Stereoselective Synthesis of Drugs and Natural Products, 2 Volume Set
John Wiley & Sons Inc (Verlag)
978-1-118-03217-6 (ISBN)
Brings together the best tested and proven stereoselective synthetic methods
Both the chemical and pharmaceutical industries are increasingly dependent on stereoselective synthetic methods and strategies for the generation of new chiral drugs and natural products that offer specific 3-D structures. With the publication of Stereoselective Synthesis of Drugs and Natural Products, researchers can turn to this comprehensive two-volume work to guide them through all the core methods for the synthesis of chiral drugs and natural products.
Stereoselective Synthesis of Drugs and Natural Products features contributions from an international team of synthetic chemists and pharmaceutical and natural product researchers. These authors have reviewed the tremendous body of literature in the field in order to compile a set of reliable, tested, and proven methods alongside step-by-step guidance. This practical resource not only explores synthetic methodology, but also reaction mechanisms and applications in medicinal chemistry and drug discovery.
The publication begins with an introductory chapter covering general principles and methodologies, nomenclature, and strategies of stereoselective synthesis. Next, it is divided into three parts:
Part One: General Methods and Strategies
Part Two: Stereoselective Synthesis by Bond Formation including
C-C bond formation
C-H bond formation
C-O bond formation
C-N bond formation
Other C-heteroatom formation and other bond formation
Part Three: Methods of Analysis and Chiral Separation
References in every chapter serve as a gateway to the literature in the field. With this publication as their guide, chemists involved in the stereoselective synthesis of drugs and natural products now have a single, expertly edited source for all the methods they need.
Vasyl Andrushko is Research Scientist at Karlsruhe Institute of Technology where he researches in the areas of organic synthetic chemistry, asymmetric catalysis with application in stereoselective drug synthesis and as well as catalysis in alternative reaction media, organometallic chemistry, supramolecular and cluster chemistry. He has published 16 papers on topics directly related to stereoselective drug synthesis. Natalia Andrushko is a scientist at the Leibniz-Institute for Catalysis at the University of Rostock where she researches in the areas of organic and bioorganic chemistry, stereoselective synthesis of drugs and asymmetric catalysis. She has published 16 papers on topics directly related to stereoselective drug synthesis.
Preface
List of contributors
List of symbols and abbreviations
PART 1: GENERAL METHODS AND STRATEGIES
Chapter 1: Principles, concepts and strategies of stereoselective synthesis
Vasyl Andrushko and Natalia Andrushko
Chapter 2: Chiral auxiliaries in drug synthesis
Stanley Chang, Shira D. Halperin, Jarod Moore and Robert Britton
Chapter 3: Solid-phase organic synthesis of drugs and natural products
Peter J. H. Scott
Chapter 4: Asymmetric phase-transfer catalysis
Kohsuke Ohmatsu, Daisuke Uraguchi, and Takashi Ooi
Chapter 5: Microwave-assisted stereoselective synthesis
Yoann Coquerel, Evelina Colacino, Jean Rodriguez, Jean Martinez and Frédéric Lamaty
Chapter 6: Application of micro reactor methodology for organic synthesis
Paul Watts and Charlotte Wiles
PART 2: STEREOSELECTIVE SYNTHESIS BY BOND FORMATION
2.1. STEREOSELECTIVE METHODS FOR C–C BOND FORMATION
Chapter 7: Asymmetric α-alkylation of aldehydes, ketones and carboxylic acids
Mark C. Kohler, Sarah E. Wengryniuk, and Don M. Coltart
Chapter 8: Asymmetric aldol reactions in the total syntheses of natural products
Seijiro Hosokawa
Chapter 9: Asymmetric Michael addition and related reactions
Pengfei Li, Jun Wang and Fuk Yee Kwong
Chapter 10: Construction of polypropionate fragments in natural product synthesis
Maris Turks, Sylvain Laclef and Pierre Vogel
Chapter 11: Organocatalytic conjugate addition in stereoselective synthesis
Adrien Quintard and Alexandre Alexakis
Chapter 12: Stereoselective Nozaki-Hiyama-Kishi reaction
Pat Guiry and Gráinne Hargaden
Chapter 13: Transition-metal-catalyzed asymmetric C–C cross-couplings in stereoselective synthesis Vasiliki Sarli
Chapter 14: Asymmetric hydroformylation, hydroxy- and alkoxycarbonylation for stereoselective synthesis
Jamie T. Durrani and Matthew L. Clarke
Chapter 15: Intramolecular oxycarbonylation in stereoselective synthesis
Tibor Gracza
Chapter 16: Stereoselective cycloaddition reactions
Tae-Kyung Lee and Jung-Mo Ahn
Chapter 17: Sigmatropic rearrangements in stereoselective synthesis
Brinton Seashore-Ludlow and Peter Somfai
Chapter 18: Ring contraction reactions in the total synthesis of biologically active natural products
Luiz F. Silva Jr.
