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einem, isomeren, methyl, octahydro, indolizin, 19375300106, harms, xxvi, isochinolin, entstehenden, 19365250107, 525, xxv, hydrazo, verbindungen, 157, 19355190113, 147, kech, xxiv, 146, 19355190112, 140, möller, xxiii, stilbazol, dicarbonester, 19355160104, 516, friedrichsen, xxii, c4o3, ihre, eignung, ein, neues, prinzip, dihydro, 155, 19345130109, xxi, verlauf, methylalkoholischer, lösung, 19345130108, 129, hydrazobenzol, 182, 19345110114, 168, 511, xix, primärprodukte, bei, 128, 19345100106, 510, 1933, xviii, chinolizins, indolizins, pseudolupinins, 150, 19335050109, 505, xvii, isochinolins, 19324980103, xvi, pyrazole, 19324980102, 294, 19314900113, 277, xiv, 276, 19314900112, 267, xiii, cumaline, 266, 19314900111, furans, 19314900110, cyclopentadiens, cyclo, hexadiens, butadiens, 242, 19314900109, 236, pyrrol, seinen, homologen, 225, 19314860112, 211, camphenilons, santens, 210, 19314860111, viii, anthracens, forme, 19314860110, 191, 1930, harren, ernst, petersen, 154, 19304780109, 137, 478, gerhard, stein, partiell, hydrierte, naphtho, anthrachinone, wasserstoff, bzw, stellung, winckler, 2372, 19290620872, 2337, tetrahydro, phthalsäure, stellungnahme, farmer, warren, eigenschaften, konjugierter, 2090, 19290620830, maleinsäure, anhydrid, arylierte, triene, fulvene, 19290620829, 2081, iii, terpenen, camphern, heterocyclischen, systemen, herren, wolfgang, lübbert, erich, naujoks, karl, röhl, harro, segeberg, 19294700106, 470, 562, 19290620318, anlagerungen, kohlenwasserstoffen, 19284600106, 460, behr, arno, homogeneous, 3527306732, 14356007, a18_215, minami, atsushi, oikawa, hideaki, 506, 30482282, 27301662, 500, antibiotics, advances, alderases, fluegel, lucas, 2444, 33492939, 8008985, chemrev, 0c00825, 2413, 121, rev, generation, cycloisomerization, tethered, triynes, baire, niu, willoughby, woods, 7419, 212, 23060191, 3538845, nature11518, 2012natur, 208h, 208, ahrendt, borths, macmillan, organocatalytic, 4244, ja000092s, 2000jachs, 4243a, 4243, versatile, 335, 10891050, ar960062n, 325, ryu, 2003, triflimide, 6390, 12785777, ja035393r, 6388, 125, shibata, lee, triflic, 3809, 11942799, ja025848x, 3808, loh, application, design, 8967, ja00023a066, 8966c, 8966, chapman, bisaha, acyloxazolidinones, 1256, ja00212a037, 1238e, 1238, james, shaw, subrata, diaminobicyclo, octane, scaffold, salen, 21462988, ol2007378, 2488, lett, tiekink, eveline, 5283, 239089361, 2066, 241097, ejoc, 202101107, 5275, hansen, yoshisada, ryoji, filippov, dmitri, marel, gijsbert, codée, jeroen, 3573, 33538169, 7901664, joc, 0c02955, 3565, openings, oxide, brinkhuis, francine, 1174, 32012430, 7187256, asia, 202000009, 1167, asian, alkali, cations, 1981, 232337915, 33759502, 1871, a0090b38, 9ab8, 4c32, 9d9a, b3d5de4e5ed3, 1c00016, 20106, 34499069, 8457343, d1cp02456f, 2021pccp, 2320095v
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t 38 1 1195 1203 doi 10 1002 cber 190503801220 issn 1099 0682 staudinger hermann 1912 die ketene in german stuttgart f enke p 58 v euler h josephson k o 1920 über kondensationen an doppelbindungen i über die kondensation von isopren mit benzochinon pdf berichte der deutschen chemischen gesellschaft a and b series 53 5 822 826 doi 10 1002 cber 19200530517 issn 1099 0682 albrecht w 1902 über cyclopentadiënchinone kondensationsversuche mit diphenylmethan dihydronaphtalin und cyclopentadiën inaugural dissertation von walther albrecht p stankiewicz buchdruckerei albrecht walther 1906 additionsproducte von cyklopentadiën und chinonen pdf justus liebigs annalen der chemie in german 348 1 2 31 49 doi 10 1002 jlac 19063480104 issn 1099 0690 woodward r b sondheimer f taub d heusler k mclamore w m 1952 the total synthesis of steroids journal of the american chemical society 74 17 4223 4251 bibcode 1952jachs 74 4223w doi 10 1021 ja01137a001 corey e j weinshenker n m schaaf t k huber w 1969 stereo controlled synthesis of prostaglandins f 2a and e 2 dl journal of the american chemical society 91 20 5675 7 doi 10 1021 ja01048a062 pmid 5808505 danishefsky s hirama m fritsch n clardy j 1979 synthesis of disodium prephenate and disodium epiprephenate stereochemistry of prephenic acid and an observation on the base catalyzed rearrangement of prephenic acid to p hydroxyphenyllactic acid journal of the american chemical society 101 23 7013 7018 bibcode 1979jachs 101 7013d doi 10 1021 ja00517a039 wender p a schaus j m white a w 1980 general methodology for cis hydroisoquinoline