메뉴 건너뛰기




Volumn 36, Issue 10, 2003, Pages 773-782

The Emergence of Allenamides in Organic Synthesis

Author keywords

[No Author keywords available]

Indexed keywords

ALLENAMIDE DERIVATIVE; ALLENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0142213273     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar030029i     Document Type: Article
Times cited : (345)

References (90)
  • 1
    • 0002266484 scopus 로고
    • Heterosubstituierte Allene and Polyallene
    • Kropf, H., Schaumann, E., Eds.; Georg Thieme Verlag: Stuttgart
    • For reviews, see: (a) Saalfrank, R. W.; Lurz, C. J. Heterosubstituierte Allene and Polyallene. In Methoden Der Organischen Chemie (Houben-Weyl); Kropf, H., Schaumann, E., Eds.; Georg Thieme Verlag: Stuttgart, 1993; pp 3093-3102.
    • (1993) Methoden Der Organischen Chemie (Houben-Weyl) , pp. 3093-3102
    • Saalfrank, R.W.1    Lurz, C.J.2
  • 3
    • 0027401155 scopus 로고
    • Alkoxyallenes-Building Blocks in Organic Synthesis
    • (c) For a review on chemistry of allenol ethers, see: Zimmer, R. Alkoxyallenes-Building Blocks in Organic Synthesis. Synthesis 1993, 165.
    • (1993) Synthesis , pp. 165
    • Zimmer, R.1
  • 4
    • 0003078710 scopus 로고
    • Base-Catalyzed Prototropic Isomerisations
    • Hubert, A. J.; Viehe, H. G. Base-Catalyzed Prototropic Isomerisations. J. Chem. Soc. 1968, 228-231.
    • (1968) J. Chem. Soc. , pp. 228-231
    • Hubert, A.J.1    Viehe, H.G.2
  • 6
    • 0026329664 scopus 로고
    • The Organocopper Route From [2-Propynylidene]morpholinium Triflates to Morpholino Allenes, 1-Morpholino-1,3-butadienes and 2-Morpholino-1-3-butadienes
    • Maas, G.; Mayer, T. The Organocopper Route From [2-Propynylidene]morpholinium Triflates to Morpholino Allenes, 1-Morpholino-1,3-butadienes and 2-Morpholino-1-3-butadienes. Synthesis 1991, 1209-1215.
    • (1991) Synthesis , pp. 1209-1215
    • Maas, G.1    Mayer, T.2
  • 8
    • 0142191967 scopus 로고
    • Lithiated 3-Trimethylsilyl-1-ethylaminopropynes
    • (b) Pennanen, S. I. Lithiated 3-Trimethylsilyl-1-ethylaminopropynes. Finn. Chem. Lett. 1984, 95-96.
    • (1984) Finn. Chem. Lett. , pp. 95-96
    • Pennanen, S.I.1
  • 9
    • 49149140321 scopus 로고
    • Synthesis of α,β-Unsaturated Aldehydes via 1-Aminopropa-1,2-dienes. Mechanistic Studies
    • An example of γ-lithiated allenamines: Craig, J. C.; Ekwuribe, N. N., Synthesis of α,β-Unsaturated Aldehydes via 1-Aminopropa-1,2-dienes. Mechanistic Studies. Tetrahedron Lett. 1980, 21, 2587-2590.
    • (1980) Tetrahedron Lett. , vol.21 , pp. 2587-2590
    • Craig, J.C.1    Ekwuribe, N.N.2
  • 11
    • 37049081117 scopus 로고
    • Site-Selective and Regioselective Cycloaddition of N-Propadienyl-anilines with Nitrile Oxides
    • For [3 + 2] cycloaddition, see: Broggini, G.; Zecchi, G., Site-Selective and Regioselective Cycloaddition of N-Propadienyl-anilines with Nitrile Oxides. J. Chem. Soc., Perkin Trans. 1 1991, 1843-1846.
    • (1991) J. Chem. Soc., Perkin Trans. 1 , pp. 1843-1846
    • Broggini, G.1    Zecchi, G.2
  • 12
    • 0025896599 scopus 로고
    • A Peculiar Reaction of Aminoallenes with Aromatic and Heteroaromatic Aldehydes
    • For [2 + 2] cycloadditions, see: (a) Niji, R.; Verkruijsse, H. D.; Harder, S.; van der Kerk, A. C. H. T. M.; Brandsma, L. A Peculiar Reaction of Aminoallenes with Aromatic and Heteroaromatic Aldehydes. Synth. Commun. 1991, 21, 653-656.
    • (1991) Synth. Commun. , vol.21 , pp. 653-656
    • Niji, R.1    Verkruijsse, H.D.2    Harder, S.3    Van der Kerk, A.C.H.T.M.4    Brandsma, L.5
  • 13
    • 37049097238 scopus 로고
    • An Unusual Ring-Enlargement in the Reactions of Acetylenic Esters and Ketones with N, N-Dimethylaminoallene
    • (b) Klop, W.; Brandsma, L., An Unusual Ring-Enlargement in the Reactions of Acetylenic Esters and Ketones with N, N-Dimethylaminoallene. J. Chem. Soc., Chem. Commun. 1983, 988-989.
