By Stanley M. Roberts, Ivan V. Kozhevnikov, Eric Derouane(eds.)
The chemist has an enormous diversity of high-tech catalysts to take advantage of while operating in fine chemical synthesis however the catalysts are in general not easy to take advantage of and require either time, ability and event to address effectively. The Catalysts for high quality Chemical Synthesis series contains demonstrated and demonstrated tactics which provide a distinct diversity assets for chemists who paintings in natural chemistry.
"... of significant worth to artificial natural chemists..." (The Chemists, summer season 2003)
quantity three within the sequence makes a speciality of catalysts for carbon-carbon bond formation and offers useful and detailed protocols on tips on how to use refined catalysts via the "inventors" and "developers" who created them. The combination of protocols and evaluation commentaries is helping the reader to simply and quickly understand and use the recent high-tech catalysts.Content:
Chapter 1 concerns of business high quality Chemical Synthesis (pages 1–12): Mark W. Hooper
Chapter 2 Alkylation and Allylation adjoining to a Carbonyl staff (pages 13–33): Fumitoshi Kakiuchi, Satoshi Ueno, Naoto Chatani, Michael North, Jose A. Fuentes, Barry Lygo and Benjamin I. Andrews
Chapter three uneven Alkylation or Amination of Allylic Esters (pages 35–57): Maria Zablocka, Marek Koprowski, Jean?Pierre Majoral, Mathieu Achard, Gerard Buono, Jerome Bayardon, Denis Sinou, Matthias Lotz, Gernot Kramer, Katja Tappe, Paul Knochel, Pierluigi Barbaro, Claudio Bianchini, Giuliano Giambastiani and Antonio Togni
Chapter four Suzuki Coupling Reactions (pages 59–90): Ana S. Abreu, Paula M. T. Ferreira, Maria?Joao R. P. Queiroz, Jie Wu, Lisha Wang, Reza Fathi, Zhen Yang, Ramon E. Huertas, John A. Soderquist, Tatsuo Ishiyama, Norio Miyaura, Bin Tao, David W. Boykin, Colin Baillie, Lijin Xu, Jianliang Xiao, Matthew L. Clarke, J. Derek Woollins, Nicholas Marion, Oscar Navarro, Roy A. Kelly and Steven P. Nolan
Chapter five Heck Coupling Reactions (pages 91–112): Peter Nilsson, Mats Larhed, Lijin Xu, Jun Mo, Jianliang Xiao, Tim G. Kilroy, Yvonne M. Malone and Patrick J. Guiry
Chapter 6 Sonogashira Coupling Reactions (pages 113–125): Anupama Datta, Herbert Plenio, Chih?An Lin and Fen?Tair Luo
Chapter 7 Cross?Coupling Reactions (pages 127–153): Jun Terao, Nobuaki Kambe, Luis A. Sarandeses, Jose Perez Sestelo, Bryan A. Frieman, Bruce H. Lipshutz, John Mancuso, Masahiro Yoshida and Mark Lautens
Chapter eight Regioselective or uneven 1,2?Addition to Aldehydes (pages 155–168): Kui?Thong Tan, Shu?Sin Chng, Hin?Soon Cheng, Teck?Peng Loh, Jens Rudolph, Carsten Bolm, Marco Lombardo, Sebastiano Licciulli, Stefano Morganti and Claudio Trombini
Chapter nine Olefin Metathesis Reactions (pages 169–180): Syuzanna Harutyunyan, Anna Michrowska, Karol Grela, Stephen J. Connon, Aideen M. Dunne, Siegfried Blechert, G. Bhaskar and B. Venkateswara Rao
Chapter 10 Cyclisation Reactions (pages 181–200): Jaime Blanco?Urgoiti, Gema Dominguez, Javier Perez?Castells, Ligang Zhao, Xiyan Lu, Minsheng He, Aiwen Lei, Xumu Zhang, Hiroshi Shinokubo, Koichiro Oshima, Antonio Rosales, Juan M. Cuerva and Enrique Oltra
Chapter eleven uneven Aldol and Michael Reactions (pages 201–223): Masakatsu Shibasaki, Shigeki Matsunaga, Naoya Kumagai, Zhuo Tang, Liu?Zhu Gong, Ai?Qiao Mi, Yao?Zhong Jiang, Masahito Watanabe, Kunihiko Murata and Takao Ikariya
Chapter 12 Stereoselective Hydroformylation, Carbonylation and Carboxylation Reactions (pages 225–250): Bernhard Breit, Martin Wills, Simon W. Breeden, Stefania Cserepi?Szucs, Jozsef Bakos, C. Ramesh, Y. Kubota, Y. Sugi, Tomoko Matsuda, Tadao Harada, Toru Nagasawa and Kaoru Nakamura
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Extra info for Catalysts for Fine Chemical Synthesis: Metal Catalysed Carbon-Carbon Bond-Forming Reactions, Volume 3
1 Synthesis of (2,6-dimethyl-phenyl)-(1-phenyl-2,3,3a,8a-tetrahydro-1H1-phospha-cyclopenta[a]inden-8-ylidene)-amines 1Rp . . . . . . . . 2 Synthesis of (E)-Methyl 2-carbomethoxy-3,5-diphenylpent-4-enoate . . . 3 Synthesis of benzyl(1,3-diphenylprop-2-enyl)amine . . . . . . . . . 4 Conclusion . . . . . . . . . . . . . . . . . . . . . . . References . . . . . . . . . . . . . . . . . . . . . . . . . . 3 JE´ROˆME BAYARDON and DENIS SINOU .
Chem. Soc. , Plaquevent, J. C. and Cahard, D. Tetrahedron: Asymmetry 2003, 14, 1671; Park, H. , Jeong, B. , Yoo, M. , Lee, J. , Park, B. , Kim, M. G. and Jew, S. S. Tetrahedron Lett. , Allbutt, B. and James, S. R. Tetrahedron Lett. 2003, 44, 5629. 2 MARIA ZABLOCKA, MAREK KOPROWSKI, JEAN-PIERRE MAJORAL, MATHIEU ACHARD and GE´RARD BUONO . . . . . . . . . . . . . . . . . . . . . . . 1 Synthesis of (2,6-dimethyl-phenyl)-(1-phenyl-2,3,3a,8a-tetrahydro-1H1-phospha-cyclopenta[a]inden-8-ylidene)-amines 1Rp .
52 ............. 53 ............. ............. 1 SYNTHESIS AND APPLICATION IN PALLADIUMCATALYSED ASYMMETRIC ALLYLIC SUBSTITUTION OF ENANTIOPURE CYCLIC b-IMINOPHOSPHINE LIGANDS MARIA ZABLOCKAa*, MAREK KOPROWSKIa, JEAN-PIERRE MAJORALb*, MATHIEU ACHARDc and GE´ RARD BUONOc* a Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland b Laboratoire de Chimie de Coordination, CNRS, 205 route de Narbonne, 31077 Toulouse Cedex, France c ENSSPICAM, CNRS, UMR 6516, Faculte´ St Je´ roˆ me, av.
Catalysts for Fine Chemical Synthesis: Metal Catalysed Carbon-Carbon Bond-Forming Reactions, Volume 3 by Stanley M. Roberts, Ivan V. Kozhevnikov, Eric Derouane(eds.)