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Volumn 15, Issue 10, 2011, Pages 1465-1481

Ethyl nosyloxycarbamate: A chameleonic aminating agent

Author keywords

Amination; Aziridines; C N bond formation; Heterocycles; Michael addition; Selectivity

Indexed keywords

ADDITION REACTIONS; AMINATION; AMINES; MOLECULES;

EID: 79955003064     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211795378092     Document Type: Article
Times cited : (13)

References (142)
  • 1
    • 0001670813 scopus 로고
    • Sulfones as chemical chameleons. Cyclization via 1,1-dipole synthons
    • Trost, B.M.; Chadiri, R.M. Sulfones as chemical chameleons. Cyclization via 1,1-dipole synthons. J. Am. Chem. Soc. 1984,106, 7260-7261.
    • (1984) J. Am. Chem. Soc , vol.106 , pp. 7260-7261
    • Trost, B.M.1    Chadiri, R.M.2
  • 2
    • 0036399768 scopus 로고    scopus 로고
    • The chemistry of the carbon-tin bond: Another chemical chameleon?
    • Quayle, P. The chemistry of the carbon-tin bond: another chemical chameleon? Main Group Met. Chem. 2002,25, 33-43.
    • (2002) Main Group Met. Chem , vol.25 , pp. 33-43
    • Quayle, P.1
  • 3
    • 0004136578 scopus 로고    scopus 로고
    • Ricci, A., Ed., Wiley-VCH: Weinheim, Germany
    • Modern Amination Methods; Ricci, A., Ed.; Wiley-VCH: Weinheim, Germany, 2000.
    • (2000) Modern Amination Methods
  • 4
    • 79955028611 scopus 로고    scopus 로고
    • Amino Group Chemistry, Ricci, A., Ed.; Wiley-VCH, Weinheim, Germany
    • Amino Group Chemistry: From Synthesis to the Life Sciences; Ricci, A., Ed.; Wiley-VCH: Weinheim, Germany, 2007.
    • (2007) From Synthesis to The Life Sciences
  • 5
    • 79955010694 scopus 로고
    • Reaction between cis and transdecalin and ethyl azidoformate
    • Chem. Abstr. 1970, 73, 120174p
    • Tardella, P.A. Reaction between cis and transdecalin and ethyl azidoformate. Atti Accad. Naz. Lincei, Cl. Sci. Fis. Mat., Rend. 1970, 48, 443-445; Chem. Abstr. 1970, 73, 120174p.
    • (1970) Atti Accad. Naz. Lincei, Cl. Sci. Fis. Mat., Rend , vol.48 , pp. 443-445
    • Tardella, P.A.1
  • 7
    • 33847800151 scopus 로고
    • Ethoxycarbonylnitrene insertion selectivity. Photolysis of ethyl azidoformate in bicyclo[4.n.0]alkanes and in al-kylcyclohexanes
    • Tardella P.A., Pellacani L. Ethoxycarbonylnitrene insertion selectivity. Photolysis of ethyl azidoformate in bicyclo[4.n.0]alkanes and in al-kylcyclohexanes. J. Org. Chem. 1976,41, 2034-2036.
    • (1976) J. Org. Chem , vol.41 , pp. 2034-2036
    • Tardella, P.A.1    Pellacani, L.2
  • 8
    • 85197361185 scopus 로고
    • Lwowski, W., Ed.; Interscience: New York, Chapter 6
    • Nitrenes; Lwowski, W., Ed.; Interscience: New York, 1970, Chapter 6.
    • (1970) Nitrenes
  • 9
    • 0000014210 scopus 로고
    • Scriven, E.F.V., Ed.; Academic Press, Inc: Orlando, FL. E.F.V., Ed.; Academic Press, Inc: Orlando, FL
    • Lwowski W. In Azides and Nitrenes Reactivity and Utility; Scriven, E.F.V., Ed.; Academic Press, Inc: Orlando, FL, 1984, pp. 205-246.
    • (1984) Azides and Nitrenes Reactivity and Utility , pp. 205-246
    • Lwowski, W.1
  • 11
    • 0005600461 scopus 로고
    • Carbethoxynitrene. Selectivity of the C-H insertion
    • Lwowski, W.; Maricich, T.J. Carbethoxynitrene. Selectivity of the C-H insertion. J. Am. Chem. Soc. 1964, 86, 3164-3165.
    • (1964) J. Am. Chem. Soc , vol.86 , pp. 3164-3165
    • Lwowski, W.1    Maricich, T.J.2
  • 12
    • 0000603208 scopus 로고
    • Carbethoxynitrene by oc elimination. Reactions with hydrocarbons
    • Lwowski, W.; Maricich, T.J. Carbethoxynitrene by oc elimination. Reactions with hydrocarbons. J. Am. Chem. Soc. 1965, 87, 3630-3637.
    • (1965) J. Am. Chem. Soc , vol.87 , pp. 3630-3637
    • Lwowski, W.1    Maricich, T.J.2
  • 13
    • 37049104185 scopus 로고
    • Unusual effect of remote sulfone group on the reactivity of the double bond in unsaturated cyclic sulfones towards ethoxycarbonylnitrene
    • Aitken R.A.; Cadogan J.I.G.; Farries H.; Gosney I.; Palmer M.H.; Simpson I.; Tinley E.J. Unusual effect of remote sulfone group on the reactivity of the double bond in unsaturated cyclic sulfones towards ethoxycarbonylnitrene. J. Chem. Soc, Chem. Commun. 1984, 791-793.
    • (1984) J. Chem. Soc, Chem. Commun , pp. 791-793
    • Aitken, R.A.1    Cadogan, J.I.G.2    Farries, H.3    Gosney, I.4    Palmer, M.H.5    Simpson, I.6    Tinley, E.J.7
  • 15
    • 85197344097 scopus 로고
    • John Wiley & Sons, Inc.: New York, 1969, Vol. 2, p. 296
    • Fieser, L.F.; Fieser, M. Reagents for Organic Synthesis; John Wiley & Sons, Inc.: New York, 1967; Vol. 1, p. 736; 1969, Vol. 2, p. 296.
    • (1967) Reagents For Organic Synthesis , vol.1 , pp. 736
    • Fieser, L.F.1    Fieser, M.2
  • 16
    • 0345768688 scopus 로고    scopus 로고
    • John Wiley & Sons, Inc.: New York, 2000, Vol. 20, p. 162
    • Ho, T.L. Fiesers' Reagents for Organic Synthesis; John Wiley & Sons, Inc.: New York, 1999, Vol. 18, p. 159; 2000, Vol. 20, p. 162.
    • (1999) Fiesers' Reagents For Organic Synthesis , vol.18 , pp. 159
    • Ho, T.L.1
  • 17
    • 85197354634 scopus 로고
    • Paquette, L.A., Ed.; John Wiley & Sons: Chichester, L.A., Ed.; John Wiley & Sons: Chichester
    • Encyclopedia of Reagents for Organic Synthesis; Paquette, L.A., Ed.; John Wiley & Sons: Chichester, 1995, Vol. 6, p. 3721.
    • (1995) Encyclopedia of Reagents for Organic Synthesis , vol.6 , pp. 3721
  • 19
    • 37049126448 scopus 로고
    • Formation of arsinimines by reactions of triphenylarsine with nitrene precursors
    • Cadogan, J.I.G.; Gosney, I. Formation of arsinimines by reactions of triphenylarsine with nitrene precursors. J. Chem. Soc, Chem. Commun. 1973, 586-587.
    • (1973) J. Chem. Soc, Chem. Commun , pp. 586-587
    • Cadogan, J.I.G.1    Gosney, I.2
  • 20
    • 0008871523 scopus 로고
    • Reactions of triarylarsines with nitrene precursors. Formation of triarylarsinimines (As,As,As-triarylarsine imides) and related compounds
    • Cadogan J.I.G.; Gosney I. Reactions of triarylarsines with nitrene precursors. Formation of triarylarsinimines (As,As,As-triarylarsine imides) and related compounds. J. Chem. Soc, Perkin Trans. 1 1974, 460-465.
