Search results
Results from the WOW.Com Content Network
strong base used in organic chemistry for the deprotonation of weakly acidic compounds Manganese dioxide: used as a pigment and as a precursor to other manganese compounds; used as a reagent in organic synthesis for the oxidation of allylic alcohols Meta-Chloroperoxybenzoic acid: used as an oxidant in organic synthesis Methyl tert-butyl ether
Download as PDF; Printable version; In other projects Wikimedia Commons ... Well-known reactions and reagents in organic chemistry include 0-9. 1,2-Wittig ...
This category was created to provide a "home" for inorganic compounds (such as NaBH 4) that are widely used in stoichiometric quantities in organic chemistry, but widely used organic reagents (such as oxalyl chloride) may belong here also. This category is not for catalysts such as Pd.
The online version is also known as e-EROS. The encyclopedia contains a description of the use of reagents used in organic chemistry. [1] [2] The eight-volume print version includes 3500 alphabetically arranged articles and the online version is regularly updated to include new reagents and catalysts.
Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).
In organometallic chemistry, organolithium reagents are chemical compounds that contain carbon–lithium (C–Li) bonds.These reagents are important in organic synthesis, and are frequently used to transfer the organic group or the lithium atom to the substrates in synthetic steps, through nucleophilic addition or simple deprotonation. [1]
"Oxidation and Reduction Reactions in Organic Chemistry". Archived from the original on 2011-06-11. "Diisobutyl Aluminum hydride (DIBAL-H) and Other Isobutyl Aluminum Alkyls (DIBAL-BOT, TIBAL) as Specialty Organic Synthesis Reagents" (PDF) .
Reactions of organocopper reagents involve species containing copper-carbon bonds acting as nucleophiles in the presence of organic electrophiles. Organocopper reagents are now commonly used in organic synthesis as mild, selective nucleophiles for substitution and conjugate addition reactions.