Ruthenium In Organic Synthesis
商品資訊
ISBN13:9783527306923
出版社:John Wiley & Sons Inc
作者:Murahashi
出版日:2004/09/14
裝訂/頁數:精裝/398頁
定價
:NT$ 13858 元優惠價
:90 折 12472 元
若需訂購本書,請電洽客服 02-25006600[分機130、131]。
商品簡介
作者簡介
名人/編輯推薦
目次
相關商品
商品簡介
In this comprehensive book, one of the leading experts, Shun-Ichi Murahashi, presents all the important facets of modern synthetic chemistry using Ruthenium, ranging from hydrogenation to metathesis. In 14 contributions, written by an international authorship, readers will find all the information they need about this fascinating and extraordinary chemistry. The result is a high quality information source and a indispensable reading for everyone working in organometallic chemistry.
From the contents:
Introduction (S.-I. Murahashi)
Hydrogenation and Transfer Hydrogenation (M. Kitamura and R. Noyori)
Oxidations (S.-I. Murahashi and N. Komiya)
Carbon-Carbon Bond Formations via Ruthenacycle Intermediates (K. Itoh)
Carbon-Carbon Bond Formation via pi-Allylruthenium Intermediates (T. Mitsudo)
Olefin Metathesis (R. H. Grubbs)
Cyclopropanation (H. Nishiyama)
Nucleophilic Addition to Alkynes and Reactions via Vinylidene Intermediates (P. Dixneuf)
Reactions via C-H Activation (N. Chatani)
Lewis Acid Reactions (E. P. Kundig)
Reactions with CO and CO2 (T. Mitsudo)
Isomerization of Organic Substrates Catalyzed by Ruthenium Complexes (H. Suzuki)
Radical Reactions (H. Nagashima)
Bond Cleavage Reactions (S. Komiya)
From the contents:
Introduction (S.-I. Murahashi)
Hydrogenation and Transfer Hydrogenation (M. Kitamura and R. Noyori)
Oxidations (S.-I. Murahashi and N. Komiya)
Carbon-Carbon Bond Formations via Ruthenacycle Intermediates (K. Itoh)
Carbon-Carbon Bond Formation via pi-Allylruthenium Intermediates (T. Mitsudo)
Olefin Metathesis (R. H. Grubbs)
Cyclopropanation (H. Nishiyama)
Nucleophilic Addition to Alkynes and Reactions via Vinylidene Intermediates (P. Dixneuf)
Reactions via C-H Activation (N. Chatani)
Lewis Acid Reactions (E. P. Kundig)
Reactions with CO and CO2 (T. Mitsudo)
Isomerization of Organic Substrates Catalyzed by Ruthenium Complexes (H. Suzuki)
Radical Reactions (H. Nagashima)
Bond Cleavage Reactions (S. Komiya)
作者簡介
Shun-Ichi Murahashi (born 1937) received his PhD from Osaka University (Japan) under Ichiro Moritani, before spending two years as a postdoctoral fellow in Ronald Breslow's group at Columbia University, New York. He joined the faculty of Osaka University upon his MS and was appointed full professor in 1979. He is now an Emeritus Professor of the university, having taken up a chair at the Okayama University of Science in 2001.
Professor Murahashi holds an honorary doctorate from the University of Rennes (France) and is the recipient of numerous scientific awards, including the Award of the Chemical Society of Japan, the Humboldt Research Award, and the Minakata-Avogadro Award.
His current research is focused on organometallic chemistry directed towards organic synthesis, biomimetic catalytic oxidation, ruthenium and palladium chemistry, and non-salt green processes.
Professor Murahashi holds an honorary doctorate from the University of Rennes (France) and is the recipient of numerous scientific awards, including the Award of the Chemical Society of Japan, the Humboldt Research Award, and the Minakata-Avogadro Award.
His current research is focused on organometallic chemistry directed towards organic synthesis, biomimetic catalytic oxidation, ruthenium and palladium chemistry, and non-salt green processes.
