By Stanley M. Roberts, Ivan V. Kozhevnikov, Eric G. Derouane(eds.)
Quantity five within the Catalysts for nice Chemical Synthesis sequence describes new systems for the regio- and stereo-controlled differences of compounds regarding oxidation or relief reactions. It describes quite a lot of catalysts, together with organometallic platforms, biocatalysts and biomimetics. This quantity additionally comprises descriptions of numerous conversions, together with: Baeyer-Villiger oxidations; Epoxidation reactions; Hydroxylation reactions; Oxidation of alcohols to aldehydes, ketones and carboxylic acids; relief of ketones; and relief of alkenes together with ?, ?-unsaturated carbonyl compounds. The e-book could be an enormous textual content for working towards man made natural chemists in and academia.
- Protocols are written in a regular layout by way of the authors who've stumbled on them
- Hints, suggestions and protection recommendation (where acceptable) is given to make sure that the tactics are reproducible
- Indications are given as to the variety of beginning fabrics used and, the place applicable, comparisons to replacement technique
- Includes suitable references to the first literature.
Chapter 1 commercial Catalysts for Regio? or Stereo?Selective Oxidations and discount rates. A evaluation of Key applied sciences and goals (pages 1–33): John Whittall
Chapter 2 uneven Hydrogenation of Alkenes, Enones, Ene?Esters and Ene?Acids (pages 35–86): Ildiko Gergely, Csaba Hegedus, Jozsef Bakos, Frederik Menges, Andreas Pfaltz, Pier Giorgio Cozzi, Jing Wu, Albert S. C. Chan, Tsuneo Imamoto, Aya Koide, Ryoichi Kuwano and Masaya Sawamura
Chapter three uneven relief of Ketones (pages 87–159): Natalia Dubrovina, Armin Borner, Kaoru Nakamura, Mikio Fujii, Yoshiteru Ida, Antonio Rosales, Juan M. Cuerva, J. Enrique Oltra, Paul H. Moran, Julian P. Henschke, Antonio Zanotti?Gerosa, Ian C. Lennon, Michel (Massoud S.) Stephan, Barbara Mohar, Martin Wills, Yingjian Xu, Gorden Docherty, Gary Woodward, Jenny Wettergren, Hans Adolfsson, Severine Jeulin, Virginie Ratovelomanana?Vidal, Jean?Pierre Genet, Estelle Burri, Silke B. Wendicke, Kay Severin, Minjie Guo, Dao Li, Yanhui sunlight, Zhaoguo Zhang, Liting Chai, Yangzhou Li, Quanrui Wang, Guangyin Wang and Gang Zhao
Chapter four Imine aid and Reductive Amination (pages 161–181): Magnus Rueping, Erli Sugiono, Cengiz Azap, Thomas Theissmann, Andrey P. Antonchick, Sharaf Nawaz Khan, Nam Ju Cho and Hong?Seok Kim
Chapter five Oxidation of basic and Secondary Alcohols (pages 183–192): Suribabu Jammi, Tharmalingan Punniyamurthy, G. B. W. L Ligthart, R. H. Meijer, J. v. Buijtenen, J. Meuldijk, J. A. J. M. Vekemans, L. A. Hulshof, Krisada Kittigowittana, Manat Pohmakotr, Vichai Reutrakul and Chutima Kuhakarn
Chapter 6 Hydroxylation, Epoxidation and comparable Reactions (pages 193–254): Yujiro Hayashi, Mitsuru Shoji, Rosaria Ciriminna, Mario Pagliaro, Tony ok. M. Shing, Gulice Y. C. Leung, To Luk, Alessandra Lattanzi, Arrigo Scettri, David Goeddel, Yian Shi, Giovanni Sartori, Alan Armstrong, Raimondo Maggi, Alessandro Mazzacani, Raffaella Sartorio, France Bigi, Belen Dominguez?Fernandez, Kazushige Hori, Keita Tani, Yasuo Tohda, Jerome Vachon, Celine Perollier, Alexandre Martinez, Jerome Lacour, Masakatsu Shibasaki, Hiroyuki Kakei, Shigeki Matsunaga, Ana Minatti, Karl Heinz Dotz, Mike R. Pitts and John Whittalld
Chapter 7 Oxidation of Ketones to Lactones or Enones (pages 255–266): Katsuji Ito, Tsutomu Katsuki, Paul Mather and John Whittall
Chapter eight Oxidative C?C Coupling (pages 267–278): Nan?Sheng Xie, Quan?Zhong Liu, Zhi?Bin Luo, Liu?Zhu Gong, Ai?Qiao Mi, Yao?Zhong Jiang, Shigeki Habaue, Tomohisa Temma, Tomoyuki Yamada, Satoshi Sakaguchi and Yasutaka Ishii
Chapter nine Oxidation of Sulfides and Sulfoxides (pages 279–302): Boyapati M. Choudary, Chinta Venkat, V. Reddy, Billakanti V. Prakash, Mannepalli L. Kantam, B. Sreedhar, Kiumar Bahrami, Vinay V. Thakur, A. Sudalai, Raffaella Del Litto, Guiseppina Roviello, Francesco Ruffo, Alessando Scarso and Giorgio Strukulxs