synthesis synthesis of reserpine journal of the american chemical society 102 19 6157 6159 bibcode 1980jachs 102 6157w doi 10 1021 ja00539a038 martin s f rueger h williamson s a grzejszczak s 1987 general strategies for the synthesis of indole alkaloids total synthesis of reserpine and α yohimbine journal of the american chemical society 109 20 6124 6134 doi 10 1021 ja00254a036 nicolaou k c yang z liu j j ueno h nantermet p g guy r k claiborne c f renaud j couladouros e a paulvannan k sorensen e j 1994 total synthesis of taxol nature 367 6464 630 4 bibcode 1994natur 367 630n doi 10 1038 367630a0 pmid 7906395 s2cid 4371975 narasaka k shimada s osoda k iwasawa n 1991 phenylboronic acid as a template in the diels alder reaction synthesis 1991 12 1171 1172 doi 10 1055 s 1991 28413 smith a b sestelo j p dormer p g 1995 total synthesis of furaquinocin c journal of the american chemical society 117 43 10755 10756 bibcode 1995jachs 11710755s doi 10 1021 ja00148a023 kozmin s a rawal v h 1998 a general strategy to aspidosperma alkaloids efficient stereocontrolled synthesis of tabersonine journal of the american chemical society 120 51 13523 13524 bibcode 1998jachs 12013523k doi 10 1021 ja983198k gibbs r a okamura w h 1988 a short enantioselective synthesis of sterpurene complete intramolecular transfer of central to axial to central chiral elements journal of the american chemical society 110 12 4062 4063 bibcode 1988jachs 110 4062g doi 10 1021 ja00220a069 charest m g siegel d r myers a g 2005 synthesis of tetracycline journal of the american chemical society 127 23 8292 3 doi 10 1021 ja052151d pmid 15941256 dauben w g kessel c r takemura k h 1980 simple efficient total synthesis of cantharidin via a high pressure diels alder reaction journal of the american chemical society 102 22 6893 6894 bibcode 1980jachs 102 6893d doi 10 1021 ja00542a060 holmes h l 1948 the diels alder reaction ethylenic and acetylenic dienophiles organic reactions vol 4 pp 60 173 doi 10 1002 0471264180 or004 02 isbn 978 0471264187 cite book isbn date incompatibility help butz l w rytina a w 1949 the diels alder reaction quinones and other cyclenones organic reactions vol 5 pp 136 192 doi 10 1002 0471264180 or005 03 isbn 978 0471264187 cite book isbn date incompatibility help kloetzel m c 1948 the diels alder reaction with maleic anhydride organic reactions vol 4 pp 1 59 doi 10 1002 0471264180 or004 01 isbn 978 0471264187 cite book isbn date incompatibility help heintzelman g r meigh i r mahajan y r weinreb s w 2005 diels alder reactions of imino dienophiles organic reactions vol 65 pp 141 599 doi 10 1002 0471264180 or065 02 isbn 978 0471264187 ciganek e 1984 the intramolecular diels alder reaction organic reactions vol 32 pp 1 374 doi 10 1002 0471264180 or032 01 isbn 978 0471264187 bibliography edit carey francis a sundberg richard j 2007 advanced organic chemistry part b reactions and synthesis 5th ed new york springer isbn 978 0387683546 external links edit english translation of diels and alder s seminal 1928 german article that won them the nobel prize english title syntheses of the hydroaromatic series german title synthesen in der hydroaromatischen reihe v t e topics in organic reactions addition reaction elimination reaction polymerization reagents rearrangement reaction redox reaction regioselectivity stereoselectivity stereospecificity substitution reaction a value alpha effect annulene anomeric effect antiaromaticity aromatic ring current aromaticity baird s rule baker nathan effect baldwin s rules bema hapothle beta silicon effect bicycloaromaticity bredt s rule bürgi dunitz angle catalytic resonance theory charge remote fragmentation charge transfer complex clar s rule conformational isomerism conjugated system conrotatory and disrotatory curtin hammett principle dynamic binding chemistry edwards equation effective molarity electromeric effect electron rich electron withdrawing group electronic effect electrophile evelyn effect flippin lodge angle free energy relationship grunwald winstein equation hammett acidity function hammett equation george s hammond hammond s postulate homoaromaticity hückel s rule hyperconjugation inductive effect kinetic isotope effect lfer solvent coefficients data page marcus theory markovnikov s rule möbius aromaticity möbius hückel concept more o ferrall jencks plot negative hyperconjugation neighbouring group participation 2 norbornyl cation nucleophile kennedy j p orton passive binding phosphaethynolate