Search results
Results From The WOW.Com Content Network
The formation of the quinoline product is influenced by the interaction of both steric and electronic effects.In a recent study, Sloop [8] investigated how substituents would influence the regioselectivity of the product as well as the rate of reaction during the rate-determining step in a modified Combes pathway, which produced trifluoromethylquinoline as the product.
The Journal of Physical Organic Chemistry is a monthly peer-reviewed scientific journal, published since 1988 by John Wiley & Sons.It covers research in physical organic chemistry in its broadest sense and is available both online and in print.
Structure of the 2-norbornyl cation, an iconic nonclassical ion. The structure was deduced from X-ray crystallography. C-C bond lengths not labeled are normal (ca. 1.5 Å). [1] In chemistry, a nonclassical ion usually refers to carbonium ions, a family of organic cations. They are characterized by delocalized three-center, two-electron bonds ...
In organic chemistry, the Baylis–Hillman, Morita–Baylis–Hillman, or MBH reaction is a carbon-carbon bond-forming reaction between an activated alkene and a carbon electrophile in the presence of a nucleophilic catalyst, such as a tertiary amine or phosphine.
The journal is published weekly, with the first issue on January 11, 2007. Like The Journal of Physical Chemistry A and B, it is published by the American Chemical Society. The journal is indexed in: Chemical Abstracts Service (CAS) and British Library. According to the Journal Citation Reports, the journal had a 2022 impact factor of 3.7. [1]
The Journal of Physical Chemistry Letters is a peer-reviewed scientific journal published by the American Chemical Society. The editor-in-chief is Gregory D. Scholes at Princeton University. The Journal of Physical Chemistry Letters covers research on all aspects of physical chemistry. George C. Schatz was editor-in-chief from 2010 to 2019.
The benzilic acid rearrangement is formally the 1,2-rearrangement of 1,2-diketones to form α-hydroxy–carboxylic acids using a base. This reaction receives its name from the reaction of benzil with potassium hydroxide to form benzilic acid. First performed by Justus von Liebig in 1838, [1] it is the first reported example of a rearrangement ...
From an ISO 4 abbreviation: This is a redirect from an ISO 4 publication title abbreviation to the unabbreviated publication title, or an article containing information about the publication.