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Copper-mediated cross-coupling reactions / (Record no. 206723)

000 -LEADER
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001 - CONTROL NUMBER
control field ocn843026114
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20171106120747.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS
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007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
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008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 130510s2013 nju ob 001 0 eng
010 ## - LIBRARY OF CONGRESS CONTROL NUMBER
LC control number 2013019308
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781118690680 (pdf)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 1118690680 (pdf)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781118690475 (epub)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 1118690478 (epub)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781118690505 ( mobi)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 1118690508 ( mobi)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Canceled/invalid ISBN 9781118060452 (hardback)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781118690659
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 1118690656
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 1118060458
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781118060452
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781299939660
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 129993966X
028 01 - PUBLISHER NUMBER
Publisher number EB00064124
Source Recorded Books
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OCLC library identifier AU@
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OCLC library identifier NLGGC
System control number 369366468
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OCLC library identifier DEBSZ
System control number 431513325
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OCLC library identifier DEBBG
System control number BV041908978
029 1# - OTHER SYSTEM CONTROL NUMBER (OCLC)
OCLC library identifier DEBBG
System control number BV043395847
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)843026114
Canceled/invalid control number (OCoLC)864918046
-- (OCoLC)876848244
040 ## - CATALOGING SOURCE
Original cataloging agency DLC
Language of cataloging eng
Description conventions rda
Transcribing agency DLC
Modifying agency YDX
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-- IDEBK
-- DG1
-- EBLCP
-- YDXCP
-- OCLCF
-- CDX
-- COO
-- CHVBK
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042 ## - AUTHENTICATION CODE
Authentication code pcc
049 ## - LOCAL HOLDINGS (OCLC)
Holding library MAIN
050 00 - LIBRARY OF CONGRESS CALL NUMBER
Classification number QD505
072 #7 - SUBJECT CATEGORY CODE
Subject category code SCI
Subject category code subdivision 013030
Source bisacsh
082 00 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 546/.652595
Edition number 23
084 ## - OTHER CLASSIFICATION NUMBER
Classification number SCI013050
Number source bisacsh
245 00 - TITLE STATEMENT
Title Copper-mediated cross-coupling reactions /
Statement of responsibility, etc. edited by Gwilherm Evano, Laboratoire de chimie organique, Service de chimie et physicochimie organiques, Université libre de Bruxelles, Brussels, Belgium, Nicolas Blanchard, Université de Strasbourg, École européenne de chimie, polymères et Matériaux, Laboratoire de chimie moléculaire associé au CNRS, Strasbourg, France.
Medium [electronic resource]
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Hoboken, New Jersey :
Name of producer, publisher, distributor, manufacturer Wiley,
Date of production, publication, distribution, manufacture, or copyright notice [2013]
300 ## - PHYSICAL DESCRIPTION
Extent 1 online resource.
336 ## - CONTENT TYPE
Content type term text
Source rdacontent
337 ## - MEDIA TYPE
Media type term computer
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term online resource
Source rdacarrier
500 ## - GENERAL NOTE
