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Volumn 15, Issue 9, 2011, Pages 1340-1362

Pyridinium ylids in heterocyclic synthesis

Author keywords

Indolizines; Nitrones; Pyranonaphthoquinones; Pyridines; Pyridinium ylid

Indexed keywords

BUILDING BLOCKES; DIHYDROFURANS; HETEROCYCLIC SYNTHESIS; INDOLIZINES; NITRONES; ORGANIC SYNTHESIS; PYRANONAPHTHOQUINONE; PYRIDINIA YLID; PYRIDINIUM; VERSATILE TOOLS;

EID: 79958233010     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211795378209     Document Type: Review
Times cited : (98)

References (171)
  • 1
    • 0003861404 scopus 로고
    • Academic Press, New York and references cited therein
    • Johnson, A.W. Ylid Chemistry 1966; Academic Press, New York and references cited therein.
    • (1966) Ylid Chemistry
    • Johnson, A.W.1
  • 2
    • 84912202540 scopus 로고
    • Uber fluorenylide und die stevenssche umlagerung
    • Wittig, G.; Felletschin, G. Uber Fluorenylide und die Stevenssche Umlagerung. Ann., 1944, 555, 133-145
    • (1944) Ann , vol.555 , pp. 133-145
    • Wittig, G.1    Felletschin, G.2
  • 3
    • 84925497165 scopus 로고
    • Zur reaktionsweise des pentaphenyl-phosphors und einiger derivate
    • Wittig, G.; Geissler, G. Zur Reaktionsweise des Pentaphenyl-phosphors und einiger Derivate. Ann., 1953, 580, 44-57.
    • (1953) Ann , vol.580 , pp. 44-57
    • Wittig, G.1    Geissler, G.2
  • 4
    • 85196228933 scopus 로고    scopus 로고
    • Asymmetric ylide reactions: Epoxidation, cyclopropanation, aziridination, olefination, and rearrangement
    • Li, A.-H.; Dai, L.-X.; Aggarwal, V.K. Asymmetric ylide reactions: Epoxidation, cyclopropanation, aziridination, olefination, and rearrangement. Chem. Rev., 1997, 97, 2341
    • Chem. Rev , vol.1997 , pp. 97
    • Li, A.-H.1    Dai, L.-X.2    Aggarwal, V.K.3
  • 5
    • 0000936734 scopus 로고
    • Ylide formation from the reaction of carbenes and carbenoids with heteroatom lone pairs
    • Padwa, A.; Hornbuckle, S.F. Ylide formation from the reaction of carbenes and carbenoids with heteroatom lone pairs. Chem. Rev., 1991, 91, 263
    • (1991) Chem. Rev , vol.91 , pp. 263
    • Padwa, A.1    Hornbuckle, S.F.2
  • 6
    • 0000171402 scopus 로고    scopus 로고
    • Stereoselective synthesis of three-membered ring compounds via ylide routes
    • Dai, L.-X.; Hou, X.-L.; Zhou, Y.-G. Stereoselective synthesis of three-membered ring compounds via ylide routes. Pure. Appl. Chem., 1999, 71, 369
    • (1999) Pure. Appl. Chem , vol.71 , pp. 369
    • Dai, L.-X.1    Hou, X.-L.2    Zhou, Y.-G.3
  • 7
    • 0001893022 scopus 로고    scopus 로고
    • Enantioselective syntheses of organosulfur compounds via [2,3]-sigmatropic rearrangements of ylides derived from di(allyl), di(propargyl), and di(benzyl) sulfide complexes; Control of carbon configuration by an easily resolved and recycled rhenium auxiliary
    • Meyer, O.; Cagle, P.C.; Weickhardt, K.; Vichard, D.; Gladysz, J.A. Enantioselective syntheses of organosulfur compounds via [2,3]-sigmatropic rearrangements of ylides derived from di(allyl), di(propargyl), and di(benzyl) sulfide complexes; Control of carbon configuration by an easily resolved and recycled rhenium auxiliary. Pure Appl. Chem., 1996, 68, 79.
    • (1996) Pure Appl. Chem , vol.68 , pp. 79
    • Meyer, O.1    Cagle, P.C.2    Weickhardt, K.3    Vichard, D.4    Gladysz, J.A.5
  • 8
    • 0000921836 scopus 로고
    • Theoretical study of the structure and reactivity of ylides of N, P, As, Sb, and Bi
    • Naito, T.; Nagase, S.; Yamataka, H. Theoretical study of the structure and reactivity of ylides of N, P, As, Sb, and Bi. J. Am. Chem. Soc., 1994, 116, 10080.
    • (1994) J. Am. Chem. Soc , vol.116 , pp. 10080
    • Naito, T.1    Nagase, S.2    Yamataka, H.3
  • 9
    • 85196230351 scopus 로고    scopus 로고
    • Ylides and ylidions - A comparative study of unusual gas-phase structures
    • Yates, B.F.; Bouma, W.J.; Radom, L. Ylides and ylidions - A comparative study of unusual gas-phase structures. J. Am. Chem. Soc., 1987, 109, 2250
    • J. Am. Chem. Soc , vol.1987 , pp. 109
    • Yates, B.F.1    Bouma, W.J.2    Radom, L.3
  • 10
    • 33845557863 scopus 로고
    • The conformations and energetics of simple ylids
    • Eades, R.A.; Gassman, P.G.; Dixon, D.A. The conformations and energetics of simple ylids. J. Am. Chem. Soc., 1981, 103, 1066
    • (1981) J. Am. Chem. Soc , vol.103 , pp. 1066
    • Eades, R.A.1    Gassman, P.G.2    Dixon, D.A.3
  • 12
    • 0012010721 scopus 로고
    • Uber enol-betaine
    • Kröhnke, F. Uber Enol-Betaine. Chem. Ber., 1935, 68, 1177-1195.
    • (1935) Chem. Ber , vol.68 , pp. 1177-1195
    • Kröhnke, F.1
  • 13
    • 84977690431 scopus 로고
    • Darstellung und eigenschaften des trimethylammonium- methylids
    • Wittig, G.; Wetterling, M. Darstellung und Eigenschaften des Trimethylammonium- methylids. Ann., 1947, 557, 193-201.
    • (1947) Ann , vol.557 , pp. 193-201
    • Wittig, G.1    Wetterling, M.2
  • 14
    • 0000778826 scopus 로고
    • The chemistry of ylids-V: Trialkylphosphoniumfluorenylides mechanism of the Wittig reaction
    • Johnson, A. Wm.; LaCount, R.B. The chemistry of ylids-V: trialkylphosphoniumfluorenylides mechanism of the Wittig reaction. Tetrahedron, 1960, 9, 130.
    • (1960) Tetrahedron , vol.9 , pp. 130
    • Wm, J.A.1    Lacount, R.B.2
  • 15
    • 0000924493 scopus 로고
    • D-orbital resonance 2. Comparative reactivity of vinyldimethylsulfonium and vinyltrimethylammonium ions
    • and references cited herein
    • Doering, W. von E.; Scheiber, K.C. D-orbital resonance 2. Comparative reactivity of vinyldimethylsulfonium and vinyltrimethylammonium ions, J. Am. Chem. Soc., 1955, 77, 514 and references cited herein
    • (1955) J. Am. Chem. Soc , vol.77 , pp. 514
    • Doering, W.1    von, E.2    Scheiber, K.C.3
  • 16
    • 0000622242 scopus 로고
    • D-orbital resonance 3. Deuterium exchange in methyl onium salts and in bicyclo [2.2.1]heptane-1-sulfonium iodide
    • Doering, W. von E.; Hoffmann, A.K. D-orbital resonance 3. Deuterium exchange in methyl onium salts and in bicyclo [2.2.1]heptane-1-sulfonium iodide. J. Am. Chem. Soc., 1955, 77, 521.
    • (1955) J. Am. Chem. Soc , vol.77 , pp. 521
    • Doering, W.1    von, E.2    Hoffmann, A.K.3
  • 17
    • 0000665165 scopus 로고
    • 197. Pyridinium ylide in organic synthesis. 1. General aspects: Methods of generation, structure and physicochemical properties
    • Litvinov, V.P. 197. Pyridinium ylide in organic synthesis. 1. General aspects: methods of generation, structure and physicochemical properties. Zh. Org. Khim, 1993, 29, 2070-2126.
    • (1993) Zh. Org. Khim , vol.29 , pp. 2070-2126
    • Litvinov, V.P.1
  • 18
    • 0007629352 scopus 로고
    • The reaction of 5,5-dihalobarbituric acids with pyridine
    • Taylor, E.C.; Paudler, W.W.; Cain, C. K. The reaction of 5,5-dihalobarbituric acids with pyridine. J. Org. Chem., 1955, 20, 264-270.
    • (1955) J. Org. Chem , vol.20 , pp. 264-270
    • Taylor, E.C.1    Paudler, W.W.2    Cain, C.K.3
  • 20
    • 84981388968 scopus 로고
    • Eine neue Synthese Substituierter Pyridine 1. Grundzuge der Synthese
    • Zecher, W.; Kröhnke, F. Eine neue Synthese Substituierter Pyridine 1. Grundzuge der Synthese. Chem. Ber., 1961, 94, 690-697;
    • (1961) Chem. Ber , vol.94 , pp. 690-697
    • Zecher, W.1    Kröhnke, F.2
  • 21
    • 0038696383 scopus 로고
    • Eine neue Synthese Substituierter Pyridine 2. Einige Varianten und Sonderfalle
    • Zecher, W.; Kröhnke, F. Eine neue Synthese Substituierter Pyridine 2. Einige Varianten und Sonderfalle. Chem. Ber., 1961, 94, 698-706
    • (1961) Chem. Ber , vol.94 , pp. 698-706
    • Zecher, W.1    Kröhnke, F.2
  • 22
    • 0038020002 scopus 로고
    • Eine neue Synthese Substituierter Pyridine 3. Pyridine aus Phenyl-phenacyl- (thio-)athern sowie aus Omega-cyan-acetophenon
    • Zecher, W.; Kröhnke, F. Eine neue Synthese Substituierter Pyridine 3. Pyridine aus Phenyl-phenacyl- (thio-)athern sowie aus Omega-cyan-acetophenon. Chem. Ber., 1961, 94, 707-712
    • (1961) Chem. Ber , vol.94 , pp. 707-712
    • Zecher, W.1    Kröhnke, F.2
  • 25
    • 0021177882 scopus 로고
    • Ylides of heterocycles 6. Ylides of barbituric acids with nicotinic acid derivatives as cationic moieties
    • Peichl, E.; Kappe, T. Ylides of heterocycles 6. Ylides of barbituric acids with nicotinic acid derivatives as cationic moieties. Arch. Pharm., 1984, 317, 946-951
    • (1984) Arch. Pharm , vol.317 , pp. 946-951
    • Peichl, E.1    Kappe, T.2
  • 26
    • 85196228892 scopus 로고
    • Reactions of uracils 11. New pyridinium and isoquinolinium ylides as well as a dispiropyrimidofuro[ 2,3-d]pyrimidine from 5,5-dichloro-1,3-dimethylbarbituric acid
    • Szilagyi, G.; Wamhoff, H.; Sohar, P. Reactions of uracils 11. New pyridinium and isoquinolinium ylides as well as a dispiropyrimidofuro[ 2,3-d]pyrimidine from 5,5-dichloro-1,3-dimethylbarbituric acid. Chem. Zeitung, 1987, 111, 144-146
    • (1987) Chem. Zeitung , vol.111 , pp. 144-146
    • Szilagyi, G.1    Wamhoff, H.2    Sohar, P.3
  • 27
    • 0017841893 scopus 로고
    • Pyrones and pyridones 74. Quinolylidene derivatives
    • Fritz, E.; Wendt, W.; Fenner, H. Pyrones and pyridones 74. Quinolylidene derivatives. Arch. Pharm., 1978, 311, 561- 568
    • (1978) Arch. Pharm , vol.311 , pp. 561-568
    • Fritz, E.1    Wendt, W.2    Fenner, H.3
  • 28
    • 79958219923 scopus 로고
    • Reaction of quinoline Noxides with barbituric acid in the presence of acetic anhydride
    • Youssif, M.M.; Sarki, S.; Hamana, M. Reaction of quinoline Noxides with barbituric acid in the presence of acetic anhydride. Heterocycles, 1981, 15, 1083-1088.
