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Scott E. Denmark
Scott Eric Denmark is an American chemist who is the Reynold C. Fuson Professor of Chemistry at the University of Illinois at Urbana-Champaign (UIUC). Denmark received an S.B. degree from MIT in 1975 and the D.Sc.Tech. degree from ETH Zurich in 1980, under the supervision of Professor Albert Eschenmoser. He joined the faculty at UIUC the same year and became an associate professor in 1986, full professor in 1987, and was named the Fuson Professor of Chemistry in 1991. He served as the president and editor-in-chief of the ''Organic Reactions'' book series between 2008 and 2018. In 2017, Denmark was elected to the American Academy of Arts and Sciences. In 2018, he was elected to the National Academy of Sciences. Early life and education Denmark was born in Lynbrook, New York in 1953. He attended MIT as an undergraduate and during his studies he was involved in research with both Richard H. Holm on ferredoxin analogs and Daniel S. Kemp on functionalized cyclophanes. He received ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
New York (state)
New York, also called New York State, is a U.S. state, state in the northeastern United States. Bordered by New England to the east, Canada to the north, and Pennsylvania and New Jersey to the south, its territory extends into both the Atlantic Ocean and the Great Lakes. New York is the List of U.S. states and territories by population, fourth-most populous state in the United States, with nearly 20 million residents, and the List of U.S. states and territories by area, 27th-largest state by area, with a total area of . New York has Geography of New York (state), a varied geography. The southeastern part of the state, known as Downstate New York, Downstate, encompasses New York City, the List of U.S. cities by population, most populous city in the United States; Long Island, with approximately 40% of the state's population, the nation's most populous island; and the cities, suburbs, and wealthy enclaves of the lower Hudson Valley. These areas are the center of the expansive New ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
ETH Zurich
ETH Zurich (; ) is a public university in Zurich, Switzerland. Founded in 1854 with the stated mission to educate engineers and scientists, the university focuses primarily on science, technology, engineering, and mathematics. ETH Zurich ranks among Europe's best universities. Like its sister institution École Polytechnique Fédérale de Lausanne, EPFL, ETH Zurich is part of the ETH Domain, Swiss Federal Institutes of Technology Domain, a consortium of universities and research institutes under the Swiss Federal Department of Economic Affairs, Education and Research. , ETH Zurich enrolled 25,380 students from over 120 countries, of which 4,425 were pursuing doctoral degrees. Students, faculty, and researchers affiliated with ETH Zurich include 22 Nobel Prize, Nobel laureates, two Fields Medalists, three Pritzker Architecture Prize, Pritzker Prize winners, and one Turing Award, Turing Award recipient, including Albert Einstein and John von Neumann. It is a founding member o ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phase-transfer Catalyst
In chemistry, a phase-transfer catalyst or PTC is a catalyst that facilitates the Phase transition, transition of a reactant from one phase (matter), phase into another phase where reaction occurs. Phase-transfer catalysis is a special form of catalysis and can act through homogeneous catalysis or heterogeneous catalysis methods depending on the catalyst used. Ionic compound, Ionic reactants are often soluble in an aqueous phase but insoluble in an organic phase in the absence of the phase-transfer catalyst. The catalyst functions like a detergent for solubilizing the salts into the organic phase. Phase-transfer catalysis refers to the acceleration of the reaction upon the addition of the phase-transfer catalyst. PTC is widely exploited industrially.Marc Halpern "Phase-Transfer Catalysis" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. Polyesters for example are prepared from acyl chlorides and Bisphenol A, bisphenol-A. Phosphothioate-based pesticides a ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Aldol Reaction