    • (1983) J. Chem. Soc., Chem. Commun. , pp. 988-989
    • Klop, W.1    Brandsma, L.2
  • 14
    • 84981567377 scopus 로고
    • Cycloaddition of (Dimethylamino)allene to Some Electrophilic Alkenes and Its Application to the Synthesis of 3-Alkylidenecyclobutenes
    • For [4 + 2] and [2 + 2] cycloadditions, see: Klop, W.; Klusener, P. A. A.; Brandsma, L., Cycloaddition of (Dimethylamino)allene to Some Electrophilic Alkenes and Its Application to the Synthesis of 3-Alkylidenecyclobutenes. Recl. J. Royal Neth. Chem. Soc. 1984, 103, 85-86.
    • (1984) Recl. J. Royal Neth. Chem. Soc. , vol.103 , pp. 85-86
    • Klop, W.1    Klusener, P.A.A.2    Brandsma, L.3
  • 15
    • 37049129566 scopus 로고
    • Base Catalysed Intramolecular Cycloadditions of Allyl 3-Phenlprop-2-ynyl Ethers and 4-Methylpent-4-en-2-ynyl Prop-2-ynyl Ethers
    • For [4 + 2] cycloadditions using allenammonium salts, see: Barlett, A. J.; Laird, T.; Ollis, W. D. Base Catalysed Intramolecular Cycloadditions of Allyl 3-Phenlprop-2-ynyl Ethers and 4-Methylpent-4-en-2-ynyl Prop-2-ynyl Ethers. J. Chem. Soc., Perkin Trans. 1 1975, 1315-1320.
    • (1975) J. Chem. Soc., Perkin Trans 1 , pp. 1315-1320
    • Barlett, A.J.1    Laird, T.2    Ollis, W.D.3
  • 16
    • 0026527408 scopus 로고
    • Thermal Isomerization of 1-Morphlino-3-phenyl-(or vinyl)-allenes. Synthesis of the [1,4]oxazino-[4,3-a]-azepine Framework
    • Mayer, T.; Maas, G., Thermal Isomerization of 1-Morphlino-3-phenyl-(or vinyl)-allenes. Synthesis of the [1,4]oxazino-[4,3-a]-azepine Framework. Tetrahedron Lett. 1992, 33, 205-208.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 205-208
    • Mayer, T.1    Maas, G.2
  • 17
    • 0001227261 scopus 로고
    • Base Catalyzed Rearrangement of Bispropargyl Sulfides, Ethers, and Amines
    • Dimerization via radical: Garratt, P. J., Base Catalyzed Rearrangement of Bispropargyl Sulfides, Ethers, and Amines. J. Am. Chem. Soc. 1975, 97, 3255-3257.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 3255-3257
    • Garratt, P.J.1
  • 18
    • 33847090113 scopus 로고
    • A New Valence Tautomerism
    • Rearrangements: N. Manisse, N.; Chuche, J., A New Valence Tautomerism. J. Am. Chem. Soc. 1977, 99, 1272-1273.
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 1272-1273
    • Manisse, N.N.1    Chuche, J.2
  • 19
    • 0033516552 scopus 로고    scopus 로고
    • Reactions of the Lithio-Derivatives of Methoxy Allene with SAMP Hydrazones. Access to Enantiopure 3-Pyrrolines
    • (a) Breuil-Desvergnes, V.; Compain, P.; Vatéle, J.-M.; Goré, J. Reactions of the Lithio-Derivatives of Methoxy Allene with SAMP Hydrazones. Access to Enantiopure 3-Pyrrolines. Tetrahedron Lett. 1999, 40, 5009-5012.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 5009-5012
    • Breuil-Desvergnes, V.1    Compain, P.2    Vatéle, J.-M.3    Goré, J.4
  • 20
    • 33748243189 scopus 로고
    • Diacetoneglucose as Auxiliary Group for the Asymmetric Hetero-Diels-Alder Reactions with Nitrosoalkenes
    • (b) Arnold, T.; Orschel, B.; Ressig, H.-U. Diacetoneglucose as Auxiliary Group for the Asymmetric Hetero-Diels-Alder Reactions with Nitrosoalkenes. Angew. Chem., Int. Ed. Engl. 1992, 31, 1033-1035.
    • (1992) Angew. Chem., Int. Ed. Engl. , vol.31 , pp. 1033-1035
    • Arnold, T.1    Orschel, B.2    Ressig, H.-U.3
  • 21
    • 0001924095 scopus 로고
    • The Synthesis and Rearrangement of an Allenamide
    • Dickinson, W. B.; Lang, P. C. The Synthesis and Rearrangement of an Allenamide. Tetrahedron Lett. 1967, 8, 3035-3040.