    • (1981) Heterocycles , vol.15 , pp. 1083-1088
    • Youssif, M.M.1    Sarki, S.2    Hamana, M.3
  • 29
    • 84982064756 scopus 로고
    • Eine Darstellungsmethode für aliphatische α,β-ungesättigte Aldehyde
    • Karrer, P.; Epprecht, A. Eine Darstellungsmethode für aliphatische α,β-ungesättigte Aldehyde. Helv. Chim. Acta 1941, 24, 1039-1045
    • (1941) Helv. Chim. Acta , vol.24 , pp. 1039-1045
    • Karrer, P.1    Epprecht, A.2
  • 30
    • 0000879718 scopus 로고
    • Syntheses using pyridinium salts
    • and references therein
    • Kröhnke, F. Syntheses using pyridinium salts. Angew. Chem. Int. Ed., 1963, 2, 380-393 and references therein.
    • (1963) Angew. Chem. Int. Ed , vol.2 , pp. 380-393
    • Kröhnke, F.1
  • 31
    • 0000538809 scopus 로고
    • The reaction of iodine with some ketones in the presence of pyridine
    • King, C.L. The reaction of iodine with some ketones in the presence of pyridine. J. Am. Chem. Soc., 1944, 66, 894-895
    • (1944) J. Am. Chem. Soc , vol.66 , pp. 894-895
    • King, C.L.1
  • 32
    • 0006256621 scopus 로고
    • The reactions of acetophenols with iodine and pyridine and the preparation of hydroxybenzoic acids
    • King, C.L. The reactions of acetophenols with iodine and pyridine and the preparation of hydroxybenzoic acids. J. Am. Chem. Soc., 1945, 67, 2089-2092
    • (1945) J. Am. Chem. Soc , vol.67 , pp. 2089-2092
    • King, C.L.1
  • 33
    • 84981750667 scopus 로고
    • Synthesen heterocyclischer aldehyde mit Hilfe von Pyridiniumsalzen
    • Ried, W.; Bender, H. Synthesen heterocyclischer aldehyde mit Hilfe von Pyridiniumsalzen. Chem. Ber., 1956, 89, 1893-1896
    • (1956) Chem. Ber , vol.89 , pp. 1893-1896
    • Ried, W.1    Bender, H.2
  • 35
    • 85196230022 scopus 로고
    • A new method for the synthesis of 4-pyridinealdehyde and its derivatives
    • Liu, M-C.; Chu, T-L. A new method for the synthesis of 4-pyridinealdehyde and its derivatives. Huaxue Xuebao, 1965, 31, 439-440
    • (1965) Huaxue Xuebao , vol.31 , pp. 439-440
    • Liu, M.-C.1    Chu, T.-L.2
  • 38
    • 84987564749 scopus 로고
    • Synthesis and electronic properties of intensely colored iron(II) complexes with new 4-substituted planar tridentate nitrogen ligans analogous to 2,2'/6',2"-terpyridine
    • Bochet, C.G.; Piguet, C.; Williams, A.F. Synthesis and electronic properties of intensely colored iron(II) complexes with new 4-substituted planar tridentate nitrogen ligans analogous to 2,2'/6',2"-terpyridine, Helv. Chim. Acta, 1993, 76, 372-384
    • (1993) Helv. Chim. Acta , vol.76 , pp. 372-384
    • Bochet, C.G.1    Piguet, C.2    Williams, A.F.3
  • 39
    • 21644454248 scopus 로고    scopus 로고
    • Pyridinium halides and their mixtures as inhibitors of steel corrosion in sulfuric acid solutions
    • Yurchenko, R.I.; Ivashchenko, S.V.; Pilipenko, T.N.; Pogrebova, I.S. Pyridinium halides and their mixtures as inhibitors of steel corrosion in sulfuric acid solutions. Russ. J. Appl. Chem., 2005, 78, 511-513.
    • (2005) Russ. J. Appl. Chem , vol.78 , pp. 511-513
    • Yurchenko, R.I.1    Ivashchenko, S.V.2    Pilipenko, T.N.3    Pogrebova, I.S.4
  • 40
    • 34250146999 scopus 로고
    • Ylides of heterocycles 4. Sulfoniumylide and pyridiniumylide of coumarin and 2-quinolone
    • Kappe, T.; Korbuly, G.; Pongratz, E. Ylides of heterocycles 4. Sulfoniumylide and pyridiniumylide of coumarin and 2-quinolone. Monatsh. Chem., 1983, 114, 303-315.
    • (1983) Monatsh. Chem , vol.114 , pp. 303-315
    • Kappe, T.1    Korbuly, G.2    Pongratz, E.3
  • 41
    • 0001224778 scopus 로고
    • Lifetimes of simple ketocarbenes
    • Toscano, J.P.; Platz, M.S. Lifetimes of simple ketocarbenes. J. Am. Chem. Soc., 1995, 117, 4712-4713.
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 4712-4713
    • Toscano, J.P.1    Platz, M.S.2
  • 42
    • 0000959320 scopus 로고
    • Structure of diazoketones. A study of hindered internal rotation
    • Kaplan, F.; Meloy, G.K. Structure of diazoketones. A study of hindered internal rotation. J. Am. Chem. Soc., 1966, 88, 950-956
    • (1966) J. Am. Chem. Soc , vol.88 , pp. 950-956
    • Kaplan, F.1    Meloy, G.K.2
  • 43
    • 0005767710 scopus 로고
    • Conformational control of decomposition pathways of alphadiazoketones
    • Kaplan, F.; Mitchell, M.L. Conformational control of decomposition pathways of alphadiazoketones. Tetrahedron Lett., 1979, 20, 759-762
    • (1979) Tetrahedron Lett , vol.20 , pp. 759-762
    • Kaplan, F.1    Mitchell, M.L.2
  • 44
    • 37049122738 scopus 로고
    • Diazoacetaldehyde as a formylcarbene - A new carbene species
    • Arnold, Z. Diazoacetaldehyde as a formylcarbene - A new carbene species. J. Chem. Soc., Chem. Commun., 1967, 299-300.
    • (1967) J. Chem. Soc., Chem. Commun , pp. 299-300
    • Arnold, Z.1
  • 45
    • 0004234620 scopus 로고
    • Brinker, U.H., Ed.; JAI Press: Greenwich, CT
    • Jackson, J.E.; Platz, M.S. In Advances in carbene chemistry; Brinker, U.H., Ed.; JAI Press: Greenwich, CT, 1994; Vol. 1, pp 89-160.
    • (1994) Advances In Carbene Chemistry , vol.1 , pp. 89-160
    • Jackson, J.E.1    Platz, M.S.2
  • 46
    • 33947461938 scopus 로고
    • Kinetics of aromatic halogenation. V. The iodination of 2,4- dichlorophenol and anisole with iodine monochloride
    • and references therein
    • Berliner, E. Kinetics of aromatic halogenation. V. The iodination of 2,4- dichlorophenol and anisole with iodine monochloride. J. Am. Chem. Soc., 1958, 81, 856-861 and references therein.
    • (1958) J. Am. Chem. Soc , vol.81 , pp. 856-861
    • Berliner, E.1
  • 47
    • 84937817044 scopus 로고
    • Preparation of a cyclopentadienylide
    • London
    • Lloyd, D.; Sneezum, J.S. Preparation of a cyclopentadienylide. Chem. Ind. (London), 1955, 1220-1221
    • (1955) Chem. Ind , pp. 1220-1221
    • Lloyd, D.1    Sneezum, J.S.2
  • 48
    • 3743129229 scopus 로고
    • The preparation of some pyridinium cyclopentadienylides
    • and referenced therein
    • Lloyd, D.; Sneezum, J.S. The preparation of some pyridinium cyclopentadienylides. Tetrahedron, 1958, 3, 334- 338 and referenced therein.
    • (1958) Tetrahedron , vol.3 , pp. 334-338
    • Lloyd, D.1    Sneezum, J.S.2
  • 51
    • 84981752280 scopus 로고
    • Das Tetracyanaethylenoxyd
    • Rieche, A.; Dietrich, P. Das Tetracyanaethylenoxyd. Chem. Ber., 1963, 96, 3044-3049
    • (1963) Chem. Ber , vol.96 , pp. 3044-3049
    • Rieche, A.1    Dietrich, P.2
  • 52
    • 0042565556 scopus 로고
    • Tetracyanoethylene oxide 1. Preparation and reaction with nucleophiles
    • Linn, W.J.; Webster, O.W.; Benson, R.E. Tetracyanoethylene oxide 1. Preparation and reaction with nucleophiles. J. Am. Chem. Soc., 1965, 87, 3651-3656.
    • (1965) J. Am. Chem. Soc , vol.87 , pp. 3651-3656
    • Linn, W.J.1    Webster, O.W.2    Benson, R.E.3
  • 53
    • 0000519370 scopus 로고    scopus 로고
    • Pyridinium ylides in organic synthesis 4. Pyridinium ylides in reactions of (Ad(N)-E) nucleophilic attachmentelimination
    • Litvinov, V.P.; Shestopalov, A.M. Pyridinium ylides in organic synthesis 4. Pyridinium ylides in reactions of (Ad(N)-E) nucleophilic attachmentelimination, Russ. J. Org. Chem., 1997, 33, 975-1014
    • (1997) Russ. J. Org. Chem , vol.33 , pp. 975-1014
    • Litvinov, V.P.1    Shestopalov, A.M.2
  • 54
    • 84986506361 scopus 로고
    • Syntheses of heterocyclic compounds using nitro ketene dithioacetal
    • Tominaga, Y.; Matsuda, Y. Syntheses of heterocyclic compounds using nitro ketene dithioacetal. J. Heterocycl. Chem., 1985, 22, 937-949.
