Transition-metal-mediated aromatic ring construction /

"Recent significant advances with transition-metal-mediated reactions have opened promising new routes to complex aromatic compounds and have been the subject of intense research in recent years. Featuring practical and efficient reactions to help organic chemists synthesize an important class...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Άλλοι συγγραφείς: Tanaka, Ken, 1967-
Μορφή: Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: Hoboken, New Jersey : Wiley, [2013]
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
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020 |a 1299731732 (MyiLibrary) 
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049 |a MAIN 
245 0 0 |a Transition-metal-mediated aromatic ring construction /  |c edited by Ken Tanaka, Tokyo University of Agriculture and Technology, Tokyo, Japan. 
264 1 |a Hoboken, New Jersey :  |b Wiley,  |c [2013] 
300 |a 1 online resource. 
336 |a text  |2 rdacontent 
337 |a computer  |2 rdamedia 
338 |a online resource  |2 rdacarrier 
520 |a "Recent significant advances with transition-metal-mediated reactions have opened promising new routes to complex aromatic compounds and have been the subject of intense research in recent years. Featuring practical and efficient reactions to help organic chemists synthesize an important class of compounds, Transition-Metal-Mediated Aromatic Ring Construction provides a valuable guide to methods, synthetic routes, and strategies to construct aromatic rings. Chapters devoted to efficient and practical reactions demonstrate how to use them for the synthesis of various complex aromatic compounds"--  |c Provided by publisher. 
520 |a "This book covers transition-metal-mediated reactions with applications for constructing aromatic rings, which are an important class of industrial chemical compounds"--  |c Provided by publisher. 
504 |a Includes bibliographical references and index. 
588 |a Description based on print version record and CIP data provided by publisher. 
505 0 |a Title Page; Copyright; Contributors; Preface; Part I: [2 + 2 + 2] and Related Cycloaddition Reactions; Chapter 1: Cobalt-Mediated [2 + 2 + 2] Cycloaddition; 1.1 INTRODUCTION; 1.2 SYNTHESIS OF BENZENES; 1.3 SYNTHESIS OF HETEROCYCLES; 1.4 MECHANISTIC ASPECTS; 1.5 SYNTHETIC APPLICATIONS; 1.6 SUMMARY AND OUTLOOK; REFERENCES; Chapter 2: Nickel-Mediated [2 + 2 + 2] Cycloaddition; 2.1 INTRODUCTION; 2.2 SYNTHESIS OF BENZENES; 2.3 CYCLOADDITION OF ALKYNES AND NITRILES; 2.4 CYCLOADDITION OF ALKYNES AND IMINES; 2.5 CYCLOADDITION OF ALKYNES AND CARBON DIOXIDE; 2.6 CYCLOADDITION OF ALKYNES AND ISOCYANATES 
