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  <titleInfo>
    <title>Principles of organic synthesis</title>
  </titleInfo>
  <name type="personal">
    <namePart>Norman, R. O. C.</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Coxon, J. M.</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="text">London</placeTerm>
    </place>
    <place>
      <placeTerm type="text">New York</placeTerm>
    </place>
    <publisher>Blackie Academic &amp; Professional</publisher>
    <dateIssued>1993</dateIssued>
    <edition>3rd ed. /</edition>
    <issuance>monographic</issuance>
  </originInfo>
  <physicalDescription>
    <extent>xv, 811 p. : ill. ;</extent>
  </physicalDescription>
  <abstract>The purpose of this book is to show how mechanistic principles can be applied both to acquiring a knowledge of organic synthetic processes and to planning the construction of organic compounds. It is designed for those who have had no more than a brief introduction to organic chemistry and who require a broad understanding of the subject.</abstract>
  <abstract>The book is in two parts. In Part I, reaction mechanism is set in its wider context of the basic principles and concepts that underlie chemical reactions: chemical thermodynamics, structural theory, theories of reaction kinetics, mechanism itself, and stereochemistry.</abstract>
  <abstract>In Part II, these principles and concepts are applied to the formation of particular types of bonds, groupings, and compounds: for example, how small molecules can be built on to give larger ones by the construction of new carbon-carbon bonds, or how one functional group can be transformed into another. The final chapter in Part II describes the planning and detailed execution of the multi-step syntheses of several complex naturally occurring compounds</abstract>
  <abstract>.</abstract>
  <abstract>There have been numerous important developments since the second edition of this book was published 15 years ago, and every chapter has been brought up to date to include them.</abstract>
  <abstract>Among the more notable are: the stereochemical control of reactions, reflecting the need to synthesize efficiently compounds with several asymmetric centres; the use of organotransition-metal reagents, leading to a new chapter; the exploitation of lithium diisopropylamide (LDA) as a base in the formation of new C-C bonds; free-radical reactions for the synthesis of C-C bonds; uses of organosilicon compounds; and subtle new protective and condensing reagents in polypeptide synthesis.</abstract>
  <abstract>The text is extensively cross-referenced and a detailed index is included.</abstract>
  <tableOfContents>1. Chemical thermodynamics -- 2. Molecular structure -- 3. Chemical kinetics -- 4. Mechanism -- 5. Stereochemistry -- 6. Formation of carbon-carbon bonds: organometallic reagents -- 7. Formation of aliphatic carbon-carbon bonds: base-catalyzed reactions -- 8. Formation of aliphatic carbon-carbon bonds: acid-catalyzed reactions -- 9. Pericyclic reactions -- 10. Formation of aliphatic carbon-nitrogen bonds -- 11. Electrophilic aromatic substitution -- 12. Nucleophilic aromatic substitution -- 13. Aromatic diazonium salts -- 14. Molecular rearrangements -- 15. Reagents containing phosphorus, sulfur, silicon or boron -- 16. Photochemical reactions -- 17. Free-radical reactions -- 18. Organotransition metal reagents -- 19. Oxidation -- 20. Reduction -- 21. The synthesis of five- and six-membered heterocyclic compounds -- 22. The syntheses of some naturally occurring compounds.</tableOfContents>
  <note>Includes index.</note>
  <subject authority="lcsh">
    <topic>Organic compounds</topic>
  </subject>
  <classification authority="ddc">547.2 NOR</classification>
  <identifier type="isbn">0751401269 (acidfree)</identifier>
  <recordInfo/>
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