    • (1985) J. Heterocycl. Chem , vol.22 , pp. 937-949
    • Tominaga, Y.1    Matsuda, Y.2
  • 55
    • 84986500870 scopus 로고
    • Synthesis of Cycl[3.2.2]azine and benzo[g]cycl[3.2.2]azine derivatives by use of the [2+8] cycloadditions reaction of indolizines and dimethyl acetylenedicarboxylate
    • Yoshinori, T.; Yoshihide, S.; Tomohiko, K.; Hiromi, G.; Yoshiro, M.; Akira, H. Synthesis of Cycl[3.2.2]azine and benzo[g]cycl[3.2.2]azine derivatives by use of the [2+8] cycloadditions reaction of indolizines and dimethyl acetylenedicarboxylate. J. Heterocycl. Chem., 1989, 26, 477-487
    • (1989) J. Heterocycl. Chem , vol.26 , pp. 477-487
    • Yoshinori, T.1    Yoshihide, S.2    Tomohiko, K.3    Hiromi, G.4    Yoshiro, M.5    Akira, H.6
  • 56
    • 0037319817 scopus 로고    scopus 로고
    • Synthesis of an annulenoannulenone, 3H-Benzo[e]cycl[3.3.2]azin-3-one
    • Yoshiro, M.; Shinya, K.; Keisuke, K.; Takashi, U.; Kouhei, Y. Synthesis of an annulenoannulenone, 3H-Benzo[e]cycl[3.3.2]azin-3-one. Heterocycles, 2003, 60, 405-411
    • (2003) Heterocycles , vol.60 , pp. 405-411
    • Yoshiro, M.1    Shinya, K.2    Keisuke, K.3    Takashi, U.4    Kouhei, Y.5
  • 57
    • 0001163813 scopus 로고
    • Synthesis of 2- methylthioindolizine-3-carbonitriles using nitro ketene dithioacetal
    • Yoshinori, T.; Yoshihide, S.; Akira, H. Synthesis of 2- methylthioindolizine-3-carbonitriles using nitro ketene dithioacetal. J. Heterocycl. Chem., 1988, 25, 1745-1749
    • (1988) J. Heterocycl. Chem , vol.25 , pp. 1745-1749
    • Yoshinori, T.1    Yoshihide, S.2    Akira, H.3
  • 60
    • 84986519266 scopus 로고
    • Nbis(methylthio)methylene derivatives. 5. New synthesis of 2-aminoindolizine and related compounds via a formal [3+3] cycloaddition reaction using Nbis(ethoxycarbonylmethylthio)-methylenephenylsulfonamides
    • Yoshinori, T.; Hiroshi, U.; Koichiro, O.; Shinya, K. Nbis(methylthio)methylene derivatives. 5. New synthesis of 2-aminoindolizine and related compounds via a formal [3+3] cycloaddition reaction using Nbis(ethoxycarbonylmethylthio)-methylenephenylsulfonamides. J. Heterocycl. Chem., 1992, 29, 209-214
    • (1992) J. Heterocycl. Chem , vol.29 , pp. 209-214
    • Yoshinori, T.1    Hiroshi, U.2    Koichiro, O.3    Shinya, K.4
  • 61
    • 84986469557 scopus 로고
    • A new synthesis of imidazo[1,2-a]pyridine and imidazo[2,1- a]isoquinoline derivatives
    • Yoshinori, T.; Shigenori, M.; Yoshihide, S.; Akira, H. A new synthesis of imidazo[1,2-a]pyridine and imidazo[2,1- a]isoquinoline derivatives. J. Heterocycl. Chem., 1987, 24, 1365-1369
    • (1987) J. Heterocycl. Chem , vol.24 , pp. 1365-1369
    • Yoshinori, T.1    Shigenori, M.2    Yoshihide, S.3    Akira, H.4
  • 62
    • 0009964304 scopus 로고
    • Reactions of pyridinium or isoquinolinium ketene dithioacetals with aromatic N-imines and S-imines
    • Yoshinori, T.; Akira, H. Reactions of pyridinium or isoquinolinium ketene dithioacetals with aromatic N-imines and S-imines. J. Heterocycl. Chem., 1988, 25, 1449-1454.
    • (1988) J. Heterocycl. Chem , vol.25 , pp. 1449-1454
    • Yoshinori, T.1    Akira, H.2
  • 63
    • 2142690327 scopus 로고
    • Optically active cyclopropanes
    • Salaün, J. Optically active cyclopropanes. Chem. Rev., 1989, 89, 1247-1270
    • (1989) Chem. Rev , vol.89 , pp. 1247-1270
    • Salaün, J.1
  • 64
    • 0001485086 scopus 로고    scopus 로고
    • Asymmetric ylide reactions: Epoxidation, cyclopropanation, aziridination, olefination, and rearrangement
    • Li, A.-H.; Dai, L.-X.; Aggarwal, V.K. Asymmetric ylide reactions: epoxidation, cyclopropanation, aziridination, olefination, and rearrangement. Chem. Rev., 1997, 97, 2341-2372
    • (1997) Chem. Rev , vol.97 , pp. 2341-2372
    • Li, A.-H.1    Dai, L.-X.2    Aggarwal, V.K.3
  • 65
    • 0345186940 scopus 로고    scopus 로고
    • Methods of Organic Chemistry (Houben-Weyl)
    • Chapters 5.2.3.4. up to 5.2.3.7, Ed. A. de Meijere, G. Thieme Verlag, Stuttgart
    • De Kimpe, N. Methods of Organic Chemistry (Houben-Weyl), Vol. E17B Carbocyclic three- membered ring compounds, Chapters 5.2.3.4. up to 5.2.3.7., pp. 1603- 1694, Ed. A. de Meijere, G. Thieme Verlag, Stuttgart (1997)
    • (1997) Carbocyclic Three- Membered Ring Compounds , vol.E17B , pp. 1603-1694
    • de Kimpe, N.1
  • 66
    • 0345186940 scopus 로고    scopus 로고
    • Methods of Organic Chemistry (Houben-Weyl)
    • Chapters 1.1.1 and 1.1.3, Ed. A. de Meijere, G. Thieme Verlag, Stuttgart
    • Zwanenburg, B.; De Kimpe, N. Methods of Organic Chemistry (Houben-Weyl), Vol. E.17A (Carbocyclic Three-Membered Ring Compounds, Chapters 1.1.1 and 1.1.3, pp. 29-40 en pp. 45-105, Ed. A. de Meijere, G. Thieme Verlag, Stuttgart (1997)
    • (1997) Carbocyclic Three-Membered Ring Compounds , vol.E.17A , pp. 29-40
    • Zwanenburg, B.1    de Kimpe, N.2
  • 67
    • 0003445429 scopus 로고    scopus 로고
    • Jacobsen, E.N., Pfaltz, A., Yamamoto, H., Eds., Springer, Berlin
    • Pfaltz, A. IN Comprehensive Asymmetric Catalysis II, Jacobsen, E.N., Pfaltz, A., Yamamoto, H., Eds., Springer, Berlin, 1999, 513-538.
    • (1999) Comprehensive Asymmetric Catalysis II , pp. 513-538
    • Pfaltz, A.1
  • 68
    • 0035828834 scopus 로고    scopus 로고
    • Synthesis of cyclopropane containing natural products
    • and references therein
    • Donaldson, W.A. Synthesis of cyclopropane containing natural products. Tetrahedron, 2001, 57, 8589-8627 and references therein.
    • (2001) Tetrahedron , vol.57 , pp. 8589-8627
    • Donaldson, W.A.1
  • 69
    • 0006879393 scopus 로고
    • New stereoselective synthesis of cyclopropanes based on pyridinium ylids
    • Shestopalov, A.M.; Shararin, Y.A.; Litvinov, V.P.; Nefedov, O.M. New stereoselective synthesis of cyclopropanes based on pyridinium ylids, Zh. Org. Khim., 1989, 25, 1111-1112
    • (1989) Zh. Org. Khim , vol.25 , pp. 1111-1112
    • Shestopalov, A.M.1    Shararin, Y.A.2    Litvinov, V.P.3    Nefedov, O.M.4
  • 70
    • 0006922811 scopus 로고
    • Regio and stereodirected synthesis of tetrahydroindolizines, tetrahydropyridine-6-olates, and cyclopropanes based upon pyridinium ylides and unsaturated nitriles
    • Shestopalov, A.M.; Litvinov, V.P.; Rodinovskaya, L.A.; Shararin, Y.A. Regio-and stereodirected synthesis of tetrahydroindolizines, tetrahydropyridine-6-olates, and cyclopropanes based upon pyridinium ylides and unsaturated nitriles. Izvest. Akad. Nauk. S.S.S.R., 1991, 146-155.
    • (1991) Izvest. Akad. Nauk. S.S.S.R , pp. 146-155
    • Shestopalov, A.M.1    Litvinov, V.P.2    Rodinovskaya, L.A.3    Shararin, Y.A.4
  • 71
    • 0034627344 scopus 로고    scopus 로고
    • Stereoselective formation of activated cyclopropanes with pyridinium ylides bearing a (-)-8-phenylmenthyl group as the chiral auxiliary
    • Kojima, S.; Fujitomo, K.; Shinohara, Y.; Shimizu, M.; Ohkata, K. Stereoselective formation of activated cyclopropanes with pyridinium ylides bearing a (-)-8-phenylmenthyl group as the chiral auxiliary. Tetrahedron Lett., 2000, 41, 9847-9951;
    • (2000) Tetrahedron Lett , vol.41 , pp. 9847-9951
    • Kojima, S.1    Fujitomo, K.2    Shinohara, Y.3    Shimizu, M.4    Ohkata, K.5
  • 72
    • 1842737308 scopus 로고    scopus 로고
    • Tereoselective synthesis of activated cyclopropanes with an alpha-pyridinium acetamide bearing an 8-phenylmenthyl group as the chiral auxiliary
    • Kojima, S.; Hiroike, K.; Ohkata, K. Stereoselective synthesis of activated cyclopropanes with an alpha-pyridinium acetamide bearing an 8-phenylmenthyl group as the chiral auxiliary. Tetrahedron Lett., 2004, 45, 3565-3568;
    • (2004) Tetrahedron Lett , vol.45 , pp. 3565-3568
    • Kojima, S.1    Hiroike, K.2    Ohkata, K.3
  • 73
    • 33646868382 scopus 로고    scopus 로고
    • The effect of substituents on the pyridine ring in the diastereoselective cyclopropanation reaction of pyridinium ylides bearing an 8-phenylmenthyl ester group
    • Kojima, S.; Fujimoto, K.; Itoh, Y.; Hiroike, K.; Murakami, M.; Ohkata, K. The effect of substituents on the pyridine ring in the diastereoselective cyclopropanation reaction of pyridinium ylides bearing an 8-phenylmenthyl ester group. Heterocycles, 2006, 67, 679-694;
    • (2006) Heterocycles , vol.67 , pp. 679-694
    • Kojima, S.1    Fujimoto, K.2    Itoh, Y.3    Hiroike, K.4    Murakami, M.5    Ohkata, K.6
  • 74
    • 33750965601 scopus 로고    scopus 로고
    • Asymmetric synthesis of activated cyclopropanes catalyzed by cinchonidine as a chiral Bronsted base
    • Kojima, S.; Suzuki, M.; Watanabe, A.; Ohkata, K. Asymmetric synthesis of activated cyclopropanes catalyzed by cinchonidine as a chiral Bronsted base. Tetrahedron Lett., 2006, 47, 9061-9065.
