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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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170 pmid 33780068 white james d shaw subrata 2011 cis 2 5 diaminobicyclo 2 2 2 octane a new scaffold for asymmetric catalysis via salen metal complexes org lett 13 9 2488 91 doi 10 1021 ol2007378 pmid 21462988 evans d a chapman k t bisaha j 1988 asymmetric diels alder cycloaddition reactions with chiral α β unsaturated n acyloxazolidinones journal of the american chemical society 110 4 1238 1256 bibcode 1988jachs 110 1238e doi 10 1021 ja00212a037 corey e j loh t p 1991 first application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective diels alder reactions journal of the american chemical society 113 23 8966 8967 bibcode 1991jachs 113 8966c doi 10 1021 ja00023a066 corey e j shibata t lee t w 2002 asymmetric diels alder reactions catalyzed by a triflic acid activated chiral oxazaborolidine journal of the american chemical society 124 15 3808 3809 doi 10 1021 ja025848x pmid 11942799 ryu d h corey e j 2003 triflimide activation of a 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cycloisomerization of tethered triynes chem rev 121 4 2413 2444 doi 10 1021 acs chemrev 0c00825 pmc 8008985 pmid 33492939 minami atsushi oikawa hideaki 2016 recent advances of diels alderases involved in natural product biosynthesis the journal of antibiotics 69 7 500 506 doi 10 1038 ja 2016 67 pmid 27301662 s2cid 30482282 behr arno 2000 organometallic compounds and homogeneous catalysis ullmann s encyclopedia of industrial chemistry doi 10 1002 14356007 a18_215 isbn 978 3527306732 diels o alder k 1928 synthesen in der hydroaromatischen reihe i mitteilung anlagerungen von di en kohlenwasserstoffen justus liebigs annalen der chemie 460 98 122 doi 10 1002 jlac 19284600106 diels o alder k 1929 synthesen in der hydroaromatischen reihe ii mitteilung über cantharidin berichte der deutschen chemischen gesellschaft 62 3 554 562 doi 10 1002 cber 19290620318 diels o alder k 1929 synthesen in der hydroaromatischen reihe iii mitteilung synthese von terpenen camphern hydroaromatischen und heterocyclischen systemen mitbearbeitet von den herren wolfgang lübbert erich naujoks franz querberitz karl röhl harro segeberg justus liebigs annalen der chemie 470 62 103 doi 10 1002 jlac 19294700106 diels o alder k 1929 synthesen in der hydroaromatischen reihe iv mitteilung über die anlagerung von maleinsäure anhydrid an arylierte diene triene und fulvene mitbearbeitet von paul pries berichte der deutschen chemischen gesellschaft 62 8 2081 2087 doi 10 1002 cber 19290620829 diels o alder k 1929 synthesen in der hydroaromatischen reihe v über δ4 tetrahydro o phthalsäure stellungnahme zu der mitteilung von e h farmer und f l warren eigenschaften konjugierter doppelbindungen vii berichte der deutschen chemischen gesellschaft 62 8 2087 2090 doi 10 1002 cber 19290620830 diels o alder k 1929 synthesen in der hydroaromatischen reihe vi mitteilung kurt alder und gerhard stein über partiell hydrierte naphtho und anthrachinone mit wasserstoff in γ bzw δ stellung mitbearbeitet von paul pries und hans winckler berichte der deutschen chemischen gesellschaft 62 8 2337 2372 doi 10 1002 cber 19290620872 diels o alder k 1930 synthesen in der hydroaromatischen reihe vii mitteilung mitbearbeitet von den harren ernst petersen und franz querberitz justus liebigs annalen der chemie 478 137 154 doi 10 1002 jlac 19304780109 diels o alder k 1931 synthesen in der hydroaromatischen reihe viii mitteilung dien synthesen des anthracens anthracen