    • (1967) Tetrahedron Lett. , vol.8 , pp. 3035-3040
    • Dickinson, W.B.1    Lang, P.C.2
  • 23
  • 24
    • 0038400404 scopus 로고
    • Studies in Claisen Rearrangement of 2-Propargylthiobenzimidazoles
    • Balasubramanian, K. K.; Venugopalan, B. Studies in Claisen Rearrangement of 2-Propargylthiobenzimidazoles. Tetrahedron Lett. 1974, 15, 2643-2644.
    • (1974) Tetrahedron Lett. , vol.15 , pp. 2643-2644
    • Balasubramanian, K.K.1    Venugopalan, B.2
  • 25
    • 0002716801 scopus 로고
    • The Preparation of N-Trichloroacetamido-1,2-dienes
    • Overman, L. E.; Marlowe, C. K.; Clizbe, L. A. The Preparation of N-Trichloroacetamido-1,2-dienes. Tetrahedron Lett. 1979, 20, 599-600.
    • (1979) Tetrahedron Lett. , vol.20 , pp. 599-600
    • Overman, L.E.1    Marlowe, C.K.2    Clizbe, L.A.3
  • 28
    • 0004305393 scopus 로고
    • Synthesis and Antibacterial Activity of Some 1-(2-Propynyl) and 1-Propadienyl Derivatives of 1,4-Dihydro-4-oxoquinoline-2-carboxylic Acids and Similar Heterocycles
    • For examples of acridone based allenamides, see: (a) Rádl, S.; Kovárová, L.; Holubeck, J. Synthesis and Antibacterial Activity of Some 1-(2-Propynyl) and 1-Propadienyl Derivatives of 1,4-Dihydro-4-oxoquinoline-2-carboxylic Acids and Similar Heterocycles. Collect. Czech. Chem. Commun. 1991, 56, 439-448.
    • (1991) Collect. Czech. Chem. Commun. , vol.56 , pp. 439-448
    • Rádl, S.1    Kovárová, L.2    Holubeck, J.3
  • 30
    • 0019848689 scopus 로고
    • Synthesis of (Allenic) N-Propadienyl- and (Acetylenic) N-(1-Propynyl)-acridones Using Phase-Transfer Catalysis
    • (c) Mahamoud, A.; Galy, J. P.; Vincent, E. J.; Barbe, J. Synthesis of (Allenic) N-Propadienyl- and (Acetylenic) N-(1-Propynyl)-acridones Using Phase-Transfer Catalysis. Synthesis 1981, 917-918.
    • (1981) Synthesis , pp. 917-918
    • Mahamoud, A.1    Galy, J.P.2    Vincent, E.J.3    Barbe, J.4
  • 31
    • 0028897714 scopus 로고
    • Synthesis, Absolute Configuration, and Enantioselectivity of Antiretroviral Effect of (R)-(-)- and (S)-(+)-Cytallene. Lipase-Catalyzed Enantio-selective Acylations N-Acylcytallenes
    • Jones, B. C. N. M.; Silverton, J. V.; Simons, C.; Megati, S.; Nishimura, H.; Maeda, Y.; Mitsuya, H.; Zemlicka, J. Synthesis, Absolute Configuration, and Enantioselectivity of Antiretroviral Effect of (R)-(-)- and (S)-(+)-Cytallene. Lipase-Catalyzed Enantio-selective Acylations N-Acylcytallenes. J. Med. Chem. 1995, 38, 1397-1405.
    • (1995) J. Med. Chem. , vol.38 , pp. 1397-1405
    • Jones, B.C.N.M.1    Silverton, J.V.2    Simons, C.3    Megati, S.4    Nishimura, H.5    Maeda, Y.6    Mitsuya, H.7    Zemlicka, J.8
  • 32
    • 0032491089 scopus 로고    scopus 로고
    • Living Coordination Polymerization of N-Allenylamides by π-Allylnickel Catalyst
    • Takagi, K.; Tomita, I.; Endo, T. Living Coordination Polymerization of N-Allenylamides by π-Allylnickel Catalyst. Macromolecules 1998, 31, 6741-6747.
    • (1998) Macromolecules , vol.31 , pp. 6741-6747
    • Takagi, K.1    Tomita, I.2    Endo, T.3
  • 33
    • 0001308717 scopus 로고    scopus 로고
    • The First Regioselective α-Deprotonation and Functionalization of Allenamides
    • Xiong, H.; Hsung, R. P.; Wei, L.-L.; Berry, C. R.; Mulder, J. A.; Stockwell, B. The First Regioselective α-Deprotonation and Functionalization of Allenamides. Org. Lett. 2000, 2, 2869-2871.
