Wulff–Dötz reaction
The Wulff–Dötz reaction (also known as the Dötz reaction or the benzannulation reaction of the Fischer carbene complexes) is the chemical reaction of an aromatic or vinylic alkoxy pentacarbonyl chromium carbene complex with an alkyne and carbon monoxide to give a Cr(CO)3-coordinated substituted phenol.[1][2][3] Several reviews have been published.[4][5][6] It is named after the German chemist Karl Heinz Dötz (b. 1943) and the American chemist William D. Wulff (b. 1949) at Michigan State University.[7] The reaction was first discovered by Karl Dötz and was extensively developed by his group and W. Wulff's group. They subsequently share the name of the reaction.
The position of the substituents is highly predictable with the largest alkyne substituent (RL) neighboring the phenol and the smallest alkyne substituent (RS) neighboring the methoxy group .[8][9] Hence, this reaction is more useful for terminal alkynes than internal alkynes.
The phenol can be liberated from the chromium complex by a mild oxidation, such as ceric ammonium nitrate or air oxidation.
Since this reaction can quickly generate complex phenolic compounds, the Wulff–Dötz reaction has been used most often in the synthesis of natural products, especially Vitamins E and K.[10][11]

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Wulff–Dötz reaction - Wikipedia, the free encyclopedia
The Wulff–Dötz reaction (also known as the Dötz reaction or the benzannulation reaction of the Fischer carbene complexes) is the chemical reaction of an ...
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Wulff-Dötz Reaction - SynArchive
Mechanism, references and reaction samples of the Wulff-Dötz Reaction.
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I. Benzannulation Reaction - Chemistry
This is a truly amazing reaction that was discovered by Karl Heinz Dötz and ... [1] For recent citations to the literature, see: Wang, H.; Wulff, W. D.; Rheingold, A. L. ...
www2.chemistry.msu.edu/faculty/wulff/myweb26/research/benzannulation.htm
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ウルフ・デッツ反応 Wulff-Dotz Reaction | Chem-Station (ケムステ)
Wulff-Dotz Reaction. 価格¥ 5,894(2015/04/11 07:41時点); 出版日2011/01/22; Perfect76ページ; ISBN-106134840769; ISBN-139786134840767; 出版社 Betascript ...
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“Dötz Benzannulation”. In: Comprehensive Organic Name Reactions ...
This reaction was initially reported by Dötz in 1975.1 It is a thermal reaction .... J. M.; Wulff, W. D.; Fumo, M. J.; Grant, E. G.; Heller, D. P.; Whitcomb, M. C. and ...
onlinelibrary.wiley.com/doi/10.1002/9780470638859.conrr200/pdf
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22 Jan 2006 ... Yiqian Lian and William D. Wulff ... recent review: K. H. Dötz et al. Chem. Soc. ... Dötz reaction leads to 1,4 relation of the two oxygen atoms.
ccc.chem.pitt.edu/wipf/Current%20Literature/Markus_2.pdf
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The Wulff–Dötz reaction is the chemical reaction of an aromatic or vinylic alkoxy pentacarbonyl chromium carbene complex with an alkyne and carbon mon...
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Wulff-Dötz reaction - Rediff Pages - Rediff.com
The Wulff-Dötz reaction (also known as the Dötz reaction or the benzannulation reaction of the Fischer carbene complexes) is the chemical reaction of an ...
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Dötz reaction | World Heritage Encyclopedia - Hawaii eBook Library
The Wulff–Dötz reaction (also known as the Dötz reaction or the benzannulation reaction of the Fischer carbene complexes) is the chemical reaction of an ...
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Wulff–Dötz reaction - Wikipedia, the free encyclopedia
The Wulff–Dötz reaction (also known as the Dötz reaction or the benzannulation reaction of the Fischer carbene ... Wulff (b. 1949) at Michigan State University.
Wulff-Dötz Reaction - SynArchive
Mechanism, references and reaction samples of the Wulff-Dötz Reaction.
