Search results
Results from the WOW.Com Content Network
Organic Reactions is a peer-reviewed book series that was established in 1942. It publishes detailed descriptions of useful organic reactions . Each article (called a chapter) is an invited review of the primary source material for the given reaction, and is written under tight editorial control, making it a secondary to tertiary‑level source.
The oldest organic reactions are combustion of organic fuels and saponification of fats to make soap. Modern organic chemistry starts with the Wöhler synthesis in 1828. In the history of the Nobel Prize in Chemistry awards have been given for the invention of specific organic reactions such as the Grignard reaction in 1912, the Diels–Alder ...
L I Smith. Organic Reactions I: The Jacobsen Reaction (Wiley, 1942) M B Smith, J March. March's Advanced Organic Chemistry (Wiley, 2001) (ISBN 0-471-58589-0) W Pötsch. Lexikon bedeutender Chemiker (VEB Bibliographisches Institut Leipzig, 1989) (ISBN 3817110553
Wiley, John & Sons, Incorporated, 1st Ed. 1962, 6th Ed. 1999 Description: A classic general textbook for an undergraduate course in inorganic chemistry Importance: This book is not only a good introduction to the subject, it was very different from earlier texts and "led to a fundamental shift in the way in which inorganic chemistry was studied ...
Before beginning any organic synthesis, it is important to understand the chemical reactions, reagents, and conditions required in each step to guarantee successful product formation. When determining optimal reaction conditions for a given synthesis, the goal is to produce an adequate yield of pure product with as few steps as possible. [ 13 ]
The aldol reaction (aldol addition) is a reaction in organic chemistry that combines two carbonyl compounds (e.g. aldehydes or ketones) to form a new β-hydroxy carbonyl compound. Its simplest form might involve the nucleophilic addition of an enolized ketone to another:
Reaction example of Chan–Lam coupling. Compound 1, a pyrrole, is coupled with aryl boronic acid, 2, to afford product 3, which is then carried forward to the target 4. The nitrile group of 2 does not poison the catalyst. Pyridine is the ligand used for the reaction. Although the reaction requires three days, it was carried out at room ...
The Gomberg–Bachmann reaction, named for the Russian-American chemist Moses Gomberg and the American chemist Werner Emmanuel Bachmann, is an aryl-aryl coupling reaction via a diazonium salt. [1] [2] [3] The arene compound (here benzene) is reacted with a diazonium salt in the presence of a base to provide the biaryl through an intermediate ...