rdf-syntax-grammar
mods:
  schema location: http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
  title info:
    title: Metal catalysed carbon-carbon bond-forming reactions
  name:
    name part: Roberts, Stanley M.
  type of resource: text
  genre: bibliography
  origin info:
    place:
      place term: enk
    place:
      place term: Chichester
    publisher: John Wiley
    date issued: ©2004
    date issued: 2004
    issuance: monographic
  language:
    language term: eng
  physical description:
    form: remote
    extent: 1 online resource (xxii, 256 pages) : illustrations
  abstract: The chemist has a vast range of high-tech catalysts to use when working in fine chemical synthesis but the catalysts are generally hard to use and require both time, skill and experience to handle properly. The Catalysts for Fine Chemical Synthesis series contains tested and validated procedures which provide a unique range resources for chemists who work in organic chemistry. "" ... of great value to synthetic organic chemists ... "" (The Chemists, Summer 2003) Volume 3 in the series focuses on catalysts for carbon-carbon bond formation and presents practical and detailed prot
  table of contents: Catalysts for Fine Chemical Synthesis Volume 3; Contents; Series Preface; Preface to Volume 3; Abbreviations; List of Chemical Names Used; 1 Considerations of Industrial Fine Chemical Synthesis; 1.1 Introduction; 1.2 Types of processes -- flow charts; 1.2.1 Classical process; 1.2.2 General catalytic process; 1.3 Costs associated with use of catalysts; 1.3.1 Catalyst fabrication costs; 1.3.2 Intellectual property right (IPR) issues; 1.3.3 Separation costs; 1.3.4 Pre-reaction/immobilisation; 1.3.5 Post reaction -- separation; 1.3.6 Industrial examples; References.
  table of contents: 2 Alkylation and Allylation Adjacent to a Carbonyl Group2.1 The RuH(2)(CO)(PPh(3))(3)-catalysed alkylation, alkenylation and arylation of aromatic ketones via carbon-hydrogen bond cleavage; 2.1.1 Preparation of carbonyldihydrotris(triphenylphosphine) ruthenium; 2.1.2 Synthesis of 8-(2-triethoxysilanylethyl)-3,4-dihydro-2H-naphthalen-1-one; 2.1.3 Synthesis of 8-(1-methyl-2-trimethylsilanylvinyl)-3,4-dihydro-2H-naphthalen-1-one; 2.1.4 Synthesis of 1-biphenyl-2-yl-2,2-dimethylpropan-1-one; 2.1.5 Conclusion; References.
  table of contents: 2.2 Catalytic, asymmetric synthesis of a, a-disubstituted amino acids using a chiral copper-salen complex as a phase transfer catalyst2.2.1 Synthesis of (chsalen); 2.2.2 Synthesis of copper(II) (chsalen); 2.2.3 Alkylation of alanine methyl ester Schiff base by chiral salen-metal catalysts, a-benzyl-alanine methyl ester; 2.2.4 Conclusion; References; 2.3 Asymmetric phase-transfer catalysed alkylation of glycine imines using cinchona alkaloid derived quaternary ammonium salts.
  table of contents: 2.3.1 Synthesis of (1S,2S,4S,5R,1 ́R)-1-(anthracen-9-ylmethyl)-5-ethyl-2-[hydroxy(quinolin-4-yl)methyl]-1-azoniabicyclo[2.2.2]octane bromide2.3.2 Synthesis of (1S,2S,4S,5R,1 ́R)-1-(anthracen-9-ylmethyl)-5-ethyl-2-[benzyloxy(quinolin-4-yl)methyl]-1-azoniabicyclo[2.2.2]octane bromide; 2.3.3 Synthesis of (2S)-tert-butyl 2-amino-4-bromopent-4-enoate; 2.3.4 Conclusion; References; 3 Asymmetric Alkylation or Amination of Allylic Esters; 3.1 Synthesis and application in palladium-catalysed asymmetric allylic substitution of enantiopure cyclic b-iminophosphine ligands.
  table of contents: 3.1.1 Synthesis of (2,6-dimethyl-phenyl)-(1-phenyl-2,3,3a,8a-tetrahydro-1H-1-phospha-cyclopenta[a]inden-8-ylidene)-amines 1R(p)3.1.2 Synthesis of (E)-Methyl 2-carbomethoxy-3,5-diphenylpent-4-enoate; 3.1.3 Synthesis of benzyl(1,3-diphenylprop-2-enyl)amine; 3.1.4 Conclusion; References; 3.2 (9H,9 ́H,10H,10 ́H,11H,11H ́,13H,13 ́H,14H,14 ́H,15H,15 ́H-perfluorotricosane-12,12 ́-diyl)bis[(4S)-4-phenyl-2-oxazoline as a ligand for asymmetric palladium-catalysed alkylation of allylic acetates in fluorous media; 3.2.1 Synthesis of 2-iodo-1-(1H,1 ́H,2H,2 ́H,3H,3 ́H-perfluorooctyl)-3-propanol.
  note: edited by Stanley M. Roberts [and others].
  note: Electronic reproduction. [Place of publication not identified] : HathiTrust Digital Library, 2010. MiAaHDL
  note: Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002. http://purl.oclc.org/DLF/benchrepro0212 MiAaHDL
  note: digitized 2010 HathiTrust Digital Library committed to preserve pda MiAaHDL
  note: Includes bibliographical references and index.
  note: English.
  subject:
    topic: Organic compounds
    topic: Synthesis
  subject:
    topic: Metal catalysts
  subject:
    topic: Chemical bonds
  subject:
    topic: Catalysts
  classification: QD262 .M48 2004eb
  classification: 547.215
  classification: O621. 3
  related item:
    title info:
      title: Metal catalysed carbon-carbon bond-forming reactions
    origin info:
      publisher: Chichester : John Wiley, ©2004
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  identifier: OverDrive, Inc.
  identifier: AECBA85C-E91C-42B2-A589-FAEB8CC86A83 OverDrive, Inc.
  identifier: http://proxy.library.tamu.edu/login
  record info:
    record content source: NhCcYBP
    record creation date: 050209
    record change date: 20260214212952.1
    record identifier: in00004678290
    language of cataloging:
      language term: eng