General note Machine generated contents note: Introduction Copper catalysis from an historical perspective: a legacy from the past Gwilherm Evano and Nicolas Blanchard PART 1 FORMATION OF C-HETEROATOM BONDS Chapter 1: Modern Ullmann-Goldberg Chemistry: Arylation of N-nucleophiles with Aryl Halides Yongwen Jiang and Dawei Ma Chapter 2: Ullmann condensation today: arylation of alcohols and thiols with aryl halides Anis Tlili and Marc Taillefer Chapter 3: Copper-Catalyzed Formation of C-P Bonds with Aryl Halides Carole Alayrac and Annie-Claude Gaumont Chapter 4: Alternative and Emerging Reagents for the Arylation of Heteronucleophiles Luc Neuville Chapter 5: Beyond Ullmann-Goldberg Chemistry: Vinylation, Alkynylation and Allenylation of Heteronucleophiles Kevin Jouvin and Gwilherm Evano Chapter 6: Aromatic/Vinylic Finkelstein Reaction Alicia Casitas and Xavi Ribas Chapter 7: Insights into the Mechanism of Modern Ullmann-Goldberg Coupling Reactions Alicia Casitas and Xavi Ribas PART 2 FORMATION OF C-C BONDS Chapter 8: Modern Copper-Catalyzed Hurtley Reaction: Efficient C-Arylation of CH-Acid Derivatives Irina P Beletskaya and Alexey Yu Fedorov Chapter 9: Copper-Catalyzed Cyanations of Aryl Halides and Related Compounds Thomas Schareina and Matthias Beller Chapter 10: Copper-Mediated Aryl-aryl Bond Formation Leading to Biaryls: A Century After Ullmann Breakthrough Yoshihiko Yamamoto Chapter 11: Copper-Catalyzed Alkynylation, Alkenylation and Allylation Reaction of Aryl Derivatives Ren-Jie Song and Jin-Heng Li Chapter 12: Copper-Catalyzed Alkynylation and Alkenylation Reaction of Alkynyl Derivatives: New Access to Diynes and Enynes Ruimao Hua Chapter 13: Copper-Mediated Alkenylation Reaction of Alkenyl Derivatives: a Straightforward Elaboration of 1,3-Dienes Hao Li, Songbai Liu, and Lanny S Liebeskind Chapter 14: Emerging Areas in Copper-Mediated Trifluoromethylations: Catalytic and Oxidative Cross-Coupling Processes Kevin Jouvin, Celine Guissart and Gwilherm Evano PART 3 APPLICATIONS OF COPPER CATALYZED CROSS COUPLING REACTIONS: HETEROCYCLES, NATURAL PRODUCTS, PROCESS AND SUSTAINABLE CHEMISTRY Chapter 15: Copper-Mediated Cyclization Reactions: New Entries to Heterocycles Daoshan Yang and Hua Fu Chapter 16: Copper-Mediated C-N Bond Forming Reactions: New Opportunities in Natural Product Synthesis Jihoon Lee and James S Panek Chapter 17: Natural Products and C-O/C-S Bond Forming Reactions: Copper Showed the Way Doron Pappo Chapter 18: Copper-Catalyzed C-C Bond Formation in Natural Product Synthesis: Elegant and Efficient Solutions to a Key Bond Disconnection Morgan Donnard and Nicolas Blanchard Chapter 19: Process Chemistry and Copper Catalysis Klaus Kunz and Norbert Lui Chapter 20: Reusable Catalysts for Copper-Mediated Coupling Reactions under Heterogeneous Conditions Zhiyong Wang, Changfeng Wan and Ye Wang .
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references and index.
505 0# - FORMATTED CONTENTS NOTE
Formatted contents note Title page; Copyright page; Foreword; Preface: Copper Catalysis from a Historical Perspective: A Legacy from the Past; The Historical and Remarkable First Discoveries by Fritz Ullmann and Irma Goldberg; Further Historical Developments: The Cyanation of Aryl Halides by Rosenmund and von Braun and the Arylation of Diketones and Malonates by Hurtley; From the Historical Discoveries to the Development of Modern Copper-Mediated Cross-Coupling Reactions; Modern Copper-Mediated Cross-Coupling Reactions and Their Impact in Organic Chemistry; Contributors; Part I: Formation of C-Heteroatom Bonds
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 1: Modern Ullmann-Goldberg Chemistry: Arylation of N-Nucleophiles with Aryl Halides1.1 Introduction; 1.2 Arylation of Amines; 1.3 Arylation of Amides, Imides, and Carbamates; 1.4 Arylation of Conjugated N-Heterocycles; 1.5 Synthesis of Anilines by Coupling with Ammonia or Synthetic Equivalents; 1.6 Conclusion and Future Prospects; 2: Ullmann Condensation Today: Arylation of Alcohols and Thiols with Aryl Halides; 2.1 Introduction; 2.2 Formation of C-O Bonds via Copper-Catalyzed Cross-Coupling Reactions with Aryl Halides
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 2.3 Formation of C-S Bonds via Copper-Catalyzed Cross-Coupling Reactions with Aryl Halides2.4 Conclusion; 3: Copper-Catalyzed Formation of C-P Bonds with Aryl Halides; 3.1 Introduction; 3.2 Arylation of Phosphines; 3.3 Arylation of Phosphine Oxides and Phosphites; 3.4 Conclusion; 4: Alternative and Emerging Reagents for the Arylation of Heteronucleophiles; 4.1 Introduction; 4.2 Chan-Lam-Evans Coupling: Copper(II)-Promoted Oxidative Aryl Transfer from Arylboron Derivatives; 4.3 Copper-Promoted Aryl Transfer from Metallated Aryl Derivatives (Nonboron)
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 4.4 Copper-Catalyzed Arylation Reactions Involving Masked S- and N-Nucleophiles4.5 Copper-Catalyzed Direct Heterofunctionalization of Aromatic C-H Bonds; 4.6 Conclusion and Future Prospects; 5: Beyond Ullmann-Goldberg Chemistry: Vinylation, Alkynylation, and Allenylation of Heteronucleophiles; 5.1 Introduction; 5.2 Copper-Mediated Alkenylation of Heteronucleophiles: Among the Best Routes to Heteroatom-Substituted Alkenes; 5.3 Alkynylation of Heteronucleophiles: The Emergence of General Methods for the Synthesis of Heteroatom-Substituted Alkynes