名人/編輯推薦
"The book presents an interesting overview of a fascinating area of reasearch...this book has definite value and is strongly recommended, both for experienced organic chemists who wish to learn about recent developments in the field of ruthenium catalysis, and for other readers who would like to understand some fundamental chemistry of ruthenium catalysis." (Angewandte Chemie I.E.)
"...a typical reader dipping into this book as reference material will find it rewarding. " (Platinum Metals Review, 2006: 50 (2), May 2006)
"...a typical reader dipping into this book as reference material will find it rewarding. " (Platinum Metals Review, 2006: 50 (2), May 2006)
目次
Preface.
List of Contributors.
1. Introduction (S.-I. Murahashi).
2. Hydrogenation and Transfer Hydrogenation (M. Kitamura and R. Noyori).
2.1 Introduction.
2.2 Hydrogenation.
2.3 Transfer Hydrogenation.
2.4 Concluding Remarks.
3. Oxidation Reactions (S.-I. Murahashi and N. Komiya).
3.1 Introduction.
3.2 Dehydrogenative Oxidation.
3.3 Oxidation with RuO4
3.4 Oxidation with Ruthenium Complex Catalysts and Oxidants.
3.5 Conclusions.
4. Carbon–Carbon Bond Formations via Ruthenacycle Intermediates (Y. Yamamoto and K. Itoh).
4.1 Introduction.
4.2 C–C Bond Formations Involving Ruthenacyclopentadiene/Ruthenacyclopentatriene.
4.3 C–C Bond Formations Involving Ruthenacyclopentene.
4.4 C–C Bond Formations Involving Ruthenacyclopentane.
4.5 C–C Bond Formations Involving Ruthenacyclopentenedione and Ruthenacyclobutenone.
4.6 Conclusion.
5. Carbon–Carbon Bond Formation via p-Allylruthenium Intermediates (T. Kondo and T. Mitsudo).
5.1 Introduction.
5.2 Synthesis, Structure, and Reactivity of α-Allylruthenium Complexes.
5.3 Catalytic Reactions via π-Allylruthenium Intermediates.
6. Ruthenium-Catalyzed Olefin Metathesis (R. H. Grubbs and T. M. Trnka).
6.1 Introduction.
6.2 Ruthenium Olefin Metathesis Catalysts.
6.3 Applications of Ruthenium-Catalyzed Olefin Metathesis in Organic Synthesis.
6.4 Summary.
7. Ruthenium-Catalyzed Cyclopropanation (H. Nishiyama).
7.1 Introduction.
7.2 Asymmetric Catalytic Cyclopropanation.
7.3 Non-Asymmetric Catalytic Cyclopropanation.
7.4 Carbene-Complexes and Mechanisms.
7.5 Conclusions.
8. Nucleophilic Additions to Alkynes and Reactions via Vinylidene Intermediates (C. Fischmeister, C. Bruneau, and P. H. Dixneuf).
8.1 Introduction.
8.2 Addition of O-Nucleophiles.
8.3 Addition of N-nucleophiles.
8.4 Addition of P-Nucleophiles: Hydrophosphination.
8.5 Hydrosilylation.
8.6 Addition of C–H Bond to Alkynes.
8.7 Conclusions.
9. Ruthenium-Catalyzed Reactions via sp C–H, sp2 C–H, sp3 C–H, and C–Halogen Bond Activations (F. Kakiuchi and N. Chatani).
