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...047084289X.ra026|chapter=Acetyl Cyanide|title=Encyclopedia of Reagents for Organic Synthesis|year=2001|last1=Morris|first1=Joel|isbn=0471936235}}</ref> ...[[carboxylate]]:<ref>{{cite journal |doi=10.1002/anie.198200361|title=The Chemistry of Acyl Cyanides|year=1982|last1=Hünig|first1=Siegfried|last2=Schaller|firs ...

|Type = Organic redox reaction The '''Fukuyama reduction''' is an [[organic reaction]] and an [[organic reduction]] in which a [[thioester]] is reduced to an [[aldehyde]] by a [[s ...

...ntheses| volume = 64| pages = 127| year = 1986}}</ref> Other reagents used for alpha-hydroxylation via enol or enolate structures include [[Davis oxazirid ...ha;-hydroxycarbonyl compounds from enolates|journal=The Journal of Organic Chemistry|volume=43|issue=2|pages=188–196|doi=10.1021/jo00396a002|issn=0022-3263}}</r ...

...apter=Darzens Halogenation |title=Comprehensive Organic Name Reactions and Reagents |date=2010 |pages=846–847 |isbn=9780471704508 }}</ref> ...compared to the usual halogenation protocol makes this reaction effective for a wide range of alcohols including those that are difficult to halogenate, ...

In [[organic chemistry]], '''methylenation''' is a [[chemical reaction]] that inserts a [[Methylen ...//pubs.acs.org/doi/abs/10.1021/jo01084a635 |journal=The Journal of Organic Chemistry |language=en |volume=24 |issue=2 |pages=264–265 |doi=10.1021/jo01084a635 |i ...

...ite book|last1=Trost|first1=B.M.|last2=Li|first2=C.-J.|title=Modern Alkyne Chemistry: Catalytic and Atom‐Economic Transformations|date=2014|publisher=Wiley VCH| The reaction proceeds with retention of the [[triple bond]]. For aldehydes and unsymmetrical ketones, the product is [[chiral]], hence there ...

{{Short description|Japanese organic chemist}} |field = [[Organic chemistry]] [[Organometallic chemistry]] ...

...nol|alcohol]], [[acetonitrile]], [[dimethylformamide]] and most of polar [[organic solvents]] ...sodium trifluoroacetate|issue=6|pages=937–940|journal=Journal of Fluorine Chemistry|volume=126|doi=10.1016/j.jfluchem.2005.04.012|date=June 2005|last1=Chang|fi ...

...ents including, [[benzene]]. It is a [[reagent]] used in the synthesis of organic and inorganic triflates. ...]/[[tetrachloromethane]] or [[Diethyl ether|ether]]/[[tetrachloromethane]] for purification. ...

...year=2010|pmid=20877810 }}</ref> limits practical application in [[organic chemistry]].<ref>C. Elschenbroich, A. Salzer ''Organometallics : A Concise Introducti ...[[organolithium compound|organolithium]] or [[Grignard reaction|Grignard]] reagents to give compounds of the form R₃Sb: ...

...ilic reactivity]], as defined by relative rate constants, with the [[Base (chemistry)|basicity]] of the nucleophile (relative to protons) and its [[polarizabili where k_b is the rate constant for nitramide decomposition by a base (B) and β_N is a parameter of t ...

...assified according to the relative location of the two thiol groups on the organic backbone. ...mercaprol.svg|[[Dimercaprol]] ("British anti-Lewisite"), an early antidote for arsenic poisoning ...

...thor3=Joseph W. Ziller |name-list-style=amp |year=1995 |title=Coordination Chemistry of Samarium Diiodide with Ethers Including the Crystal Structure of Tetrahy ...arris |author3=André B. Charette|encyclopedia=Encyclopedia of Reagents for Organic Synthesis |year=2005 |doi=10.1002/047084289X.rs004.pub2|isbn=0471936235}}</ ...

...60052a001}}</ref><ref>Chakrabartty, in Trahanovsky, ''Oxidation in Organic Chemistry'', pp. 343–370, Academic Press, New York, '''1978'''</ref> The reaction can Substrates are broadly limited to methyl ketones and secondary [[Alcohol (chemistry)|alcohol]]s oxidizable to methyl ketones, such as [[isopropanol]]. The only ...

{{Short description|Organic compound containing at least one covalent carbon-iodine bond}} ...nes are organoiodine compounds that are required for health and the reason for government-mandated [[iodized salt|iodization]] of salt. ...

...te]] of the metal remain unchanged.<ref name="Brown">{{cite book|title=The chemistry of the metal-carbon bond, vol. 2|year=1985|publisher=John Wiley & Sons|auth ...idth=300|caption=Examples of type 1,1 (a) and 1,2 (b) resulting geometries for insertion reactions ...

...]]s.<ref>{{Cite encyclopedia|encyclopedia = [[Encyclopedia of Reagents for Organic Synthesis]]|last1 = Little|first1 = Sarah|last2 = Trice|first2 = Jane|title The reaction of [[boron trichloride]] with [[alcohol (chemistry)|alcohol]]s was reported in 1931, and was used to prepare dimethoxyboron ch ...

....wiley.com/doi/10.1002/047084289X.rl141 |work=Encyclopedia of Reagents for Organic Synthesis |editor-last=John Wiley & Sons, Ltd |access-date=2023-11-18 |plac ...3 |title=Trapping Lithium Selenides with Evolving Heterogeneous Interfaces for High‐Power Lithium‐Ion Capacitors |url=https://onlinelibrary.wiley.com/doi/ ...

...small group of chemists, the anion is abbreviated as TFPB otherwise, short for '''T'''etrakis[3,5-bis(tri'''F'''luoromethyl)'''P'''henyl]'''B'''orate.<ref ...one]]s.<ref name = catalyst>{{cite journal|title = Palladium(II) catalysts for living alternating copolymerization of olefins and carbon monoxide|first1 = ...

...n]]).<ref>Ham, Peter "Zinc amalgam" in e-EROS Encyclopedia of Reagents for Organic Synthesis (2001). {{doi|10.1002/047084289X.rz003}}</ref> It is the reducing agent in the [[Jones reductor]], used in analytical chemistry. Formerly the zinc plates of dry [[battery (electric)|batteries]] were amal ...