Wulff-Dötz reaction - Rediff Pages - Rediff.com
It is named after the German chemist Karl Heinz Dötz (b. 1943) and the American chemist William D. Wulff (b. 1949) at Michigan State University. The reaction ...
I. Benzannulation Reaction - Chemistry
This is a truly amazing reaction that was discovered by Karl Heinz Dötz and ... [1] For recent citations to the literature, see: Wang, H.; Wulff, W. D.; Rheingold, A. L. ...
Dötz reaction - Javascript Version
It is named after the German chemist Karl Heinz Dötz (b. 1943) and the American chemist William D. Wulff (b. 1949) at Michigan State University. The reaction ...
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It is named after the German chemist Karl Heinz Dötz (b. 1943) and the American chemist William D. Wulff (b. 1949) at Michigan State University. The reaction ...
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It is named after the German chemist Karl Heinz Dötz (b. 1943) and the American chemist William D. Wulff (b. 1949) at Michigan State University. The reaction ...
Books on the term Wulff–Dötz reaction
Wulff-Dotz Reaction
Lambert M Surhone, Mariam T Tennoe, Susan F Henssonow, 2011
The reaction was first discovered by Karl Dotz and was extensively developed by his group and W. Wulff's group. They subsequently share the name of the reaction.
Blood Reaction A Vampire Novel
Blood Reaction A Vampire Novel
DL Atha, 2011
Annalice, a single mother and physician, is ready to immerse herself in the mundane chores of her farm as a diversion from her hectic professional life. But she becomes the victim of a home invasion, the supernatural kind. Vindictive and cruel, Asa, a century old vampire, takes brutal control of her life and home.Forcing her to strike a bargain in ...
Name Reactions: A Collection of Detailed Mechanisms and ...
Jie Jack Li, 2014
Dötz, K. H. Angew. Chem. Int. Ed. 1975, 14, 644645. Karl H. Dötz (1943) was a professor at the University of Munich in Germany. 2. Wulff, W. D. In Advances in Metal-Organic Chemistry; Liebeskind, L. S., Ed.; JAI Press, Greenwich, CT; 1989;  ...
Mass Spectrometry Studies of Fischer Carbenes and Traceless ...
Keith A. Korthals, 2007
CHAPTER TWO AXIAL AND PLANAR INTERACTIONS IN RELATION TO THE WULFF-DOTZ BENZANNULATION REACTION We are interested in the construction of axial and planar diastereomers such as those shown in Scheme 2.8.
Reaction (Reflection Series)
Reaction (Reflection Series)
Jessica Roberts, 2012
Harmony… I’ve previously had that in my life, but only once, briefly, a while ago. It was during the time I’d started my first year of college. My own apartment, a new old car, and a life free of deadbeat stepfathers, all of which was fulfilling enough. But if it wasn’t, I also had a best friend, soul mate, and boyfriend all in one. Yes, life was n...
Transition-Metal-Med... Aromatic Ring Construction
Transition-Metal-Med... Aromatic Ring Construction
Ken Tanaka, 2013
State-of-the-science methods, synthetic routes, and strategies to construct aromatic ringsThe development of new reactions for the synthesis of aromatic compounds is a highly active research area in organic synthesis, providing new functional organic materials, functional reagents, and biologically active compounds. Recently, significant advances i...
Name Reactions for Carbocyclic Ring Formations
Jie Jack Li, 2010
6 The DBR has been extensively developed by Dotz and William D. Wulff, and is often reffered to as the Wulff-Dotz reaction. 4. 8.3 Mechanism Rs%RL | 8-:--_RL Cr(CO)4 R1 \ x R2 1 11 12 Cr(CO)5 _CO R2 +co R2 (OC)3Cr RL (OC)3Cr R|_ ...