9.1 Introduction.
9.2 Activation of sp2 C–H Bonds.
9.3 Addition of C–H Bonds in Aldehydes to C–C Multiple Bonds and Related Reactions.
9.4 Activation of sp3 C–H Bonds.
9.5 Addition of sp C–H Bonds in Acetylenes to C–C Multiple Bonds.
9.6 Catalytic Reactions Involving Carbon-Halogen Bond Cleavage.
9.7 Conclusions.
10. Ruthenium Lewis Acid-Catalyzed Reactions (R. F. R. Jazzar and E. P. Kündig).
10.1 Introduction.
10.2 Ethers, Acetals, Carboxylic Acid Derivatives, and Epoxides.
10.3 Ru-Promoted Additions to C=O and C”N Bonds.
10.4 Activation of Organo-Sulfur Derivatives.
10.5 Halide Substitution for Fluoride.
10.6 Cycloaddition Reactions.
11. Ruthenium-Catalyzed Reactions with CO and CO2 (T. Mitsudo and T. Kondo).
11.1 Introduction.
11.2 Reactions with Carbon Monoxide.
11.3 Reactions with Carbon Dioxide.
12. Isomerization of Organic Substrates Catalyzed by Ruthenium Complexes (H. Suzuki and T. Takao).
12.1 Introduction.
12.2 Isomerization of Alkenyl Alcohols to Aldehydes and Ketones.
12.3 Isomerization of Propargyl Alcohols and Ethers.
12.4 Isomerization of Functionalized Alkenes.
12.5 Cycloisomerization of 1,6-Enynes and 1,6-Dienes.
12.6 Racemization of Secondary Alcohols.
12.7 Olefin Isomerization Promoted by the Grubbs Catalyst.
13. Ruthenium-Promoted Radical Reactions (H. Nagashima).
13.1 Introduction and Historical Background.
13.2 Ruthenium-catalyzed Kharasch Addition (ATRA) in Organic Synthesis.
13.3 Ruthenium-catalyzed Intramolecular Kharasch Addition (ATRC) in Organic Synthesis.
13.4 Ruthenium-catalyzed Addition of Sulfonyl Chlorides to Alkenes in Organic Synthesis.
13.5 Ruthenium-catalyzed Addition of Organic Halides and Sulfonylchlorides in Polymer Synthesis: ATRP.
13.6 Summary and Perspective.
14. Ruthenium-Catalyzed Bond Cleavage Reactions (S. Komiya and M. Hirano).
14.1 Introduction.
14.2 C–H Bond Activation Reactions.
14.3 C–C Bond-Activation Reactions.
14.4 Cleavage Reactions of Other Single Bonds.
14.5 Conclusions.
Index.
List of Contributors.
1. Introduction (S.-I. Murahashi).
2. Hydrogenation and Transfer Hydrogenation (M. Kitamura and R. Noyori).
2.1 Introduction.
2.2 Hydrogenation.
2.3 Transfer Hydrogenation.
2.4 Concluding Remarks.
3. Oxidation Reactions (S.-I. Murahashi and N. Komiya).
3.1 Introduction.
3.2 Dehydrogenative Oxidation.
3.3 Oxidation with RuO4
3.4 Oxidation with Ruthenium Complex Catalysts and Oxidants.
3.5 Conclusions.
4. Carbon–Carbon Bond Formations via Ruthenacycle Intermediates (Y. Yamamoto and K. Itoh).
4.1 Introduction.
4.2 C–C Bond Formations Involving Ruthenacyclopentadiene/Ruthenacyclopentatriene.
4.3 C–C Bond Formations Involving Ruthenacyclopentene.
4.4 C–C Bond Formations Involving Ruthenacyclopentane.
4.5 C–C Bond Formations Involving Ruthenacyclopentenedione and Ruthenacyclobutenone.
4.6 Conclusion.
5. Carbon–Carbon Bond Formation via p-Allylruthenium Intermediates (T. Kondo and T. Mitsudo).
5.1 Introduction.
5.2 Synthesis, Structure, and Reactivity of α-Allylruthenium Complexes.
5.3 Catalytic Reactions via π-Allylruthenium Intermediates.
6. Ruthenium-Catalyzed Olefin Metathesis (R. H. Grubbs and T. M. Trnka).
6.1 Introduction.
6.2 Ruthenium Olefin Metathesis Catalysts.
6.3 Applications of Ruthenium-Catalyzed Olefin Metathesis in Organic Synthesis.
6.4 Summary.
7. Ruthenium-Catalyzed Cyclopropanation (H. Nishiyama).
7.1 Introduction.
7.2 Asymmetric Catalytic Cyclopropanation.
7.3 Non-Asymmetric Catalytic Cyclopropanation.
7.4 Carbene-Complexes and Mechanisms.
7.5 Conclusions.
8. Nucleophilic Additions to Alkynes and Reactions via Vinylidene Intermediates (C. Fischmeister, C. Bruneau, and P. H. Dixneuf).