    • (2006) Tetrahedron Lett , vol.47 , pp. 9061-9065
    • Kojima, S.1    Suzuki, M.2    Watanabe, A.3    Ohkata, K.4
  • 75
    • 0030727607 scopus 로고    scopus 로고
    • Transformations of resin-bound pyridinium ylides 1. A stereoselective synthesis of 2,2,3-trisubstituted cyclopropanecarboxylates
    • Vo, N.H.; Eyermann, C.J.; Hodge, C.N. Transformations of resin-bound pyridinium ylides 1. A stereoselective synthesis of 2,2,3-trisubstituted cyclopropanecarboxylates. Tetrahedron Lett., 1997, 38, 7951-7954.
    • (1997) Tetrahedron Lett , vol.38 , pp. 7951-7954
    • Vo, N.H.1    Eyermann, C.J.2    Hodge, C.N.3
  • 77
    • 33751386721 scopus 로고
    • Stereoselective synthesis of 2,5-dihydrofurans by sequential SN2' cleavage of alkynyloxiranes and AG+-catalyzed cyclization of the allenylcarbinol products
    • Marshall, J.A.; Pinney, K. Stereoselective synthesis of 2,5-dihydrofurans by sequential SN2' cleavage of alkynyloxiranes and AG+-catalyzed cyclization of the allenylcarbinol products. J. Org. Chem., 1993, 58, 7180-7184;
    • (1993) J. Org. Chem , vol.58 , pp. 7180-7184
    • Marshall, J.A.1    Pinney, K.2
  • 78
    • 0028226421 scopus 로고
    • Synthesis of the pseudopterane 2,5-furanocyclic ringsystem by [2,3] Wittig ring contraction of bridged furan and dihydrofuran propargylic ethers
    • Marshall, J.A.; Yu, B. Synthesis of the pseudopterane 2,5-furanocyclic ringsystem by [2,3] Wittig ring contraction of bridged furan and dihydrofuran propargylic ethers. J. Org. Chem., 1994, 59, 324-331;
    • (1994) J. Org. Chem , vol.59 , pp. 324-331
    • Marshall, J.A.1    Yu, B.2
  • 79
    • 0028905974 scopus 로고
    • Zirconocene-catalyzed kinetic resolution of dihydrofurans
    • Visser, M.S.; Hoveyda, A.H. Zirconocene-catalyzed kinetic resolution of dihydrofurans, Tetrahedron, 1995, 51, 4383-4394;
    • (1995) Tetrahedron , vol.51 , pp. 4383-4394
    • Visser, M.S.1    Hoveyda, A.H.2
  • 80
    • 0031467338 scopus 로고    scopus 로고
    • Hydroxylated alpha-vinylpyrrolidines from sugar-derived 2,5- dihydrofurans. Synthesis of (1S, 2S, 8aR) 1, 2-dihydroxyindolizidine by ring closing olefin metathesis
    • Paolucci, C.; Musiani, L.; Venturelli, F.; Fava, A. Hydroxylated alpha-vinylpyrrolidines from sugar-derived 2,5- dihydrofurans. Synthesis of (1S, 2S, 8aR) 1, 2-dihydroxyindolizidine by ring closing olefin metathesis. Synthesis, 1997, 1415-1419;
    • (1997) Synthesis , pp. 1415-1419
    • Paolucci, C.1    Musiani, L.2    Venturelli, F.3    Fava, A.4
  • 81
    • 0032581698 scopus 로고    scopus 로고
    • An efficient one-pot synthesis of dialkyl 2,5-dihydrofuran- 2,3-dicarboxylates mediated by vinyltriphenylphosphonium salt
    • Yavari, I.; Mosslemin, M.H. An efficient one-pot synthesis of dialkyl 2,5-dihydrofuran- 2,3-dicarboxylates mediated by vinyltriphenylphosphonium salt. Tetrahedron, 1998 54, 9169-9174;
    • (1998) Tetrahedron , vol.54 , pp. 9169-9174
    • Yavari, I.1    Mosslemin, M.H.2
  • 82
    • 0039627909 scopus 로고    scopus 로고
    • A straight synthesis of 2-alpha-substituted N-tosylaminomethyl-2,5-dihydrofurans by the reaction of N-sulfonylimines with arsonium 4-hydroxyl-cis-2- butenylides
    • Li, A.; Deng, W.; Dai, L.; Hou, X. A straight synthesis of 2-alpha-substituted N-tosylaminomethyl-2,5-dihydrofurans by the reaction of N-sulfonylimines with arsonium 4-hydroxyl-cis-2- butenylides. Chin. J. Chem., 1999 17, 300-304;
    • (1999) Chin. J. Chem , vol.17 , pp. 300-304
    • Li, A.1    Deng, W.2    Dai, L.3    Hou, X.4
  • 83
    • 0033583006 scopus 로고    scopus 로고
    • Reaction of oxazirconacyclopentenes with propynoates. A new pathway for the formation of 2,5-dihydrofuran derivatives
    • Xi, C.J.; Kotora, M.; Takahashi, T. Reaction of oxazirconacyclopentenes with propynoates. A new pathway for the formation of 2,5-dihydrofuran derivatives. Tetrahedron Lett., 1999, 40, 2375-2378;
    • (1999) Tetrahedron Lett , vol.40 , pp. 2375-2378
    • Xi, C.J.1    Kotora, M.2    Takahashi, T.3
  • 84
    • 0034638688 scopus 로고    scopus 로고
    • Efficient synthesis of 4-(2'- alkenyl)-2,5-dihydrofurans via PdCl2-catalyzed coupling-cyclization reaction of 2,3-allenols with allylic halides
    • Ma, S.; Gao, W. Efficient synthesis of 4-(2'- alkenyl)-2,5-dihydrofurans via PdCl2-catalyzed coupling-cyclization reaction of 2,3-allenols with allylic halides. Tetrahedron Lett., 2000, 41, 8933-8936;
    • (2000) Tetrahedron Lett , vol.41 , pp. 8933-8936
    • Ma, S.1    Gao, W.2
  • 85
    • 0035804517 scopus 로고    scopus 로고
    • 2,5-Dimethoxy-2,5-dihydrofuran and vinyl ethers in the synthesis of functionalised 2-alkylfurans
    • Malanga, C.; Mannucci, S. 2,5-Dimethoxy-2,5-dihydrofuran and vinyl ethers in the synthesis of functionalised 2-alkylfurans. Tetrahedron Lett., 2001, 42, 2023-2025.
    • (2001) Tetrahedron Lett , vol.42 , pp. 2023-2025
    • Malanga, C.1    Mannucci, S.2
  • 86
    • 28444441995 scopus 로고    scopus 로고
    • Synthesis of dihydrofurans substituted in the 2-position
    • Kilroy, T.G.; O'Sullivan, T.P.; Guiry, P.J. Synthesis of dihydrofurans substituted in the 2-position. Eur. J. Org. Chem., 2005, 4929-4949.
    • (2005) Eur. J. Org. Chem , pp. 4929-4949
    • Kilroy, T.G.1    O'Sullivan, T.P.2    Guiry, P.J.3
  • 87
    • 33644525335 scopus 로고    scopus 로고
    • Pyridinium ylides in the synthesis of 2,3- dihydrofurans
    • Chuang, C.-P.; Tsai, A.-I. Pyridinium ylides in the synthesis of 2,3- dihydrofurans. Synthesis, 2006, 675-679.
    • (2006) Synthesis , pp. 675-679
    • Chuang, C.-P.1    Tsai, A.-I.2
  • 88
    • 84981756103 scopus 로고
    • Uber eine neue Methode zur Darstellung von alpha-Pyridonen und die Synthese des Nicotellins
    • Thesing, J.; Muller, A. Uber eine neue Methode zur Darstellung von alpha-Pyridonen und die Synthese des Nicotellins. Chem. Ber., 1957, 90, 711-723;
    • (1957) Chem. Ber , vol.90 , pp. 711-723
    • Thesing, J.1    Muller, A.2
  • 89
    • 37049097663 scopus 로고
    • A Preparation of tetrahydroindolizines from pyridinium and isoquinolinium ylids
    • Katritzky, A.R.; Grzeskowiak, N.E.; Builla, J. A Preparation of tetrahydroindolizines from pyridinium and isoquinolinium ylids. J. Chem. Soc., Perkin Trans. 1, 1981, 1180-1185;
    • (1981) J. Chem. Soc., Perkin Trans , vol.1 , pp. 1180-1185
    • Katritzky, A.R.1    Grzeskowiak, N.E.2    Builla, J.3
  • 90
    • 0346601498 scopus 로고
    • Stereochemical formation aspects of substituted hydrogenated 3-(1-pyridionio)-6-pyridinethiolates and synthesis of 4,6- diaryl-3-cyano-2(1H)-pyridinethiones on their basis
    • Shestopalov, A.M.; Shararin, Y.A.; Promomenkov, V.K. Stereochemical formation aspects of substituted hydrogenated 3-(1-pyridionio)-6-pyridinethiolates and synthesis of 4,6- diaryl-3-cyano-2(1H)-pyridinethiones on their basis. Khim. Geterotsikl. Soedin., 1990, 370-375;
    • (1990) Khim. Geterotsikl. Soedin , pp. 370-375
    • Shestopalov, A.M.1    Shararin, Y.A.2    Promomenkov, V.K.3
  • 91
    • 0025729637 scopus 로고
    • Stereoselective synthesis of trans-4,5-substituted 1,4,5,6-tetrahydropyridine-2-(olates)thiolates
    • Shestopalov, A.M.; Litvinov, V.P.; Rodinovskaya, L.A.; Sharanin, Y.A. Stereoselective synthesis of trans-4,5-substituted 1,4,5,6-tetrahydropyridine-2-(olates)thiolates. Synthesis, 1991, 402-404.