Metal Carbenes in Organic Synthesis (Topics in Organometallic Chemistry)
Metal Carbenes in Organic Synthesis (Topics in Organometallic Chemistry)
Karl Heinz Dötz, 2013
Metal carbene complexes have made their way from organometallic curiosities to valuable reagents and catalysts. They offer novel synthetic opportunities in carbon carbon bond formation based on either carbene-centered reactions or on metal-templated processes which makes them indispensable in modern synthetic methodology. The most prominent metal c...
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A diastereoselective synthesis of an arene chromiumtricarbonyl complex via a Dötz reaction
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Kuldeep's Blog: Reactions
This is a list of Named / Unnamed Reactions and Links to various websites 0-9 * 1,3-dipolar cycloaddition A * Abramovitch-Shapiro tryptamine synthesis * Acetoacetic ester condensation * Achmatowicz reaction * Acyloin condensation * Adams catalyst * Adkins catalyst * Adkins-Peterson reaction * Akabori amino acid reaction * Alder ene reaction * Alder-Stein rules * Aldol addition * Aldol condensation * Algar-Flynn-Oyamada reaction * Allan-Robinson reaction * Allylic rearrangement * Amadori rearrangement * Angeli-Rimini reaction * Andrussov oxidation * Appel reaction * Arbuzov reaction, Arbusow reaction * Arens-van Dorp synthesis, Isler modification * Arndt-Eistert synthesis * Auwers synthesis * Azo coupling B * Baeyer-Drewson indigo synthesis * Baeyer-Villiger oxidation * Baeyer-Villiger rearrangement * Bakeland process (Bakelite) * Baker-Venkataraman rearrangement * Baker-Venkataraman transformation * Bally-Scholl synthesis * Balz-Schiemann reaction * Bamberger rearrangement * Bamberger triazine synthesis * Bamford-Stevens reaction * Barbier-Wieland degradation * Bardhan-Senguph phenanthrene synthesis * Bartoli indole synthesis * Bartoli reaction * Barton reaction * Barton-Kellogg reaction * Barton-McCombie reaction, Barton deoxygenation * Baudisch reaction * Bayer test * Baylis-Hillman reaction * Bechamp reaction * Bechamp reduction * Beckmann fragmentation * Beckmann rearrangement * Bellus-Claisen rearrangement * Belousov-Zhabotinsky reaction * Benary reaction * Benzidine rearrangement * Benzilic acid rearrangement * Benzoin condensation * Bergman cyclization * Bergmann azlactone peptide synthesis * Bergmann degradation * Bergmann-Zervas carbobenzoxy method * Bernthsen acridine synthesis * Bestmann's reagent * Betti reaction * Biginelli pyrimidine synthesis * Biginelli reaction * Birch reduction * Bischler-Möhlau indole synthesis * Bischler-Napieralski reaction * Blaise ketone synthesis * Blaise reaction * Blanc reaction * Blanc chloromethylation * Bodroux reaction * Bodroux-Chichibabin aldehyde synthesis * Bogert-Cook synthesis * Bohn-Schmidt reaction * Boord olefin synthesis * Borodin reaction * Borsche-Drechsel cyclization * Bosch-Meiser urea process * Bouveault aldehyde synthesis * Bouveault-Blanc reduction * Boyland-Sims oxidation * Boyer Reaction * Bredt's rule * Brown hydroboration * Bucherer carbazole synthesis * Bucherer reaction * Bucherer–Bergs reaction * Buchner ring enlargement * Buchner-Curtius-Schlotterbeck reaction * Buchwald-Hartwig amination * Bunnett reaction C * Cadiot-Chodkiewicz coupling * Camps quinoline synthesis * Cannizzaro reaction * Carroll reaction * Catalytic reforming * CBS reduction * Chan-Lam coupling * Chapman rearrangement * Chichibabin