    • (1974) J. Chem. Soc, Perkin Trans , vol.1 , pp. 460-465
    • Cadogan, J.I.G.1    Gosney, I.2
  • 21
    • 49549163770 scopus 로고
    • Interaction of hexyl azide and (ethoxycarbonyl)nitrene
    • Gibson H.H.; Bundy C.H.; Gaddy H.R, III Interaction of hexyl azide and (ethoxycarbonyl)nitrene. Tetrahedron Lett. 1973, 3801-3804.
    • (1973) Tetrahedron Lett , pp. 3801-3804
    • Gibson, H.H.1    Bundy, C.H.2    Gaddy, H.R.3
  • 22
    • 33847089632 scopus 로고
    • Reaction of organic azides with ethoxycarbonylnitrene
    • Gibson, H.H., Jr.; Gaddy, H.R, III; Blankenship, C.S. Reaction of organic azides with ethoxycarbonylnitrene. J. Org. Chem. 1977, 42, 2443-2448.
    • (1977) J. Org. Chem , vol.42 , pp. 2443-2448
    • Gibson Jr., H.H.1    Gaddy, H.R.2    Blankenship, C.S.3
  • 23
    • 37049128382 scopus 로고
    • Reactivity of organophosphorus compounds. XXX. Iminophospholes and a new synthesis of benzo-furazans via intramolecular rearrangement of 1-o-(nitroarylimino)-1,2,5-triphenylphospholes
    • Cadogan J.I.G.; Scott R.J.; Gee R.D.; Gosney I. Reactivity of organophosphorus compounds. XXX. Iminophospholes and a new synthesis of benzo-furazans via intramolecular rearrangement of 1-o-(nitroarylimino)-1,2,5-triphenylphospholes. J. Chem. Soc, Perkin Trans. 1 1974, 1694-1702.
    • (1974) J. Chem. Soc, Perkin Trans , vol.1 , pp. 1694-1702
    • Cadogan, J.I.G.1    Scott, R.J.2    Gee, R.D.3    Gosney, I.4
  • 24
    • 0001301107 scopus 로고
    • Reaction of carbethoxynitrene with allenes
    • Bingham, E.M.; Gilbert, J.C. Reaction of carbethoxynitrene with allenes. J. Org. Chem. 1975, 40, 224-228.
    • (1975) J. Org. Chem , vol.40 , pp. 224-228
    • Bingham, E.M.1    Gilbert, J.C.2
  • 25
    • 0009997961 scopus 로고
    • Propellanes. XXIX. Electrophilic reactions of 11,13-dioxo-12-methyl-12-aza[4.4.3]propella-3,8-diene: Attack by nitrenes
    • Ruettimann, A.; Ginsburg, D. Propellanes. XXIX. Electrophilic reactions of 11,13-dioxo-12-methyl-12-aza[4.4.3]propella-3,8-diene: attack by nitrenes. Tetrahedron 1976, 32, 1009-1011.
    • (1976) Tetrahedron , vol.32 , pp. 1009-1011
    • Ruettimann, A.1    Ginsburg, D.2
  • 26
    • 33947094853 scopus 로고
    • N-aminoporphyrins. Preparation and metal complexes. Structure of N-tosylamino-5,10,15,20- tetraphenylporphinatonickel(II)
    • Callot H.J.; Chevrier B.; Weiss R. N-aminoporphyrins. Preparation and metal complexes. Structure of N-tosylamino-5,10,15,20- tetraphenylporphinatonickel(II). J. Am. Chem. Soc. 1978,100, 4733-4741.
    • (1978) J. Am. Chem. Soc , vol.100 , pp. 4733-4741
    • Callot, H.J.1    Chevrier, B.2    Weiss, R.3
  • 27
    • 33645598406 scopus 로고
    • Thermolysis of ethyl azidoformate in 2,3-dimethyl-2-butene. Example of a simple olefin giving a dominant 1,2,3-A2-triazoline intermediate
    • Nicholas P.P.; Goodrich B.F. Thermolysis of ethyl azidoformate in 2,3-dimethyl-2-butene. Example of a simple olefin giving a dominant 1,2,3-A2-triazoline intermediate. J. Org. Chem. 1975, 40, 3396-3398.
    • (1975) J. Org. Chem , vol.40 , pp. 3396-3398
    • Nicholas, P.P.1    Goodrich, B.F.2
  • 28
    • 30944469027 scopus 로고
    • Hexakis [jl-(ethyl chlorocarbamato-N,O)]-(J. 4-oxo-tetrazinc and its thermolysis in simple olefins
    • Nicholas, P.P.; Goodrich, B.F. Hexakis [jl-(ethyl chlorocarbamato-N,O)]-(J. 4-oxo-tetrazinc and its thermolysis in simple olefins. J. Org. Chem. 1979, 44, 2126-2130.
    • (1979) J. Org. Chem , vol.44 , pp. 2126-2130
    • Nicholas, P.P.1    Goodrich, B.F.2
  • 29
    • 85197347260 scopus 로고
    • Crosslinking or chain-lengthening hydrocarbon polymers
    • DE 2708584. Chem. Abstr. 1977, 87, 185859
    • Brooks, J.L.; Budziarek, R Crosslinking or chain-lengthening hydrocarbon polymers. Ger. Offen. 1977, DE 2708584. Chem. Abstr. 1977, 87, 185859.
    • (1977) Ger. Offen
    • Brooks, J.L.1    Budziarek, R.2
  • 30
    • 79954991348 scopus 로고
    • Reaction of tetraethylammonium fluoride
    • Hayami, J.; Ono, N.; Kaji, A. Reaction of tetraethylammonium fluoride. Nippon Kagaku Zasshi, 1971, 92, 87-90.
    • (1971) Nippon Kagaku Zasshi , vol.92 , pp. 87-90
    • Hayami, J.1    Ono, N.2    Kaji, A.3
  • 31
    • 27944468425 scopus 로고
    • Electroreduction of N-haloamides. Part III. The electrochemical reduction of N-fluorourethans in acetonitrile. The generation of carbethoxynitrene
    • Lessard, J.; Berube, D. Electroreduction of N-haloamides. Part III. The electrochemical reduction of N-fluorourethans in acetonitrile. The generation of carbethoxynitrene. Can. J. Chem. 1984, 62, 768-777.
    • (1984) Can J. Chem , vol.62 , pp. 768-777
    • Lessard, J.1    Berube, D.2
  • 32
    • 0041062051 scopus 로고
    • Inversion of the mechanism of epimination and epoxidation of activated olefins
    • Zeifman Yu.V.; Rokhlin E.M.; Utebaev U.; Knunyants I.L. Inversion of the mechanism of epimination and epoxidation of activated olefins. Dokl. Akad. Nauk SSSR, 1976,226, 1337-1340.
    • (1976) Dokl. Akad. Nauk SSSR , vol.226 , pp. 1337-1340
    • Zeifman, Y.V.1    Rokhlin, E.M.2    Utebaev, U.3    Knunyants, I.L.4
  • 33
    • 84956249451 scopus 로고
    • Fluorine-containing heterocumulenes. Communication 17. Epimination of bis(trifluoromethyl)ketene anil
    • Ter-Gabrielyan E.G.; Gambaryan N.P.; Zeifman Yu.V. Fluorine-containing heterocumulenes. Communication 17. Epimination of bis(trifluoromethyl)ketene anil. Izv. Akad. Nauk SSSR, Ser. Khim. 1978, 1888-1891.
    • (1978) Izv. Akad. Nauk SSSR, Ser. Khim , pp. 1888-1891
    • Ter-Gabrielyan, E.G.1    Gambaryan, N.P.2    Zeifman, Y.V.3
  • 34
    • 0040151071 scopus 로고
    • The reaction of organoboranes with ethyl β-nitrobenzenesulfonoxycarbamate under two-phase conditions. A convenient synthesis of ethyl N-alkylcarbamates from olefins via hydroboration
    • Akimoto, I.; Suzuki, A. The reaction of organoboranes with ethyl β- nitrobenzenesulfonoxycarbamate under two-phase conditions. A convenient synthesis of ethyl N-alkylcarbamates from olefins via hydroboration. Synth. Commun. 1981, 11, 475-480.