    • (1991) Synthesis , pp. 402-404
    • Shestopalov, A.M.1    Litvinov, V.P.2    Rodinovskaya, L.A.3    Sharanin, Y.A.4
  • 92
    • 0026572651 scopus 로고
    • Synthesis of C2-symmetry 2,2'- bipyridine and 1,10-phenanthroline chiral ligands bearig the 6,6- dimethylnorpinan-2-aryl group
    • Chelucci, G.; Falorni, M.; Giacomelli, G. Synthesis of C2-symmetry 2,2'- bipyridine and 1,10-phenanthroline chiral ligands bearig the 6,6- dimethylnorpinan-2-aryl group. Tetrahedron, 1992, 48, 3653-3658.
    • (1992) Tetrahedron , vol.48 , pp. 3653-3658
    • Chelucci, G.1    Falorni, M.2    Giacomelli, G.3
  • 93
    • 85023210227 scopus 로고
    • John Wiley & Sons, New York
    • Elderfield, R.C. In Heterocyclic Compounds, John Wiley & Sons, New York, 1950, Vol. 1, pp 455-472;
    • (1950) Heterocyclic Compounds , vol.1 , pp. 455-472
    • Elderfield, R.C.1
  • 94
    • 84876212924 scopus 로고
    • The chemistry of heterocyclic compounds
    • Interscience Publishers, New York
    • Klingsberg, E. The chemistry of heterocyclic compounds, Vol. 1, "Pyridine and its Derivatives", Interscience Publishers, New York, 1960, p. 477.
    • (1960) Pyridine and Its Derivatives , vol.1 , pp. 477
    • Klingsberg, E.1
  • 95
    • 0000043331 scopus 로고
    • Syntheses using pyridinium salts
    • Kröhnke, F. Syntheses using pyridinium salts, Angew. Chem. Int. Ed., 1963, 2, 225-238;
    • (1963) Angew. Chem. Int. Ed , vol.2 , pp. 225-238
    • Kröhnke, F.1
  • 96
    • 0002417273 scopus 로고
    • Synthesis using pyridinium salts 5. Specific synthesis of pyridines and oligopyridines
    • and references cited therein
    • Kröhnke, F. Synthesis using pyridinium salts 5. Specific synthesis of pyridines and oligopyridines. Synthesis, 1976, 1-24 and references cited therein.
    • (1976) Synthesis , pp. 1-24
    • Kröhnke, F.1
  • 97
    • 0037119317 scopus 로고    scopus 로고
    • Macromolecules containing bipyridine and terpyridine metal complexes: Towards metallosupramolecular polymers
    • and cited references therein
    • Schubert, U.S.; Eschbaumer, C. Macromolecules containing bipyridine and terpyridine metal complexes: Towards metallosupramolecular polymers. Angew. Chem. Int. Ed., 2002, 41, 2893-2926 and cited references therein.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 2893-2926
    • Schubert, U.S.1    Eschbaumer, C.2
  • 98
    • 84952138084 scopus 로고
    • Synthetic neuromuscular- and ganglionblocking agents - N-alkylated bipyridyls, bipiperidyls and their methylene and ethylene homologues
    • Beyerman, H.C.; Bontekoe, J.S. Synthetic neuromuscular- and ganglionblocking agents - N-alkylated bipyridyls, bipiperidyls and their methylene and ethylene homologues. Recl. Trav. Chim. Pays-Bas, 1955, 74, 1395-1404.
    • (1955) Recl. Trav. Chim. Pays-Bas , vol.74 , pp. 1395-1404
    • Beyerman, H.C.1    Bontekoe, J.S.2
  • 99
    • 32144447243 scopus 로고    scopus 로고
    • Synthesis and single-crystal X-ray characterization of 4,4"-functionalized 4'-(4- bromophenyl)-2,2':6',2"-terpyridines
    • Eryazici, I.; Moorefield, C.N.; Durmus, S.; Newkome, G.R. Synthesis and single-crystal X-ray characterization of 4,4"-functionalized 4'-(4- bromophenyl)-2,2':6',2"-terpyridines. J. Org. Chem., 2006, 71, 1009-1014.
    • (2006) J. Org. Chem , vol.71 , pp. 1009-1014
    • Eryazici, I.1    Moorefield, C.N.2    Durmus, S.3    Newkome, G.R.4
  • 100
    • 0035803142 scopus 로고    scopus 로고
    • Ru(II) complexes of polyarylated terpyridines: Unexpected side-chain C-metallation and photo sensitization of electron transfer
    • Mikel, C.; Potvin, P.G. Ru(II) complexes of polyarylated terpyridines: unexpected side-chain C-metallation and photo sensitization of electron transfer. Inorg. Chim. Acta, 2001, 325, 1-8.
    • (2001) Inorg. Chim. Acta , vol.325 , pp. 1-8
    • Mikel, C.1    Potvin, P.G.2
  • 101
    • 0000334457 scopus 로고
    • Synthesis of halogenated terpyridines and incorporation of the terpyridine nucleus into a polyethereal macrocycle
    • Newkome, G.R.; Hager, D.C.; Kiefer, G.E. Synthesis of halogenated terpyridines and incorporation of the terpyridine nucleus into a polyethereal macrocycle. J. Org. Chem., 1986, 51, 850-853;
    • (1986) J. Org. Chem , vol.51 , pp. 850-853
    • Newkome, G.R.1    Hager, D.C.2    Kiefer, G.E.3
  • 102
    • 33748648029 scopus 로고    scopus 로고
    • Novel synthesis of substituted 4'-hydroxy-2, 2':6', 2"- terpyridines
    • Fallahpour, R.-A.; Constable, E.C. Novel synthesis of substituted 4'-hydroxy-2, 2':6', 2"- terpyridines. J. Chem. Soc., Perkin Trans. I 1997, 2264-2264;
    • (1997) J. Chem. Soc., Perkin Trans , vol.1 , pp. 2264-2264
    • Fallahpour, R.-A.1    Constable, E.C.2
  • 103
    • 0001609363 scopus 로고    scopus 로고
    • Ruthenium(II) complexes of novel 4'- ethoxy- and 4'-hydroxy-5,5"-dimethyl-2,2':6',2"-terpyridines: X-ray crystal structures of 4'-ethoxy-5,5"-dimethyl-2,2":6',2"-terpyridine and the ruthenium(II) complex of 4'-ethoxy-5,5"-dimethyl-2,2':6',2"-terpyridine with 4'- chloro-2,2':6',2"'-terpyridine
    • Fallahpour, R.-A.; Neuburger, M.; Zehnder, M. Ruthenium(II) complexes of novel 4'- ethoxy- and 4'-hydroxy-5,5"-dimethyl-2,2':6',2"-terpyridines: X-ray crystal structures of 4'-ethoxy-5,5"-dimethyl-2,2":6',2"-terpyridine and the ruthenium(II) complex of 4'-ethoxy-5,5"-dimethyl-2,2':6',2"-terpyridine with 4'- chloro-2,2':6',2"'-terpyridine. Polyhedron, 1999, 18, 2445-2454.
    • (1999) Polyhedron , vol.18 , pp. 2445-2454
    • Fallahpour, R.-A.1    Neuburger, M.2    Zehnder, M.3
  • 104
    • 21144476629 scopus 로고
    • Preparation of new organic luminophores based on diacetylpyridines
    • Lhotak, P.; Kurfurst, A. Preparation of new organic luminophores based on diacetylpyridines. Collect. Czech. Chem. Commun., 1992, 57, 1937-1946;
    • (1992) Collect. Czech. Chem. Commun , vol.57 , pp. 1937-1946
    • Lhotak, P.1    Kurfurst, A.2
  • 105
    • 1642433452 scopus 로고    scopus 로고
    • Zinc(II) and ruthenium(II) complexes of novel fluorene substituted terpyridine ligands: Synthesis, spectroscopy and electrochemistry
    • Thomas, K.R.J.; Lin, J.T.; Chang, C.-P.; Chuen, C.-H.; Cheng, C.-C. Zinc(II) and ruthenium(II) complexes of novel fluorene substituted terpyridine ligands: Synthesis, spectroscopy and electrochemistry. J. Chin. Chem. Soc., 2002, 49, 833-840.
    • (2002) J. Chin. Chem. Soc , vol.49 , pp. 833-840
    • Thomas, K.R.J.1    Lin, J.T.2    Chang, C.-P.3    Chuen, C.-H.4    Cheng, C.-C.5
  • 106
    • 0001103421 scopus 로고
    • Pyridines. VI. Polypyridyls by the chichibabin synthesis
    • Frank, R.L.; Riener, E.F. Pyridines. VI. Polypyridyls by the chichibabin synthesis. J. Am. Chem. Soc., 1950, 72, 4182-4183.
    • (1950) J. Am. Chem. Soc , vol.72 , pp. 4182-4183
    • Frank, R.L.1    Riener, E.F.2
  • 107
    • 0025232882 scopus 로고
    • Spontaneous assembly of a double-helical binuclear complex of 2,2'-6',2"-6",2"'-6"',2"",6"",2""'-sexipyridine
    • Constable, E.C.; Ward, M.D. Spontaneous assembly of a double-helical binuclear complex of 2,2'-6',2"-6",2"'-6"',2"",6"",2""'-sexipyridine. J. Am. Chem. Soc., 1990, 112, 1256-1258;
    • (1990) J. Am. Chem. Soc , vol.112 , pp. 1256-1258
    • Constable, E.C.1    Ward, M.D.2
  • 108
    • 0001401952 scopus 로고    scopus 로고
    • Synthesis of cyclo-2,2':4',4":2",2"':4"',4"":2"",2""':4""',4-sexipyridine
    • Kelly, T.R.; Lee, Y.-J.; Mears, R.J. Synthesis of cyclo-2,2':4',4":2",2"':4"',4"":2"",2""':4""',4-sexipyridine. J. Org. Chem., 1997, 62, 2774-2781.
    • (1997) J. Org. Chem , vol.62 , pp. 2774-2781
    • Kelly, T.R.1    Lee, Y.-J.2    Mears, R.J.3
  • 109
    • 0000611145 scopus 로고
    • Dimetallic, trimetallic and tetrametallic double-stranded helical complexes derived from alkylthio-substituted septipyridines - Synthesis, structure and redox properties
    • Potts, K.T.; Keshavarzk, M.; Tham, F.S.; Raiford, K.A.G.; Arana, C.; Abruna, H.D. Dimetallic, trimetallic and tetrametallic double-stranded helical complexes derived from alkylthio-substituted septipyridines - Synthesis, structure and redox properties. Inorg. Chem., 1993, 32, 5477-5484.
