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Volumn 33, Issue 3, 2000, Pages 157-169

Recovery of carbonyl compounds from N,N-dialkylhydrazones

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE; HYDRAZONE DERIVATIVE; NATURAL PRODUCT;

EID: 0034104711     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar990062y     Document Type: Article
Times cited : (130)

References (79)
  • 1
    • 0000434949 scopus 로고
    • Alkylation of chiral hydrazones
    • Morrison, J. D., Ed.; Academic Press: Orlando, FL
    • (a) Enders, D. Alkylation of Chiral Hydrazones. In Asymmetric Synthesis; Morrison, J. D., Ed.; Academic Press: Orlando, FL, 1984; Vol. 3, pp 275-339.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 275-339
    • Enders, D.1
  • 2
    • 0001306216 scopus 로고
    • Preparation of aldehydes by reduction of nitriles with diisobutylaluminiumhydride
    • Zakharkin, L. I.; Khorlina, I. M. Preparation of Aldehydes by Reduction of Nitriles with Diisobutylaluminiumhydride. Dokl. Akad. Nauk. S.S.S.R. 1957, 116, 422-424; Chem. Abstr. 1958, 52, 8040f.
    • (1957) Dokl. Akad. Nauk. S.S.S.R. , vol.116 , pp. 422-424
    • Zakharkin, L.I.1    Khorlina, I.M.2
  • 3
    • 4243859953 scopus 로고
    • Zakharkin, L. I.; Khorlina, I. M. Preparation of Aldehydes by Reduction of Nitriles with Diisobutylaluminiumhydride. Dokl. Akad. Nauk. S.S.S.R. 1957, 116, 422-424; Chem. Abstr. 1958, 52, 8040f.
    • (1958) Chem. Abstr. , vol.52
  • 4
    • 84982456512 scopus 로고
    • Asymmetrische synthesen via metallierte chirale hydrazone. Enantioselektive alkylierung von cyclischen ketonen und aldehyden
    • (a) Enders, D.; Eichenauer, H. Asymmetrische Synthesen via metallierte chirale Hydrazone. Enantioselektive Alkylierung von cyclischen Ketonen und Aldehyden. Chem. Ber. 1979, 112, 2933-2960.
    • (1979) Chem. Ber. , vol.112 , pp. 2933-2960
    • Enders, D.1    Eichenauer, H.2
  • 5
    • 0032572844 scopus 로고    scopus 로고
    • Enantioselective synthesis of α-sulfenylated ketones and aldehydes via α-thiolation of metalated SAMP/RAMP-hydrazones
    • Enders, D.; Schafer, T.; Mies, W. Enantioselective Synthesis of α-Sulfenylated Ketones and Aldehydes via α-Thiolation of Metalated SAMP/RAMP-Hydrazones. Tetrahedron 1998, 54, 10239-10252.
    • (1998) Tetrahedron , vol.54 , pp. 10239-10252
    • Enders, D.1    Schafer, T.2    Mies, W.3
  • 6
    • 0032552052 scopus 로고    scopus 로고
    • Electrophilic amination of hydrazones: A new synthetic route to protected α-hydrazino and α-aminoketones
    • Enders, D.; Joseph, R.; Poiesz, C. Electrophilic Amination of Hydrazones: A New Synthetic Route to Protected α-Hydrazino and α-Aminoketones. Tetrahedron 1998, 54, 10069-10078.
    • (1998) Tetrahedron , vol.54 , pp. 10069-10078
    • Enders, D.1    Joseph, R.2    Poiesz, C.3
  • 7
    • 33748810344 scopus 로고    scopus 로고
    • Enantioselective synthesis of α-phosphino ketones and 2-phosphino-alcohols
    • Enders, D.; Berg, T.; Raabe, G.; Runsink, J. Enantioselective Synthesis of α-Phosphino Ketones and 2-Phosphino-Alcohols. Liebigs Ann./Recl. 1997, 345-363.
    • (1997) Liebigs Ann./Recl. , pp. 345-363
    • Enders, D.1    Berg, T.2    Raabe, G.3    Runsink, J.4
  • 13
    • 84982453292 scopus 로고
    • Mild cleavage of N,N-dimethylhydrazones to carbonyl compounds with singlet oxygen
    • (a) Friedrich, E.; Lutz, W.; Eichenauer, H.; Enders, D. Mild Cleavage of N,N-Dimethylhydrazones to Carbonyl Compounds with Singlet Oxygen. Synthesis 1977, 893-894.