    • (1981) Synth. Commun , vol.11 , pp. 475-480
    • Akimoto, I.1    Suzuki, A.2
  • 36
    • 0000185359 scopus 로고
    • Reactions of vinylsilanes with ethoxycarbonylnitrene under phase-transfer conditions; a novel route to silicon-containing aziridines
    • Lukevics, E.; Dirnens, V.V.; Gol'dberg, Yu. Sh.; Liepinsh E.E. Reactions of vinylsilanes with ethoxycarbonylnitrene under phase-transfer conditions; a novel route to silicon-containing aziridines. J. Organomet. Chem. 1986, 316, 249-254.
    • (1986) J. Organomet. Chem , vol.316 , pp. 249-254
    • Lukevics, E.1    Dirnens, V.V.2    Gol'dberg, Y.S.3    Liepinsh, E.E.4
  • 37
    • 0042797300 scopus 로고
    • Generation of carbethoxynitrene by α elimination and its reactions with olefins under two-phase conditions
    • Send M.; Namba T.; Kise H. Generation of carbethoxynitrene by α elimination and its reactions with olefins under two-phase conditions. J. Org. Chem. 1978, 43, 3345-3348.
    • (1978) J. Org. Chem , vol.43 , pp. 3345-3348
    • Send, M.1    Namba, T.2    Kise, H.3
  • 38
    • 79955045296 scopus 로고
    • Electronic state of ethoxycarbonylnitrene generated by α-elimination under two-phase conditions
    • Send, M.; Namba, T.; Kise, H. Electronic state of ethoxycarbonylnitrene generated by α-elimination under two-phase conditions. Bull. Chem. Soc Jpn. 1979, 52, 2975-2977.
    • (1979) Bull. Chem. Soc Jpn , vol.52 , pp. 2975-2977
    • Send, M.1    Namba, T.2    Kise, H.3
  • 40
    • 33746482902 scopus 로고    scopus 로고
    • Pyrolysis of tricyclic cyclobutane-fused sulfolanes as a route to cis-1,2-divinyl compounds and their Cope-derived products
    • Aitken, R.A.; Cadogan, J.I.G.; Gosney, I.; Humphries, CM.; McLaughlin, L.M.; Wyse, S.J. Pyrolysis of tricyclic cyclobutane-fused sulfolanes as a route to cis-1,2-divinyl compounds and their Cope-derived products. J. Chem. Soc, Perkin Trans. 1 1999, 605-614.
    • (1999) J. Chem. Soc, Perkin Trans , vol.1 , pp. 605-614
    • Aitken, R.A.1    Cadogan, J.I.G.2    Gosney, I.3    Humphries, C.M.4    McLaughlin, L.M.5    Wyse, S.J.6
  • 44
    • 33845559300 scopus 로고
    • Regioselectivity of the (ethoxy-carbonylnitrene insertion reaction on monochloro- and dichloroalkanes and cycloalkanes
    • and references therein
    • D'Epifanio L.; Pellacani L.; Tardella P.A. Regioselectivity of the (ethoxy-carbonylnitrene insertion reaction on monochloro- and dichloroalkanes and cycloalkanes. J. Org. Chem. 1979, 44, 3605-3607 and references therein.
    • (1979) J. Org. Chem , vol.44 , pp. 3605-3607
    • D'Epifanio, L.1    Pellacani, L.2    Tardella, P.A.3
  • 45
    • 0342481424 scopus 로고
    • Ethoxycarbonylnitrene addition to vinyl chlorides. Synthesis and thermal rearrangement of α-chloroaziridines
    • Pellacani, L.; Persia, F.; Tardella, P.A. Ethoxycarbonylnitrene addition to vinyl chlorides. Synthesis and thermal rearrangement of α-chloroaziridines. Tetrahedron Lett. 1980,21, 4967-4970.
    • (1980) Tetrahedron Lett , vol.21 , pp. 4967-4970
    • Pellacani, L.1    Persia, F.2    Tardella, P.A.3
  • 46
    • 0010690282 scopus 로고
    • Degradation of aminimides obtained from enamines and (ethoxycarbonyl)nitrene
    • Pellacani, L.; Pulcini, P.; Tardella, P.A. Degradation of aminimides obtained from enamines and (ethoxycarbonyl)nitrene. J. Org. Chem. 1982, 47, 5023-5025.
    • (1982) J. Org. Chem , vol.47 , pp. 5023-5025
    • Pellacani, L.1    Pulcini, P.2    Tardella, P.A.3
  • 47
    • 4544264241 scopus 로고
    • N-Protected a amino ketones from enamines and (ethoxycarbonyl)nitrene
    • Fioravanti, S.; Loreto, M.A.; Pellacani, L.; Tardella, P.A. N-Protected a amino ketones from enamines and (ethoxycarbonyl)nitrene. J. Org. Chem. 1985,50, 5365-5368.
    • (1985) J. Org. Chem , vol.50 , pp. 5365-5368
    • Fioravanti, S.1    Loreto, M.A.2    Pellacani, L.3    Tardella, P.A.4
  • 48
    • 0001827558 scopus 로고    scopus 로고
    • Regio- and stereoselectivity in the amination of cyclohexanone enamines
    • Fioravanti, S.; Pellacani, L.; Tardella, P.A. Regio- and stereoselectivity in the amination of cyclohexanone enamines. Gazz. Chim. Ital. 1997, 127, 41-44.
    • (1997) Gazz. Chim. Ital , vol.127 , pp. 41-44
    • Fioravanti, S.1    Pellacani, L.2    Tardella, P.A.3
  • 52
    • 0025867083 scopus 로고
    • Asymmetric formation of carbon-nitrogen bonds in chiral enol ethers
    • Fioravanti, S.; Loreto, M.A.; Pellacani, L.; Tardella, P.A. Asymmetric formation of carbon-nitrogen bonds in chiral enol ethers. Tetrahedron, 1991, 47, 5877-5882.
    • (1991) Tetrahedron , vol.47 , pp. 5877-5882
    • Fioravanti, S.1    Loreto, M.A.2    Pellacani, L.3    Tardella, P.A.4
  • 53
    • 0027253980 scopus 로고
    • A novel route to N-substituted allylamines by the reaction of allylsilanes with (ethoxycarbonyl)nitrene
    • Fioravanti, S.; Loreto, M.A.; Pellacani, L.; Raimondi, S.; Tardella, P.A. A novel route to N-substituted allylamines by the reaction of allylsilanes with (ethoxycarbonyl)nitrene. Tetrahedron Lett. 1993,34, 4101-4104.
    • (1993) Tetrahedron Lett , vol.34 , pp. 4101-4104
    • Fioravanti, S.1    Loreto, M.A.2    Pellacani, L.3    Raimondi, S.4    Tardella, P.A.5
  • 54
    • 0028880397 scopus 로고
    • Stereochemistry in reactions of chiral cyclic allylsilanes with (ethoxycarbonyl)nitrene. A new route to chiral N-substituted allylamines
    • Loreto, M.A.; Tardella, P.A.; Tofani, D. Stereochemistry in reactions of chiral cyclic allylsilanes with (ethoxycarbonyl)nitrene. A new route to chiral N-substituted allylamines. Tetrahedron Lett. 1995, 36, 8295-8298.
    • (1995) Tetrahedron Lett , vol.36 , pp. 8295-8298
    • Loreto, M.A.1    Tardella, P.A.2    Tofani, D.3
  • 56
    • 0020402194 scopus 로고
    • Synthetic studies on 2-N-substituted cephems. I. Reaction of 2-cephem with (ethoxycarbonyl)nitrene
    • Hoshide, Y.; Ogawa, H. Synthetic studies on 2-N-substituted cephems. I. Reaction of 2-cephem with (ethoxycarbonyl)nitrene. Yakugaku Zasshi, 1982, 102, 816-822.
    • (1982) Yakugaku Zasshi , vol.102 , pp. 816-822
    • Hoshide, Y.1    Ogawa, H.2
  • 57
    • 84985052810 scopus 로고
    • Azimines. VI. 1-(Alkoxycarbonyl)-2,3-dialkyl- and -2,3-diarylazimines. Helv
    • Leuenberger, C; Hoesch, L.; Dreiding, A.S. Azimines. VI. 1-(Alkoxycarbonyl)-2,3-dialkyl- and -2,3-diarylazimines. Helv. Chim. Acta 1982,65, 217-228.