    • (1993) Inorg. Chem , vol.32 , pp. 5477-5484
    • Potts, K.T.1    Keshavarzk, M.2    Tham, F.S.3    Raiford, K.A.G.4    Arana, C.5    Abruna, H.D.6
  • 110
    • 0031550599 scopus 로고    scopus 로고
    • A convergent approach to a solubilised septipyridine
    • Constable, E.C.; Smith, D.R. A convergent approach to a solubilised septipyridine. Tetrahedron, 1997, 53, 1715-1720.
    • (1997) Tetrahedron , vol.53 , pp. 1715-1720
    • Constable, E.C.1    Smith, D.R.2
  • 111
    • 33846369081 scopus 로고    scopus 로고
    • Synthesis of polycyclic indolizine derivatives via one-pot tandem reactions of N-ylides with dichloro substituted α,β-unsaturated carbonyl compounds
    • Liu, Y.; Hu H.-Y.; Liu, Q.-J.; Hu, H.-W.; Xu, J.-H. Synthesis of polycyclic indolizine derivatives via one-pot tandem reactions of N-ylides with dichloro substituted α,β-unsaturated carbonyl compounds. Tetrahedron, 2007, 63, 2024-2033.
    • (2007) Tetrahedron , vol.63 , pp. 2024-2033
    • Liu, Y.1    Hu, H.-Y.2    Liu, Q.-J.3    Hu, H.-W.4    Xu, J.-H.5
  • 112
    • 17844379479 scopus 로고    scopus 로고
    • Synthesis of some new indolizines
    • Sarkunam, K.; Nallu, M. Synthesis of some new indolizines. J. Heterocycl. Chem., 2005, 42, 5-11;
    • (2005) J. Heterocycl. Chem , vol.42 , pp. 5-11
    • Sarkunam, K.1    Nallu, M.2
  • 113
    • 2542421781 scopus 로고    scopus 로고
    • Synthesis of monofluorinated indolizines and their derivatives by the 1,3- dipolar reaction of N-ylides with fluorinated vinyl tosylates
    • Fang, X.; Wu, Y.-M.; Deng, J.; Wang, S.-W. Synthesis of monofluorinated indolizines and their derivatives by the 1,3- dipolar reaction of N-ylides with fluorinated vinyl tosylates. Tetrahedron, 2004, 60, 5487-5493;
    • (2004) Tetrahedron , vol.60 , pp. 5487-5493
    • Fang, X.1    Wu, Y.-M.2    Deng, J.3    Wang, S.-W.4
  • 114
    • 0037238451 scopus 로고    scopus 로고
    • Synthesis of fluorinated indolizines and 4H-pyrrolo[1,2-alpha]benzimidazoles via 1,3-dipolar cycloaddition of fluoroalkenes to N-ylides
    • Wu, K.; Chen, Q.-Y. Synthesis of fluorinated indolizines and 4H-pyrrolo[1,2-alpha]benzimidazoles via 1,3-dipolar cycloaddition of fluoroalkenes to N-ylides. Synthesis, 2003, 35-40;
    • (2003) Synthesis , pp. 35-40
    • Wu, K.1    Chen, Q.-Y.2
  • 115
    • 0032979272 scopus 로고    scopus 로고
    • Synthesis of 5-(2-phenylethenyl)indolizines by selective intermolecular 1,3-dipolar cycloaddition of 2-(2-phenylethenyl)pyridinium N-ylide with alkenes promoted by tetrakis-pyridine cobalt(II) dichromate
    • Zhou, J.; Hu, Y.; Hu, H Synthesis of 5-(2-phenylethenyl)indolizines by selective intermolecular 1,3-dipolar cycloaddition of 2-(2-phenylethenyl)pyridinium N-ylide with alkenes promoted by tetrakis-pyridine cobalt(II) dichromate. J. Chem. Res. S., 1999, 136-137;
    • (1999) J. Chem. Res. S , pp. 136-137
    • Zhou, J.1    Hu, Y.2    Hu, H.3
  • 116
    • 0030959037 scopus 로고    scopus 로고
    • A convenient synthesis of 1-acylindolizines by 1,3-dipolar cycloaddition reactions of pyridinium ylides and α,β-unsaturated aldehydes or ketones in the presence of tetrakis-pyridine cobalt dichromate
    • Zhang, X.; Cao, W.; Wei, X.; Hu, H. A convenient synthesis of 1-acylindolizines by 1,3-dipolar cycloaddition reactions of pyridinium ylides and α,β-unsaturated aldehydes or ketones in the presence of tetrakis-pyridine cobalt dichromate. Synth. Commun., 1997, 27, 1395- 1403;
    • (1997) Synth. Commun , vol.27 , pp. 1395-1403
    • Zhang, X.1    Cao, W.2    Wei, X.3    Hu, H.4
  • 117
    • 37049074960 scopus 로고
    • A facile one-step synthesis of aromatic indolizines by 1,3-dipolar cycloaddition of pyridinium and related heteroaromatic ylides with alkenes in the presence of TPCD [Copy4(HCrO4)2]
    • Wei, X.; Hu, Y.; Li, T.; Hu, H. A facile one-step synthesis of aromatic indolizines by 1,3-dipolar cycloaddition of pyridinium and related heteroaromatic ylides with alkenes in the presence of TPCD [Copy4(HCrO4)2]. J. Chem. Soc., Perk. Trans. 1, 1993, 20, 2487-2489;
    • (1993) J. Chem. Soc., Perk. Trans. 1 , vol.20 , pp. 2487-2489
    • Wei, X.1    Hu, Y.2    Li, T.3    Hu, H.4
  • 118
    • 84986487115 scopus 로고
    • Regioselectivity in the 1,3-dipolar cycloaddition reaction of unsymmetric pyridinium dicyanomethylides with dimethyl acetylenedicarboxylate and methyl propiolate - An example of dipole-dipole control of regioselectivity
    • Matsumoto, K.; Ikemi, Y.; Konishi, H.; Shi, X.; Uchida, T.; Aoyama, K. Regioselectivity in the 1,3-dipolar cycloaddition reaction of unsymmetric pyridinium dicyanomethylides with dimethyl acetylenedicarboxylate and methyl propiolate - An example of dipole-dipole control of regioselectivity. J. Heterocycl. Chem., 1988, 25, 689-692;
    • (1988) J. Heterocycl. Chem , vol.25 , pp. 689-692
    • Matsumoto, K.1    Ikemi, Y.2    Konishi, H.3    Shi, X.4    Uchida, T.5    Aoyama, K.6
  • 119
    • 85196232060 scopus 로고
    • 1,3- Dipolar cycloadditions of pyridinium and diazinium dicyanomethylids with bis(trimethylsilyl)acetylene as an acetylene equivalent in 1,3-dipolar cycloaddition
    • Ikemi, Y.; Matsumoto, K.; Uchida, T. 1,3- Dipolar cycloadditions of pyridinium and diazinium dicyanomethylids with bis(trimethylsilyl)acetylene as an acetylene equivalent in 1,3-dipolar cycloaddition. Heterocycles, 1983, 20, 1009-1012;
    • (1983) Heterocycles , vol.20 , pp. 1009-1012
    • Ikemi, Y.1    Matsumoto, K.2    Uchida, T.3
  • 120
    • 0342975599 scopus 로고
    • Generation and 1,3-dipolar behaviour of pyridinium arylsulfonylmethylides - Simple route to indolizines
    • Abramovitch, R. A.; Alexanian, V. Generation and 1,3-dipolar behaviour of pyridinium arylsulfonylmethylides - Simple route to indolizines. J. Org. Chem., 1976, 41, 2144- 2148;
    • (1976) J. Org. Chem , vol.41 , pp. 2144-2148
    • Abramovitch, R.A.1    Alexanian, V.2
  • 121
    • 84982412162 scopus 로고
    • Indolizines form phenacylcyclimonium salts
    • Fröhlich, J.; Kröhnke, F. Indolizines form phenacylcyclimonium salts. Chem. Ber., 1971, 104, 1621-1628;
    • (1971) Chem. Ber , vol.104 , pp. 1621-1628
    • Fröhlich, J.1    Kröhnke, F.2
  • 122
    • 84982064242 scopus 로고
    • Synthesis of fluoranthenes and related aromatic polycycles by means of pyridinium salts
    • Curtze, J.R.; Duchardt, K.H.; Kröhnke, F. Synthesis of fluoranthenes and related aromatic polycycles by means of pyridinium salts. Chem. Ber., 1979, 112, 2197-2208;
    • (1979) Chem. Ber , vol.112 , pp. 2197-2208
    • Curtze, J.R.1    Duchardt, K.H.2    Kröhnke, F.3
  • 123
    • 0001257642 scopus 로고
    • Formation of pyrrocolines by reaction of dimethyl acetylenecarboxylate with heterocyclic zwitterions
    • Boekelheide, V.; Fahrenholtz, K. Formation of pyrrocolines by reaction of dimethyl acetylenecarboxylate with heterocyclic zwitterions. J. Am. Chem. Soc., 1961, 83, 458-462.
    • (1961) J. Am. Chem. Soc , vol.83 , pp. 458-462
    • Boekelheid, V.1    Fahrenholt, K.2
  • 124
    • 0033527813 scopus 로고    scopus 로고
    • Synthesis of indolizine derivatives by the reaction of 2-(2'-pyridyl)-pyridinium ylides with ethylenic dipolarophiles
    • Druta, I.I.; Andrei, M.A.; Ganj, C.I.; Aburel, P.S. Synthesis of indolizine derivatives by the reaction of 2-(2'-pyridyl)-pyridinium ylides with ethylenic dipolarophiles. Tetrahedron, 1999, 55, 13063-13070;
    • (1999) Tetrahedron , vol.55 , pp. 13063-13070
    • Druta, I.I.1    Andrei, M.A.2    Ganj, C.I.3    Aburel, P.S.4
  • 125
    • 0032485366 scopus 로고    scopus 로고
    • Synthesis of 5-(2'-pyridyl)-indolizines by the reaction of 2-(2'-pyridyl)-pyridiniumylides with activated alkynes
    • Druta, I.I.; Andrei, M.A.; Aburel, P.S. Synthesis of 5-(2'-pyridyl)-indolizines by the reaction of 2-(2'-pyridyl)-pyridiniumylides with activated alkynes. Tetrahedron, 1998, 54, 2107-2112.
    • (1998) Tetrahedron , vol.54 , pp. 2107-2112
    • Druta, I.I.1    Andrei, M.A.2    Aburel, P.S.3
  • 126
    • 0000033912 scopus 로고    scopus 로고
    • Preparation of 1- trifluoroacetyl indolizines and their derivatives via the cycloaddition of pyridinium N-ylides with 4-4-ethoxyl-1,1,1-trifluorobut-3-enone
    • Zhu, S.-z.; Qin, C.-y.; Wang, Y.-L.; Chu, Q.-l. Preparation of 1- trifluoroacetyl indolizines and their derivatives via the cycloaddition of pyridinium N-ylides with 4-4-ethoxyl-1,1,1-trifluorobut-3-enone. J. Fluorine Chem., 1999, 99, 183-187.