    • (2000) Org. Lett. , vol.2 , pp. 2869-2871
    • Xiong, H.1    Hsung, R.P.2    Wei, L.-L.3    Berry, C.R.4    Mulder, J.A.5    Stockwell, B.6
  • 34
    • 0036242254 scopus 로고    scopus 로고
    • Metallations and Reactions with Electrophiles of 4-Isopropyl-5,5-diphenyloxazolidin-2-one (DIOZ) with N-Allyl and N-Propargyl Substituents: Chiral Homo-enolate Reagents
    • Gaul, C.; Seebach, D. Metallations and Reactions with Electrophiles of 4-Isopropyl-5,5-diphenyloxazolidin-2-one (DIOZ) with N-Allyl and N-Propargyl Substituents: Chiral Homo-enolate Reagents. Helv. Chim. Acta 2002, 85, 963-978.
    • (2002) Helv. Chim. Acta , vol.85 , pp. 963-978
    • Gaul, C.1    Seebach, D.2
  • 35
    • 84986492906 scopus 로고
    • Base-Catalyzed Cyclization of N-Propargylamides to Oxazoles
    • Nilsson, B. M.; Hacksell, U. Base-Catalyzed Cyclization of N-Propargylamides to Oxazoles. J. Heterocycl. Chem. 1989, 26, 269-275.
    • (1989) J. Heterocycl. Chem. , vol.26 , pp. 269-275
    • Nilsson, B.M.1    Hacksell, U.2
  • 36
    • 0026517986 scopus 로고
    • The Transformation of a Chromene Derivative into Benzofurans via Allene Intermediates
    • Gericke, R.; Lues, I. The Transformation of a Chromene Derivative into Benzofurans via Allene Intermediates. Tetrahedron Lett. 1992, 33, 1871-1874.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 1871-1874
    • Gericke, R.1    Lues, I.2
  • 38
    • 0026651014 scopus 로고
    • A New Strategy for the Conversion of Penams into Cephems via Allene Chemistry
    • (a) Farina, V.; Kant, J. A New Strategy for the Conversion of Penams into Cephems via Allene Chemistry. Tetrahedron Lett. 1992, 33, 3559-3562.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 3559-3562
    • Farina, V.1    Kant, J.2
  • 39
    • 0026777049 scopus 로고
    • A Stereocontrolled Synthesis of Cefprozil Related Cephems via Allenylazetidiones
    • (b) Kant, J.; Farina, V. A Stereocontrolled Synthesis of Cefprozil and Related Cephems via Allenylazetidiones. Tetrahedron Lett. 1992, 33, 3563-3566.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 3563-3566
    • Kant, J.1    Farina, V.2
  • 40
    • 0029936663 scopus 로고    scopus 로고
    • Iodocyclization of 3-Alkynyl- and 3-Allenyl-2-(Substituted Amino)-1-imidazolin-4-ones
    • Noguchi, M.; Okada, H.; Wantanabe, M.; Okuda, K.; Nakamura, O. Iodocyclization of 3-Alkynyl- and 3-Allenyl-2-(Substituted Amino)-1-imidazolin-4-ones. Tetrahedron 1996, 52, 6581-6590.
    • (1996) Tetrahedron , vol.52 , pp. 6581-6590
    • Noguchi, M.1    Okada, H.2    Wantanabe, M.3    Okuda, K.4    Nakamura, O.5
  • 43
    • 0032576866 scopus 로고    scopus 로고
    • Cascade and Sequential Palladium Catalysed Cyclisation-Azide Capture-1,3-Dipolar Cycloaddition Route to Complex Triazoles
    • (c) Gardiner, M.; Grigg, R.; Sridharan, V.; Vicker, N. Cascade and Sequential Palladium Catalysed Cyclisation-Azide Capture-1,3-Dipolar Cycloaddition Route to Complex Triazoles. Tetrahedron Lett. 1998, 39, 435-438.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 435-438
    • Gardiner, M.1    Grigg, R.2    Sridharan, V.3    Vicker, N.4
  • 45
    • 0030583479 scopus 로고    scopus 로고
    • Sequential Hydrostannylation-Cyclisation of δ and ω-Allenyl Aryl Halides. Cyclisation at the Proximal Carbon
    • Grigg, R.; Sansano, J. M. Sequential Hydrostannylation-Cyclisation of δ and ω-Allenyl Aryl Halides. Cyclisation at the Proximal Carbon. Tetrahedron 1996, 52, 13441-13454.
    • (1996) Tetrahedron , vol.52 , pp. 13441-13454
    • Grigg, R.1    Sansano, J.M.2
  • 46
    • 0035822074 scopus 로고    scopus 로고
    • Synthesis of Spiro- and Fused Heterocycles by Palladium Catalysed Carbo and Hetero-annulation Cascades of Allenes
    • Grigg, R.; Köppen, I.; Rasparini, M.; Sridharan, V. Synthesis of Spiro- and Fused Heterocycles by Palladium Catalysed Carbo and Hetero-annulation Cascades of Allenes. Chem. Commun. 2001, 964-965.
