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    <subfield code="a">Transition-metal-mediated aromatic ring construction /</subfield>
    <subfield code="c">edited by Ken Tanaka, Tokyo University of Agriculture and Technology, Tokyo, Japan.</subfield>
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    <subfield code="a">Includes bibliographical references and index.</subfield>
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    <subfield code="a">Title Page; Copyright; Contributors; Preface; Part I: [2 + 2 + 2] and Related Cycloaddition Reactions; Chapter 1: Cobalt-Mediated [2&#xA0;+&#xA0;2&#xA0;+&#xA0;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&#xA0;+&#xA0;2&#xA0;+&#xA0;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</subfield>
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    <subfield code="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&#xA0;+&#xA0;2&#xA0;+&#xA0;2]&#xA0;Cycloaddition; 3.1 INTRODUCTION; 3.2 SYNTHESIS OF BENZENES; 3.3 SYNTHESIS OF HETEROCYCLES; 3.4 MECHANISM OF RUTHENIUM-CATALYZED [2&#xA0;+&#xA0;2&#xA0;+&#xA0;2] CYCLOADDITIONS; 3.5 SYNTHETIC APPLICATIONS; 3.6 SUMMARY AND OUTLOOK; REFERENCES; Chapter 4: Rhodium-Mediated [2&#xA0;+&#xA0;2&#xA0;+&#xA0;2]&#xA0;Cycloaddition; 4.1 INTRODUCTION; 4.2 SYNTHESIS OF BENZENES; 4.3 SYNTHESIS OF PYRIDINES</subfield>
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    <subfield code="a">4.4 SYNTHESIS OF PYRIDONES AND RELATED HETEROCYCLES4.5 SUMMARY AND OUTLOOK; REFERENCES; Chapter 5: Iridium-Mediated [2&#xA0;+&#xA0;2&#xA0;+&#xA0;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&#xA0;+&#xA0;2&#xA0;+&#xA0;2] and Related Cycloadditions Mediated by Other Transition Metals; 6.1 INTRODUCTION; 6.2 PALLADIUM-CATALYZED [2&#xA0;+&#xA0;2&#xA0;+&#xA0;2] AND [2&#xA0;+&#xA0;2&#xA0;+&#xA0;1] CYCLOADDITIONS; 6.3 IRON-CATALYZED [2&#xA0;+&#xA0;2&#xA0;+&#xA0;2] CYCLOADDITION; 6.4 MANGANESE-CATALYZED [2&#xA0;+&#xA0;2&#xA0;+&#xA0;2] CYCLOADDITION</subfield>
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    <subfield code="a">6.5 RHENIUM-CATALYZED [2&#xA0;+&#xA0;2&#xA0;+&#xA0;2], [2&#xA0;+&#xA0;1&#xA0;+&#xA0;2&#xA0;+&#xA0;1], AND [2&#xA0;+&#xA0;2&#xA0;+&#xA0;1&#xA0;+&#xA0;1] CYCLOADDITIONS6.6 OTHER TRANSITION-METAL-CATALYZED [2&#xA0;+&#xA0;2&#xA0;+&#xA0;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&#xA0;+&#xA0;2&#xA0;+&#xA0;2] Cycloaddition; 8.1 INTRODUCTION; 8.2 COBALT-CATALYZED [2&#xA0;+&#xA0;2&#xA0;+&#xA0;2] CYCLOADDITION; 8.3 RHODIUM-CATALYZED [2&#xA0;+&#xA0;2&#xA0;+&#xA0;2] CYCLOADDITION</subfield>
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