    • (1977) Synthesis , pp. 893-894
    • Friedrich, E.1    Lutz, W.2    Eichenauer, H.3    Enders, D.4
  • 14
    • 0001510437 scopus 로고
    • Regiospezifische und enantioselektive aldol-reaktionen
    • (b) Eichenajer, H.; Friedrich, E.; Lutz, W.; Enders, D. Regiospezifische und Enantioselektive Aldol-Reaktionen. Angew. Chem. 1978, 90, 219-220; Angew. Chem., Int. Ed. Engl. 1978, 17, 206-207.
    • (1978) Angew. Chem. , vol.90 , pp. 219-220
    • Eichenauer, H.1    Friedrich, E.2    Lutz, W.3    Enders, D.4
  • 15
    • 84985609994 scopus 로고
    • (b) Eichenauer, H.; Friedrich, E.; Lutz, W.; Enders, D. Regiospezifische und Enantioselektive Aldol-Reaktionen. Angew. Chem. 1978, 90, 219-220; Angew. Chem., Int. Ed. Engl. 1978, 17, 206-207.
    • (1978) Angew. Chem., Int. Ed. Engl. , vol.17 , pp. 206-207
  • 16
    • 0029821708 scopus 로고    scopus 로고
    • Studies directed toward the synthesis of ulapualide A. Asymmetric synthesis of the C26-C42 fragment
    • Panek, J. S.; Beresis, R. T.; Celatka, C. A. Studies Directed toward the Synthesis of Ulapualide A. Asymmetric Synthesis of the C26-C42 Fragment. J. Org. Chem. 1996, 61, 6494-6495.
    • (1996) J. Org. Chem. , vol.61 , pp. 6494-6495
    • Panek, J.S.1    Beresis, R.T.2    Celatka, C.A.3
  • 17
    • 0006549099 scopus 로고
    • Mild and efficient oxidative cleavage of N,N-dialkylhydrazones to ketones with perborate
    • (a) Enders, D.; Bhushan, V. Mild and Efficient Oxidative Cleavage of N,N-Dialkylhydrazones to Ketones with Perborate. Z. Naturforsch. 1987, 42b, 1595-1596.
    • (1987) Z. Naturforsch , vol.42 B , pp. 1595-1596
    • Enders, D.1    Bhushan, V.2
  • 18
    • 0342679641 scopus 로고
    • Functional group oxidation using sodium perborate
    • (b) McKillop, A.; Tarbin, J. A. Functional Group Oxidation Using Sodium Perborate. Tetrahedron 1987, 43, 1753-1758.
    • (1987) Tetrahedron , vol.43 , pp. 1753-1758
    • McKillop, A.1    Tarbin, J.A.2
  • 19
    • 0028102188 scopus 로고
    • Facile cleavage of N,N-dimethylhydrazones to ketones using tetrabutylammonium peroxydisulfate
    • Choi, H. C.; Kim, Y. A. Facile Cleavage of N,N-Dimethylhydrazones to Ketones using Tetrabutylammonium Peroxydisulfate. Synth. Commun. 1994, 24, 2307-2311.
    • (1994) Synth. Commun. , vol.24 , pp. 2307-2311
    • Choi, H.C.1    Kim, Y.A.2
  • 20
    • 0030592698 scopus 로고    scopus 로고
    • Oxidation of hydrazones by hypervalent organoiodine reagents: Regeneration of the carbonyl group and facile syntheses of α-acetoxy and α-alkoxy azo compounds
    • Barton, D. H. R.; Jaszberenyi, J. C.; Liu, W.; Shinada, T. Oxidation of Hydrazones by Hypervalent Organoiodine Reagents: Regeneration of the Carbonyl Group and Facile Syntheses of α-Acetoxy and α-Alkoxy Azo Compounds. Tetrahedron 1996, 52, 14673-14688.
    • (1996) Tetrahedron , vol.52 , pp. 14673-14688
    • Barton, D.H.R.1    Jaszberenyi, J.C.2    Liu, W.3    Shinada, T.4
  • 21
    • 0002094569 scopus 로고
    • Oxidation reactions using magnesium monoperoxyphthalate: A comparison with m-chloroperoxybenzoic acid
    • Brougham, P.; Cooper, M. S.; Cummerson, D. A.; Heaney, H.; Thompson, N. Oxidation Reactions Using Magnesium Monoperoxyphthalate: A Comparison with m-Chloroperoxybenzoic Acid. Synthesis 1987, 1015-1017.