    • (2001) Chem. Commun. , pp. 964-965
    • Grigg, R.1    Köppen, I.2    Rasparini, M.3    Sridharan, V.4
  • 49
    • 0030726933 scopus 로고    scopus 로고
    • Pronounced Chemo-, Regio-, and Stereoselective [2 + 2] Cycloaddition Reaction of Allenes Toward Alkenes and Alkynes
    • Kimura, M.; Horino, Y.; Wakamiya, Y.; Okajima, T.; Tamaru, Y. Pronounced Chemo-, Regio-, and Stereoselective [2 + 2] Cycloaddition Reaction of Allenes Toward Alkenes and Alkynes. J. Am. Chem. Soc. 1997, 119, 10869-10870.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 10869-10870
    • Kimura, M.1    Horino, Y.2    Wakamiya, Y.3    Okajima, T.4    Tamaru, Y.5
  • 50
    • 0030995589 scopus 로고    scopus 로고
    • Efficient Synthesis of 4-Ethenylidene-2-oxazolidiones via Palladium Catalyzed Amino Cyclization of 2-Butyn-1,4-diol Biscarbamates
    • Kimura, M.; Wakamiya, Y.; Horino, Y.; Tamaru, Y. Efficient Synthesis of 4-Ethenylidene-2-oxazolidiones via Palladium Catalyzed Amino Cyclization of 2-Butyn-1,4-diol Biscarbamates. Tetrahedron Lett. 1997, 38, 3963-3966.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 3963-3966
    • Kimura, M.1    Wakamiya, Y.2    Horino, Y.3    Tamaru, Y.4
  • 51
    • 0033555653 scopus 로고    scopus 로고
    • Efficient Entry to Tetrahydropyridines: Addition to Enol Ethers to Allenesulfonamides Involving a Novel 1,3-Sulfonyl Shift
    • Horino, Y.; Kimura, M.; Wakamiya, Y.; Okajima, T.; Tamaru, Y. Efficient Entry to Tetrahydropyridines: Addition to Enol Ethers to Allenesulfonamides Involving a Novel 1,3-Sulfonyl Shift. Angew. Chem., Int. Ed. Engl. 1999, 38, 121-123.
    • (1999) Angew. Chem., Int. Ed. Engl. , vol.38 , pp. 121-123
    • Horino, Y.1    Kimura, M.2    Wakamiya, Y.3    Okajima, T.4    Tamaru, Y.5
  • 52
    • 0033578602 scopus 로고    scopus 로고
    • Inverse Demand [4 + 2] Cycloaddition Reactions of Allenamides. Reactivity Scopes of an Electron Deficient variant of Allenamines
    • Wei, L.-L.; Xiong, H.; Douglas, C. J.; Hsung, R. P. Inverse Demand [4 + 2] Cycloaddition Reactions of Allenamides. Reactivity Scopes of an Electron Deficient variant of Allenamines. Tetrahedron Lett. 1999, 40, 6903-6907.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 6903-6907
    • Wei, L.-L.1    Xiong, H.2    Douglas, C.J.3    Hsung, R.P.4
  • 53
    • 0001703383 scopus 로고    scopus 로고
    • First Stereoselective Inverse Demand [4 + 2] Cycloaddition Reactions of Novel Chiral Allenamides with Heterodienes
    • Wei, L.-L.; Hsung, R. P.; Xiong, H.; Mulder, J. A.; Nkansah, N. T. First Stereoselective Inverse Demand [4 + 2] Cycloaddition Reactions of Novel Chiral Allenamides with Heterodienes. Org. Lett. 1999, 1, 2145-2148.
    • (1999) Org. Lett. , vol.1 , pp. 2145-2148
    • Wei, L.-L.1    Hsung, R.P.2    Xiong, H.3    Mulder, J.A.4    Nkansah, N.T.5
  • 56
    • 0037124403 scopus 로고    scopus 로고
    • Chiral Enamide. Part 1. Epoxidations of Chiral Enamides. A Viable Approach to Chiral Nitrogenstablized Oxyallyl Cations in [4+3] Cycloadditions
    • (b) Xiong, H.; Hsung, R. P.; Shen, L.; Hahn, J. M. Chiral Enamide. Part 1. Epoxidations of Chiral Enamides. A Viable Approach to Chiral Nitrogenstablized Oxyallyl Cations in [4+3] Cycloadditions. Tetrahedron Lett. 2002, 43, 4449-4453.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 4449-4453
    • Xiong, H.1    Hsung, R.P.2    Shen, L.3    Hahn, J.M.4
  • 58
    • 0142161034 scopus 로고
    • An Improved Synthesis of Oxotremorine
    • Bebbington, A.; Shakeshaft, D. An Improved Synthesis of Oxotremorine. J. Med. Chem. 1965, 8, 274-275.