505 8 |a 2.7 CYCLOADDITION OF ALKYNES AND CARBODIIMIDE2.8 CYCLOADDITION OF DIYNES AND KETENES; 2.9 CYCLOADDITION OF ARYNES; 2.10 MECHANISM; 2.11 SUMMARY AND OUTLOOK; REFERENCES; Chapter 3: Ruthenium-Mediated [2 + 2 + 2] Cycloaddition; 3.1 INTRODUCTION; 3.2 SYNTHESIS OF BENZENES; 3.3 SYNTHESIS OF HETEROCYCLES; 3.4 MECHANISM OF RUTHENIUM-CATALYZED [2 + 2 + 2] CYCLOADDITIONS; 3.5 SYNTHETIC APPLICATIONS; 3.6 SUMMARY AND OUTLOOK; REFERENCES; Chapter 4: Rhodium-Mediated [2 + 2 + 2] Cycloaddition; 4.1 INTRODUCTION; 4.2 SYNTHESIS OF BENZENES; 4.3 SYNTHESIS OF PYRIDINES 
505 8 |a 4.4 SYNTHESIS OF PYRIDONES AND RELATED HETEROCYCLES4.5 SUMMARY AND OUTLOOK; REFERENCES; Chapter 5: Iridium-Mediated [2 + 2 + 2] Cycloaddition; 5.1 INTRODUCTION; 5.2 SYNTHESIS OF BENZENE DERIVATIVES; 5.3 SYNTHESIS OF HETEROCYCLIC COMPOUNDS; 5.4 MECHANISTIC ASPECTS; 5.5 SUMMARY AND OUTLOOK; REFERENCES; Chapter 6: [2 + 2 + 2] and Related Cycloadditions Mediated by Other Transition Metals; 6.1 INTRODUCTION; 6.2 PALLADIUM-CATALYZED [2 + 2 + 2] AND [2 + 2 + 1] CYCLOADDITIONS; 6.3 IRON-CATALYZED [2 + 2 + 2] CYCLOADDITION; 6.4 MANGANESE-CATALYZED [2 + 2 + 2] CYCLOADDITION 
505 8 |a 6.5 RHENIUM-CATALYZED [2 + 2 + 2], [2 + 1 + 2 + 1], AND [2 + 2 + 1 + 1] CYCLOADDITIONS6.6 OTHER TRANSITION-METAL-CATALYZED [2 + 2 + 2] CYCLOADDITION; 6.7 SUMMARY AND OUTLOOK; REFERENCES; Chapter 7: Application to the Synthesis of Natural Products; 7.1 INTRODUCTION; 7.2 CONSTRUCTION OF BENZENE RINGS; 7.3 CONSTRUCTION OF A HETEROCYCLIC RING; 7.4 MISCELLANEOUS; 7.5 SUMMARY AND OUTLOOK; REFERENCES; Chapter 8: Synthesis of Planar Chiral Aromatic Compounds via [2 + 2 + 2] Cycloaddition; 8.1 INTRODUCTION; 8.2 COBALT-CATALYZED [2 + 2 + 2] CYCLOADDITION; 8.3 RHODIUM-CATALYZED [2 + 2 + 2] CYCLOADDITION 
505 8 |a 8.4 ENANTIOSELECTIVE [2 + 2 + 2] CYCLOADDITION8.5 SUMMARY AND OUTLOOK; REFERENCES; Chapter 9: Synthesis of Axially Chiral Aromatic Compounds via [2 + 2 + 2] Cycloaddition; 9.1 INTRODUCTION; 9.2 COBALT-CATALYZED ENANTIOSELECTIVE [2 + 2 + 2] CYCLOADDITION; 9.3 IRIDIUM-CATALYZED ENANTIOSELECTIVE [2 + 2 + 2] CYCLOADDITION; 9.4 RHODIUM-CATALYZED ENANTIOSELECTIVE [2 + 2 + 2] CYCLOADDITION; 9.5 ENANTIOSELECTIVE SYNTHESIS OF AXIALLY CHIRAL ANILIDES AND BEZAMIDES; 9.6 SUMMARY AND OUTLOOK; REFERENCES; Chapter 10: Synthesis of Helically Chiral Aromatic Compounds via [2 + 2 + 2] Cycloaddition 
650 0 |a Aromatic compounds  |x Synthesis. 
650 0 |a Transition metal catalysts. 
650 7 |a SCIENCE / Chemistry / Organic.  |2 bisacsh 
650 7 |a Aromatic compounds  |x Synthesis.  |2 fast  |0 (OCoLC)fst00815028 
650 7 |a Transition metal catalysts.  |2 fast  |0 (OCoLC)fst01154758 
655 4 |a Electronic books. 
655 0 |a Electronic books. 
655 7 |a Electronic books.  |2 local 
700 1 |a Tanaka, Ken,  |d 1967- 
776 0 8 |i Print version:  |t Transition-metal-mediated aromatic ring construction  |d Hoboken, New Jersey : Wiley, [2013]  |z 9781118148921  |w (DLC) 2012049882 
856 4 0 |u https://doi.org/10.1002/9781118629871  |z Full Text via HEAL-Link 
994 |a 92  |b DG1