    • (1982) Chim. Acta , vol.65 , pp. 217-228
    • Leuenberger, C.1    Hoesch, L.2    Dreiding, A.S.3
  • 58
    • 84985726429 scopus 로고
    • Hydrogen cyanide N-methylide: Preparation, spectroscopic identification, and its relationship to other C2H3N isomers
    • Maier, G.; Schmidt, C; Reisenauer, H.P.; Endlein, E.; Becker, D.; Eckwert, J.; Hess, B.A., Jr.; Schaad, L.J. Hydrogen cyanide N-methylide: preparation, spectroscopic identification, and its relationship to other C2H3N isomers. Chem. Ber. 1993,126, 2337-2352.
    • (1993) Chem. Ber , vol.126 , pp. 2337-2352
    • Maier, G.1    Schmidt, C.2    Reisenauer, H.P.3    Endlein, E.4    Becker, D.5    Eckwert, J.6    Hess Jr., B.A.7    Schaad, L.J.8
  • 59
    • 33748591453 scopus 로고
    • Chemical repercussions of orbital interactions through bond and through space. The reactivity of the double bond in unsaturated cyclic sulfones towards aziridine formation and epoxidation
    • Aitken, R.A.; Gosney, I.; Farries, H.; Palmer, M.H.; Simpson, I.; Cadogan, J.I.G.; Tinley, E.J. Chemical repercussions of orbital interactions through bond and through space. The reactivity of the double bond in unsaturated cyclic sulfones towards aziridine formation and epoxidation. Tetrahedron, 1984,40, 2487-2503.
    • (1984) Tetrahedron , vol.40 , pp. 2487-2503
    • Aitken, R.A.1    Gosney, I.2    Farries, H.3    Palmer, M.H.4    Simpson, I.5    Cadogan, J.I.G.6    Tinley, E.J.7
  • 60
    • 0342648465 scopus 로고
    • Chemical repercussions of orbital interactions through bond and through space. Effect of remote substituents on the addition of nitrenes to bicyclic olefins
    • Aitken, R.A.; Gosney, I.; Farries, H.; Palmer, M.H.; Simpson, I.; Cadogan, J.I.G.; Tinley, E.J. Chemical repercussions of orbital interactions through bond and through space. Effect of remote substituents on the addition of nitrenes to bicyclic olefins. Tetrahedron 1985, 41, 1329-1346.
    • (1985) Tetrahedron , vol.41 , pp. 1329-1346
    • Aitken, R.A.1    Gosney, I.2    Farries, H.3    Palmer, M.H.4    Simpson, I.5    Cadogan, J.I.G.6    Tinley, E.J.7
  • 61
    • 2642715027 scopus 로고
    • Generation of ethoxycarbon-ylnitrene in a solid-liquid two-phase system in the presence of a phase transfer catalyst or under ultrasonic irradiation
    • Dirnens, V.V.; Gol'dberg, Yu.Sh.; Lukevics, E. Generation of ethoxycarbon-ylnitrene in a solid-liquid two-phase system in the presence of a phase transfer catalyst or under ultrasonic irradiation. Dokl. Akad. Nauk SSSR 1988, 298, 116-118.
    • (1988) Dokl. Akad. Nauk SSSR , vol.298 , pp. 116-118
    • Dirnens, V.V.1    Gol'dberg, Y.S.2    Lukevics, E.3
  • 62
  • 63
    • 0028295197 scopus 로고
    • Improved amination by ethyl N-{[(4-nitrophenyl)sulfonyl]oxy}carbamate in the presence of inorganic oxides or carbonates
    • Barani, M.; Fioravanti, S.; Loreto, M.A.; Pellacani, L.; Tardella, P.A. Improved amination by ethyl N-{[(4-nitrophenyl)sulfonyl]oxy}carbamate in the presence of inorganic oxides or carbonates. Tetrahedron 1994, 50, 3829-3834.
    • (1994) Tetrahedron , vol.50 , pp. 3829-3834
    • Barani, M.1    Fioravanti, S.2    Loreto, M.A.3    Pellacani, L.4    Tardella, P.A.5
  • 64
    • 0028131522 scopus 로고
    • Cs2CO3 or CaO as promoters of ethyl N-{[(4-methylphenyl)sulfonyl]oxy}carbamate in amination reactions
    • Barani, M.; Fioravanti, S.; Pellacani, L.; Tardella, P.A. Cs2CO3 or CaO as promoters of ethyl N-{[(4-methylphenyl)sulfonyl]oxy}carbamate in amination reactions. Tetrahedron 1994, 50, 11235-11238.
    • (1994) Tetrahedron , vol.50 , pp. 11235-11238
    • Barani, M.1    Fioravanti, S.2    Pellacani, L.3    Tardella, P.A.4
  • 67
    • 4544359931 scopus 로고    scopus 로고
    • Electrophilic α-animation of carbonyl compounds
    • Erdik, E. Electrophilic α-animation of carbonyl compounds. Tetrahedron 2004, 60, 8747-8782.
    • (2004) Tetrahedron , vol.60 , pp. 8747-8782
    • Erdik, E.1
  • 69
    • 0033529723 scopus 로고    scopus 로고
    • Synthesis of hydroxamic esters via alkoxyami- nocarbonylation of β-dicarbonyl compounds
    • Hanessian, S.; Johnstone, S. Synthesis of hydroxamic esters via alkoxyami- nocarbonylation of β-dicarbonyl compounds. J. Org. Chem. 1999, 64, 5896-5903.
    • (1999) J. Org. Chem , vol.64 , pp. 5896-5903
    • Hanessian, S.1    Johnstone, S.2
  • 70
    • 84954262458 scopus 로고
    • Ureas from Lossen rearrangements of hydroxamic acids induced by β-toluenesulfonyl chloride or 2-chloro-1-methylpyridinium iodide in the presence of amines: A correction
    • Pihuleac J.; Bauer, L. Ureas from Lossen rearrangements of hydroxamic acids induced by β-toluenesulfonyl chloride or 2-chloro-1-methylpyridinium iodide in the presence of amines: a correction. Synthesis 1989, 61-64
    • (1989) Synthesis , pp. 61-64
    • Pihuleac, J.1    Bauer, L.2
  • 72
    • 0012478328 scopus 로고
    • Novel synthesis of β-hydroxyvaline
    • Berse, C; Bessette, P. Novel synthesis of β-hydroxyvaline. Can. J. Chem. 1971,49, 2610-2611.
    • (1971) Can. J. Chem , vol.49 , pp. 2610-2611
    • Berse, C.1    Bessette, P.2
  • 73
    • 0034705615 scopus 로고    scopus 로고
    • Aziridination of chiral 3-(2,2-dimethyl-1,3-dioxolan-4-yl)-2-propenoate esters
    • Fazio, A.; Loreto, M.A.; Tardella, P.A.; Tofani, D. Aziridination of chiral 3-(2,2-dimethyl-1,3-dioxolan-4-yl)-2-propenoate esters. Tetrahedron 2000, 56, 4515-4519.
    • (2000) Tetrahedron , vol.56 , pp. 4515-4519
    • Fazio, A.1    Loreto, M.A.2    Tardella, P.A.3    Tofani, D.4
  • 74
    • 0035843407 scopus 로고    scopus 로고
    • Aziridination of α, β-unsaturated phosphonic esters
    • Fazio, A.; Loreto, M.A.; Tardella, P.A. Aziridination of α, β-unsaturated phosphonic esters. Tetrahedron Lett. 2001, 42, 2185-2187.
    • (2001) Tetrahedron Lett , vol.42 , pp. 2185-2187
    • Fazio, A.1    Loreto, M.A.2    Tardella, P.A.3
  • 75
    • 0037505338 scopus 로고    scopus 로고
    • Synthesis of α-amino γ-butyrolactone derivatives by aziridination of α-ylidene γ-butyrolactones
    • Gasperi, T.; Loreto, M.A.; Tardella, P.A.; Veri, E. Synthesis of α-amino γ-butyrolactone derivatives by aziridination of α-ylidene γ-butyrolactones. Tetrahedron Lett. 2003, 44, 4953-4956.
