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Agents, reducing

I began graduate studies at the University of Chicago in 1936. At that time, the structure of diborane was a subject of considerable study and [Pg.3]

I soon discovered that simple aldehydes and ketones react rapidly with diborane at 0° C. Hydrolysis then produces the corresponding alcohol. [Pg.3]

My thesis was completed in 1938 and the results were published in 1939 Hydrides of Boron. XI. The Reaction of Diborane with Organic Compounds Containing a Carbonyl Group (3). [Pg.3]

Interest in this development among organic chemists was minimal. Diborane was a chemical rarity at the time, available only in milligram quantities through complex procedures. [Pg.3]

Most recently, various halide ions were utilized for shape control. Bromide ions were used to synthesize Rh nanocubes [29]. Nal was added to synthesize PtcPdi c nanocubes, whereas substituting Nat with NaCl produced PtPd nanooctahedra [30]. [Pg.26]


Andrews deration An important titration for the estimation of reducing agents. The reducing agent is dissolved In concentrated hydrochloric acid and titrated with potassium iodale(V) solution. A drop of carbon tetrachloride is added to the solution and the end point is indicated by the disappearance of the iodine colour from this layer. The reducing agent is oxidized and the iodate reduced to ICl, i.e. a 4-eiectron change. [Pg.34]

Benedict solution Aqueous solution of Na2C03, CuSO, and sodium citrate used for testing for reducing agents, particularly sugars, which give red-yellow colours or precipitates. [Pg.54]

Chromium(IJ) chloride, chromous chloride, CrCl2- White solid (Cr plus HCl gas) dissolving to give a blue solution. Forms hydrates, widely used as a reducing agent. [Pg.98]

Europium(TTI) salts are typical lanthanide derivatives. Europium(ll) salts are pale yellow in colour and are strong reducing agents but stable in water. EuX2 are prepared from EuX -hEu (X=C1, Br, I) or EuFa + Ca EuCl2 forms a dihydrale. EUSO4 is prepared by electrolytic reduction of Eu(III) in sulphuric acid. Eu(II) is probably the most stable +2 stale of the lanthanides... [Pg.170]

Germanium chlorides. GeCl4, m.p. —49°C, b.p. 86" C (Ge plus CI2) is hydrolysed by water. GeClj, colourless reducing agent (GeCU plus Ge). [Pg.189]

NH4)2Fe(S04)2,6H20. Pale green crystalline solid used as a standard reducing agent (e.g. for KMn04). More stable than FeS04. [Pg.222]

LiAKOBujaH. A selective reducing agent for converting RCOCl to aldehydes and reducing steroid ketones. See aluminium hydride. [Pg.241]

Hi at 500" C. Stable crystalline compound, gives LiOH and Hi with water (may ignite in moist atmosphere). Used as a source of Hi, as a reducing agent, and for the preparation of hydrides. [Pg.242]

Hypophosphorous acid, H3PO2, H2P(0)0H. A monobasic acid. Ba(H2P02)2 is formed when white phosphorus is dissolved in Ba(OH)2 solution. H3PO2 and its salts are strong reducing agents. [Pg.309]

Phosphorous acid, H3PO3, HP(0)(0H)2-A dibasic acid (PCI3 plus cold water), strong reducing agent. [Pg.309]


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ALKOXYALUMINATE REDUCING AGENTS