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 5.4 Allenylation of Heteronucleophiles: New Tools for the Synthesis of Allenamides5.5 Conclusion and Future Prospects; 6: Aromatic/Vinylic Finkelstein Reaction; 6.1 Introduction; 6.2 Copper-Mediated Halogen Exchange Reactions in Aryl Halides; 6.3 Most Recent Developments and Overview; 7: Insights into the Mechanism of Modern Ullmann-Goldberg Coupling Reactions; 7.1 General View and Key Mechanistic Aspects; 7.2 Oxidation State of Copper Catalysts; 7.3 Identity of the Active Copper(I) Complex; 7.4 Activation Mode of Aryl Halides by Copper Complexes
520 ## - SUMMARY, ETC.
Summary, etc. "Providing insight into the use of copper in cross-coupling reactions as a cost-efficient alternative to palladium, Copper-Mediated Cross Coupling Reactions provides a complete up-to-date collection of the available catalytic systems and processes. This essential reference covers a broad scope of copper-mediated reactions, their variations, key advances, improvements, and an array of applications that have revolutionized copper catalysis for any industry involving organic synthesis. The text discusses recently developed methods for conducting copper-mediated reactions with supported catalysts, which allow for recyclable and reusable systems"--
Assigning source Provided by publisher.
520 ## - SUMMARY, ETC.
Summary, etc. "This book is divided into three parts: Formation of C-Heteroatom Bonds, Formation of C-C Bonds, and Applications of Copper Catalyzed Cross Coupling Reactions: Heterocycles, Natural Products, Process and Sustainable Chemistry"--
Assigning source Provided by publisher.
588 ## - SOURCE OF DESCRIPTION NOTE
Source of description note Description based on print version record and CIP data provided by publisher.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Copper catalysts.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Copper
General subdivision Reactivity.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Chemical bonds.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Organic compounds
General subdivision Synthesis.
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element SCIENCE / Chemistry / Physical & Theoretical.
Source of heading or term bisacsh
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Chemical bonds.
Source of heading or term fast
Authority record control number (OCoLC)fst00852856
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Copper catalysts.
Source of heading or term fast
Authority record control number (OCoLC)fst00878447
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Copper
General subdivision Reactivity.
Source of heading or term fast
Authority record control number (OCoLC)fst00878394
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Organic compounds
General subdivision Synthesis.
Source of heading or term fast
Authority record control number (OCoLC)fst01047668
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Katalysator.
Authority record control number (DE-588)4029919-3
Source of heading or term gnd
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Kupfer.
Authority record control number (DE-588)4033734-0
Source of heading or term gnd
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Kreuzkupplungsreaktion.
Authority record control number (DE-588)1033635499
Source of heading or term gnd
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Organische Synthese.
Authority record control number (DE-588)4075695-6
Source of heading or term gnd
655 #4 - INDEX TERM--GENRE/FORM
Genre/form data or focus term Electronic books.
655 #0 - INDEX TERM--GENRE/FORM
Genre/form data or focus term Electronic books.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Evano, Gwilherm,
Relator term editor of compilation.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Blanchard, Nicolas,
Relator term editor of compilation.
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Print version:
Title Copper-mediated cross-coupling reactions
Place, publisher, and date of publication Hoboken, New Jersey : Wiley, [2013]
International Standard Book Number 9781118060452
Record control number (DLC) 2013011111
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier http://onlinelibrary.wiley.com/book/10.1002/9781118690659
Public note Wiley Online Library
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Books

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Last Updated on September 15, 2019
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