Reductions in organic chemistry /

Saved in:
Bibliographic Details
Author / Creator:Hudlicky, Milos, 1919-
Edition:2nd ed.
Imprint:Washington, DC : American Chemical Society, [1996]
Description:xxvi, 429 p. : ill. ; 24 cm.
Language:English
Series:ACS monograph 188
Subject:
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/2570920
Hidden Bibliographic Details
ISBN:0841233446
Notes:Includes bibliographical references (p. 323-365) and indexes.
Table of Contents:
  • Preface to the First Edition
  • Preface to the Second Edition
  • Introduction
  • Safety First
  • Abbreviations and Proprietary Names
  • Categories of Reductions:Catalytic Hydrogenation
  • Reduction with Hydrides and Complex Hydrides
  • Electroreduction and Reductions with Metals
  • Reductions with Metal Compounds
  • Reductions with Nonmetal Compounds
  • Reduction of Specific Types of Organic Compounds
  • Reduction of Hydrocarbons and Aromatic Heterocycles
  • Reduction of Halogen Derivatives of Hydrocarbons and Basic Heterocycles
  • Reduction of Nitro, Nitroso, Diazo, and Azido Derivatives of Hydrocarbons and Basic Heterocycles
  • Reduction of Sulfur Compounds (Except Sulfur Derivatives of Aldehydes, Ketones,and Acids)
  • Reduction of Amines and Their Derivatives and of Phosphorus Compounds
  • Reduction of Aldehydes and Their Derivatives
  • Reduction of Ketones and Their Derivatives
  • Reduction of Carboxylic Acids
  • Reduction of Acyl Chlorides and Acid Anhydrides
  • Reduction of Nitriles
  • Reduction of Organometallic Compounds
  • Correlation Tables
  • Reduction of Alkanes, Alkenes, Alkadienes, and Alkynes
  • Reduction of Aromatic Hydrocarbons
  • Reduction of Heterocyclic Aromatic Compounds
  • Reduction of Halogen Compounds
  • Reduction of Nitro Compounds
  • Reduction of Nitroso, Diazonium and Azido Compounds
  • Reduction of Alcohols and Phenols
  • Reduction of Ethers
  • Reduction of Epoxides, Peroxides, and Ozonides
  • Reduction of Sulfur Compounds (Except Sulfur Derivatives of Aldehydes, Ketones,and Acids)
  • Reduction of Amines and Their Derivatives
  • Reduction of Phosphorus Compounds
  • Reduction of Aldehydes
  • Reduction of Derivatives of Aldehydes
  • Reduction of Ketones
  • Reduction of Substitution Derivatives of Ketones
  • Reduction of Hydroxy Ketones, Diketones, and Quinones
  • Reduction of Ketals, Thioketals, Ketimines, Ketoximes, and Hydrazones
  • Reduction of Carboxylic Acids
  • Reduction of Derivatives of Carboxylic Acids
  • Reduction of Acyl Chlorides and Acid Anhydrides
  • Reduction of Esters of Carboxylic Acids
  • Reduction of Esters of Unsaturated Carboxylic Acids
  • Reduction of Substitution Derivatives of Esters
  • Reduction of Functionalized Esters
  • Reduction of Amides, Lactams, and Imides
  • Reduction of Amidines, Thioamides, Imidoyl Chlorides and Hydrazides
  • Reduction of Nitriles
  • Catalytic Hydrogenation with Hydrogen Generated from Sodium Borohydride
  • Catalytic Hydrogenation Under Elevated Pressure
  • Preparation of Palladium Catalyst
  • Preparation of the Lindlar Catalyst
  • Reduction with Raney Nickel
  • Desulfurization with Raney Nickel
  • Preparation of Nickel Catalyst
  • Catalytic Transfer of Hydrogen
  • Homogeneous Hydrogenation
  • Preparation of Alane (Aluminum Hydride)
  • Preparation of Lithium Tris(tert-butoxy)aluminum Hydride
  • Analysis of Hydrides and Complex Hydrides
  • Reduction with Lithium Triethoxylaluminum Hydride
  • Reduction with Lithium Tris-tert-butoxyaluminum Hydride
  • Reduction with Lithium Aluminum Hydride and Diethylamine
  • Reduction with Lithium (1,1''-Binaphthyl-2,2''-dioxy)ethoxyaluminum Hydride
  • Reduction with Alane (Aluminum Hydride) In Situ
  • Reduction with Diisobutylalane
  • Reduction with Borane
  • Reduction with Borane In Situ
  • Reduction with Thexylchloroborane-Dimethyl Sulfide
  • Reduction with Sodium Borohydride
  • Reduction with Zinc Borohydride
  • Reduction with Sodium Cyanoborohydride
  • Reduction with Triethylsilane
  • Reduction with Zinc Borohydride
  • Reduction with Triethylsilane
  • Reduction with Stannanes
  • Electrolytic Reduction
  • Reduction with Sodium(Birch Reduction) Reduction with Sodium
  • Reduction with Sodium Naphthalene
  • Reduction with Sodium Amalgam
  • Reduction with Nickel-Aluminum Alloy
  • Reduction with Zinc (Clemmensen Reduction)
  • Reduction with Zinc in Alkaline Solution
  • Reduction with Zinc and Sodium Iodide
  • Reduction with Iron
  • Reduction with Tin
  • Reduction with Stannous Chloride
  • Reduction with Chromous Chloride
  • Reduction with Vanadous Chloride
  • Reduction with Hydriodic Acid
  • Reduction with Sulfur Dioxide
  • Reduciton with Sodium Sulfite
  • Reduciton with Sodium Hydrosulfite (Dithionite)
  • Reduction with Sodium dithionite in the Presence of a Phase-Transfer Catalyst
  • Reduction with Hydrazine
  • Reduction with Hypophosphorous Acid
  • Reduction with Ammonium Hypophosphite
  • Reduction with Trialky