polar effect polyfluorene ring strain σ aromaticity spherical aromaticity spiroaromaticity steric effects superaromaticity swain lupton equation taft equation thorpe ingold effect vinylogy walsh diagram woodward hoffmann rules woodward s rules y aromaticity yukawa tsuno equation zaitsev s rule σ bishomoaromaticity list of organic reactions carbon carbon bond forming reactions acetoacetic ester synthesis acyloin condensation aldol condensation aldol reaction alkane metathesis alkyne metathesis alkyne trimerisation alkynylation allan robinson reaction arndt eistert reaction auwers synthesis aza baylis hillman reaction barbier reaction barton kellogg reaction baylis hillman reaction benary reaction bergman cyclization biginelli reaction bingel reaction blaise ketone synthesis blaise reaction blanc chloromethylation bodroux chichibabin aldehyde synthesis bouveault aldehyde synthesis bucherer bergs reaction buchner ring expansion cadiot chodkiewicz coupling carbonyl allylation carbonyl olefin metathesis castro stephens coupling chan rearrangement chan lam coupling claisen condensation claisen rearrangement claisen schmidt condensation combes quinoline synthesis corey fuchs reaction corey house synthesis coupling reaction cross coupling reaction cross dehydrogenative coupling cross coupling partner dakin west reaction darzens reaction diels alder reaction doebner reaction wulff dötz reaction ene reaction enyne metathesis ethenolysis favorskii reaction ferrier carbocyclization friedel crafts reaction fujimoto belleau reaction fujiwara moritani reaction fukuyama coupling gabriel colman rearrangement gattermann reaction glaser coupling grignard reaction grignard reagent hammick reaction heck reaction henry reaction heterogeneous metal catalyzed cross coupling high dilution principle hiyama coupling homologation reaction horner wadsworth emmons reaction hydrocyanation hydrovinylation hydroxymethylation ivanov reaction johnson corey chaykovsky reaction julia olefination julia kocienski olefination kauffmann olefination knoevenagel condensation knorr pyrrole synthesis kolbe schmitt reaction kowalski ester homologation kulinkovich reaction kumada coupling liebeskind srogl coupling malonic ester synthesis mannich reaction mcmurry reaction meerwein arylation methylenation michael reaction minisci reaction mizoroki heck vs reductive heck nef isocyanide reaction nef synthesis negishi coupling nierenstein reaction nitro mannich reaction nozaki hiyama kishi reaction olefin conversion technology olefin metathesis palladium nhc complex passerini reaction peterson olefination pfitzinger reaction piancatelli rearrangement pinacol coupling reaction prins reaction quelet reaction ramberg bäcklund reaction rauhut currier reaction reformatsky reaction reimer tiemann reaction rieche formylation ring closing metathesis robinson annulation sakurai reaction seyferth gilbert homologation shapiro reaction sonogashira coupling stetter reaction stille reaction stollé synthesis stork enamine alkylation suzuki reaction takai olefination thermal rearrangement of aromatic hydrocarbons thorpe reaction ugi reaction ullmann reaction wagner jauregg reaction weinreb ketone synthesis wittig reaction wurtz reaction wurtz fittig reaction zincke suhl reaction homologation reactions arndt eistert reaction hooker reaction kiliani fischer synthesis kowalski ester homologation methoxymethylenetriphenylphosphorane seyferth gilbert homologation wittig reaction olefination reactions bamford stevens reaction barton kellogg reaction boord olefin synthesis chugaev elimination cope reaction corey winter olefin synthesis dehydrohalogenation elimination reaction grieco elimination hofmann elimination horner wadsworth emmons reaction hydrazone iodination julia olefination julia kocienski olefination kauffmann olefination mcmurry reaction peterson olefination ramberg bäcklund reaction shapiro reaction takai olefination wittig reaction carbon heteroatom bond forming reactions azo coupling bartoli indole synthesis boudouard reaction cadogan sundberg indole synthesis diazonium compound esterification grignard reagent haloform reaction hegedus indole synthesis hurd mori 1 2 3 thiadiazole synthesis kharasch sosnovsky reaction knorr pyrrole synthesis leimgruber batcho indole synthesis mukaiyama hydration nenitzescu indole synthesis oxymercuration reaction reed reaction schotten baumann reaction ullmann condensation williamson ether synthesis yamaguchi esterification