forme justus liebigs annalen der chemie 486 191 202 doi 10 1002 jlac 19314860110 diels o alder k 1931 synthesen in der hydroaromatischen reihe ix mitteilung synthese des camphenilons und des santens justus liebigs annalen der chemie 486 202 210 doi 10 1002 jlac 19314860111 diels o alder k 1931 synthesen in der hydroaromatischen reihe x mitteilung dien synthesen ︁ mit pyrrol und seinen homologen justus liebigs annalen der chemie 486 211 225 doi 10 1002 jlac 19314860112 diels o alder k 1931 synthesen in der hydroaromatischen reihe xi mitteilung dien synthesen ︁ des cyclopentadiens cyclo hexadiens und butadiens mit acetylen dicarbonsäure und ihren estern justus liebigs annalen der chemie 490 236 242 doi 10 1002 jlac 19314900109 diels o alder k 1931 synthesen in der hydroaromatischen reihe xii mitteilung dien synthesen ︁ sauerstoffhaltiger heteroringe 2 dien synthesen des furans justus liebigs annalen der chemie 490 243 257 doi 10 1002 jlac 19314900110 diels o alder k 1931 synthesen in der hydroaromatischen reihe xiii mitteilung dien synthesen ︁ sauerstoffhaltiger heteroringe 3 dien synthesen der cumaline justus liebigs annalen der chemie 490 257 266 doi 10 1002 jlac 19314900111 diels o alder k 1931 synthesen in der hydroaromatischen reihe xiv mitteilung dien synthesen ︁ stickstoffhaltiger heteroringe 2 dien synthesen der pyrrole mit acetylen dicarbonsäure und mit ihren estern justus liebigs annalen der chemie 490 267 276 doi 10 1002 jlac 19314900112 diels o alder k 1931 synthesen in der hydroaromatischen reihe xv mitteilung dien synthesen ︁ stickstoffhaltiger heteroringe 3 dien synthesen der indole justus liebigs annalen der chemie 490 277 294 doi 10 1002 jlac 19314900113 diels o alder k 1932 synthesen in der hydroaromatischen reihe xvi mitteilung dien synthesen ︁ stickstoffhaltiger heteroringe 4 dien synthesen der pyrrole imidazole und pyrazole justus liebigs annalen der chemie 498 1 15 doi 10 1002 jlac 19324980102 diels o alder k 1932 synthesen in der hydroaromatischen reihe xvii mitteilung dien synthesen ︁ stickstoffhaltiger heteroringe 5 dien synthesen des pyridins chinolins chinaldins und isochinolins justus liebigs annalen der chemie 498 16 49 doi 10 1002 jlac 19324980103 diels o alder k 1933 synthesen in der hydroaromatischen reihe xviii dien synthesen ︁ stickstoffhaltiger heteroringe 6 dien synthesen des pyridins zur kenntnis des chinolizins indolizins norlupinans und pseudolupinins justus liebigs annalen der chemie 505 103 150 doi 10 1002 jlac 19335050109 diels o alder k 1934 synthesen in der hydroaromatischen reihe xix dien synthesen ︁ stickstoffhaltiger heteroringe 7 zur kenntnis der primärprodukte bei den dien synthesen des pyridins chinolins und chinaldins justus liebigs annalen der chemie 510 87 128 doi 10 1002 jlac 19345100106 diels o reese j 1934 synthesen in der hydroaromatischen reihe xx über die anlagerung von acetylen dicarbonsäureester an hydrazobenzol justus liebigs annalen der chemie 511 168 182 doi 10 1002 jlac 19345110114 diels o meyer r 1934 synthesen in der hydroaromatischen reihe xxi dien synthesen ︁ stickstoffhaltiger heteroringe 8 über den verlauf der dien synthese des pyridins in methylalkoholischer lösung justus liebigs annalen der chemie 513 129 145 doi 10 1002 jlac 19345130108 diels o friedrichsen w 1934 synthesen in der hydroaromatischen reihe xxii über die anthracen c4o3 addukte ihre eignung zu dien synthesen und ein neues prinzip zur synthese von phtalsäuren und dihydro phtalsäuren justus liebigs annalen der chemie 513 145 155 doi 10 1002 jlac 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