Action of Reducing Agents

Admixtures water-reducing agents

Alcohols as reducing agents

Alcohols reducing agents

Aldehydes reducing agents

Alkali iodides, reducing agents

Alkali metals as reducing agents

Alkali polysulfides, reducing agents

Alkali sulfides, reducing agents

Aluminum hydride reducing agents

Amalgams, as reducing agents

Ammonia as reducing agent

Ammonium hydrogen sulfide, reducing agent

Ammonium sulfide, reducing agent

Ammonium sulfide, reducing agent reduction

Analyses environmental, reducing agent

As reducing agent

Ascorbic acid (vitamin reducing agent

Asymmetric reducing agent

Atomic reducing agent for SnS

Auxiliary reducing agent

Bleaching of silk with reducing agents

Borane as reducing agent

Boranes as reducing agents

Borohydride compound reducing agents

Borohydrides, chiral, asymmetric reducing agents

CHATGILIALOGLU Reducing Agent

CNT as a Reducing Agent

Cadmium-based reducing agents

Calcium borohydride reducing agents

Camphor chiral modification of reducing agents

Capping-reducing agent

Carbon as a reducing agent

Carbon as reducing agent

Carbon monoxide as a reducing agent

Carbon monoxide as reducing agent

Carbon monoxide reducing agent

Catalytically excited hydrogen as reducing agent

Chelating agents reduced catalyst

Chemical reaction reducing agents

Chemoselective reducing agents

Chemoselective reducing agents aldehydes

Chemoselective reducing agents ketones

Chiral reducing agents

Cholesterol-reducing agents

Colloid reducing agents

Complex reducing agents

Complex reducing agents alkyl halides

Complex reducing agents desulfurizations

Complex reducing agents reduction

Complex reducing agents unsaturated carbonyl compounds

DIBAL reducing agent

Diimide reducing agent

Diisobutylaluminium hydride reducing agent

Drag reducing agents

Electroless DMAB reducing agent

Electroless hypophosphite reducing agent

Electrophilic reducing agents

Ethanol reducing agent

Ethyl phosphite reducing agent

Excipient reducing agents

Exogenous reducing agents

Fatty acid reducing agents

Flash reducing agents

Formate reducing agent

Formates, as reducing agents

From metal salt, reducing agent and ligand

Gas reducing agent

Gastric secretions agents that reduce

Glucose reducing agent

H2 as reducing agent

Hard reducing agent

Heavy metal reducing agents

Hydrated electron reducing agent

Hydrazine reducing agent

Hydrazine, as reducing agent

Hydride reducing agents

Hydride transfer reducing agent

Hydrides, as reducing agents

Hydrocarbons as reducing agent

Hydrogen as a reducing agent

Hydrogen as a reducing agent catalytic hydrogenation

Hydrogen as reducing agent

Hydrogen iodide reducing agent

Hydrogen peroxide as a reducing agent

Hydroorganosilanes as Reducing Agents

Hypophosphite-reducing agents

Important oxidizing and reducing agents

Influences of Reducing Agents

Iodide reducing agent

Iodides, alkaline, reducing agents

IpcBH as chiral reducing agent

Iron powder as reducing agent

Iron reducing agents

Ketones hydride reducing agents

Lewis acid reducing agent

Lithium aluminum hydride as reducing agent

Lithium aluminum hydride reducing agent for

Lithium aluminum hydride reducing agent for aldehydes and ketones

Lithium as reducing agent

Lithium derivatives Reducing agents)

Lithium reducing agent

Lithium reducing agent, acting

Macrocyclic reducing agents

Magnesium reducing agent

Metal hydride reagents reducing agents

Metallic reducing agents

Metals as reducing agents

Methane reducing agent

Methyl mercaptan, reducing agent

Mimicking a naturally occurring reducing agent

NaBH4 as the Reducing Agent

NaBH4 reducing agent

Nicotinamide, 1,4-dihydrobiomimetic reducing agents heterocycle reduction

Nicotinamide, 1,4-dihydrobiomimetic reducing agents hydride donors

Nicotinamide, 1,4-dihydrobiomimetic reducing agents reaction with water

Nucleophilic reducing agents

One-electron reducing agent

Organic compounds, reducing agents

Organometallic compounds reducing agents

Other reducing agents

Oxidation-reduction reactions reducing agent

Oxidizing and Reducing Agents

POLYMERIC REDUCING AGENT

Palladium catalysts reducing agents

Phosphonium iodide reducing agent

Phosphorus compounds, reducing agents

Photosynthesis reducing agent

Polar, 206 reducing agent

Poly reducing agent

Polymer reducing agents, preparation

Polymer-bound reducing agents

Polymer-bound reducing agents, polymeric

Polymeric Organotin Dihydride Reagent as a Reducing Agent

Potassium Graphite Intercalates as Reducing Agents

Potassium reducing agent

Preparation of Rieke Magnesium Using Potassium or Sodium as Reducing Agent

Radical-based reducing agents

Reaction Reducing agent

Reactions Involving Radicals, Electron-Deficient Species, Reducing Agents, and at Surfaces

