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Journal of the Chemical Society C: Organic (1966–1971) Journal of the Chemical Society D: Chemical Communications (1969–1971) From 1972 until 1996 Journal of the Chemical Society, Dalton Transactions (1972–1996) (formerly J. Chem. Soc. A) Journal of the Chemical Society, Faraday Transactions (1972–1989) (formerly J. Chem. Soc. B)
The Journal of the American Chemical Society (also known as JACS) is a weekly peer-reviewed scientific journal that was established in 1879 by the American Chemical Society. [1] The journal has absorbed two other publications in its history, the Journal of Analytical and Applied Chemistry (July 1893) and the American Chemical Journal (January ...
The journal began its publication in 1905 as Transactions of the Faraday Society.When the society merged with the other chemistry societies of the United Kingdom to form the Royal Society of Chemistry, the publication of the journal was transferred to the Chemical Society in 1972 as part of the merger negotiations.
In 1874, a group of American chemists gathered at the Joseph Priestley House to mark the 100th anniversary of Priestley's discovery of oxygen.Although there was an American scientific society at that time (the American Association for the Advancement of Science, founded in 1848), the growth of chemistry in the U.S. prompted those assembled to consider founding a new society that would focus ...
In organic chemistry, the oxy-Cope rearrangement is a chemical reaction.It involves reorganization of the skeleton of certain unsaturated alcohols. It is a variation of the Cope rearrangement in which 1,5-dien-3-ols are converted to unsaturated carbonyl compounds by a mechanism typical for such a [3,3]-sigmatropic rearrangement.
Chemical Society Reviews is a biweekly peer-reviewed scientific journal published by the Royal Society of Chemistry, for review articles on topics of current interest in chemistry. Its predecessors were Quarterly Reviews, Chemical Society (1947–1971) and Royal Institute of Chemistry, Reviews (1968–1971); it maintained its current title ...
A notable variant of the Huisgen 1,3-dipolar cycloaddition is the copper(I) catalyzed variant, no longer a true concerted cycloaddition, in which organic azides and terminal alkynes are united to afford 1,4-regioisomers of 1,2,3-triazoles as sole products (substitution at positions 1' and 4' as shown above).
Ketene cycloadditions proceed by a concerted, [2+2] cycloaddition mechanism. Ketenes, unlike most alkenes, can align antarafacially with respect to other alkenes. Thus, the suprafacial- antarafacial geometry required for concerted, thermal [2+2] cycloaddition can be achieved in reactions of ketenes. [4]