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Name reactions : a collection of detailed mechanisms and synthetic applications / Jie Jack Li.

By: Material type: TextTextPublication details: Cham ; New York : Springer, c2014.Edition: 5th edDescription: xxii, 681 p. : ill. (some color) : 24 cmContent type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
ISBN:
  • 9783319039787 (alk. paper)
  • 3319039784 (alk. paper)
Subject(s): DDC classification:
  • 22 547.2 L.J.N
LOC classification:
  • QD291 .L5 2014
Online resources:
Contents:
From the content: Alder ene reaction.-Aldol condensation.-Algar-Flynn-Oyamada reaction.-Allan-Robinson reaction.-Arndt-Eistert homologation.-Baeyer-Villiger oxidation.-Baker-Venkataraman rearrangement.-Bamford-Stevens reaction.-Baran reagents.-Barbier reaction.-Bargellini reaction.-Bartoli indole synthesis.-Barton radical decarboxylation.-Barton-McCombie deoxygenation.-Barton nitrite photolysis.-Barton-Zard reaction.-Batcho-Leimgruber indole synthesis.-Baylis-Hillman reaction.-Beckmann rearrangement.-Abnormal Beckmann rearrangement.-Beirut reaction.-Benzilic acid rearrangement.-Benzoin condensation.-Bergman cyclization.-Biginelli reaction.-Birch reduction.-Bischler-Mohlau indole synthesis.-Bischler-Napieralski reaction.-Blaise reaction.-Blum-Ittah aziridine synthesis.-Boekelheide reaction.-Boger pyridine synthesis.-Borch reductive amination.-Borsche-Drechsel cyclization.-Boulton-Katritzky rearrangement.-Bouveault aldehyde synthesis.-Bouveault-Blanc reduction.
Summary: In this fifth edition the author has added twenty-seven new name reactions to reflect the recent advances in organic chemistry. Each reaction is delineated by its detailed step-by-step, electron-pushing mechanism and supplemented with the original and the latest references, especially from review articles.-- Source other than Library of Congress.
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Includes bibliographical references and index.

From the content: Alder ene reaction.-Aldol condensation.-Algar-Flynn-Oyamada reaction.-Allan-Robinson reaction.-Arndt-Eistert homologation.-Baeyer-Villiger oxidation.-Baker-Venkataraman rearrangement.-Bamford-Stevens reaction.-Baran reagents.-Barbier reaction.-Bargellini reaction.-Bartoli indole synthesis.-Barton radical decarboxylation.-Barton-McCombie deoxygenation.-Barton nitrite photolysis.-Barton-Zard reaction.-Batcho-Leimgruber indole synthesis.-Baylis-Hillman reaction.-Beckmann rearrangement.-Abnormal Beckmann rearrangement.-Beirut reaction.-Benzilic acid rearrangement.-Benzoin condensation.-Bergman cyclization.-Biginelli reaction.-Birch reduction.-Bischler-Mohlau indole synthesis.-Bischler-Napieralski reaction.-Blaise reaction.-Blum-Ittah aziridine synthesis.-Boekelheide reaction.-Boger pyridine synthesis.-Borch reductive amination.-Borsche-Drechsel cyclization.-Boulton-Katritzky rearrangement.-Bouveault aldehyde synthesis.-Bouveault-Blanc reduction.

In this fifth edition the author has added twenty-seven new name reactions to reflect the recent advances in organic chemistry. Each reaction is delineated by its detailed step-by-step, electron-pushing mechanism and supplemented with the original and the latest references, especially from review articles.-- Source other than Library of Congress.

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