Chapter 19: Electrocyclic reactions in stereoselective synthesis
Marcus A. Tius
Chapter 20: Transannular cyclization in natural product total synthesis
Jiong Yang and Haoran Xue
Chapter 21: Cascade reactions in stereoselective synthesis
Bor-Cherng Hong and Nitin S. Dange
Chapter 22: Sulfur dioxide: a powerful tool for the stereoselective construction of C-C bonds
Pierre Vogel, Dean Markovic and Mâris Turks
Chapter 23: Transition metal C-H activation: application to stereoselective synthesis of natural products and drugs
Mickaël Jean and Pierre van de Weghe
Chapter 24: Metathesis reactions in drug and natural product synthesis
Akio Saito, Yuji Hanzawa
Chapter 25: Radicals in stereoselective C-C bond formation
Josep Bonjoch, Ben Bradshaw and Faïza Diaba
Chapter 26: Trifluoromethyl (CF3) group insertion methods in stereoselective synthesis
Tsutomu Konno
Chapter 27: Stereoselective organocatalyzed C–C bond-forming reactions
Kazuo Nagasawa and Koji Yasui
Chapter 28: Enzyme-catalysed stereoselective C–C bond formation reactions in total syntheses
Adeline Ranoux and Ulf Hanefeld
2.2. STEREOSELECTIVE METHODS FOR C–H BOND FORMATION
Chapter 29: Stereoselective hydrogenation of C=C bonds: application to drug and natural product synthesis
Natalia Andrushko and Vasyl Andrushko
Chapter 30: Asymmetric hydrogenation of C=O and C=N bonds in stereoselective synthesis
Natalia Andrushko and Vasyl Andrushko
Chapter 31: Asymmetric protonation of carbanions and polar double bonds: application to total syntheses
Thomas Poisson and Shu Kobayashi
Chapter 32: Organocatalytic reduction in stereoselective synthesis
Felix Kortmann and Adriaan Minnaard
Chapter 33: Biocatalytic asymmetric reduction of C=O and activated C=C bonds in stereoselective synthesis
Tomoko Matsuda, Rio Yamanaka and Kaoru Nakamura
2.3. STEREOSELECTIVE METHODS FOR C–O BOND FORMATION
Chapter 34: Transition-metal-catalyzed stereoselective oxidations in drug and natural product synthesis
Alessandro Scarso and Giorgio Strukul
Chapter 35: Asymmetric epoxidation in stereoselective synthesis
Zhicai Yang
Chapter 36: Biocatalytic asymmetric oxidations in stereoselective synthesis
Anett Schallmey, Pablo Dominguez de Maria and Paula Bracco
Chapter 37: Ether transfer methodology: application to the synthesis of polyketide natural products
Eric Stefan and Richard E. Taylor
Chapter 38: Stereoselective formation of 2-deoxyglycosidic bonds in biologically active natural products
Daisuke Takahashi and Kazunobu Toshima
2.4. STEREOSELECTIVE METHODS FOR C–N BOND FORMATION
Chapter 39: Asymmetric hydroamination and reductive amination in total synthesis
Manas K. Ghorai, Deo Prakash Tiwari and Aditya Bhattacharyya
Chapter 40: Carboamination and alkylative cyclization with C-N bond formation in stereoselective syntheses
Manas K. Ghorai, Sandipan Halder and Sauvik Samanta
Chapter 41: Cycloadditions with stereoselective C-N bond formation in total syntheses
Guillaume Vincent
2.5. STEREOSELECTIVE FORMATION OF OTHER C–HETEROATOM AND OTHER BONDS
Chapter 42: Stereoselective halogenations
Chong Kiat Tan, Yi Zhao, Jing Zhou and Ying-Yeung Yeung
Chapter 43: Stereoselective synthesis of halogenated natural products
Takehiko Yoshimitsu
Chapter 44: Asymmetric fluorination methods: application in the stereoselective synthesis of fluorinated drugs
Vincent Bizet and Dominique Cahard
Chapter 45: Enzymatic halogenation in stereoselective synthesis
Cormac D. Murphy and Benjamin R. Clark
Chapter 46: Stereoselective carbon–sulfur (C–S) bond formation
Kyungsoo Oh
Chapter 47: Stereoselective methods for carbon-phosphorus (C–P) bond formation
Marcin Kalek and Jacek Stawinski
Chapter 48: Transition-metal-catalyzed asymmetric sulfoxidation in drug and natural product synthesis
Alessandro Scarso and Giorgio Strukul
PART 3: METHODS OF ANALYSIS AND CHIRAL SEPARATION
Chapter 49: NMR-Spectroscopy in drug and natural product analysis
Stanisuaw Witkowski and Iwona Wawer
Chapter 50: Determination of enantiomeric purity and absolute configuration by NMR spectroscopy
Thomas J. Wenzel
Chapter 51: Solid-state NMR spectroscopy in drug design and discovery
David A. Middleton and Simon G. Patching
Chapter 52: Capillary electrophoresis in chiral separations
Ans Hendrickx, Debby Mangelings and Yvan Vander Heyden
Chapter 53: Determination of absolute configuration using chiroptical methods
Joao Marcos Batista, Jr.
Chapter 54: Chiral chromatographic methods in the analysis and purification of enantiomers
Arnau Novell and Cristina Minguillón
Chapter 55: X-Ray crystallography and 1H NMR anisotropy methods for determination of absolute configurations
Nobuyuki Harada
Chapter 56: Crystallization based separation of enantiomers
Yaling Wang and Alex Chen
Chapter 57: Enzymatic dynamic kinetic resolution in stereoselective synthesis
Francisca Rebolledo, Javier González-Sabín, and Vicente Gotor
Subject index
| Verlagsort | New York |
|---|---|
| Sprache | englisch |
| Maße | 236 x 310 mm |
| Gewicht | 6623 g |
| Themenwelt | Naturwissenschaften ► Chemie ► Organische Chemie |
| Technik | |
| ISBN-10 | 1-118-03217-9 / 1118032179 |
| ISBN-13 | 978-1-118-03217-6 / 9781118032176 |
| Zustand | Neuware |
| Haben Sie eine Frage zum Produkt? |
aus dem Bereich