The aldol reaction (aldol addition) is a Chemical reaction, reaction in organic chemistry that combines two Carbonyl group, 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 Enolate, enolized ketone to another: These products are known as ''aldols'', from the ''ald''ehyde + alcoh''ol'', a structural motif seen in many of the products. The use of aldehyde in the name comes from its history: aldehydes are more reactive than ketones, so that the reaction was discovered first with them. The aldol reaction is paradigmatic in organic chemistry and one of the most common means of forming carbon–carbon bonds in organic chemistry. It lends its name to the family of aldol reactions and similar techniques analyze a whole family of carbonyl α-substitution reactions, as well as the Claisen condensation, diketone condensations. Scope Aldol structural units are found in many importa ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Nitroalkene
A nitroalkene, or nitro olefin, is a functional group combining the functionality of its constituent parts, an alkene and nitro group, while displaying its own chemical properties through polar effect, alkene activation, making the functional group useful in specialty reactions such as the Michael reaction or Diels-Alder additions. Synthesis Nitroalkenes are synthesized by various means, notable examples include: * Nitroaldol reactions such as the Henry reaction: : * Nitration of an alkene with nitryl iodide generated ''in-situ'' from silver nitrite and elemental iodine: * Direct nitration of alkenes with nitric oxide and an aluminum oxide catalyst in acidic conditions: *Direct nitration of alkenes with Clayfen (Iron(III) nitrate supported on Montmorillonite clay): * Dehydration of nitro-alcohols: Reactions Nitroalkenes are useful Precursor (chemistry), intermediates for various chemical functionalities. * A nitroalkene behaving as a Michael acceptor in the synthesis of Ly ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Frederick Stanley Kipping
(Frederic) Stanley Kipping FRS (16 August 1863 – 1 May 1949) was an English chemist. He undertook much of the pioneering work on silicon polymers and coined the term silicone. Life He was born in Salford, Lancashire, England, the son of James Kipping, a Bank of England official, and Julia Du Val, a daughter of painter Charles Allen Du Val. He was educated at Manchester Grammar School before enrolling in 1879 at Owens College (now Manchester University) for an external degree from the University of London. After working for the local gas company for a short time he went in 1886 to Germany to work under William Henry Perkin, Jr. in the laboratories of Adolf von Baeyer at Munich University. Back in England, he took a position as demonstrator for Perkin, who had been appointed professor at Heriot-Watt College, Edinburgh. In 1890, Kipping was appointed chief demonstrator in chemistry for the City and Guilds of London Institute, where he worked for the chemist Henry Edward Armst ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Claisen Rearrangement
The Claisen rearrangement is a powerful carbon–carbon chemical bond, bond-forming chemical reaction discovered by Rainer Ludwig Claisen. The heating of an allyl Vinyl group, vinyl ether will initiate a Sigmatropic reaction, [3,3]-sigmatropic rearrangement to give a γ,δ-unsaturated carbonyl, driven by exergonically favored carbonyl CO bond formation with Δ(Δf''H'') ca. . Mechanism The Claisen rearrangement is an exothermic, concerted (bond cleavage and recombination) pericyclic reaction. Woodward–Hoffmann rules show a suprafacial, stereospecific reaction pathway. The kinetics are of the first order and the whole transformation proceeds through a highly ordered cyclic transition state and is intramolecular. Crossover experiment (chemistry), Crossover experiments eliminate the possibility of the rearrangement occurring via an intermolecular reaction mechanism and are consistent with an intramolecular process. There are substantial solvent effects observed in the Claisen ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Nazarov Cyclization Reaction
The Nazarov cyclization reaction (often referred to as simply the Nazarov cyclization) is a chemical reaction used in organic chemistry for the synthesis of cyclopentenones. The reaction is typically divided into ''classical'' and ''modern'' variants, depending on the reagents and substrate (chemistry), substrates employed. It was originally discovered by Ivan Nikolaevich Nazarov (1906–1957) in 1941 while studying the rearrangements of allyl vinyl ketones. As originally described, the Nazarov cyclization involves the activation of a divinyl ketone using a stoichiometric Lewis acid or protic acid promoter. The key step of the reaction mechanism involves a cationic 4π-electrocyclic reaction, electrocyclic ring closure which forms the cyclopentenone product (See Nazarov cyclization reaction#Mechanism, Mechanism below). As the reaction has been developed, variants involving substrates other than divinyl ketones and promoters other than Lewis acids have been subsumed under the nam ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclophane
In organic chemistry, a cyclophane is a hydrocarbon consisting of an aromatic unit (typically a benzene ring) and a Catenation, chain that forms a bridge (chemical), bridge between two non-adjacent positions of the aromatic ring. More complex derivatives with multiple aromatic units and bridges forming cagelike structures are also known. Cyclophanes are well-studied examples of Strain (chemistry), strained organic compounds. [n]-Cyclophanes Structures Paracyclophanes adopt the boat conformation normally observed in cyclohexanes. Smaller value of n lead to greater distortions. X-ray crystallography on '[6]paracyclophane' shows that the aromatic bridgehead carbon atom makes an angle of 20.5° with the plane. The benzyl carbons deviate by another 20.2°. The carbon-to-carbon bond length alternation has increased from 0 for benzene to 39 picometer, pm. Despite their distorted structures, cyclophanes retain their aromaticity, as determined by UV-vis spectroscopy. Reactivity With re ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Daniel S
Daniel commonly refers to: * Daniel (given name), a masculine given name and a surname * List of people named Daniel * List of people with surname Daniel * Daniel (biblical figure) * Book of Daniel, a biblical apocalypse, "an account of the activities and visions of Daniel" Daniel may also refer to: Arts and entertainment Literature * ''Daniel'' (Old English poem), an adaptation of the Book of Daniel * ''Daniel'', a 2006 novel by Richard Adams * ''Daniel'' (Mankell novel), 2007 Music * "Daniel" (Bat for Lashes song) (2009) * "Daniel" (Elton John song) (1973) * "Daniel", a song from '' Beautiful Creature'' by Juliana Hatfield * ''Daniel'' (album), a 2024 album by Real Estate Other arts and entertainment * ''Daniel'' (1983 film), by Sidney Lumet * ''Daniel'' (2019 film), a Danish film * Daniel (comics), a character in the ''Endless'' series Businesses * Daniel (department store), in the United Kingdom * H & R Daniel, a producer of English porcelain between 1827 and ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ferredoxin
Ferredoxins (from Latin ''ferrum'': iron + redox, often abbreviated "fd") are iron–sulfur proteins that mediate electron transfer in a range of metabolic reactions. The term "ferredoxin" was coined by D.C. Wharton of the DuPont Co. and applied to the "iron protein" first purified in 1962 by Mortenson, Valentine, and Carnahan from the anaerobic organism, anaerobic bacterium ''Clostridium pasteurianum''. Another redox protein, isolated from spinach chloroplasts, was termed "chloroplast ferredoxin". The chloroplast ferredoxin is involved in both cyclic and non-cyclic photophosphorylation reactions of photosynthesis. In non-cyclic photophosphorylation, ferredoxin is the last electron acceptor thus reducing the enzyme NADP+ reductase. It accepts electrons produced from sunlight-Electron excitation, excited chlorophyll and transfers them to the enzyme ferredoxin: NADP+ oxidoreductase . Ferredoxins are small proteins containing iron and sulfur atoms organized as iron–sulfur clusters ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Richard H
Richard is a male given name. It originates, via Old French, from Old Frankish and is a compound of the words descending from Proto-Germanic language">Proto-Germanic ''*rīk-'' 'ruler, leader, king' and ''*hardu-'' 'strong, brave, hardy', and it therefore means 'strong in rule'. Nicknames include " Richie", " Dick", " Dickon", " Dickie", " Rich", " Rick", "Rico (name), Rico", " Ricky", and more. Richard is a common English (the name was introduced into England by the Normans), German and French male name. It's also used in many more languages, particularly Germanic, such as Norwegian, Danish, Swedish, Icelandic, and Dutch, as well as other languages including Irish, Scottish, Welsh and Finnish. Richard is cognate with variants of the name in other European languages, such as the Swedish "Rickard", the Portuguese and Spanish "Ricardo" and the Italian "Riccardo" (see comprehensive variant list below). People named Richard Multiple people with the same name * Richard Ander ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