    • (1965) J. Med. Chem. , vol.8 , pp. 274-275
    • Bebbington, A.1    Shakeshaft, D.2
  • 59
    • 0035801916 scopus 로고    scopus 로고
    • Recent Advances in the Chemistry of Ynamines and Ynamides
    • For a recent review, see: Hsung, R. P.; Zificsak, C. A.; Mulder, J. A.; Rameshkumar, C.; Wei, L.-L. Recent Advances in the Chemistry of Ynamines and Ynamides. Tetrahedron 2001, 57, 7575-7606.
    • (2001) Tetrahedron , vol.57 , pp. 7575-7606
    • Hsung, R.P.1    Zificsak, C.A.2    Mulder, J.A.3    Rameshkumar, C.4    Wei, L.-L.5
  • 60
    • 0000868359 scopus 로고
    • 1-Hetero-1-alkine,-polyine bzw. 1,2-Dihetero-ethine
    • Kropf, H., Schaumann, E., Eds.; Georg Thieme Verlag: Stuttgart
    • For other reviews, see: (a) Himbert, G. 1-Hetero-1-alkine,-polyine bzw. 1,2-Dihetero-ethine. In Methoden Der Organischen Chemie (Houben-Weyl); Kropf, H., Schaumann, E., Eds.; Georg Thieme Verlag: Stuttgart, 1993; Vol. E15, pp 3267-3443.
    • (1993) Methoden Der Organischen Chemie (Houben-Weyl) , vol.E15 , pp. 3267-3443
    • Himbert, G.1
  • 61
    • 0000130007 scopus 로고
    • Ynamines: A Versatile Tool in Organic Synthesis
    • (b) Ficini, J. Ynamines: A Versatile Tool in Organic Synthesis. Tetrahedron 1976, 32, 1448-1486.
    • (1976) Tetrahedron , vol.32 , pp. 1448-1486
    • Ficini, J.1
  • 62
    • 0001541454 scopus 로고    scopus 로고
    • Lewis Acid Promoted Hetero [2 + 2] Cycloaddition Reactions of Aldehydes with 10-Propynyl-9(10H)-acridone
    • Hsung, R. P.; Zificsak, C.; Wei, L.-L.; Douglas, C. J.; Xiong, H.; Mulder, J. A. Lewis Acid Promoted Hetero [2 + 2] Cycloaddition Reactions of Aldehydes with 10-Propynyl-9(10H)-acridone. Org. Lett. 1999, 1, 1237-1240.
    • (1999) Org. Lett. , vol.1 , pp. 1237-1240
    • Hsung, R.P.1    Zificsak, C.2    Wei, L.-L.3    Douglas, C.J.4    Xiong, H.5    Mulder, J.A.6
  • 63
    • 0000645684 scopus 로고    scopus 로고
    • The First Successful Base-Promoted Isomerization of Propargyl Amides to Chiral Ynamides
    • Huang, J.; Xiong, H.; Hsung, R. P.; Rameshkumar. C.; Mulder, J. A.; Grebe, T. P. The First Successful Base-Promoted Isomerization of Propargyl Amides to Chiral Ynamides. Org. Lett. 2002, 4, 2417-2420.
    • (2002) Org. Lett. , vol.4 , pp. 2417-2420
    • Huang, J.1    Xiong, H.2    Hsung, R.P.3    Rameshkumar, C.4    Mulder, J.A.5    Grebe, T.P.6
  • 64
    • 0000967977 scopus 로고    scopus 로고
    • The First Highly Stereoselective Ficini-Claisen Rearrangement Using Chiral Ynamides
    • Mulder, J. A.; Hsung, R. P.; Frederick, M. O.; Tracey, M. R.; Zificsak, C. A. The First Highly Stereoselective Ficini-Claisen Rearrangement Using Chiral Ynamides. Org. Lett. 2002, 4, 1383-1386.
    • (2002) Org. Lett. , vol.4 , pp. 1383-1386
    • Mulder, J.A.1    Hsung, R.P.2    Frederick, M.O.3    Tracey, M.R.4    Zificsak, C.A.5
  • 67
    • 0000605653 scopus 로고
    • An Unusual Reaction of Propargyl Bromide
    • Zaugg, H. E.; Swett, L. R.; Stone, G. R. An Unusual Reaction of Propargyl Bromide. J. Org. Chem. 1958, 23, 1389-1390.
    • (1958) J. Org. Chem. , vol.23 , pp. 1389-1390
    • Zaugg, H.E.1    Swett, L.R.2    Stone, G.R.3
  • 68
    • 0001327733 scopus 로고
    • Heterocyclic Ynammonium Salts
    • (a) Katritzky, A. R.; Ramer, W. H. Heterocyclic Ynammonium Salts. J. Org. Chem. 1985, 50, 852-856.