degradation reactions barbier wieland degradation bergmann degradation edman degradation emde degradation gallagher hollander degradation hofmann rearrangement hooker reaction isosaccharinic acid marker degradation ruff degradation strecker degradation von braun amide degradation weerman degradation wohl degradation organic redox reactions acyloin condensation adkins peterson reaction akabori amino acid reaction alcohol oxidation algar flynn oyamada reaction amide reduction andrussow process angeli rimini reaction aromatization autoxidation baeyer villiger oxidation barton mccombie deoxygenation bechamp reduction benkeser reaction bergmann degradation birch reduction bohn schmidt reaction bosch reaction bouveault blanc reduction boyland sims oxidation cannizzaro reaction carbonyl reduction clemmensen reduction collins oxidation corey itsuno reduction corey kim oxidation corey winter olefin synthesis criegee oxidation dakin oxidation davis oxidation deoxygenation dess martin oxidation dna oxidation elbs persulfate oxidation emde degradation eschweiler clarke reaction étard reaction fischer tropsch process fleming tamao oxidation fukuyama reduction ganem oxidation glycol cleavage griesbaum coozonolysis grundmann aldehyde synthesis haloform reaction hydrogenation hydrogenolysis hydroxylation jones oxidation kiliani fischer synthesis kolbe electrolysis kornblum oxidation kornblum delamare rearrangement leuckart reaction ley oxidation lindgren oxidation lipid peroxidation lombardo methylenation luche reduction markó lam deoxygenation mcfadyen stevens reaction meerwein ponndorf verley reduction methionine sulfoxide miyaura borylation mozingo reduction noyori asymmetric hydrogenation omega oxidation oppenauer oxidation oxygen rebound mechanism ozonolysis parikh doering oxidation pinnick oxidation prévost reaction reduction of nitro compounds reductive amination riley oxidation rosenmund reduction rubottom oxidation sabatier reaction sarett oxidation selenoxide elimination shapiro reaction sharpless asymmetric dihydroxylation epoxidation of allylic alcohols sharpless epoxidation sharpless oxyamination stahl oxidation staudinger reaction stephen aldehyde synthesis swern oxidation transfer hydrogenation wacker process wharton reaction whiting reaction wohl aue reaction wolff kishner reduction wolffenstein böters reaction zinin reaction rearrangement reactions 1 2 rearrangement 1 2 wittig rearrangement 2 3 sigmatropic rearrangement 2 3 wittig rearrangement achmatowicz reaction alkyne zipper reaction allen millar trippett rearrangement allylic rearrangement alpha ketol rearrangement amadori rearrangement arndt eistert reaction aza cope rearrangement baker venkataraman rearrangement bamberger rearrangement banert cascade beckmann rearrangement benzilic acid rearrangement bergman cyclization bergmann degradation boekelheide reaction brook rearrangement buchner ring expansion carroll rearrangement chan rearrangement claisen rearrangement cope rearrangement corey fuchs reaction cornforth rearrangement criegee rearrangement curtius rearrangement demjanov rearrangement di π methane rearrangement dimroth rearrangement divinylcyclopropane cycloheptadiene rearrangement dowd beckwith ring expansion reaction electrocyclic reaction ene reaction enyne metathesis favorskii reaction favorskii rearrangement ferrier carbocyclization ferrier rearrangement fischer hepp rearrangement fries rearrangement fritsch buttenberg wiechell rearrangement gabriel colman rearrangement group transfer reaction halogen dance rearrangement hayashi rearrangement hofmann rearrangement hofmann martius rearrangement ireland claisen rearrangement jacobsen rearrangement kornblum delamare rearrangement kowalski ester homologation lobry de bruyn van ekenstein transformation lossen rearrangement mcfadyen stevens reaction mclafferty rearrangement meyer schuster rearrangement mislow evans rearrangement mumm rearrangement myers allene synthesis nazarov cyclization reaction neber rearrangement newman kwart rearrangement overman rearrangement oxy cope rearrangement pericyclic reaction piancatelli rearrangement pinacol rearrangement pummerer rearrangement ramberg bäcklund reaction ring expansion and contraction ring closing metathesis rupe reaction schmidt reaction semipinacol rearrangement seyferth gilbert homologation sigmatropic reaction skattebøl rearrangement smiles rearrangement sommelet hauser rearrangement stevens...
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