    • (1987) Synthesis , pp. 1015-1017
    • Brougham, P.1    Cooper, M.S.2    Cummerson, D.A.3    Heaney, H.4    Thompson, N.5
  • 22
    • 0027535784 scopus 로고
    • Simple and efficient conversion of N,N-dimethylhydrazones and aldehydes to nitriles
    • Fernández, R.; Gasch, C.; Lassaletta, J. M.; Llera, J. M.; Vázquez, J. Simple and Efficient Conversion of N,N-Dimethylhydrazones and Aldehydes to Nitriles. Tetrahedron Lett. 1993, 34, 141-144.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 141-144
    • Fernández, R.1    Gasch, C.2    Lassaletta, J.M.3    Llera, J.M.4    Vázquez, J.5
  • 23
    • 84989588794 scopus 로고
    • Plant, A. Oxidative cleavage of N,N-dialkylhydrazones to ketones with magnesium monoperoxyphthalate
    • Enders, D.; Plant, A. Oxidative Cleavage of N,N-Dialkylhydrazones to Ketones with Magnesium Monoperoxyphthalate. Synlett 1990, 725-726.
    • (1990) Synlett , pp. 725-726
    • Enders, D.1
  • 24
    • 0001876562 scopus 로고
    • Enantioselective synthesis of α-substituted nitriles by oxidative cleavage of aldehyde SAMP-hydrazones with magnesium monoperoxyphthalate
    • Enders, D.; Plant, A. Enantioselective Synthesis of α-Substituted Nitriles by Oxidative Cleavage of Aldehyde SAMP-Hydrazones with Magnesium Monoperoxyphthalate. Synlett 1994, 1054-1056.
    • (1994) Synlett , pp. 1054-1056
    • Enders, D.1    Plant, A.2
  • 25
    • 0001886335 scopus 로고    scopus 로고
    • Variation der ringgrösse von epothilonen-totalsynthese von [14]-, [15]-, [17]-, und [18] epothilon A
    • Nicolaou, K. C.; Sarabia, F.; Ninkovic, S.; Ray, M.; Finlay, V.; Boddy, C. N. C, Variation der Ringgrösse von Epothilonen-Totalsynthese von [14]-, [15]-, [17]-, und [18] Epothilon A. Angew. Chem. 1998, 110, 85-89; Angew. Chem., Int. Ed. 1998, 37, 81-84.
    • (1998) Angew. Chem. , vol.110 , pp. 85-89
    • Nicolaou, K.C.1    Sarabia, F.2    Ninkovic, S.3    Ray, M.4    Finlay, V.5    Boddy, C.N.C.6
  • 26
    • 0003184017 scopus 로고    scopus 로고
    • Nicolaou, K. C.; Sarabia, F.; Ninkovic, S.; Ray, M.; Finlay, V.; Boddy, C. N. C, Variation der Ringgrösse von Epothilonen-Totalsynthese von [14]-, [15]-, [17]-, und [18] Epothilon A. Angew. Chem. 1998, 110, 85-89; Angew. Chem., Int. Ed. 1998, 37, 81-84.
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 81-84
  • 27
    • 0034647038 scopus 로고    scopus 로고
    • Diastereo- and enantioselective total synthesis of stigmatellin A
    • in press
    • Enders, D.; Geibel, G.; Osborne, S. Diastereo- and Enantioselective Total Synthesis of Stigmatellin A. Chem. Eur. J. 2000, in press.
    • (2000) Chem. Eur. J.
    • Enders, D.1    Geibel, G.2    Osborne, S.3
  • 28
    • 84986710185 scopus 로고
    • Conversion of aldehydes into nitriles via oxidation of their dimethylhydrazones
    • Said, S. B.; Skarzewski, J.; Mlochowski, J. Conversion of Aldehydes into Nitriles via Oxidation of their Dimethylhydrazones. Synthesis 1989, 223-224.
    • (1989) Synthesis , pp. 223-224
    • Said, S.B.1    Skarzewski, J.2    Mlochowski, J.3
  • 29
    • 0009976739 scopus 로고
    • A convenient method for hydrazone hydrolysis
    • Duraisamy, M.; Walborsky, H. M. A Convenient Method for Hydrazone Hydrolysis. J. Org. Chem. 1984, 49, 3410-3411.
    • (1984) J. Org. Chem. , vol.49 , pp. 3410-3411
    • Duraisamy, M.1    Walborsky, H.M.2
  • 30
    • 84956130826 scopus 로고
    • Praparative ergebnisse der umsetzung von hydrazinderivaten und hydrazonen mit peressigsäure
    • Horner, L.; Fernekess, H. Praparative Ergebnisse der Umsetzung von Hydrazinderivaten und Hydrazonen mit Peressigsäure. Chem. Ber. 1961, 94, 712-724.
