Ads
related to: common organic chemistry portal
Search results
Results From The WOW.Com Content Network
An example of a common reaction is a substitution reaction written as: Nu ... Organic-Chemistry.org, Organic Chemistry Portal – Recent Abstracts and (Name)Reactions;
Cadiot–Chodkiewicz coupling; Cadogan-Sundberg indole synthesis; Camps quinoline synthesis; Cannizzaro reaction; Carbohydrate acetalisation; Carbonyl reduction
The Weinreb ketone synthesis or Weinreb–Nahm ketone synthesis is a chemical reaction used in organic chemistry to make carbon–carbon bonds. It was discovered in 1981 by Steven M. Weinreb and Steven Nahm as a method to synthesize ketones. [1]
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).
A name reaction (or named reaction) is a chemical reaction named after its discoverer(s) or developer(s). Among the tens of thousands of organic reactions that are known, hundreds of such reactions are typically identified by the eponym. [1]
Organic Chemistry Portal RSC ontology ID The Wohl–Ziegler reaction [1] [2] is a chemical reaction that involves the allylic or benzylic bromination of hydrocarbons ...
The Williamson ether synthesis is a common organic reaction in industrial synthesis and in undergraduate teaching laboratories. Yields for these ether syntheses are traditionally low when reaction times are shortened, which can be the case with undergraduate laboratory class periods.
Organic Chemistry Portal rubottom-oxidation The Rubottom oxidation is a useful, high-yielding chemical reaction between silyl enol ethers and peroxyacids to give the corresponding α-hydroxy carbonyl product.