    • (1985) J. Org. Chem. , vol.50 , pp. 852-856
    • Katritzky, A.R.1    Ramer, W.H.2
  • 69
    • 0028281308 scopus 로고
    • Phase-Transfer-Catalyzed Alkylative Eliminations
    • (b) Majumdar, K. C.; Ghouh, S. K. Phase-Transfer-Catalyzed Alkylative Eliminations. Synth. Commun. 1994, 24, 217-231.
    • (1994) Synth. Commun. , vol.24 , pp. 217-231
    • Majumdar, K.C.1    Ghouh, S.K.2
  • 70
    • 0034967347 scopus 로고    scopus 로고
    • Facile Synthesis of Bicyclic and Tricyclic Skeletons by Cycloisomerizations of Hept-1-en-6-ynes and 4,9-Diheteradodeca-1,11-dien-6-ynes
    • van Boxtel, L. J.; Korbe, S.; Noltemeyer, M.; de Meijere, A. Facile Synthesis of Bicyclic and Tricyclic Skeletons by Cycloisomerizations of Hept-1-en-6-ynes and 4,9-Diheteradodeca-1,11-dien-6-ynes. Eur. J. Org. Chem. 2001, 2283-2292.
    • (2001) Eur. J. Org. Chem. , pp. 2283-2292
    • Van Boxtel, L.J.1    Korbe, S.2    Noltemeyer, M.3    De Meijere, A.4
  • 71
    • 0025025682 scopus 로고
    • Convenient Synthesis of Densely Functionalized N-Substituted 4-Methylene-2-oxazolidinoe
    • Kimura, M.; Kure, S.; Yoshida, Z.; Tanaka, S.; Fugami, K.; Tamaru, Y. Convenient Synthesis of Densely Functionalized N-Substituted 4-Methylene-2-oxazolidinoe. Tetrahedron Lett. 1990, 31, 4887-4890.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 4887-4890
    • Kimura, M.1    Kure, S.2    Yoshida, Z.3    Tanaka, S.4    Fugami, K.5    Tamaru, Y.6
  • 73
    • 0035898813 scopus 로고    scopus 로고
    • Construction of a Carbapenam Skeleton Using Palladium-Catalyzed Cyclization
    • (b) Kozawa, Y.; Mori, M. Construction of a Carbapenam Skeleton Using Palladium-Catalyzed Cyclization. Tetrahedron Lett. 2001, 42, 4869-4873.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4869-4873
    • Kozawa, Y.1    Mori, M.2
  • 74
    • 0034686072 scopus 로고    scopus 로고
    • Recent Advances in the Pauson-Khand Reaction and Related [2+2+1] Cycloadditions
    • For an excellent review, see: Brummond, K. M.; Kent, J. L. Recent Advances in the Pauson-Khand Reaction and Related [2+2+1] Cycloadditions. Tetrahedron 2000, 56, 3263-3283.
    • (2000) Tetrahedron , vol.56 , pp. 3263-3283
    • Brummond, K.M.1    Kent, J.L.2
  • 75
    • 1542763298 scopus 로고
    • Ring-Closing Metathesis and Related Processes in Organic Synthesis
    • (a) Grubbs, R. H.; Miller, S. J.; Fu, G. C. Ring-Closing Metathesis and Related Processes in Organic Synthesis. Acc. Chem. Res. 1995, 28, 446-452.
    • (1995) Acc. Chem. Res. , vol.28 , pp. 446-452
    • Grubbs, R.H.1    Miller, S.J.2    Fu, G.C.3
  • 76
    • 0033516491 scopus 로고    scopus 로고
    • Olefin Metathesis by Molybdenum Imido Alkylidene Catalysts
    • (b) Schrock, R. R. Olefin Metathesis by Molybdenum Imido Alkylidene Catalysts. Tetrahedron 1999, 55, 8141-8153.
    • (1999) Tetrahedron , vol.55 , pp. 8141-8153
    • Schrock, R.R.1
  • 77
    • 22944431654 scopus 로고
    • Chemistry of Allene Oxides
    • Chan, T. H.; Ong, B. S. Chemistry of Allene Oxides. Tetrahedron 1980, 36, 2269-2289.
    • (1980) Tetrahedron , vol.36 , pp. 2269-2289
    • Chan, T.H.1    Ong, B.S.2
  • 78
    • 0037178958 scopus 로고    scopus 로고
    • Synthesis of Functionalized Lactones by the DMDO Oxidation of Allenic Acid
    • Crandall, J. K.; Rambo, E. Synthesis of Functionalized Lactones by the DMDO Oxidation of Allenic Acid. Tetrahedron 2002, 58, 7027-7036.