    • (1961) Chem. Ber. , vol.94 , pp. 712-724
    • Horner, L.1    Fernekess, H.2
  • 31
    • 0029306043 scopus 로고
    • Bulk synthesis of two-dimensional polymers: The molecular recognition approach
    • Stupp, S. I.; Son, S.; Li, L. S.; Lin, H. C.; Keser, M. Bulk Synthesis of Two-Dimensional Polymers: The Molecular Recognition Approach. J. Am. Chem. Soc. 1995, 117, 5212-5227.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5212-5227
    • Stupp, S.I.1    Son, S.2    Li, L.S.3    Lin, H.C.4    Keser, M.5
  • 32
    • 33947332270 scopus 로고
    • Oxidation of aldehyde N,N-dialkylhydrazones with hydrogen peroxide. A new nitrile synthesis
    • Smith, R. F.; Albright, J. A.; Waring, A. M. Oxidation of Aldehyde N,N-Dialkylhydrazones with Hydrogen Peroxide. A New Nitrile Synthesis. J. Org. Chem. 1966, 31, 4100-4102.
    • (1966) J. Org. Chem. , vol.31 , pp. 4100-4102
    • Smith, R.F.1    Albright, J.A.2    Waring, A.M.3
  • 33
    • 0001510437 scopus 로고
    • Regiospezifische und enantioselektive aldol-reaktionen
    • Eichenauer, H.; Friedrich, E.; Lutz, W.; Enders, D. Regiospezifische und Enantioselektive Aldol-Reaktionen. Angew. Chem. 1978, 90 219-220; Angew. Chem., Int. Ed. Engl. 1978, 17, 206-207.
    • (1978) Angew. Chem. , vol.90 , pp. 219-220
    • Eichenauer, H.1    Friedrich, E.2    Lutz, W.3    Enders, D.4
  • 34
    • 84985609994 scopus 로고
    • Eichenauer, H.; Friedrich, E.; Lutz, W.; Enders, D. Regiospezifische und Enantioselektive Aldol-Reaktionen. Angew. Chem. 1978, 90 219-220; Angew. Chem., Int. Ed. Engl. 1978, 17, 206-207.
    • (1978) Angew. Chem., Int. Ed. Engl. , vol.17 , pp. 206-207
  • 35
    • 0001045674 scopus 로고
    • On the facile regeneration of carbonyl compounds by oxidative cleavage of hydrazones using dioxiranes
    • (a) Altamura, A.; Curci, R.; Edwards, J. O. On the Facile Regeneration of Carbonyl Compounds by Oxidative Cleavage of Hydrazones using Dioxiranes. J. Org. Chem. 1993, 58, 7289-7293.
    • (1993) J. Org. Chem. , vol.58 , pp. 7289-7293
    • Altamura, A.1    Curci, R.2    Edwards, J.O.3
  • 36
    • 0032473909 scopus 로고    scopus 로고
    • High-yield synthesis of nitriles by oxidation of aldehyde N,N-dimethylhydrazones with dimethyldioxirane
    • (b) Altamura, A.; D'Accolti, L.; Detomaso, A.; Dinoi, A.; Fiorentino, M.; Fusco, C.; Curci, R. High-yield Synthesis of Nitriles by Oxidation of Aldehyde N,N-Dimethylhydrazones with Dimethyldioxirane. Tetrahedron Lett. 1998, 39, 2009-2012.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2009-2012
    • Altamura, A.1    D'Accolti, L.2    Detomaso, A.3    Dinoi, A.4    Fiorentino, M.5    Fusco, C.6    Curci, R.7
  • 37
    • 0002779931 scopus 로고
    • 3) or molybdenum hexafluoride and reductive cleavage of oximes with molybdenyl chloride/zinc
    • 3) or Molybdenum Hexafluoride and Reductive Cleavage of Oximes with Molybdenyl Chloride/Zinc. Synthesis 1976, 808-809.
    • (1976) Synthesis , pp. 808-809
    • Olah, G.A.1    Welch, J.2    Prakash, G.K.S.3    Ho, T.L.4
  • 38
    • 0003092411 scopus 로고
    • The oxidative cleavage of hydrazones and oximes with cobalt(III) trifluoride
    • Olah, G. A.; Welch, J.; Henninger, M. The Oxidative Cleavage of Hydrazones and Oximes with Cobalt(III) Trifluoride. Synthesis 1977, 308-309.