    • (2003) Tetrahedron Lett , vol.44 , pp. 4953-4956
    • Gasperi, T.1    Loreto, M.A.2    Tardella, P.A.3    Veri, E.4
  • 76
    • 31344465974 scopus 로고    scopus 로고
    • Spiroaziridines from 4-substituted α-ylidene-γ-butyrolactones
    • Gasperi, T.; Loreto, M.A.; Migliorini, A.; Tardella, P.A. Spiroaziridines from 4-substituted α-ylidene-γ-butyrolactones. Heterocycles 2005, 65, 1447-1454.
    • (2005) Heterocycles , vol.65 , pp. 1447-1454
    • Gasperi, T.1    Loreto, M.A.2    Migliorini, A.3    Tardella, P.A.4
  • 77
    • 33751334378 scopus 로고    scopus 로고
    • Oc Amino-α-vinyl-'γ-butyrolactone derivatives from a {[(trimethylsilyl)methyl]alkylidene}-γ-butyrolactones
    • Capuzzi, M.; Gambacorta, A.; Gasperi, T.; Loreto, M.A.; Tardella, P.A. oc Amino-α-vinyl-'γ-butyrolactone derivatives from a {[(trimethylsilyl)methyl]alkylidene}-γ-butyrolactones. Eur. J. Org. Chem. 2006, 5076-5082.
    • (2006) Eur. J. Org. Chem , pp. 5076-5082
    • Capuzzi, M.1    Gambacorta, A.2    Gasperi, T.3    Loreto, M.A.4    Tardella, P.A.5
  • 78
    • 34250676971 scopus 로고    scopus 로고
    • Novel spirohet erocycles by aziridination of α-methylene-γ- and -8-lactams
    • Loreto, M.A.; Migliorini, A.; Tardella, P.A.; Gambacorta, A. Novel spirohet erocycles by aziridination of α-methylene-γ- and -8-lactams. Eur. J. Org. Chem. 2007, 2365-2371.
    • (2007) Eur. J. Org. Chem , pp. 2365-2371
    • Loreto, M.A.1    Migliorini, A.2    Tardella, P.A.3    Gambacorta, A.4
  • 79
    • 71549115446 scopus 로고    scopus 로고
    • Synthesis of functionalized spiroaziridine-oxindoles from 3-ylideneoxindoles: An easy route to 3-(aminoalkyl)oxindoles
    • Ammetto, I.; Gasperi, T.; Loreto, M.A.; Migliorini, A.; Palmarelli, F.; Tardella, P.A. Synthesis of functionalized spiroaziridine-oxindoles from 3-ylideneoxindoles: an easy route to 3-(aminoalkyl)oxindoles. Eur. J. Org. Chem. 2009, 6189-6197.
    • (2009) Eur. J. Org. Chem , pp. 6189-6197
    • Ammetto, I.1    Gasperi, T.2    Loreto, M.A.3    Migliorini, A.4    Palmarelli, F.5    Tardella, P.A.6
  • 80
    • 0030813267 scopus 로고    scopus 로고
    • β,γ-Unsaturated α- amino ester derivatives by amination of γ-silylated α,β-unsaturated esters
    • Loreto, M.A.; Pompei, F.; Tardella, P.A.; Tofani, D. P, γ-Unsaturated α- amino ester derivatives by amination of γ-silylated α,β-unsaturated esters. Tetrahedron 1997, 53, 15853-15858.
    • (1997) Tetrahedron , vol.53 , pp. 15853-15858
    • Loreto, M.A.1    Pompei, F.2    Tardella, P.A.3    Tofani, D.4
  • 81
    • 0141991215 scopus 로고    scopus 로고
    • Synthesis of β, β-branched β-amino ester derivatives through spiroaziridination of (αtrimethylsilanylmethyl)cyclohexylidene esters
    • Gasperi, T.; Loreto, M.A.; Tardella, P.A. Synthesis of β, β-branched β-amino ester derivatives through spiroaziridination of (α-trimethylsilanylmethyl)cyclohexylidene esters. Tetrahedron Lett. 2003, 44, 8467-8470.
    • (2003) Tetrahedron Lett , vol.44 , pp. 8467-8470
    • Gasperi, T.1    Loreto, M.A.2    Tardella, P.A.3
  • 82
    • 33644642296 scopus 로고    scopus 로고
    • α--Methylene-β-amino ketone derivatives from β-ketoallylsilanes
    • Loreto, M.A.; Migliorini, A.; Tardella, P.A. α-Methylene-β-amino ketone derivatives from β-ketoallylsilanes. J. Org. Chem. 2006, 71, 2163-2166.
    • (2006) J. Org. Chem , vol.71 , pp. 2163-2166
    • Loreto, M.A.1    Migliorini, A.2    Tardella, P.A.3
  • 83
    • 0035858739 scopus 로고    scopus 로고
    • α-Methylene β-amino phosphonic ester derivatives by amination of (1-trimethylsilanylmethyl-vinyl) phosphonic esters
    • Loreto, M.A.; Pompili, C; Tardella, P.A. α-Methylene β-amino phosphonic ester derivatives by amination of (1-trimethylsilanylmethyl-vinyl) phosphonic esters. Tetrahedron 2001, 57, 4423-4427.
    • (2001) Tetrahedron , vol.57 , pp. 4423-4427
    • Loreto, M.A.1    Pompili, C.2    Tardella, P.A.3
  • 84
    • 0037090207 scopus 로고    scopus 로고
    • Amination of oc, 3- unsaturated (2-trimethylsilanylmethyl) carboxylic esters
    • Gasperi, T.; Loreto, M.A.; Tardella, P.A.; Gambacorta, A. Amination of oc, 3- unsaturated (2-trimethylsilanylmethyl) carboxylic esters. Tetrahedron Lett. 2002,43, 3017-3020.
    • (2002) Tetrahedron Lett , vol.43 , pp. 3017-3020
    • Gasperi, T.1    Loreto, M.A.2    Tardella, P.A.3    Gambacorta, A.4
  • 85
    • 0009480764 scopus 로고    scopus 로고
    • 2-Ethoxycarbonyl-2-fluoroaziridines: Methyl- ene-bridged (Ca to N) α-fluoro-α-amino acids analogues
    • Usuki, Y.; Fukuda, Y.; Iio, H. 2-Ethoxycarbonyl-2-fluoroaziridines: methyl- ene-bridged (Ca to N) α-fluoro-α-amino acids analogues. ITE Lett. Batteries New Technol. Med. 2001,2, 237-240.
    • (2001) ITE Lett. Batteries New Technol. Med , vol.2 , pp. 237-240
    • Usuki, Y.1    Fukuda, Y.2    Iio, H.3
  • 86
    • 85197357153 scopus 로고    scopus 로고
    • A short and facile synthesis of vinylglycine derivatives
    • Bellassoued, M.; Grugier, J.; Fromentin, P. A short and facile synthesis of vinylglycine derivatives. Phys. Chem. News 2004,17, 139-140.
    • (2004) Phys. Chem. News , vol.17 , pp. 139-140
    • Bellassoued, M.1    Grugier, J.2    Fromentin, P.3
  • 90
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H.C.; Finn, M.G.; Sharpless, K.B. Click chemistry: diverse chemical function from a few good reactions. Angew. Chem., Int. Ed. Engl. 2001, 40, 2004-2021.
    • (2001) Angew. Chem. Int. Ed. Engl , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 91
    • 34250811485 scopus 로고    scopus 로고
    • The rise of azide-alkyne 1,3-dipolar 'click' cycloaddition and its application to polymer science and surface modification
    • Evans, RA. The rise of azide-alkyne 1,3-dipolar 'click' cycloaddition and its application to polymer science and surface modification. Aust. J. Chem. 2007,60, 384-395.
    • (2007) Aust. J. Chem , vol.60 , pp. 384-395
    • Evans, R.A.1
  • 92
    • 0001139468 scopus 로고
    • MIRC (Michael Initiated Ring Closure) reactions. Formation of three, five, six, and seven membered rings
    • Little, R.D.; Dawson, J.R MIRC (Michael Initiated Ring Closure) reactions. Formation of three, five, six, and seven membered rings. Tetrahedron Lett. 1980, 21, 2609-2612.