8.1 Introduction.
8.2 Addition of O-Nucleophiles.
8.3 Addition of N-nucleophiles.
8.4 Addition of P-Nucleophiles: Hydrophosphination.
8.5 Hydrosilylation.
8.6 Addition of C–H Bond to Alkynes.
8.7 Conclusions.
9. Ruthenium-Catalyzed Reactions via sp C–H, sp2 C–H, sp3 C–H, and C–Halogen Bond Activations (F. Kakiuchi and N. Chatani).
9.1 Introduction.
9.2 Activation of sp2 C–H Bonds.
9.3 Addition of C–H Bonds in Aldehydes to C–C Multiple Bonds and Related Reactions.
9.4 Activation of sp3 C–H Bonds.
9.5 Addition of sp C–H Bonds in Acetylenes to C–C Multiple Bonds.
9.6 Catalytic Reactions Involving Carbon-Halogen Bond Cleavage.
9.7 Conclusions.
10. Ruthenium Lewis Acid-Catalyzed Reactions (R. F. R. Jazzar and E. P. Kündig).
10.1 Introduction.
10.2 Ethers, Acetals, Carboxylic Acid Derivatives, and Epoxides.
10.3 Ru-Promoted Additions to C=O and C”N Bonds.
10.4 Activation of Organo-Sulfur Derivatives.
10.5 Halide Substitution for Fluoride.
10.6 Cycloaddition Reactions.
11. Ruthenium-Catalyzed Reactions with CO and CO2 (T. Mitsudo and T. Kondo).
11.1 Introduction.
11.2 Reactions with Carbon Monoxide.
11.3 Reactions with Carbon Dioxide.
12. Isomerization of Organic Substrates Catalyzed by Ruthenium Complexes (H. Suzuki and T. Takao).
12.1 Introduction.
12.2 Isomerization of Alkenyl Alcohols to Aldehydes and Ketones.
12.3 Isomerization of Propargyl Alcohols and Ethers.
12.4 Isomerization of Functionalized Alkenes.
12.5 Cycloisomerization of 1,6-Enynes and 1,6-Dienes.
12.6 Racemization of Secondary Alcohols.
12.7 Olefin Isomerization Promoted by the Grubbs Catalyst.
13. Ruthenium-Promoted Radical Reactions (H. Nagashima).
13.1 Introduction and Historical Background.
13.2 Ruthenium-catalyzed Kharasch Addition (ATRA) in Organic Synthesis.
13.3 Ruthenium-catalyzed Intramolecular Kharasch Addition (ATRC) in Organic Synthesis.
13.4 Ruthenium-catalyzed Addition of Sulfonyl Chlorides to Alkenes in Organic Synthesis.
13.5 Ruthenium-catalyzed Addition of Organic Halides and Sulfonylchlorides in Polymer Synthesis: ATRP.
13.6 Summary and Perspective.
14. Ruthenium-Catalyzed Bond Cleavage Reactions (S. Komiya and M. Hirano).
14.1 Introduction.
14.2 C–H Bond Activation Reactions.
14.3 C–C Bond-Activation Reactions.
14.4 Cleavage Reactions of Other Single Bonds.
14.5 Conclusions.
Index.
主題書展
更多
主題書展
更多書展今日66折
您曾經瀏覽過的商品
購物須知
外文書商品之書封,為出版社提供之樣本。實際出貨商品,以出版社所提供之現有版本為主。部份書籍,因出版社供應狀況特殊,匯率將依實際狀況做調整。
無庫存之商品,在您完成訂單程序之後,將以空運的方式為你下單調貨。為了縮短等待的時間,建議您將外文書與其他商品分開下單,以獲得最快的取貨速度,平均調貨時間為1~2個月。
為了保護您的權益,「三民網路書店」提供會員七日商品鑑賞期(收到商品為起始日)。
若要辦理退貨,請在商品鑑賞期內寄回,且商品必須是全新狀態與完整包裝(商品、附件、發票、隨貨贈品等)否則恕不接受退貨。