    • (1977) Synthesis , pp. 308-309
    • Olah, G.A.1    Welch, J.2    Henninger, M.3
  • 39
    • 84944154170 scopus 로고
    • Tungsten hexafluoride, a mild oxidizing agent for the cleavage of hydrazones
    • Olah, G. A.; Prakash, G. K. S.; Ho, T. L. Tungsten Hexafluoride, a Mild Oxidizing Agent for the Cleavage of Hydrazones. Synthesis 1976, 809-810.
    • (1976) Synthesis , pp. 809-810
    • Olah, G.A.1    Prakash, G.K.S.2    Ho, T.L.3
  • 40
    • 0010557998 scopus 로고
    • Uranium hexafluoride, a convenient new oxidizing agent for organic synthesis
    • Olah, G. A.; Welch, J.; Ho, T. L. Uranium Hexafluoride, a Convenient New Oxidizing Agent for Organic Synthesis. J. Am. Chem. Soc. 1976, 98, 6717-6718.
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 6717-6718
    • Olah, G.A.1    Welch, J.2    Ho, T.L.3
  • 41
    • 84985152091 scopus 로고
    • Oxidative cleavage of oximes and dimethylhydrazones with nitronium and nitrosonium salts
    • Olah, G. A.; Ho, T. L. Oxidative Cleavage of Oximes and Dimethylhydrazones with Nitronium and Nitrosonium Salts. Synthesis 1976, 610-611.
    • (1976) Synthesis , pp. 610-611
    • Olah, G.A.1    Ho, T.L.2
  • 42
    • 0001265156 scopus 로고
    • Conversion of N,N-dimethylhydrazones to carbonyl compounds by clay-supported ferric nitrate
    • Laszlo, P.; Polla, E. Conversion of N,N-Dimethylhydrazones to Carbonyl Compounds by Clay-Supported Ferric Nitrate. Tetrahedron Lett. 1984, 25, 3309-3312.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 3309-3312
    • Laszlo, P.1    Polla, E.2
  • 43
    • 0000161976 scopus 로고    scopus 로고
    • MTO catalyzed oxidation of aldehyde N,N-dimethylhydrazones with hydrogenperoxide: High yield formation of nitriles and N-methylene-N-methyl N-oxide
    • Rudler, H.; Denise, B. MTO Catalyzed Oxidation of Aldehyde N,N-Dimethylhydrazones with Hydrogenperoxide: High Yield Formation of Nitriles and N-Methylene-N-Methyl N-Oxide. J. Chem. Soc., Chem. Commun. 1998, 2145-2146.
    • (1998) J. Chem. Soc., Chem. Commun. , pp. 2145-2146
    • Rudler, H.1    Denise, B.2
  • 44
    • 0343987016 scopus 로고
    • Cleavage of aldehyde hydrazonium iodides under mild conditions. A convenient route to chiral nitriles of high enantiomeric purity
    • Moore, J. S.; Stupp, S. I. Cleavage of Aldehyde Hydrazonium Iodides under Mild Conditions. A Convenient Route to Chiral Nitriles of High Enantiomeric Purity. J. Org. Chem. 1990, 55, 3377-3381.
    • (1990) J. Org. Chem. , vol.55 , pp. 3377-3381
    • Moore, J.S.1    Stupp, S.I.2
  • 45
    • 0032532257 scopus 로고    scopus 로고
    • An elimination reaction of N-carbomethoxy-N,N-dimethylhydrazonium salts to alkyl nitriles
    • Xiao, Z.; Timberlake, J. W. An Elimination Reaction of N-Carbomethoxy-N,N-dimethylhydrazonium Salts to Alkyl Nitriles. Tetrahedron 1998, 54, 12715-12720.
    • (1998) Tetrahedron , vol.54 , pp. 12715-12720
    • Xiao, Z.1    Timberlake, J.W.2
  • 47
    • 0026541239 scopus 로고
    • On attempted Diels-Alder reaction of 1-ethoxycarbonylindole-3-carboxaldehyde N,N-dimethylhydrazone
    • (b) Biswas, G. K.; Nath, A. C.; Mukherjee, B.; Patra, A.; Chakrabarty, M. On Attempted Diels-Alder Reaction of 1-Ethoxycarbonylindole-3-carboxaldehyde N,N-Dimethylhydrazone. Tetrahedron Lett. 1992, 33, 117-118.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 117-118
    • Biswas, G.K.1    Nath, A.C.2    Mukherjee, B.3    Patra, A.4    Chakrabarty, M.5
  • 48
    • 0009832716 scopus 로고
    • The reactivity of 2-formylthiophene, 1-methyl-2-formylpyrrole, benzaldehyde and 2-formylfurane N,N-dimethylhydrazones with dimethyl acetylenedicarboxylate
    • Gonzales, M. E.; Sancho, P.; Soriano, C.; Ballesteros, R.; Abarca, B.; Sepulveda, J. The Reactivity of 2-Formylthiophene, 1-Methyl-2-formylpyrrole, Benzaldehyde and 2-Formylfurane N,N-Dimethylhydrazones with Dimethyl Acetylenedicarboxylate. Heterocycles 1988, 27, 1227-1231.
