a Cr
- Page 508 and 509:
11.8 Sugar Metal Carbenes as Organo
- Page 510 and 511:
References zation reactions that al
- Page 512 and 513:
35 (a) C.A. Merlic, Y. You, D.M. Mc
- Page 514 and 515:
D. R. Cefalo, P. J. Bonitatebus Jr.
- Page 516 and 517:
12 Functionalized Organozirconium a
- Page 518 and 519:
12.2 Functionalized Organozirconoce
- Page 520 and 521:
Ph O (H)ZrCp Ph O 2Cl Ph O O O 92 %
- Page 522 and 523:
12.2 Functionalized Organozirconoce
- Page 524 and 525:
i-PrO O OBu-t O H N Scheme 12.15 H
- Page 526 and 527:
BnO Scheme 12.19 O BnO + 27 28 Cp 2
- Page 528 and 529:
12.2 Functionalized Organozirconoce
- Page 530 and 531:
R 1 O O O R R1 R 2 Scheme 12.28 R P
- Page 532 and 533:
12.2 Functionalized Organozirconoce
- Page 534 and 535:
12.3 Functionalized Organotitanium
- Page 536 and 537:
12.3 Functionalized Organotitanium
- Page 538 and 539:
t-BuOOC Scheme 12.44 O CH 3 7.5 mol
- Page 540 and 541:
12.3 Functionalized Organotitanium
- Page 542 and 543:
H 13C 6 O R Scheme 12.52 SiMe 3 O T
- Page 544 and 545:
12.3 Functionalized Organotitanium
- Page 546 and 547:
O O OEt 87 Scheme 12.59 Scheme 12.6
- Page 548 and 549:
12.3 Functionalized Organotitanium
- Page 550 and 551:
12.3 Functionalized Organotitanium
- Page 552 and 553:
40 A. M. Sun, X. Huang, Heteroatom
- Page 554 and 555:
13 Manganese Organometallics for th
- Page 556 and 557:
13.2.2 Preparation of Organomangane
- Page 558 and 559:
13.3 1,2-Addition to Aldehydes and
- Page 560 and 561:
13.3.2 Manganese-Mediated Barbier-
- Page 562 and 563:
HeptMnX + HeptMnX + Scheme 13.17 Cl
- Page 564 and 565:
13.4 Preparation of Ketones by Acyl
- Page 566 and 567:
Me 3Si Cl ( ) 3 R Li 80% 82% Scheme
- Page 568 and 569:
13.5 1,4-Addition of Organomanganes
- Page 570 and 571:
BuM BuMgCl BuMnCl BuMgCl BuCu BuCu
- Page 572 and 573:
13.6 Transition-Metal-Catalyzed Cro
- Page 574 and 575:
13.6 Transition-Metal-Catalyzed Cro
- Page 576 and 577:
I Cl Scheme 13.56 MeO MnCl (1.2 equ
- Page 578 and 579:
13.7 Manganese-Mediated Cross-coupl
- Page 580 and 581:
13 C. Boucley, G. Cahiez, unpublish
- Page 582 and 583:
570 14 Polyfunctional Electrophilic
- Page 584 and 585:
572 14 Polyfunctional Electrophilic
- Page 586 and 587:
η5 η6 η4 η7 574 14 Polyfunction
- Page 588 and 589:
576 14 Polyfunctional Electrophilic
- Page 590 and 591:
578 14 Polyfunctional Electrophilic
- Page 592 and 593:
580 14 Polyfunctional Electrophilic
- Page 594 and 595:
582 14 Polyfunctional Electrophilic
- Page 596 and 597:
584 14 Polyfunctional Electrophilic
- Page 598 and 599:
586 14 Polyfunctional Electrophilic
- Page 600 and 601:
588 14 Polyfunctional Electrophilic
- Page 602 and 603:
590 14 Polyfunctional Electrophilic
- Page 604 and 605:
592 14 Polyfunctional Electrophilic
- Page 606 and 607:
51 594 CO 2Me + Fe(CO)3 CO2Me 14 Po
- Page 608 and 609:
596 14 Polyfunctional Electrophilic
- Page 610 and 611:
598 14 Polyfunctional Electrophilic
- Page 612 and 613:
Table 14.1 Examples of synthetic ap
- Page 614 and 615:
602 Entry Target molecule Disconnec
- Page 616 and 617:
Entry Target molecule Disconnection
- Page 618 and 619:
Entry Target molecule Disconnection
- Page 620 and 621:
Entry Target molecule Disconnection
- Page 622 and 623:
Target molecule Disconnections Mult
- Page 624 and 625:
612 14 Polyfunctional Electrophilic
- Page 626 and 627:
614 14 Polyfunctional Electrophilic
- Page 628 and 629:
616 14 Polyfunctional Electrophilic
- Page 630 and 631:
618 14 Polyfunctional Electrophilic
- Page 632 and 633:
620 14 Polyfunctional Electrophilic
- Page 634 and 635:
622 14 Polyfunctional Electrophilic
- Page 636 and 637:
624 14 Polyfunctional Electrophilic
- Page 638 and 639:
626 14 Polyfunctional Electrophilic
- Page 640 and 641:
15 Polyfunctional Zinc, Cobalt and
- Page 642 and 643:
Trifluoromethylzinc compounds prepa
- Page 644 and 645:
15.3 Electrochemical Synthesis and
- Page 646 and 647:
15.3.2 Carbon±Carbon Bond Formatio
- Page 648 and 649:
Cl Cl NC + MeO2C 1eq 2eq e, CoX 2 c
- Page 650 and 651:
1eq Br FG + R 2eq OAc e, CoX 2 cat
- Page 652 and 653:
Cl O + O e, FeBr 2(Bpy) n DMF, Fe a
- Page 654 and 655:
15.4 Electrosynthesis of Compounds
- Page 656 and 657:
15.4 Electrosynthesis of Compounds
- Page 658 and 659:
FG CuCN/LiCl ZnBr 0ºC CuZnBrCN 15.
- Page 660 and 661:
15.4 Electrosynthesis of Compounds
- Page 662 and 663:
15.5 General Conclusion (industrial
- Page 664 and 665:
17 Durandetti, M.; Devaud, M.; Peri
- Page 666 and 667:
I2 Index b-alkoxyalkylidenemalonic,
- Page 668 and 669:
I4 Index boronic ester 47 4-boronyl
- Page 670 and 671:
I6 Index cyclohexadiene 415 cyclohe
- Page 672 and 673:
I8 Index fluoroalkenylstannane 206
- Page 674 and 675:
I10 Index iron-catalyzed carbolithi
- Page 676 and 677:
I12 Index nickel-catalyzed carbozin
- Page 678 and 679:
I14 Index psicosecarbene complexes
- Page 680 and 681:
I16 Index Suzuki-Miyaura reaction a