    • (1999) J. Fluorine Chem , vol.99 , pp. 183-187
    • Zhu, S.-Z.1    Qin, C.-Y.2    Wang, Y.-L.3    Chu, Q.-L.4
  • 127
    • 85178961265 scopus 로고
    • Tautomerie in der Pyridin-Reihe
    • Chichibabin, A.E. Tautomerie in der Pyridin-Reihe. Chem. Ber., 1927, 60, 1607-1617;
    • (1927) Chem. Ber , vol.60 , pp. 1607-1617
    • Chichibabin, A.E.1
  • 128
    • 84993869502 scopus 로고
    • Methods for construction of the indolizine nucleus
    • Uchida, T.; Matsumoto, K. Methods for construction of the indolizine nucleus. Synthesis, 1976, 209-239;
    • (1976) Synthesis , pp. 209-239
    • Uchida, T.1    Matsumoto, K.2
  • 130
    • 0242383403 scopus 로고    scopus 로고
    • A practical parallel synthesis of 2-substituted indolizines
    • Chai, W.; Kwok, A.; Wong, V.; Carruthers, N.I.; Wu, J. A practical parallel synthesis of 2-substituted indolizines. Synlett, 2003, 2086-2088;
    • (2003) Synlett , pp. 2086-2088
    • Chai, W.1    Kwok, A.2    Wong, V.3    Carruthers, N.I.4    Wu, J.5
  • 131
    • 0035917326 scopus 로고    scopus 로고
    • Chichibabin indolizine synthesis revisited: Synthesis of indolizinones by solvolysis of 4- alkoxycarbonyl-3-oxotetrahydroquinolizinium ylides
    • Kostik, E.; Abiko, A.; Oku, A. Chichibabin indolizine synthesis revisited: Synthesis of indolizinones by solvolysis of 4- alkoxycarbonyl-3-oxotetrahydroquinolizinium ylides. J. Org. Chem., 2001, 66, 2618-2623;
    • (2001) J. Org. Chem , vol.66 , pp. 2618-2623
    • Kostik, E.1    Abiko, A.2    Oku, A.3
  • 132
    • 33644788991 scopus 로고    scopus 로고
    • An improved synthesis of some 5-substituted indolizines using regiospecific lithiation
    • Kuznetosv, A.G.; Bush, A.; Rybakov, V.B.; Babaev, E.V. An improved synthesis of some 5-substituted indolizines using regiospecific lithiation. Molecules, 2005, 10, 1074-1083.
    • (2005) Molecules , vol.10 , pp. 1074-1083
    • Kuznetosv, A.G.1    Bush, A.2    Rybakov, V.B.3    Babaev, E.V.4
  • 133
    • 0042566349 scopus 로고    scopus 로고
    • A novel microwave-mediated one-pot synthesis of indolizines via a three-component reaction
    • Bora, U.; Saikia, A.; Bouah, R. A novel microwave-mediated one-pot synthesis of indolizines via a three-component reaction. Org. Lett., 2003, 5, 435- 438.
    • (2003) Org. Lett , vol.5 , pp. 435-438
    • Bora, U.1    Saikia, A.2    Bouah, R.3
  • 134
    • 0031209335 scopus 로고    scopus 로고
    • Syntheses and characterization of new styryl fluorescent dyes from DAMN
    • Jaung, J.Y.; Matsuoka, M.; Fukunishi, K. Syntheses and characterization of new styryl fluorescent dyes from DAMN. Part II, Dyes and pigments, 1997, 34, 255-266;
    • (1997) Part II, Dyes and Pigments , vol.34 , pp. 255-266
    • Jaung, J.Y.1    Matsuoka, M.2    Fukunishi, K.3
  • 135
    • 0032010448 scopus 로고    scopus 로고
    • Dicyanopyrazine studies. Syntheses and characterization of new bis-styryl fluorescent dyes from DAMN
    • Jaung, J.Y.; Matsuoka, M.; Fukunishi, K. Dicyanopyrazine studies. Syntheses and characterization of new bis-styryl fluorescent dyes from DAMN. Part III Dyes and pigments, 1998, 36, 395-405;
    • (1998) Part III Dyes and Pigments , vol.36 , pp. 395-405
    • Jaung, J.Y.1    Matsuoka, M.2    Fukunishi, K.3
  • 136
    • 0032036073 scopus 로고    scopus 로고
    • Dicyanopyrazine studies. Part IV: Syntheses and solid state absorption spectra of new dicyanopyrazine dyes derived from dichlorodicyanopyrazine and Fisher's type bases
    • Jaung, J.Y. Matsuoka, M.; Fukunishi, K. Dicyanopyrazine studies. Part IV: Syntheses and solid state absorption spectra of new dicyanopyrazine dyes derived from dichlorodicyanopyrazine and Fisher's type bases. Dyes and pigments, 1998, 37, 135-144.
    • (1998) Dyes and Pigments , vol.37 , pp. 135-144
    • Jaung, J.Y.1    Matsuoka, M.2    Fukunishi, K.3
  • 137
    • 0347004674 scopus 로고    scopus 로고
    • 1,3-Dipolar cycloaddition reactions of pyridinium azomethine ylides containing 5,6-dicyanopyrazines
    • Jaung, J.Y.; Jung, Y.S. 1,3-Dipolar cycloaddition reactions of pyridinium azomethine ylides containing 5,6-dicyanopyrazines. Bull. Korean Chem. Soc., 2003, 24, 1565-1566;
    • (2003) Bull. Korean Chem. Soc , vol.24 , pp. 1565-1566
    • Jaung, J.Y.1    Jung, Y.S.2
  • 138
    • 10644244455 scopus 로고    scopus 로고
    • Halochromism of pyridinium azomethine ylides stabilized by dicyanopyrazine group
    • Jung, Y.S.; Jaung, J.Y. Halochromism of pyridinium azomethine ylides stabilized by dicyanopyrazine group. Dyes and pigments, 2005, 65, 205-209.
    • (2005) Dyes and Pigments , vol.65 , pp. 205-209
    • Jung, Y.S.1    Jaung, J.Y.2
  • 140
    • 84937193770 scopus 로고
    • S. Patai and Z. Rappoport, Eds., John Wiley & sons, New York
    • Naruta, Y.; Maruyama, K. The chemistry of quinoid compounds, Vol II, S. Patai and Z. Rappoport, Eds., John Wiley & sons, New York, 1988, p. 241- 402.
    • (1988) The Chemistry of Quinoid Compounds , vol.2 , pp. 241-402
    • Naruta, Y.1    Maruyama, K.2
  • 141
    • 37049110186 scopus 로고
    • Alkylation of quinones by carbanions - Uze of pyridinium ylids to insert phenacyl, acetonyl and related groups
    • Aldersley, M.F.; Dean, F.M.; Nayyirmazhir, R. Alkylation of quinones by carbanions - Uze of pyridinium ylids to insert phenacyl, acetonyl and related groups. J. Chem. Soc., Perkin Trans. I, 1983, 1753-1757;
    • (1983) J. Chem. Soc., Perkin Trans. I , pp. 1753-1757
    • Aldersley, M.F.1    Dean, F.M.2    Nayyirmazhir, R.3
  • 142
    • 37049073764 scopus 로고
    • Adducts from quinones and diazoalkanes 10. 2-Diazopropane and 2-methyl-1,4-naphthoquinone - Structures and conformations of novel vinylic quinones and epoxides
    • Aldersley, M.F.; Dean, F.M.; Mann, B.E. Adducts from quinones and diazoalkanes 10. 2-Diazopropane and 2-methyl-1,4-naphthoquinone - Structures and conformations of novel vinylic quinones and epoxides. J. Chem. Soc., Perkin Trans. I, 1986, 2217-2222;
    • (1986) J. Chem. Soc., Perkin Trans. I , pp. 2217-2222
    • Aldersley, M.F.1    Dean, F.M.2    Mann, B.E.3
  • 143
    • 0001007853 scopus 로고
    • Derivatives of naphtho[2,3-c]pyran-5,10-dione - A simple synthesis and a note of their chromogenic properties
    • Aldersley, M.F.; Dean, F.M.; Hanzah, A.S. Derivatives of naphtho[2,3-c]pyran-5,10-dione - A simple synthesis and a note of their chromogenic properties. Tetrahedron Lett., 1986, 27, 255-258;
    • (1986) Tetrahedron Lett , vol.27 , pp. 255-258
    • Aldersley, M.F.1    Dean, F.M.2    Hanzah, A.S.3
  • 144
    • 37049080295 scopus 로고
    • Pyridinium ylids in syntheses of naphthopyrandiones and in regioselective syntheses of acylated anthraquinones related to fungal and bacterial metabolites
    • Aldersley, M.F.; Chishti, S.H.; Dean, F.M.; Douglas, M.E.; Ennis, D.S. Pyridinium ylids in syntheses of naphthopyrandiones and in regioselective syntheses of acylated anthraquinones related to fungal and bacterial metabolites. J. Chem. Soc., Perkin Trans. I, 1990, 2163-2174.
    • (1990) J. Chem. Soc., Perkin Trans. I , pp. 2163-2174
    • Aldersley, M.F.1    Chishti, S.H.2    Dean, F.M.3    Douglas, M.E.4    Ennis, D.S.5
  • 145
    • 0034737427 scopus 로고    scopus 로고
    • Synthetic strategies towards pyranonaphthoquinone antibiotics
    • Brimble, M.A.; Nairn, M.R.; Prabaharan, H. Synthetic strategies towards pyranonaphthoquinone antibiotics. Tetrahedron, 2000, 56, 1937-1992;
    • (2000) Tetrahedron , vol.56 , pp. 1937-1992
    • Brimble, M.A.1    Nairn, M.R.2    Prabaharan, H.3
  • 146
    • 34247130452 scopus 로고    scopus 로고
    • A survey of synthetic routes towards the pyranonaphthoquinone antibiotic pentalongin and syntheses of the corresponding nitrogen derivatives
    • Claessens, S.; Verniest, G.; Jacobs, J.; Van Hende, E.; Habonimana, P.; Nguyen Van, T.; Van Puyvelde, L.; De Kimpe, N. A survey of synthetic routes towards the pyranonaphthoquinone antibiotic pentalongin and syntheses of the corresponding nitrogen derivatives. Synlett, 2007, 829-850.
    • (2007) Synlett , pp. 829-850
    • Claessens, S.1    Verniest, G.2    Jacobs, J.3    van Hende, E.4    Habonimana, P.5    van Nguyen, T.6    van Puyvelde, L.7    de Kimpe, N.8
  • 147
    • 33947296590 scopus 로고
    • Basicity of N-ylides
    • Philips, W.G.; Ratts, K.W. Basicity of N-ylides. J. Org. Chem., 1970, 35, 3144-3147.