Reactions of oxaziridines with nucleophiles and reducing agents

Reactions with Nucleophiles and Reducing Agents

Reactions with Oxidising and Reducing Agents

Reactions with Reducing Agents

Reactivity of hydride-transfer reducing agents

Redox reactions reducing agents

Redox reducing agents

Reduced Species/Reducing Agent/Reductant

Reduced state Reducing agents

Reducing Agent for the Transition Metal

Reducing Agents Based on Group 4 and Aqueous Media

Reducing Agents For Metallurgy and Good Health

Reducing agent A reactant

Reducing agent A substance that

Reducing agent The substance that reduces

Reducing agent alkali metals

Reducing agent alkaline earth agents

Reducing agent defined

Reducing agent ferrous sulfamate

Reducing agent holding reductants

Reducing agent in displacement reactions

Reducing agent metal alkyls

Reducing agent or reductant

Reducing agent powerful

Reducing agent recognizing

Reducing agent relative strengths

Reducing agent strengths

Reducing agent, ascorbic acid

Reducing agent, definition

Reducing agent, equivalent mass

Reducing agent, hindered

Reducing agent, hindered Reduction

Reducing agent, hindered chemoselectivity

Reducing agent, reductant

Reducing agent, sodium borohydride

Reducing agents Et3SiH

Reducing agents Grignards

Reducing agents Group

Reducing agents LiAlH

Reducing agents Subject

Reducing agents U3+ ion

Reducing agents alkylamine

Reducing agents amines

Reducing agents and processes

Reducing agents antioxidants

Reducing agents bleaches

Reducing agents borohydride

Reducing agents bulky

Reducing agents carbon

Reducing agents catecholborane

Reducing agents compounds

Reducing agents diastereoselectivity

Reducing agents diisobutylaluminum hydride

Reducing agents dimethyl sulfide

Reducing agents disulfide reduction

Reducing agents dithionites

Reducing agents effect on iodo-beads

Reducing agents for biosynthesis

Reducing agents for reductive

Reducing agents group 1 metals

Reducing agents group 13-based

Reducing agents hydrogen

Reducing agents hydrogen peroxide in alkaline solution

Reducing agents identification

Reducing agents in metallurgy

Reducing agents in organic chemistry

Reducing agents ionic-phase

Reducing agents lithium aluminium hydride

Reducing agents lithium aluminum hydride

Reducing agents lithium tetrahydridoaluminate

Reducing agents mercury hydrides

Reducing agents metal hydrides

Reducing agents metals

Reducing agents naphthalide salts

Reducing agents nuclear spin

Reducing agents organoboron compounds

Reducing agents organotin hydrides

Reducing agents persistence

Reducing agents phosphorus oxoacids and salts

Reducing agents polymer-supported

Reducing agents polymeric quaternary ammonium

Reducing agents reductive amination

Reducing agents samarium diiodide

Reducing agents silane reactions

Reducing agents sodium amalgam

Reducing agents sodium hydrosulphite

Reducing agents sodium naphthalide

Reducing agents sodium thiosulphate

Reducing agents sugars

Reducing agents sulfites

Reducing agents summary

Reducing agents thiol

Reducing agents thiols

Reducing agents three-component reactions

Reducing agents tin dichloride

Reducing agents titanium compounds

Reducing agents transition metals

Reducing agents, acetal stability

Reducing agents, chemical

Reducing agents, complex hydrides

Reducing agents, culture media

Reducing agents, enzyme

Reducing agents, enzyme activation

Reducing agents, ligands

Reducing agents, oxidation-reduction

Reducing agents, oxidation-reduction potentials

Reducing agents, solid supported

Reducing or oxidizing agent

Reducing/oxidizing agents

Reduction Reactions and Reducing Agents

Reduction samarium diiodide reducing agent

Reduction with chiral reducing agents

Reduction, reducing agent

Reduction-deposition reducing agents

Reinforcement bond water-reducing agents

Related Reducing Agents

Relative Strengths of Oxidizing and Reducing Agents

Relative reactivity of hydride-donor reducing agents

Rieke Zinc as a Reducing Agent for Common Organic Functional Groups

Scott 1 Reducing Agents

Selected Usage of Hydride Reducing Agents

Serum lipid reducing agents

Shrinkage-reducing agent

Silanes as Reducing Agents Hydrosilylation

Silanes as reducing agents

Silicon and Related Reducing Agents

Silicon hydride reducing agent

Silylated cyclohexadiene reducing agent

Single electron reducing agent

Sodium borohydride as a reducing agent

Sodium borohydride as reducing agent

Sodium formate as reducing agent

Sodium formate as reducing agent preparation of palladium catalyst

Sodium hydrosulfite reducing agent

Sodium iodide reducing agent

Sodium polysulfide as agent to reduce

Sodium polysulfide as agent to reduce l,3-dinitro-4,6-diaminobenzene

Sodium sulfite reducing agent

Solid reducing agents

Solid-Supported Reducing Agents and Their Applications

Stereoselectivity of hydride reducing agents

Stoichiometric reducing agents

Strengths of Oxidizing and Reducing Agents

Strong reducing agents

Sulfur Reducing Agents

Sulfur dioxide reducing agent

Sulfur-type reducing agents

Supplemental activator and reducing agent

The s-Block Metals as Reducing Agents

Tin as reducing agent

Tin, as reducing agent for complex

Tin, as reducing agent for complex W chlorides

Titrations with Other Reducing Agents

Titrations with Reducing Agents

Trialkyl phosphites reducing agents

Trialkylborohydrides, as reducing agents

Trichlorosilane, as reducing agent

Triethyl phosphite reducing agent

Triethylsilane reducing agent

Triethylsilane, as reducing agent

Triphenylphosphine reducing agent

Tris phosphine reducing agent

Tris silane reducing agent

Vanadium complexes reducing agents

Voltaic cells oxidizing and reducing agents

Water as reducing agent

Water-reducing agents

Water-reducing agents compressive strength

Water-reducing agents effect

Water-reducing agents standard deviation

Water-reducing agents workability

Weak reducing agents

With Bases, Nucleophiles, and Reducing Agents

With Reducing Agents

Workability retarding water-reducing agents

Zinc Complex Reducing Agents

Zinc, as reducing agent

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