    • (1988) Heterocycles , vol.27 , pp. 1227-1231
    • Gonzales, M.E.1    Sancho, P.2    Soriano, C.3    Ballesteros, R.4    Abarca, B.5    Sepulveda, J.6
  • 49
    • 0002002903 scopus 로고
    • Facile conversion of N,N-dimethylhydrazones to carbonyl compounds by cupric ion-catalyzed hydrolysis
    • Corey, E. J.; Knapp, S. Facile Conversion of N,N-Dimethylhydrazones to Carbonyl Compounds by Cupric Ion-Catalyzed Hydrolysis. Tetrahedron Lett. 1976, 3667-3668.
    • (1976) Tetrahedron Lett. , pp. 3667-3668
    • Corey, E.J.1    Knapp, S.2
  • 51
    • 0032980696 scopus 로고    scopus 로고
    • Copper(II) chloride mediated racemization-free hydrolysis of α-alkylated ketone SAMP-hydrazones
    • Enders, D.; Hundertmark, T.; Lazny, R. Copper(II) Chloride Mediated Racemization-Free Hydrolysis of α-Alkylated Ketone SAMP-Hydrazones. Synth. Commun. 1999, 28, 27-33.
    • (1999) Synth. Commun. , vol.28 , pp. 27-33
    • Enders, D.1    Hundertmark, T.2    Lazny, R.3
  • 52
    • 0031012432 scopus 로고    scopus 로고
    • Synthesis and biological activities of degraded limonoids, (±)-fraxinellonone and its related compounds
    • Okamura, H.; Yamauchi, K.; Miyawaki, K.; Iwagawa, T.; Nakatani, M. Synthesis and Biological Activities of Degraded Limonoids, (±)-Fraxinellonone and Its Related Compounds. Tetrahedron Lett. 1997, 38, 263-266.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 263-266
    • Okamura, H.1    Yamauchi, K.2    Miyawaki, K.3    Iwagawa, T.4    Nakatani, M.5
  • 53
    • 0343456051 scopus 로고
    • Controlled access to furanose precursors related to sesquiterpene lactones
    • Georges, M.; Fraser-Reid, B. Controlled Access to Furanose Precursors Related to Sesquiterpene Lactones. J. Org. Chem. 1985, 50, 5754-5758.
    • (1985) J. Org. Chem. , vol.50 , pp. 5754-5758
    • Georges, M.1    Fraser-Reid, B.2
  • 55
    • 0002853558 scopus 로고    scopus 로고
    • Mild racemization free cleavage of ketone SAMP-hydrazones with oxalic acid-recycling of the chiral auxiliary
    • Enders, D.; Hundertmark, T.; Lazny, R. Mild Racemization Free Cleavage of Ketone SAMP-Hydrazones with Oxalic Acid-Recycling of the Chiral Auxiliary. Synlett 1998, 721-722.
    • (1998) Synlett , pp. 721-722
    • Enders, D.1    Hundertmark, T.2    Lazny, R.3
  • 56
    • 0000864299 scopus 로고    scopus 로고
    • Synthesis of racemic 3,5-O-benzylidene-2-deoxypentoses from 2-phenyl-1,3-dioxan-5-one hydrate
    • Ulven, T.; Sørbye, K. A.; Carlsen, P. H. J. Synthesis of Racemic 3,5-O-Benzylidene-2-deoxypentoses from 2-Phenyl-1,3-dioxan-5-one Hydrate. Acta Chem. Scand. 1997, 51, 1041-1044.
