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: Green sustainable process for chemical and environmental engineering and science
    sub title: organic synthesis in water and supercritical water
  title info:
    title: Organic synthesis in water and supercritical water
  name:
    name part: Inamuddin
    name part: 1980-
    role:
      role term: editor.
  name:
    name part: Boddula, Rajender
    role:
      role term: editor.
  name:
    name part: Asiri, Abdullah M.
    role:
      role term: editor.
  name:
    name part: ScienceDirect (Online service)
  type of resource: text
  genre: Electronic books.
  origin info:
    place:
      place term: ne
    date issued: 2020
    issuance: monographic
  language:
    language term: eng
  physical description:
    form: remote
    extent: 1 online resource
  abstract: Green Sustainable Process for Chemical and Environmental Engineering and Science: Organic Synthesis in Water and Supercritical Water provides an in-depth review of purification and extraction methods for medicinal, analytical, engineering and bioactive compounds utilizing green chemistry protocols.
  table of contents: 2.9. Aqueous intramolecular D-A reaction in the total synthesis -- 2.10. [3+2] Cycloaddition reactions in water -- 2.11. [4+3] Cycloaddition reaction -- 2.12. [2+2+2] Cycloadditions -- 2.13. [5+2] Cycloadditions -- 3. Cycloaddition reactions ``on-water´´ -- 4. Concluding remarks -- Acknowledgments -- References -- Chapter 4: Hydrogenation reactions in water -- 1. Introduction -- 2. Types of hydrogenation -- 2.1. Catalytic hydrogenation -- 2.2. Transfer hydrogenation -- 2.3. Asymmetric hydrogenation -- 2.4. Asymmetric transfer hydrogenation -- 2.5. Electrocatalytic hydrogenation -- 2.6. Selective hydrogenation -- 2.6.1. Chemoselective hydrogenation -- 2.6.2. Diastereoselective hydrogenation -- 2.6.3. Regioselective hydrogenation -- 2.7. Other hydrogenation -- 3. Water as hydrogen donor -- 3.1. Synthesis of aliphatic compounds -- 3.2. Synthesis of aromatic compounds -- 3.3. Synthesis of carbonyl compounds -- 3.4. Synthesis of alcohols, ethers, sugars, nitro and nitril compounds -- 3.5. Synthesis of bio-oils, fossil fuel, and cellulose -- 4. Water as solvent -- 4.1. Synthesis of aliphatic compounds -- 4.2. Synthesis of aromatic compounds -- 4.3. Synthesis of carbonyl compounds -- 4.4. Synthesis of alcohols, ethers, sugars, nitro, and nitril compounds -- 5. Conclusion -- References -- Chapter 5: Magnetically separable nanocatalyzed synthesis of bioactive heterocycles in water -- 1. Introduction -- 2. Synthesis of nitrogen-containing heterocycles -- 2.1. Synthesis of N-substituted pyrroles -- 2.2. Synthesis of 1,4-dihydropyridines -- 2.3. Synthesis of hexahydroquinoline carboxylates -- 2.4. Synthesis of quinolines -- 2.5. Synthesis of acridine-1,8(2H,5H)-diones -- 2.6. Synthesis of benzo[d]imidazoles -- 2.7. Synthesis of imidazo[1,2-a]pyridines -- 2.8. Synthesis of quinoxalines -- 2.9. Synthesis of 1,2,3-triazoles.
  table of contents: 5. Factors affecting CC coupling reactions in water -- 5.1. Catalyst -- 5.2. Bimetallic catalysts -- 5.3. Base and concentration effect -- 5.4. Light water/heavy water -- 5.5. Energy source -- 5.6. Additives and transfer agents -- 6. Specific CC coupling reactions -- 6.1. Mizoroki-Heck reaction -- 6.2. Hiyama reaction -- 6.3. Suzuki-Miyaura reaction -- 6.4. Sonogashira-Hagihara reaction -- 6.5. Stille reaction -- 6.6. Negishi reaction -- 7. Applications in synthesis -- 7.1. Derivatization of biomolecules -- 7.2. Bioactive molecules -- 8. Conclusions -- References -- Index.
  note: edited by Inamuddin, Rajender Boddula and Abdulah M. Asiri.
  subject:
    topic: Green chemistry
  subject:
    topic: Chimie verte
  subject:
    topic: Green chemistry
  classification: TP155.2.E58
  classification: 660.028/6
  identifier: 9780128195420
  identifier: 0128195428
  identifier: http://proxy.library.tamu.edu/login
  record info:
    record content source: OPELS
    record creation date: 200715
    record change date: 20260327165035.2
    record identifier: in00005767006
    language of cataloging:
      language term: eng