    • (1980) Tetrahedron Lett , vol.21 , pp. 2609-2612
    • Little, R.D.1    Dawson, J.R.2
  • 93
    • 0036064894 scopus 로고    scopus 로고
    • Synthesis of substituted cyclopropyl-phosphonates by Michael Induced Ring Closure (MIRC) reactions
    • Stevens, C.V.; Van Heecke, G.; Barbero, C; Patora, K.; De Kimpe, N.; Verhe R Synthesis of substituted cyclopropyl-phosphonates by Michael Induced Ring Closure (MIRC) reactions. Synlett 2002, 1089-1092.
    • (2002) Synlett , pp. 1089-1092
    • Stevens, C.V.1    van Heecke, G.2    Barbero, C.3    Patora, K.4    de Kimpe, N.5    Verhe, R.6
  • 94
    • 0025728161 scopus 로고
    • Electrophilic amination: First direct transfer of NHBoc with lithium tert-butyl-N-tosyloxycarbamate
    • Genêt, J.P.; Mallart, S.; Greck, C; Piveteau, E. Electrophilic amination: first direct transfer of NHBoc with lithium tert-butyl-N-tosyloxycarbamate. Tetrahedron Lett. 1991, 32, 2359-2362.
    • (1991) Tetrahedron Lett , vol.32 , pp. 2359-2362
    • Genêt, J.P.1    Mallart, S.2    Greck, C.3    Piveteau, E.4
  • 95
    • 0026521029 scopus 로고
    • A convenient synthesis of N-Boc protected primary amines via the reaction of organoboranes with lithium or potassium tert-butyl-N-tosyloxycarbamate
    • Genêt, J.P.; Hajicek, J.; Bischoff L.; Greck, C. A convenient synthesis of N-Boc protected primary amines via the reaction of organoboranes with lithium or potassium tert-butyl-N-tosyloxycarbamate. Tetrahedron Lett. 1992, 33, 2677-2680.
    • (1992) Tetrahedron Lett , vol.33 , pp. 2677-2680
    • Genêt, J.P.1    Hajicek, J.2    Bischoff, L.3    Greck, C.4
  • 96
    • 0001678784 scopus 로고
    • Electrophilic amination of carbanions with metalated t-butyl-N-tosyloxycarbamate
    • Greck, C; Bischoff, L.; Girard, A.; Hajicek, J.; Genêt, J.P. Electrophilic amination of carbanions with metalated t-butyl-N-tosyloxycarbamate. Bull. Soc. Chim. Fr. 1994,131, 429-433.
    • (1994) Bull. Soc. Chim. Fr , vol.131 , pp. 429-433
    • Greck, C.1    Bischoff, L.2    Girard, A.3    Hajicek, J.4    Genêt, J.P.5
  • 97
    • 0003074072 scopus 로고
    • Tert-Butyl lithio[(mesitylsulfonyl)oxy]carbamate-3THF: Structure of nitrenoids in crystals
    • Angew. Chem., Int. Ed. Engl. 1994, 33, 115-117
    • Boche, G.; Boie, C; Bosold, F.; Harms, K.; Marsch, M. tert-Butyl lithio[(mesitylsulfonyl)oxy]carbamate-3THF: structure of nitrenoids in crystals. Angew. Chem. 1994,106, 90-91; Angew. Chem., Int. Ed. Engl. 1994, 33, 115-117.
    • (1994) Angew. Chem , vol.106 , pp. 90-91
    • Boche, G.1    Boie, C.2    Bosold, F.3    Harms, K.4    Marsch, M.5
  • 98
    • 0842328414 scopus 로고    scopus 로고
    • Aza-Michael addition of nosyloxycarbamates to 2-(trifluoromethyl)acrylates
    • Colantoni, D.; Fioravanti, S.; Pellacani, L.; Tardella, P.A. Aza-Michael addition of nosyloxycarbamates to 2-(trifluoromethyl)acrylates. Org. Lett. 2004,6, 197-200.
    • (2004) Org. Lett , vol.6 , pp. 197-200
    • Colantoni, D.1    Fioravanti, S.2    Pellacani, L.3    Tardella, P.A.4
  • 99
    • 0006287027 scopus 로고
    • Synthesis of primary amines by the reaction of α-methylhydroxylamine with organomagnesium and organolith-ium compounds
    • Sheverdina, N.I.; Kocheskov, K.A. Synthesis of primary amines by the reaction of α-methylhydroxylamine with organomagnesium and organolith-ium compounds. Zh. Obsh. Khim. 1938, 8, 1825-1830.
    • (1938) Zh. Obsh. Khim , vol.8 , pp. 1825-1830
    • Sheverdina, N.I.1    Kocheskov, K.A.2
  • 100
    • 33845185611 scopus 로고
    • Electrophilic amination of carbanions
    • Erdik, E.; Ay, M. Electrophilic amination of carbanions. Chem. Rev. 1989, 89, 1947-1980.
    • (1989) Chem. Rev , vol.89 , pp. 1947-1980
    • Erdik, E.1    Ay, M.2
  • 101
    • 84874097945 scopus 로고    scopus 로고
    • Electrophilic amination of carbanions, enolates, and their surrogates
    • Ciganek, E. Electrophilic amination of carbanions, enolates, and their surrogates. Org. React. 2008, 72, 1-366.
    • (2008) Org. React , vol.72 , pp. 1-366
    • Ciganek, E.1
  • 102
    • 44449149726 scopus 로고    scopus 로고
    • Carbon-nitrogen bond-forming reactions of dialkyl azodicarboxylate. A promising synthetic strategy
    • Nair, V.; Biju, A.T.; Mathew, S.C.; Babu, B.P. Carbon-nitrogen bond-forming reactions of dialkyl azodicarboxylate. A promising synthetic strategy. Chem. Asian J. 2008,3, 810-820.
    • (2008) Chem. Asian J , vol.3 , pp. 810-820
    • Nair, V.1    Biju, A.T.2    Mathew, S.C.3    Babu, B.P.4
  • 104
    • 73149091235 scopus 로고    scopus 로고
    • An unexpected highly stereoselective bisaziridination of (E, E)-1,4-dialkyl-2,3-dinitrobutadienes followed by a nitro group driven ring enlargement
    • Ciogli, A.; Fioravanti, S.; Gasparrini, F.; Pellacani, L.; Rizzato, E.; Spinelli, D.; Tardella P.A. An unexpected highly stereoselective bisaziridination of (E, E)-1,4-dialkyl-2,3-dinitrobutadienes followed by a nitro group driven ring enlargement. J. Org. Chem. 2009, 74, 9314-9318.
    • (2009) J. Org. Chem , vol.74 , pp. 9314-9318
    • Ciogli, A.1    Fioravanti, S.2    Gasparrini, F.3    Pellacani, L.4    Rizzato, E.5    Spinelli, D.6    Tardella, P.A.7
  • 105
    • 0034796434 scopus 로고    scopus 로고
    • A facile synthesis of N-alkoxycarbonylaziridines from olefins bearing two geminal electron-withdrawing groups
    • Fioravanti, S.; Morreale, A.; Pellacani, L.; Tardella, P.A. A facile synthesis of N-alkoxycarbonylaziridines from olefins bearing two geminal electron-withdrawing groups. Synthesis 2001, 1975-1978.
    • (2001) Synthesis , pp. 1975-1978
    • Fioravanti, S.1    Morreale, A.2    Pellacani, L.3    Tardella, P.A.4
  • 107
    • 0344738565 scopus 로고    scopus 로고
    • Aza-MIRC reactions of sulfonyl-activated hydroxycarbamates with α,β-difunctionalized acrylates
    • Fioravanti, S.; Morreale, A.; Pellacani, L.; Tardella, P.A. Aza-MIRC reactions of sulfonyl-activated hydroxycarbamates with α,β-difunctionalized acrylates. Eur. J. Org. Chem. 2003, 4549-4552.
    • (2003) Eur. J. Org. Chem , pp. 4549-4552
    • Fioravanti, S.1    Morreale, A.2    Pellacani, L.3    Tardella, P.A.4
  • 110
    • 4143113646 scopus 로고    scopus 로고
    • Cinchona alkaloids in the asymmetric synthesis of 2-(phenylsulfanyl)aziridines
    • Fioravanti, S.; Mascia, M.G.; Pellacani, L.; Tardella, P.A. Cinchona alkaloids in the asymmetric synthesis of 2-(phenylsulfanyl)aziridines. Tetrahedron 2004, 60, 8073-8077.