    • (1970) J. Org. Chem , vol.35 , pp. 3144-3147
    • Philips, W.G.1    Ratts, K.W.2
  • 148
    • 0033548008 scopus 로고    scopus 로고
    • Synthesis of 3-alkyl- and 3- aryl-2-aza-anthraquinones
    • Kesteleyn, B.; Nguyen Van, T.; De Kimpe, N. Synthesis of 3-alkyl- and 3- aryl-2-aza-anthraquinones. Tetrahedron, 1999, 55, 2091-2102.
    • (1999) Tetrahedron , vol.55 , pp. 2091-2102
    • Kesteleyn, B.1    van Nguyen, T.2    de Kimpe, N.3
  • 149
    • 85196229335 scopus 로고    scopus 로고
    • Isagarin, a new type of tetracyclic naphthoquinone from the roots of Pentas longiflora
    • Van Puyvelde, L.; El-Hady, S.; De Kimpe, N.; Ferreau-Dupont, J.; Declercq, J.P. Isagarin, a new type of tetracyclic naphthoquinone from the roots of Pentas longiflora. J. Nat. Prod., 1998, 64, 438-440.
    • (1998) J. Nat. Prod , vol.64 , pp. 438-440
    • van Puyvelde, L.1    El-Hady, S.2    de Kimpe, N.3    Ferreau-Dupont, J.4    Declercq, J.P.5
  • 150
    • 0033593254 scopus 로고    scopus 로고
    • Synthesis of isagarin, a new type of tetracyclic naphthoquinone from Pentas longiflora
    • Kesteleyn, B.; Van Puyvelde, L.; De Kimpe, N. Synthesis of isagarin, a new type of tetracyclic naphthoquinone from Pentas longiflora. J. Org. Chem., 1999, 64, 438-440.
    • (1999) J. Org. Chem , vol.64 , pp. 438-440
    • Kesteleyn, B.1    van Puyvelde, L.2    de Kimpe, N.3
  • 151
    • 33846807716 scopus 로고    scopus 로고
    • New synthesis of N-substituted benz[g]isoquinoline-3,5,10(2H)-triones
    • Jacobs, J.; Claessens, S.; Kesteleyn, B.; Huygen, K.; De Kimpe, N. New synthesis of N-substituted benz[g]isoquinoline-3,5,10(2H)-triones. Tetrahedron, 2007, 63, 2503-2510.
    • (2007) Tetrahedron , vol.63 , pp. 2503-2510
    • Jacobs, J.1    Claessens, S.2    Kesteleyn, B.3    Huygen, K.4    de Kimpe, N.5
  • 152
    • 58149152847 scopus 로고    scopus 로고
    • New and highly efficient synthesis of 3-substituted 1- hydroxybenz[g]isoquinoline-5,10-diones
    • Jacobs, J.; Claessens, S.; Mbala Mavinga, B.; Huygen, K.; De Kimpe, N. New and highly efficient synthesis of 3-substituted 1- hydroxybenz[g]isoquinoline-5,10-diones. Tetrahedron, 2009, 65, 1193-1199.
    • (2009) Tetrahedron , vol.65 , pp. 1193-1199
    • Jacobs, J.1    Claessens, S.2    Mbala, M.B.3    Huygen, K.4    de Kimpe, N.5
  • 153
    • 18744414266 scopus 로고    scopus 로고
    • New developments in nucleophilic additions to nitrones
    • Merino, P. New developments in nucleophilic additions to nitrones. Comptes Rendus Chimie, 2005, 8, 775-788;
    • (2005) Comptes Rendus Chimie , vol.8 , pp. 775-788
    • Merino, P.1
  • 154
    • 2942669882 scopus 로고    scopus 로고
    • Nitrone in L-lyxose series: Cycloaddition way for the synthesis of new C-alpha-fucosides
    • Chevrier, C.; LeNouen, D.; Neuburger, M.; Defoin, A.; Tarnus, C. Nitrone in L-lyxose series: cycloaddition way for the synthesis of new C-alpha-fucosides. Tetrahedron Lett., 2004, 45, 5363-5366.
    • (2004) Tetrahedron Lett , vol.45 , pp. 5363-5366
    • Chevrier, C.1    Lenouen, D.2    Neuburger, M.3    Defoin, A.4    Tarnus, C.5
  • 156
    • 0000178124 scopus 로고
    • Functionalized nitrones - Highly stereoselective and regioselective synthesis of DL-Retronecine
    • Tufariello, J.J.; Lee, G.E. Functionalized nitrones - Highly stereoselective and regioselective synthesis of DL-Retronecine. J. Am. Chem. Soc., 1980, 102, 373-374;
    • (1980) J. Am. Chem. Soc , vol.102 , pp. 373-374
    • Tufariello, J.J.1    Lee, G.E.2
  • 157
    • 84984195854 scopus 로고
    • Aminyl oxides (nitroxides) 37. Formation of vinylaminyl oxides substituted by electron- acceptor groups and related radicals as studied by electron-spinresonance spectroscopy
    • Aurich, H.G.; Schmidt, M.; Schwerzel, T. Aminyl oxides (nitroxides) 37. Formation of vinylaminyl oxides substituted by electron- acceptor groups and related radicals as studied by electron-spinresonance spectroscopy. Chem. Ber., 1985, 118, 1086-1104.
    • (1985) Chem. Ber , vol.118 , pp. 1086-1104
    • Aurich, H.G.1    Schmidt, M.2    Schwerzel, T.3
  • 158
    • 0000814757 scopus 로고
    • Oxidation of imines to nitrones by the permanganate ion
    • Christensen, D.; Jorgensen, K.A. Oxidation of imines to nitrones by the permanganate ion, J. Org. Chem., 1989, 54, 126-131;
    • (1989) J. Org. Chem , vol.54 , pp. 126-131
    • Christensen, D.1    Jorgensen, K.A.2
  • 160
    • 33751553196 scopus 로고
    • Tngstatecatalyzed oxidation of secondary amines to nitrones - Alpha-substitution of secondary amines via nitrones
    • Murahashi, S.-I.; Mitsui, H.; Shiota, T.; Tsuda, T.; Watanabe, S. Tngstatecatalyzed oxidation of secondary amines to nitrones - Alpha-substitution of secondary amines via nitrones. J. Org. Chem., 1990, 55, 1736-1744.
    • (1990) J. Org. Chem , vol.55 , pp. 1736-1744
    • Murahashi, S.-I.1    Mitsui, H.2    Shiota, T.3    Tsuda, T.4    Watanabe, S.5
  • 161
    • 0000361728 scopus 로고
    • An efficiënt synthesis of 5-membered cyclic nitrones from gamma-nitroketones
    • Zschiesche, R.; Reissig, H.V. An efficiënt synthesis of 5-membered cyclic nitrones from gamma-nitroketones. Tetrahedron Lett., 1988, 29, 1685-1686.
    • (1988) Tetrahedron Lett , vol.29 , pp. 1685-1686
    • Zschiesche, R.1    Reissig, H.V.2
  • 164
    • 85171876059 scopus 로고
    • Uber α-Keto-aldinitrone und eine neue Darstellungsweise von α-Keto-aldehyden
    • Kröhnke, F.; Borner, E. Uber α-Keto-aldinitrone und eine neue Darstellungsweise von α-Keto-aldehyden. Chem. Ber., 1936, 69, 2006-2016.
    • (1936) Chem. Ber , vol.69 , pp. 2006-2016
    • Kröhnke, F.1    Borner, E.2
  • 166
    • 0030825651 scopus 로고    scopus 로고
    • The first 1,7-electrocyclizations of butadienyl pyridinium ylides: Stereoselective formation of 1,2-annulated 2,3- dihydroazepines
    • Marx, K.; Eberbach, W. The first 1,7-electrocyclizations of butadienyl pyridinium ylides: stereoselective formation of 1,2-annulated 2,3- dihydroazepines. Tetrahedron, 1997, 53, 14687-14700
    • (1997) Tetrahedron , vol.53 , pp. 14687-14700
    • Marx, K.1    Eberbach, W.2
  • 167
    • 0034595709 scopus 로고    scopus 로고
    • 8-Phenyl-10,10a-dihydropyridol[1,2-a]azepines by 1,7- electrocyclization of conjugated pyridinium ylides - Rationalization of the periselectivity
    • Marx, K. Eberbach, W. 8-Phenyl-10,10a-dihydropyridol[1,2-a]azepines by 1,7- electrocyclization of conjugated pyridinium ylides - Rationalization of the periselectivity. Chem. Eur. J., 2000, 6, 2063-2068.
    • (2000) Chem. Eur. J , vol.6 , pp. 2063-2068
    • Marx, K.1    Eberbach, W.2
  • 168
    • 33745051395 scopus 로고    scopus 로고
    • Cascade reactions of nitrogen- and phosphorus-containing ylides with methyl diazoacetate and in situ generated diazocyclopropane
    • Tomilov, Y.V.; Platonov, D.N., Dorokhov, D.V.; Kostyuchenko, L.V. Cascade reactions of nitrogen- and phosphorus-containing ylides with methyl diazoacetate and in situ generated diazocyclopropane. Russ. Chem. Bull., 2006, 55, 112-117.
    • (2006) Russ. Chem. Bull , vol.55 , pp. 112-117
    • Tomilov, Y.V.1    Platonov, D.N.2    Dorokhov, D.V.3    Kostyuchenko, L.V.4
  • 169
    • 0007585171 scopus 로고    scopus 로고
    • Michael addition versus 1,3- cycloaddition reactions of pyridinium ylides with (arylmethylene)isoxazol-5- ones: Diastereoselective formation of 4-[1-aryl-2-(1- pyridinio)ethyl]isoxazolium-5-olates
    • Risitano, F.; Grassi, G.; Bruno, G.; Nicolo, F. Michael addition versus 1,3- cycloaddition reactions of pyridinium ylides with (arylmethylene)isoxazol-5- ones: diastereoselective formation of 4-[1-aryl-2-(1- pyridinio)ethyl]isoxazolium-5-olates, Ann., 1997, 441-445
    • (1997) Ann , pp. 441-445
    • Risitano, F.1    Grassi, G.2    Bruno, G.3    Nicolo, F.4
  • 170
    • 0015320843 scopus 로고
    • Novel antihelmintic agents 6. Pyrantel analogs with activity against whipworm
    • McFarland, J.W.; Howes, H.L. Novel antihelmintic agents 6. Pyrantel analogs with activity against whipworm. J. Med. Chem., 1972, 15, 365-368.
    • (1972) J. Med. Chem , vol.15 , pp. 365-368
    • McFarland, J.W.1    Howes, H.L.2


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