    • (2002) Tetrahedron , vol.58 , pp. 7027-7036
    • Crandall, J.K.1    Rambo, E.2
  • 79
    • 0001113076 scopus 로고
    • Silylketone Chemistry. Synthesis and Reactions of Olefinic and Acetylenic Silyl Ketones
    • Reich, H. J.; Kelly, M. J. Silylketone Chemistry. Synthesis and Reactions of Olefinic and Acetylenic Silyl Ketones. J. Am. Chem. Soc. 1982, 104, 1119-1120.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 1119-1120
    • Reich, H.J.1    Kelly, M.J.2
  • 81
    • 0001241382 scopus 로고
    • Novel Methods for the Synthesis of C-Aryl Glycoside Natural Products
    • Parker, K. A. Novel Methods for the Synthesis of C-Aryl Glycoside Natural Products. Pure Appl. Chem. 1994, 66, 2135-2138.
    • (1994) Pure Appl. Chem. , vol.66 , pp. 2135-2138
    • Parker, K.A.1
  • 82
    • 0038731303 scopus 로고    scopus 로고
    • A Lewis-Acid Mediated Stereoselective Removal of An Anomeric Urea Substituent
    • Berry, C. R.; Rameshkumar, C.; Tracey, M. R.; Wei, L.-L.; Hsung, R. P. A Lewis-Acid Mediated Stereoselective Removal of An Anomeric Urea Substituent. Synlett 2003, 791-796.
    • (2003) Synlett , pp. 791-796
    • Berry, C.R.1    Rameshkumar, C.2    Tracey, M.R.3    Wei, L.-L.4    Hsung, R.P.5
  • 83
    • 0037623735 scopus 로고    scopus 로고
    • Pyranyl Heterocycles from Inverse Electron Demand Hetero [4 + 2] Cycloaddition Reactions of Chiral Allenamides
    • Rameshkumar, C.; Hsung, R. P. Pyranyl Heterocycles from Inverse Electron Demand Hetero [4 + 2] Cycloaddition Reactions of Chiral Allenamides. Synlett 2003, 1241-1246.
    • (2003) Synlett , pp. 1241-1246
    • Rameshkumar, C.1    Hsung, R.P.2
  • 84
    • 0037474651 scopus 로고    scopus 로고
    • Cycloaddition Reactions of Vinyl Oxocarbenium Ions
    • For reviews, see: (a) Harmata, M.; Rashatasakhon, P. Cycloaddition Reactions of Vinyl Oxocarbenium Ions. Tetrahedron 2003, 59, 2371-2395.
    • (2003) Tetrahedron , vol.59 , pp. 2371-2395
    • Harmata, M.1    Rashatasakhon, P.2
  • 85
    • 0034871416 scopus 로고    scopus 로고
    • Exploration of Fundamental and Synthetic Aspects of the Intramolecular 4+3 Cycloaddition Reaction
    • (b) Harmata, M., Exploration of Fundamental and Synthetic Aspects of the Intramolecular 4+3 Cycloaddition Reaction. Acc. Chem. Res. 2001, 34, 595-605.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 595-605
    • Harmata, M.1
  • 86
    • 0001475961 scopus 로고    scopus 로고
    • Heteroatom-Stabilized Allylic Cation in 4 + 3 Cycloaddition Reactions
    • Also see: Harmata, M., Heteroatom-Stabilized Allylic Cation in 4 + 3 Cycloaddition Reactions. Recent Res. Dev. Org. Chem. 1997, 1, pp523-535.
    • (1997) Recent Res. Dev. Org. Chem. , vol.1 , pp. 523-535
    • Harmata, M.1
  • 87
    • 33845184642 scopus 로고
    • Cycloaddition Reactions of Heteroaromatic Six-Membered Rings
    • Katritzky, A. R.; Dennis, N. Cycloaddition Reactions of Heteroaromatic Six-Membered Rings. Chem. Rev. 1989, 89, 827-861.
    • (1989) Chem. Rev. , vol.89 , pp. 827-861
    • Katritzky, A.R.1    Dennis, N.2
  • 88
    • 0000059785 scopus 로고    scopus 로고
    • Cycloaddition Reactions of a Nitrogen-Substituted Oxyallyl Cation with Cyclopentadiene and Substituted Furans
    • Walters, M. A.; Arcand, H. R. Cycloaddition Reactions of a Nitrogen-Substituted Oxyallyl Cation with Cyclopentadiene and Substituted Furans. J. Org. Chem. 1996, 61, 1478-1486.
    • (1996) J. Org. Chem. , vol.61 , pp. 1478-1486
    • Walters, M.A.1    Arcand, H.R.2
  • 89
    • 0035825779 scopus 로고    scopus 로고
    • On the Inherent Instability of α-Amino α′-Fluoro Ketones. Evidence for Their Transformation to Reactive Oxyvinyliminium Ion Intermediates
    • For other elegant studies on nitrogen-substituted oxyallyls, see: (a) Myers, A. G.; Barbay, J. K., On the Inherent Instability of α-Amino α′-Fluoro Ketones. Evidence for Their Transformation to Reactive Oxyvinyliminium Ion Intermediates. Org. Lett. 2001, 3, 425-428.
    • (2001) Org. Lett. , vol.3 , pp. 425-428
    • Myers, A.G.1    Barbay, J.K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.