    • (2004) Tetrahedron , vol.60 , pp. 8073-8077
    • Fioravanti, S.1    Mascia, M.G.2    Pellacani, L.3    Tardella, P.A.4
  • 111
    • 0346501852 scopus 로고    scopus 로고
    • Functionalized enones as starting materials for the construction of aziridine scaffolds
    • Fioravanti, S.; Morreale, A.; Pellacani, L.; Tardella, P.A. Functionalized enones as starting materials for the construction of aziridine scaffolds. Mol. Diversity 2003, 6, 177-180.
    • (2003) Mol. Diversity , vol.6 , pp. 177-180
    • Fioravanti, S.1    Morreale, A.2    Pellacani, L.3    Tardella, P.A.4
  • 113
    • 27444448119 scopus 로고    scopus 로고
    • Efficient synthesis of 4-cyano-2,3-dihydrooxazoles by direct animation of 2-alkylidene-3-oxo-nitriles
    • Burini, E.; Fioravanti, S.; Morreale, A.; Pellacani, L.; Tardella, P.A. Efficient synthesis of 4-cyano-2,3-dihydrooxazoles by direct animation of 2-alkylidene-3-oxo-nitriles. Synlett 2005, 2673-2675.
    • (2005) Synlett , pp. 2673-2675
    • Burini, E.1    Fioravanti, S.2    Morreale, A.3    Pellacani, L.4    Tardella, P.A.5
  • 114
    • 34848827407 scopus 로고    scopus 로고
    • A novel deacylation during the amination of trifluoromethyl β-dicarbonyl compounds
    • Fioravanti, S.; Pellacani, L.; Ramadori, F.; Tardella, P.A. A novel deacylation during the amination of trifluoromethyl β-dicarbonyl compounds. Tetrahedron Lett. 2007, 48, 7821-7824.
    • (2007) Tetrahedron Lett , vol.48 , pp. 7821-7824
    • Fioravanti, S.1    Pellacani, L.2    Ramadori, F.3    Tardella, P.A.4
  • 115
    • 27744502047 scopus 로고    scopus 로고
    • Unexpected and expeditious entry into trifluoromethyl aziridines from substituted β-dicarbonyl compounds
    • Colantoni, D.; Fioravanti, S.; Pellacani, L.; Tardella, P.A. Unexpected and expeditious entry into trifluoromethyl aziridines from substituted β-dicarbonyl compounds. J. Org. Chem. 2005, 70, 9648-9650.
    • (2005) J. Org. Chem , vol.70 , pp. 9648-9650
    • Colantoni, D.1    Fioravanti, S.2    Pellacani, L.3    Tardella, P.A.4
  • 117
    • 17444396338 scopus 로고    scopus 로고
    • Aziridines versus vinyl carbamates from the direct amination of electron-withdrawing group-substituted trifluoromethyl enoates
    • Fioravanti, S.; Colantoni, D.; Pellacani, L.; Tardella, P.A. Aziridines versus vinyl carbamates from the direct amination of electron-withdrawing group-substituted trifluoromethyl enoates. J. Org. Chem. 2005, 70, 3296-3298.
    • (2005) J. Org. Chem , vol.70 , pp. 3296-3298
    • Fioravanti, S.1    Colantoni, D.2    Pellacani, L.3    Tardella, P.A.4
  • 118
    • 0037424739 scopus 로고    scopus 로고
    • Reagent-controlled diastereoselective aminations with a new chiral nosyloxycarbamate
    • Fioravanti, S.; Morreale, A.; Pellacani, L.; Tardella, P.A. Reagent-controlled diastereoselective aminations with a new chiral nosyloxycarbamate. Tetrahedron Lett. 2003, 44, 3031-3034.
    • (2003) Tetrahedron Lett , vol.44 , pp. 3031-3034
    • Fioravanti, S.1    Morreale, A.2    Pellacani, L.3    Tardella, P.A.4
  • 119
    • 0000332869 scopus 로고
    • Stereochemistry of sulfur compounds. VII. Course of substitution at sulfur attached to four different ligands
    • Jones, M.R.; Cram, D.J. Stereochemistry of sulfur compounds. VII. Course of substitution at sulfur attached to four different ligands. J. Am. Chem. Soc. 1974, 96, 2183-2190.
    • (1974) J. Am. Chem. Soc , vol.96 , pp. 2183-2190
    • Jones, M.R.1    Cram, D.J.2
  • 120
    • 77956695661 scopus 로고
    • Asymmetric total synthesis of (+)-7-deoxypancratistatin
    • Tian, X.; Maurya, R.; Konigsberger, K.; Hudlicky, T. Asymmetric total synthesis of (+)-7-deoxypancratistatin. Synlett 1995, 1125-1126.
    • (1995) Synlett , pp. 1125-1126
    • Tian, X.1    Maurya, R.2    Konigsberger, K.3    Hudlicky, T.4
  • 121
    • 0033234137 scopus 로고    scopus 로고
    • Preparation of racemic and enantiopure arenesulfonimidoyl azoles - new compounds chiral on sulfur
    • Kugle, R.; Hocke, H.; Schulz, M.; Schilke, F. Preparation of racemic and enantiopure arenesulfonimidoyl azoles - new compounds chiral on sulfur. Phosphorus, Sulfur Silicon Relat. Elem. 1999, 149, 179-206.
    • (1999) Phosphorus, Sulfur Silicon Relat. Elem , vol.149 , pp. 179-206
    • Kugle, R.1    Hocke, H.2    Schulz, M.3    Schilke, F.4
  • 122
    • 85197351402 scopus 로고    scopus 로고
    • Preparation of pancratistatins and processes for their production
    • WO 9716453, Chem. Abstr. 1997, 127, 17845
    • Hudlicky, T.; Koenigsberger, K.; Mclamore, S.D.; Maurya, R. Preparation of pancratistatins and processes for their production. PCT Int. Appl. 1997, WO 9716453, Chem. Abstr. 1997, 127, 17845.
    • (1997) PCT Int. Appl
    • Hudlicky, T.1    Koenigsberger, K.2    McLamore, S.D.3    Maurya, R.4
  • 123
    • 0029798274 scopus 로고    scopus 로고
    • Toluene dioxygenase-mediated cis-dihydroxylation of aromatics in enanti-oselective synthesis. asymmetric total syntheses of pancratistatin and 7-deoxypancratistatin, promising antitumor agents
    • Hudlicky, T.; Tian, X.; Koenigsberger, K.; Maurya, R.; Rouden, J.; Fan, B. Toluene dioxygenase-mediated cis-dihydroxylation of aromatics in enanti-oselective synthesis. asymmetric total syntheses of pancratistatin and 7-deoxypancratistatin, promising antitumor agents. J. Am. Chem. Soc. 1996, 118, 10752-10765.
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 10752-10765
    • Hudlicky, T.1    Tian, X.2    Koenigsberger, K.3    Maurya, R.4    Rouden, J.5    Fan, B.6
  • 124
    • 34047121324 scopus 로고
    • Reactions of alkoxycarbonylnitrenes with tertiary amines. I. Reaction of methoxycarbonylnitrene with triethylamine
    • Abdul Hai S.M. Reactions of alkoxycarbonylnitrenes with tertiary amines. I. Reaction of methoxycarbonylnitrene with triethylamine. Pak. J. Sci. Ind. Res. 1974, 17, 59-64.
    • (1974) Pak. J. Sci. Ind. Res , vol.17 , pp. 59-64
    • Abdul Hai, S.M.1
  • 125
    • 0030912584 scopus 로고    scopus 로고
    • Intramolecular ring cleavage of chiral terpenoid-derived oxazinone via asymmetric anti-aldol reaction: Unexpected entry to a N-substituted tetrahydro-1,3-oxazine-2,4-dione derivative
    • Abbas, T.R.; Cadogan, J.I.G.; Doyle, A.A.; Gosney, I.; Hodgson, P.K.G.; Howells, G.E.; Hulme, A.N.; Parsons, S.; Sadler, I.H. Intramolecular ring cleavage of chiral terpenoid-derived oxazinone via asymmetric anti-aldol reaction: unexpected entry to a N-substituted tetrahydro-1,3-oxazine-2,4-dione derivative. Tetrahedron Lett. 1997, 38, 4917-4920.