    • (1997) Acta Chem. Scand. , vol.51 , pp. 1041-1044
    • Ulven, T.1    Sørbye, K.A.2    Carlsen, P.H.J.3
  • 58
    • 0020263079 scopus 로고
    • Synthesis and absolute stereochemistry of serricornin [(4S, 6S, 7S)-4,6-dimethyl-7-hydroxy-3-nonanone]
    • Mori, K.; Niomi, H. Synthesis and Absolute Stereochemistry of Serricornin [(4S, 6S, 7S)-4,6-Dimethyl-7-hydroxy-3-nonanone]. Tetrahedron 1982, 38, 3705-3711.
    • (1982) Tetrahedron , vol.38 , pp. 3705-3711
    • Mori, K.1    Niomi, H.2
  • 61
    • 0029968678 scopus 로고    scopus 로고
    • A short asymmetric synthesis of both enantiomers of ramulosin and its analogues
    • Enders, D.; Kaiser, A. A Short Asymmetric Synthesis of Both Enantiomers of Ramulosin and Its Analogues. Synthesis 1996, 209-214.
    • (1996) Synthesis , pp. 209-214
    • Enders, D.1    Kaiser, A.2
  • 62
    • 85082662655 scopus 로고
    • Selective cleavage of dimethylhydrazones to the carbonyl compounds using silica gel and its application in the synthesis of (Z)-9-tetradecenyl acetate
    • (a) Mitra, R. B.; Bhaskar Reddy, G. Selective Cleavage of Dimethylhydrazones to the Carbonyl Compounds Using Silica Gel and its Application in the Synthesis of (Z)-9-Tetradecenyl Acetate. Synthesis 1989, 694-698.
    • (1989) Synthesis , pp. 694-698
    • Mitra, R.B.1    Bhaskar Reddy, G.2
  • 63
    • 8644264844 scopus 로고
    • A simple and efficient heterogeneous hydrolysis of N,N-dimethylhydrazone derivatives
    • (b) Kotsuki, H.; Miyazaki, A.; Kadota, I.; Ochi, M. A Simple and Efficient Heterogeneous Hydrolysis of N,N-Dimethylhydrazone Derivatives. J. Chem. Soc., Perkin Trans. 1 1990, 420-430.
    • (1990) J. Chem. Soc., Perkin Trans. 1 , vol.1 , pp. 420-430
    • Kotsuki, H.1    Miyazaki, A.2    Kadota, I.3    Ochi, M.4
  • 64
    • 0002668641 scopus 로고    scopus 로고
    • 3+-Catalyzed regeneration of carbonyl compounds from hydrazones under microwave irradiation
    • 3+-Catalyzed Regeneration of Carbonyl Compounds from Hydrazones under Microwave Irradiation. Synlett 1997, 1251-1252.
    • (1997) Synlett , pp. 1251-1252
  • 65
    • 0010490629 scopus 로고    scopus 로고
    • Palladium catalyzed hydrolysis of dimethylhydrazones to carbonyl compounds
    • Mino, T.; Hirota, T.; Yamashita, M. Palladium Catalyzed Hydrolysis of Dimethylhydrazones to Carbonyl Compounds. Synlett 1996, 999-1000.
    • (1996) Synlett , pp. 999-1000
    • Mino, T.1    Hirota, T.2    Yamashita, M.3
  • 66
    • 0001952336 scopus 로고
    • Mild nonoxidative procedure for the hydrolysis of dimethylhydrazones
    • Gawley, R. E.; Termine, E. J. Mild Nonoxidative Procedure for the Hydrolysis of Dimethylhydrazones. Synth. Commun. 1982, 12, 15-18.
    • (1982) Synth. Commun. , vol.12 , pp. 15-18
    • Gawley, R.E.1    Termine, E.J.2
  • 67
    • 0000698739 scopus 로고
    • Enantioselektive synthese 3-substituierter 2-ketoester
    • (a) Enders, D.; Dyker, H.; Raabe, G. Enantioselektive Synthese 3-substituierter 2-Ketoester. Angew. Chem. 1992, 104, 649-651; Angew. Chem., Int. Ed. Engl. 1992, 31, 618-620.
    • (1992) Angew. Chem. , vol.104 , pp. 649-651
    • Enders, D.1    Dyker, H.2    Raabe, G.3
  • 68
    • 0026661322 scopus 로고
    • (a) Enders, D.; Dyker, H.; Raabe, G. Enantioselektive Synthese 3-substituierter 2-Ketoester. Angew. Chem. 1992, 104, 649-651; Angew. Chem., Int. Ed. Engl. 1992, 31, 618-620.