pyridine synthesis * Chichibabin reaction * Chugaev elimination * Ciamician-Dennstedt rearrangement * Claisen condensation * Claisen rearrangement * Claisen-Schmidt condensation * Clemmensen reduction * Collins-Reagent * Combes quinoline synthesis * Conia reaction * Conrad-Limpach synthesis * Corey-Gilman-Ganem oxidation * Cook-Heilbron thiazole synthesis * Cope elimination * Cope rearrangement * Corey reagent * Corey-Bakshi-Shibata reduction * Corey-Fuchs reaction * Corey-Kim oxidation * Corey-Posner, Whitesides-House reaction * Corey-Winter olefin synthesis * Corey-Winter reaction * Coupling reaction * Craig method * Cram's rule of asymmetric induction * Creighton process * Criegee reaction * Criegee rearrangement * Cross metathesis * Crum Brown-Gibson rule * Curtius degradation * Curtius rearrangement, Curtius reaction D * Dakin reaction * Dakin-West reaction * Danheiser Annulation * Darapsky degradation * Darzens condensation, Darzens-Claisen reaction, Glycidic ester condensation * Darzens synthesis of unsaturated ketones * Darzens tetralin synthesis * Delepine reaction * Demjanov rearrangement * Demjanow desamination * Dess-Martin oxidation * Diazotisation * DIBAL-H selective reduction * Dieckmann condensation * Dieckmann reaction * Diels-Alder reaction * Diels Reese reaction * Dienol benzene rearrangement * Dienone phenol rearrangement * Dimroth rearrangement * Di-pi-methane rearrangement * Directed ortho metalation * Doebner modification * Doebner reaction * Doebner-Miller reaction, Beyer method for quinolines * Doering-LaFlamme carbon chain extension * Dötz reaction * Dowd-Beckwith ring expansion reaction * Duff reaction * Dutt-Wormall reaction E * E1cB elimination reaction * Eder reaction * Edman degradation * Eglinton reaction * Ehrlich-Sachs reaction * Einhorn variant * Einhorn-Brunner reaction * Elbs persulfate oxidation * Elbs reaction * Elimination reaction * Emde degradation * Emmert reaction * Ene reaction * Epoxidation * Erlenmeyer synthesis, Azlactone synthesis * Erlenmeyer-Plöchl azlactone and amino acid synthesis * Eschenmoser fragmentation * Eschweiler-Clarke reaction * Ester pyrolysis * Étard reaction * Evans aldol F * Favorskii reaction * Favorskii rearrangement * Favorskii-Babayan synthesis * Feist-Benary synthesis * Fenton reaction * Ferrario reaction * Ferrier carbocyclization * Ferrier rearrangement * Finkelstein reaction * Fischer indole synthesis * Fischer oxazole synthesis * Fischer peptide synthesis * Fischer phenylhydrazine and oxazone reaction * Fischer glycosidation * Fischer-Hepp rearrangement * Fischer-Speier esterification * Fischer Tropsch synthesis * Fleming-Tamao oxidation * Flood reaction * Forster reaction * Forster-Decker method * Franchimont reaction * Frankland synthesis * Frankland-Duppa reaction * Freund reaction * Friedel-Crafts Acylation * Friedel-Crafts Alkylation * Friedländer synthesis * Fries rearrangement * Fritsch-Buttenberg-Wiechell rearrangement * Fujimoto-Belleau reaction * Fukuyama coupling * Fukuyama indole synthesis G * Gabriel ethylenimine method * Gabriel synthesis * Gabriel-Colman rearrangement, Gabriel isoquinoline synthesis * Gallagher-Hollander degradation * Gassman indole synthesis * Gastaldi synthesis * Gattermann aldehyde synthesis * Gattermann Koch reaction * Gattermann reaction * Gewald reaction * Gibbs phthalic anhydride process * Gilman reagent * Glaser coupling * Glycol cleavage * Gogte synthesis * Gomberg-Bachmann reaction * Gomberg-Bachmann-Hey reaction * Gomberg-Free radical reaction * Gould-Jacobs reaction * Graebe-Ullmann synthesis * Grignard degradation * Grignard reaction * Grob fragmentation * Grubbs' catalyst in Olefin metathesis * Grundmann aldehyde synthesis * Gryszkiewicz-Trochimowski and McCombie method * Guareschi-Thorpe condensation * Guerbet reaction * Gutknecht pyrazine synthesis H * Haller-Bauer reaction * Haloform reaction * Hammett equation * Hammick reaction * Hammond-Principle or Hammond postulate * Hantzsch pyrrole synthesis * Hantzsch dihydropyridine synthesis, Hantzsch pyridine synthesis * Hantzsch Pyridine synthesis, Gattermann-Skita synthesis, Guareschi-Thorpe condensation, Knoevenagel-Fries modification * Hantzsch-Collidin-synthesis * Harber-Weiss reaction * Harries Ozonide reaction * Haworth Methylation * Haworth Phenanthrene synthesis * Haworth-reaction * Hay coupling * Hayashi rearrangement * Heck reaction * Helferich method * Hell-Volhard-Zelinsky halogenation * Hemetsberger indole synthesis * Hemetsberger-Knittel synthesis * Henkel reaction, Raecke process, Henkel process * Henry reaction, Kamlet reaction * Herz reaction, Herz compounds * Herzig-Meyer alkimide group determination * Heumann indigo synthesis * Hinsberg indole synthesis * Hinsberg oxindole synthesis * Hinsberg reaction * Hinsberg separation * Hinsberg sulfone synthesis * Hoch-Campbell ethylenimine synthesis * Hock rearrangement * Hofmann degradation, Exhaustive methylation * Hofmann Elimination * Hofmann Isonitrile synthesis, Carbylamine reaction * Hofmann produkt * Hofmann rearrangement * Hofmann-Löffler reaction, Löffler-Freytag reaction, Hofmann-Löffler-Freytag reaction * Hofmann-Martius rearrangement * Hofmann's Rule * Hofmann-Sand reaction * Homo rearrangement of steroids * Hooker reaction * Horner-Wadsworth-Emmons reaction * Hoesch reaction * Hosomi-Sakurai reaction * Houben-Fischer synthesis * Hunsdiecker reaction * Hydroboration * Hydrohalogenation I * Ing-Manske procedure * Ipso substitution * Ivanov reagent, Ivanov reaction J * Jacobsen rearrangement * Janovsky reaction * Japp-Klingemann reaction * Japp-Maitland condensation * Johnson-Claisen rearrangement * Jones oxidation * Jordan-Ullmann-Goldberg synthesis * Julia olefination * Julia-Lythgoe olefination K * Kabachnik–Fields reaction * Kiliani-Fischer synthesis * Kindler reaction * Kishner cyclopropane synthesis * Knoevenagel condensation * Knorr pyrazole synthesis * Knorr pyrrole synthesis * Knorr quinoline synthesis * Koch-Haaf reaction * Kochi reaction * Koenigs-Knorr reaction * Kolbe electrolysis * Kolbe-Schmitt reaction * Kornblum oxidation * Kornblum–DeLaMare rearrangement * Kowalski ester homologation * Krapcho decarboxylation * Kröhnke aldehyde synthesis * Kröhnke oxidation * Kröhnke pyridine synthesis * Kucherov reaction * Kuhn-Winterstein reaction * Kulinkovich reaction * Kumada coupling L * Larock indole synthesis * Lebedev process * Lehmstedt-Tanasescu reaction * Leimgruber-Batcho indole synthesis * Letts nitrile synthesis * Leuckart reaction * Leuckart thiophenol reaction * Leuckart-Wallach reaction * Leuckart amide synthesis * Levinstein process * Ley Oxidation * Lieben iodoform reaction, Haloform reaction * Liebeskind-Srogl coupling * Lindlar catalyst * Lobry-de Bruyn-van Ekenstein transformation * Lossen rearrangement * Luche reduction M * Madelung synthesis * Malaprade reaction, Periodic acid oxidation * Malonic ester synthesis * Mannich reaction * Markó-Lam deoxygenation * Markovnikov's rule, Markownikoff rule, Markownikow rule * Martinet dioxindole synthesis * McDougall monoprotection * McFadyen-Stevens reaction * McMurry reaction * Meerwein arylation * Meerwein-Ponndorf-Verley reduction * Meisenheimer rearrangement * Meissenheimer complex * Menshutkin reaction * Metal-ion-catalyzed σ-bond rearrangement * Mesylation * Merckwald asymmetric synthesis * Meyer and Hartmann reaction * Meyer reaction * Meyer synthesis * Meyer–Schuster rearrangement * Michael addition * Michael addition, Michael system * Michael condensation * Michaelis-Arbuzov reaction * Mignonac reaction * Milas hydroxylation of olefins * Mitsunobu reaction * Mukaiyama aldol addition * Mukaiyama reaction * Myers' asymmetric alkylation N * Nametkin rearrangement * Nazarov cyclization reaction * Neber rearrangement * Nef reaction * Negishi coupling * Negishi-Zipper reaction * Nenitzescu indole synthesis * Nenitzescu reductive acylation * Nicholas reaction * Niementowski quinazoline synthesis * Niementowski quinoline synthesis * Nierenstein reaction * Nitroaldol reaction * Normant reagents * Noyori asymmetric hydrogenation * Nozaki-Hiyama-Kishi Nickel/Chromium Coupling reaction * Nucleophilic acyl substitution O * Ohira–Bestmann reaction * Olefin metathesis * Oppenauer oxidation * Ostromyslenskii reaction, Ostromisslenskii reaction * Oxidative decarboxylation * Oxo synthesis * Oxy-Cope rearrangement * Oxymercuration * Ozonolysis P * Paal-Knorr pyrrole synthesis * Paal-Knorr synthesis * Paneth technique * Passerini reaction * Paterno-Büchi reaction * Pauson-Khand reaction * Pechmann condensation * Pechmann pyrazole synthesis * Pellizzari reaction * Pelouze synthesis * Perkin alicyclic synthesis * Perkin reaction * Perkin rearrangement * Perkow reaction * Petasis reaction * Petasis reagent * Peterson olefination * Peterson reaction * Petrenko-Kritschenko piperidone synthesis * Pfau-Plattner azulene synthesis * Pfitzinger reaction * Pfitzner-Moffatt oxidation * Pictet-Gams isoquinoline synthesis * Pictet-Hubert reaction * Pictet-Spengler tetrahydroisoquinoline synthesis * Pictet-Spengler reaction * Piloty-Robinson pyrrole synthesis * Pinacol coupling reaction * Pinacol rearrangement * Pinner amidine synthesis * Pinner method for ortho esters * Pinner reaction * Pinner triazine synthesis * Piria reaction * Pitzer strain * Polonovski reaction * Pomeranz-Fritsch reaction * Ponzio reaction * Prelog strain * Prevost reaction * Prileschajew reaction * Prilezhaev reaction * Prins reaction * Prinzbach synthesis * Pschorr reaction * Pummerer rearrangement * Purdie methylation, Irvine-Purdie methylation Q R * Ramberg-Backlund reaction * Raney-Nickel * Rap-Stoermer condensation * Raschig phenol process * Rauhut–Currier reaction * Reed reaction * Reformatskii reaction * Reilly-Hickinbottom rearrangement * Reimer-Tiemann reaction * Reissert indole synthesis * Reissert reaction, Reissert compound * Reppe synthesis * Retropinacol rearrangement * Riemschneider thiocarbamate synthesis * Riley oxidations * Ring closing metathesis * Ring opening metathesis * Ritter reaction * Robinson annulation * Robinson-Gabriel synthesis * Robinson Schopf reaction * Rosenmund reaction * Rosenmund reduction * Rosenmund-von Braun synthesis * Rothemund reaction * Rupe rearrangement * Rubottom oxidation * Ruff-Fenton degradation * Ruzicka large ring synthesis S * Sakurai reaction * Salol reaction * Sandheimer * Sandmeyer