    • (1997) Tetrahedron Lett , vol.38 , pp. 4917-4920
    • Abbas, T.R.1    Cadogan, J.I.G.2    Doyle, A.A.3    Gosney, I.4    Hodgson, P.K.G.5    Howells, G.E.6    Hulme, A.N.7    Parsons, S.8    Sadler, I.H.9
  • 126
    • 0026697882 scopus 로고
    • Enantiospecific preparation of [(2R,6S)-endo]-4-aza-1,10,10-trimethyl-3-oxatricyclo[5.2.1.02,6]decan-4-one by a nitrene-mediated route from [(1S)-endo]-(-)-borneol and its utility as a chiral auxiliary in some asymmetric transformations
    • Banks, M.R.; Blake, A.J.; Cadogan, J.I.G.; Dawson, I.M.; Gosney, I.; Grant, K.J.; Gaur, S.; Hodgson, P.K.G.; Knight, K.S.; Smith, G.W. Enantiospecific preparation of [(2R,6S)-endo]-4-aza-1,10,10-trimethyl-3-oxatricyclo[5.2.1.02,6]decan-4-one by a nitrene-mediated route from [(1S)-endo]-(-)-borneol and its utility as a chiral auxiliary in some asymmetric transformations. Tetrahedron 1992, 48, 7979-8006.
    • (1992) Tetrahedron , vol.48 , pp. 7979-8006
    • Banks, M.R.1    Blake, A.J.2    Cadogan, J.I.G.3    Dawson, I.M.4    Gosney, I.5    Grant, K.J.6    Gaur, S.7    Hodgson, P.K.G.8    Knight, K.S.9    Smith, G.W.10
  • 127
    • 26844569944 scopus 로고    scopus 로고
    • N-Tosyloxycarbamates as a source of metal nitrenes: Rhodium-catalyzed C-H insertion and aziridination reactions
    • Lebel, H.; Huard, K.; Lectard, S. N-Tosyloxycarbamates as a source of metal nitrenes: rhodium-catalyzed C-H insertion and aziridination reactions. J. Am. Chem. Soc. 2005, 127, 14198-14199.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 14198-14199
    • Lebel, H.1    Huard, K.2    Lectard, S.3
  • 128
    • 53849147524 scopus 로고    scopus 로고
    • N-Tosyloxycarbamates as reagents in rhodium-catalyzed C-H amination reactions
    • Huard, K.; Lebel, H. N-Tosyloxycarbamates as reagents in rhodium-catalyzed C-H amination reactions. Chem. Eur. J. 2008, 14, 6222-6230.
    • (2008) Chem. Eur. J , vol.14 , pp. 6222-6230
    • Huard, K.1    Lebel, H.2
  • 131
    • 66949130991 scopus 로고    scopus 로고
    • O-Arylsulfonyl hydroxylamines via a decarboxylative rearrangement
    • Fioravanti, S.; Pellacani, L.; Tardella, P.A. O-Arylsulfonyl hydroxylamines via a decarboxylative rearrangement. Tetrahedron 2009, 65, 5747-5751.
    • (2009) Tetrahedron , vol.65 , pp. 5747-5751
    • Fioravanti, S.1    Pellacani, L.2    Tardella, P.A.3
  • 132
    • 0037067548 scopus 로고    scopus 로고
    • Diastereoselective aziridination of chiral α-carbonyl enoates
    • Fioravanti, S.; Morreale, A.; Pellacani, L.; Tardella, P.A. Diastereoselective aziridination of chiral α-carbonyl enoates. J. Org. Chem. 2002, 67, 4972-4974.
    • (2002) J. Org. Chem , vol.67 , pp. 4972-4974
    • Fioravanti, S.1    Morreale, A.2    Pellacani, L.3    Tardella, P.A.4
  • 133
    • 18744388906 scopus 로고    scopus 로고
    • Can functionalized N-acyloxy aziridines be easily deprotected?
    • Fioravanti, S.; Morreale, A.; Pellacani, L.; Tardella, P.A. Can functionalized N-acyloxy aziridines be easily deprotected? C. R. Chim. 2005, 8, 845-847.
    • (2005) C. R. Chim , vol.8 , pp. 845-847
    • Fioravanti, S.1    Morreale, A.2    Pellacani, L.3    Tardella, P.A.4
  • 134
    • 33845273838 scopus 로고    scopus 로고
    • Parallel solution-phase synthesis of acrylonitrile scaffolds carrying L-α-amino acidic or D-glycosyl residues
    • Fioravanti, S.; Pellacani, L.; Tardella P.A.; Morreale, A.; Del Signore, G. Parallel solution-phase synthesis of acrylonitrile scaffolds carrying L-α-amino acidic or D-glycosyl residues. J. Comb. Chem. 2006, 8, 808-811.
    • (2006) J. Comb. Chem , vol.8 , pp. 808-811
    • Fioravanti, S.1    Pellacani, L.2    Tardella, P.A.3    Morreale, A.4    del Signore, G.5
  • 138
    • 0037958127 scopus 로고
    • Preparation and reactivity of allyl N-[(arylsulfonyl)oxy]carbamates, new reagents for electrophilic transfer of an NHalloc group
    • Greck, C; Bischoff, L.; Ferreira, F.; Genêt, J.P. Preparation and reactivity of allyl N-[(arylsulfonyl)oxy]carbamates, new reagents for electrophilic transfer of an NHalloc group. J. Org. Chem. 1995, 60, 7010-7012.
    • (1995) J. Org. Chem , vol.60 , pp. 7010-7012
    • Greck, C.1    Bischoff, L.2    Ferreira, F.3    Genêt, J.P.4
  • 139
    • 85197362683 scopus 로고    scopus 로고
    • Rappoport, Z. and Liebman, J. F., Eds., (The Chemistry of Functional Groups, Patai, S. and Rappoport, Z., Eds.), Wiley: Chichester, Chapt. 8
    • Erdik E. In The Chemistry of Hydroxylamines, Oximes and Hydroxamic Acids, Part 1, Rappoport, Z. and Liebman, J. F., Eds., (The Chemistry of Functional Groups, Patai, S. and Rappoport, Z., Eds.), Wiley: Chichester, Chapt. 8, 2009.
    • (2009) The Chemistry of Hydroxylamines, Oximes and Hydroxamic Acids, Part 1
    • Erdik, E.1
  • 140
    • 67650025090 scopus 로고    scopus 로고
    • Product subclass 5: Aziridines. Science of Synthesis
    • Schau-mann, E., Enders, D., Eds.; Georg Thieme Verlag, Stuttgart, New York, 2009
    • Sweeney J. B. Product subclass 5: aziridines. Science of Synthesis; Schau-mann, E., Enders, D., Eds.; Georg Thieme Verlag, Stuttgart, New York, 2009, Volume Date 2008, 40a, pp. 643-772.
    • (2008) Volume Date , vol.40 , pp. 643-772
    • Sweeney, J.B.1
  • 141
    • 71549115446 scopus 로고    scopus 로고
    • Synthesis of functionalized spiroaziridine-oxindoles from 3-ylideneoxindoles: An easy route to 3-(aminoalkyl)oxindoles
    • Ammetto, I.; Gasperi, T.; Loreto, M. A.; Migliorini, A.; Palmarelli, F.; Tardella, P. A. Synthesis of functionalized spiroaziridine-oxindoles from 3-ylideneoxindoles: an easy route to 3-(aminoalkyl)oxindoles. Eur. J. Org. Chem. 2009, 6189-6197.
    • (2009) Eur. J. Org. Chem , pp. 6189-6197
    • Ammetto, I.1    Gasperi, T.2    Loreto, M.A.3    Migliorini, A.4    Palmarelli, F.5    Tardella, P.A.6
  • 142
    • 77956620860 scopus 로고    scopus 로고
    • Pd-Catalyzed intermolecular ortho-C-H amidation of anilides by N-nosyloxycarbamate
    • Ng, K.-H.; Chan, A. S. C; Yu, W.-Y. Pd-Catalyzed intermolecular ortho-C-H amidation of anilides by N-nosyloxycarbamate. J. Am. Chem. Soc. 2010, 132, 12862-12864.
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 12862-12864
    • Ng, K.-H.1    Chan, A.S.C.2    Yu, W.-Y.3


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