    • (1992) Angew. Chem., Int. Ed. Engl. , vol.31 , pp. 618-620
  • 69
    • 0002988180 scopus 로고
    • Enantio- and diastereoselective synthesis of 3-substituted cyclic hemiketals of ω-hydroxy-2-oxoesters
    • (b) Enders, D.; Dyker, H.; Raabe, G.; Runsink, J. Enantio- and Diastereoselective Synthesis of 3-Substituted Cyclic Hemiketals of ω-Hydroxy-2-oxoesters. Synlett 1992, 901-903.
    • (1992) Synlett , pp. 901-903
    • Enders, D.1    Dyker, H.2    Raabe, G.3    Runsink, J.4
  • 71
    • 0025845905 scopus 로고
    • Efficient enzymatic hydrazone hydrolysis by baker's yeast
    • Kamal, A.; Rao, M. V.; Meshram, H. M. Efficient Enzymatic Hydrazone Hydrolysis by Baker's Yeast. Tetrahedron Lett. 1991, 32, 2657-2658.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 2657-2658
    • Kamal, A.1    Rao, M.V.2    Meshram, H.M.3
  • 72
    • 0000664225 scopus 로고
    • The reduction of oximes with tervalent titanium. A mild deoximation procedure and the partial synthesis of erythromycylamine
    • Timms, G. H.; Wildsmith, E. The Reduction of Oximes with Tervalent Titanium. A Mild Deoximation Procedure and the Partial Synthesis of Erythromycylamine. Tetrahedron Lett. 1971, 195-198.
    • (1971) Tetrahedron Lett. , pp. 195-198
    • Timms, G.H.1    Wildsmith, E.2
  • 73
    • 0016807508 scopus 로고
    • Cleavage of steroidal tosylhydrazones with titanous chloride under mild conditions
    • Chandrasekhar, B. P.; Sunthankar, S. V.; Telang, S. G. Cleavage of Steroidal Tosylhydrazones with Titanous Chloride under Mild Conditions. Chem. Ind. 1975, 87-88.
    • (1975) Chem. Ind. , pp. 87-88
    • Chandrasekhar, B.P.1    Sunthankar, S.V.2    Telang, S.G.3
  • 74
    • 0011157467 scopus 로고
    • A method for cleaving 2,4-dinitrophenylhydrazones to ketones
    • McMurry, J. E.; Silvestri, M. A Method for Cleaving 2,4-Dinitrophenylhydrazones to Ketones. J. Org. Chem. 1975, 40, 1502-1504.
    • (1975) J. Org. Chem. , vol.40 , pp. 1502-1504
    • McMurry, J.E.1    Silvestri, M.2
  • 75
    • 0002340639 scopus 로고    scopus 로고
    • Enantioselective synthesis of planar chiral ortho-functionalised ferrocenylketones
    • (a) Enders, D.; Peters, R.; Lochtman, R.; Runsink, J. Enantioselective Synthesis of Planar Chiral ortho-Functionalised Ferrocenylketones. Synlett 1997, 1462-1464.
    • (1997) Synlett , pp. 1462-1464
    • Enders, D.1    Peters, R.2    Lochtman, R.3    Runsink, J.4
  • 76
    • 0343986985 scopus 로고    scopus 로고
    • Dissertation, RWTH Aachen
    • (b) Peters, R. Dissertation, RWTH Aachen, 2000.
    • (2000)
    • Peters, R.1
  • 77
    • 0343551032 scopus 로고
    • Recovery of carbonyl compounds from their dinitrophenylhydrazones
    • Casnati, G. Recovery of Carbonyl Compounds from their dinitrophenylhydrazones. Chem. Abstr. 1958, 52, 17159.
    • (1958) Chem. Abstr. , vol.52 , pp. 17159
    • Casnati, G.1
  • 78
    • 0001289476 scopus 로고
    • Reaction of oxime O-acetates with chromous acetate. A method for the conversion of ketoximes to ketones under mild conditions
    • Corey, E. J.; Richman, J. E. Reaction of Oxime O-Acetates with Chromous Acetate. A Method for the Conversion of Ketoximes to Ketones under Mild Conditions. J. Am. Chem. Soc. 1970, 92, 5276-5277.
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 5276-5277
    • Corey, E.J.1    Richman, J.E.2
  • 79
    • 0002417456 scopus 로고
    • Reductive cleavage of oximes with vanadium(II) chloride
    • Olah, G. A.; Arvanaghi, M.; Prakash, G. K. S. Reductive Cleavage of Oximes with Vanadium(II) Chloride. Synthesis 1980, 220.
    • (1980) Synthesis , pp. 220
    • Olah, G.A.1    Arvanaghi, M.2    Prakash, G.K.S.3


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