diphenylurea isatin synthesis * Sandmeyer isonitrosoacetanilide isatin synthesis * Sandmeyer reaction * Sanger reagent * Sarett oxidation * Saytzeff rule, Saytzeff's Rule * Schiemann reaction * Schlenk equilibrium * Schlosser modification * Schlosser variant * Schmidlin ketene synthesis * Schmidt degradation * Schmidt reaction * Scholl reaction * Schorigin Shorygin reaction, Shorygin reaction, Wanklyn reaction * Schotten-Baumann reaction * Semidine rearrangement * Semmler-Wolff reaction * Seyferth-Gilbert homologation * Shapiro reaction * Sharpless asymmetric dihydroxylation * Sharpless epoxidation * Sharpless oxyamination or aminohydroxylation * Simmons-Smith reaction * Simonini reaction * Simonis chromone cyclization * Skraup chinolin synthesis * Skraup reaction * Smiles rearrangement * SNAr nucleophilic aromatic substitution * SN1 * SN2 * SNi * Sommelet reaction * Sonn-Müller method * Sonogashira coupling * Sørensen formol titration * Staedel-Rugheimer pyrazine synthesis * Staudinger reaction * Stephen aldehyde synthesis * Stetter reaction * Stevens rearrangement * Stieglitz rearrangement * Stille coupling * Stobbe condensation * Stollé synthesis * Stork acylation * Stork enamine alkylation * Strecker amino acid synthesis * Strecker degradation * Strecker sulfite alkylation * Strecker synthesis * Suzuki coupling * Swain equation * Swarts reaction * Swern oxidation T * Tamao oxidation * Tafel rearrangement * Takai olefination * Tebbe olefination * ter Meer reaction * Thiele reaction * Thorpe reaction * Tiemann rearrangement * Tiffeneau ring enlargement reaction * Tiffeneau-Demjanow rearrangement * Tischtschenko reaction * Tishchenko reaction, Tischischenko-Claisen reaction * Tollens reagent * Trapp mixture * Traube purine synthesis * Truce-Smiles rearrangement * Tscherniac-Einhorn reaction * Tschitschibabin reaction * Tschugajeff reaction * Twitchell process * Tyrer sulfonation process U * Ugi reaction * Ullmann reaction * Upjohn dihydroxylation * Urech cyanohydrin method * Urech hydantoin synthesis V * Van Slyke determination * Varrentrapp reaction * Vilsmeier reaction * Vilsmeier-Haack reaction * Voight amination * Volhard-Erdmann cyclization * von Braun amide degradation * von Braun reaction * von Richter cinnoline synthesis * von Richter reaction W * Wacker-Tsuji oxidation * Wagner-Jauregg reaction * Wagner-Meerwein rearrangement * Walden inversion * Wallach rearrangement * Weerman degradation * Weinreb ketone synthesis * Wenker ring closure * Wenker synthesis * Wessely-Moser rearrangement * Westphalen-Lettré rearrangement * Wharton reaction * Whiting reaction * Wichterle reaction * Widman-Stoermer synthesis * Wilkinson catalyst * Willgerodt rearrangement * Willgerodt-Kindler reaction * Williamson ether synthesis * Winstein reaction * Wittig reaction * Wittig rearrangement * Wittig-Horner reaction * Wohl degradation * Wohl-Aue reaction * Wohler synthesis * Wohl-Ziegler reaction * Wolffenstein-Böters reaction * Wolff rearrangement * Wolff-Kishner reduction * Woodward cis-hydroxylation * Woodward-Hoffmann rule * Wulff-Dötz reaction * Wurtz coupling, Wurtz reaction * Wurtz-Fittig reaction Y * Yamaguchi esterification Z * Zeisel determination * Zerevitinov determination, Zerewitinoff determination * Ziegler condensation * Ziegler method * Zimmermann reaction * Zincke disulfide cleavage * Zinke nitration * Zincke reaction * Zincke-Suhl reaction.
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