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Volumn 34, Issue 7, 2004, Pages 1337-1347

Synthesis of Functionalized N-Arylsulfonyl Aziridines from α,β-Unsaturated Esters, Amides, Ketones, and Nitriles Using N,N-Dichloroarylsulfonamides as Nitrogen Source

Author keywords

Alkenes; Aziridination; N Arylsulfonyl aziridine; P Toluenesulfonamide

Indexed keywords

2 ACETYL 3 PHENYL N (4 TOLUENESULFONYL)AZIRIDINE; 2 BENZOYL 3 [4 CHLOROPHENYL N (4 TOLUENESULFONYL)AZIRIDINE]; 2 CYANO 3 PHENYL N (4 TOLUENESULFONYL)AZIRIDINE; 2 CYANO N (4 TOLUENESULFONYL)AZIRIDINE; ALKENE; AMIDE; AZIRIDINE DERIVATIVE; COPPER DERIVATIVE; ESTER; KETONE; METHYL 3,3 DIMETHYL N (4 TOLUENESULFONYL)AZIRIDINE 2 CARBOXYLATE; N (4 TOLUENESULFONYL) 2 METHOXYCARBONYL 3 (4 CHLOROPHENYL)AZIRIDINE; N (4 TOLUENESULFONYL) 2 METHOXYCARBONYL 3 (4 NITROPHENYL)AZIRIDINE; N (4 TOLUENESULFONYL) 2 METHOXYCARBONYL 3 PHENYLAZIRIDINE; N (4 TOLUENESULFONYL) 2 METHOXYCARBONYLAZIRIDINE; N (4 TOLUENESULFONYL)AZIRIDINE 2 CARBOXAMIDE; NITRILE; NITROGEN; SODIUM HYDROXIDE; SULFONAMIDE; UNCLASSIFIED DRUG;

EID: 1842585948     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120030324     Document Type: Article
Times cited : (26)

References (50)
  • 1
    • 0033800394 scopus 로고    scopus 로고
    • Recent synthetic applications of chiral aziridines
    • (a) McCoull, W.; Davis, F.A. Recent synthetic applications of chiral aziridines. Synthesis 2000, 1, 1347-1365;
    • (2000) Synthesis , vol.1 , pp. 1347-1365
    • McCoull, W.1    Davis, F.A.2
  • 2
    • 33748605775 scopus 로고
    • Chiral aziridines - Their synthetic use in stereoselective transformations
    • (b) Tanner, D. Chiral aziridines - their synthetic use in stereoselective transformations. Angew. Chem. Int. Ed. Engl. 1994, 33, 599-619.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 599-619
    • Tanner, D.1
  • 3
    • 0028272321 scopus 로고
    • 2-Symmetric bis(aziridines): A new class of chiral ligands for transition metal-mediated asymmetric synthesis
    • 2-Symmetric bis(aziridines): a new class of chiral ligands for transition metal-mediated asymmetric synthesis. Tetrahedron Lett. 1994, 35 (26), 4631-4634;
    • (1994) Tetrahedron Lett. , vol.35 , Issue.26 , pp. 4631-4634
    • Tanner, D.1    Andersson, P.G.2    Harden, A.3    Somfai, P.4
  • 4
    • 0001238773 scopus 로고    scopus 로고
    • Simple aziridino alcohols as chiral ligands. Enantioselective additions of diethylzinc to N-diphenylphosphinoylimines
    • (b) Andersson, P.G.; Guijarro, D.; Tanner, D. Simple aziridino alcohols as chiral ligands. Enantioselective additions of diethylzinc to N-diphenylphosphinoylimines. Synlett. 1996 (8), 727-728;
    • (1996) Synlett , Issue.8 , pp. 727-728
    • Andersson, P.G.1    Guijarro, D.2    Tanner, D.3
  • 5
    • 0032212416 scopus 로고    scopus 로고
    • Aziridino alcohols as catalysts for the enantio-selective addition of diethylzinc to aldehydes
    • (c) Tanner, D.; Korno, H.T.; Guijarro, D.; Andersson, P.G. Aziridino alcohols as catalysts for the enantio-selective addition of diethylzinc to aldehydes. Tetrahedron 1998, 54 (47), 14213-14232.
    • (1998) Tetrahedron , vol.54 , Issue.47 , pp. 14213-14232
    • Tanner, D.1    Korno, H.T.2    Guijarro, D.3    Andersson, P.G.4
  • 6
    • 0001806627 scopus 로고
    • Aziridines
    • Hassner, A., Ed.; Wiley: New York
    • (a) Deyrup, J.A. Aziridines. In The Chemistry of Heterocyclic Compounds; Hassner, A., Ed.; Wiley: New York, 1983; Vol. 42, 1-214;
    • (1983) The Chemistry of Heterocyclic Compounds , vol.42 , pp. 1-214
    • Deyrup, J.A.1
  • 7
    • 84943392701 scopus 로고
    • Aziridines, azirines and fused ring derivatives
    • Lwowski, W., Ed.; Pergamon: Oxford
    • (b) Padwa, A.; Woolhouse, A.D. Aziridines, azirines and fused ring derivatives. In Comprehensive Heterocyclic Chemistry; Lwowski, W., Ed.; Pergamon: Oxford, 1984; Vol. 7, 47-93;
    • (1984) Comprehensive Heterocyclic Chemistry , vol.7 , pp. 47-93
    • Padwa, A.1    Woolhouse, A.D.2
  • 9
    • 0002686438 scopus 로고    scopus 로고
    • Aziridines and azirines: Fused-ring derivatives
    • Padwa, A., Ed.; Pergamon: Oxford
    • (d) Rai, K.M.L.; Hassner, A. Aziridines and azirines: fused-ring derivatives. In Comprehensive Heterocyclic Chemistry II; Padwa, A., Ed.; Pergamon: Oxford, 1996; Vol. 1A, 61-96.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.1 A , pp. 61-96
    • Rai, K.M.L.1    Hassner, A.2
  • 10
    • 37049088477 scopus 로고
    • Methylene transfer from dimethyloxosulfonium methylide to N-arylsulfonylaziridines: Stereospecific synthesis of N-arylsulfonylazetidines
    • (a) Nadir, U.K.; Sharma, R.L.; Koul, V.K. Methylene transfer from dimethyloxosulfonium methylide to N-arylsulfonylaziridines: stereospecific synthesis of N-arylsulfonylazetidines. J. Chem. Soc. Perkin Transaction I 1991, 8, 2015-2019;
    • (1991) J. Chem. Soc. Perkin Transaction I , vol.8 , pp. 2015-2019
    • Nadir, U.K.1    Sharma, R.L.2    Koul, V.K.3
  • 11
    • 37049082796 scopus 로고
    • Reaction of N-arylsulfonylaziridines with dimethylsulfoniumethoxycarbonyl methylide: Regio- and stereo-selective synthesis of 1-arylsulfonyl-2-ethoxycarbonyl azetidines
    • (b) Nadir, U.K.; Arora, A. Reaction of N-arylsulfonylaziridines with dimethylsulfoniumethoxycarbonyl methylide: regio- and stereo-selective synthesis of 1-arylsulfonyl-2-ethoxycarbonyl azetidines. J. Chem. Soc. Perkin Transaction I 1995, 20, 2605-2609.
    • (1995) J. Chem. Soc. Perkin Transaction I , vol.20 , pp. 2605-2609
    • Nadir, U.K.1    Arora, A.2
  • 12
    • 0027078738 scopus 로고
    • Regiospecific cycloaddition reaction of 2-aryl and 2-alkyl 1-arenesulfonylaziridines with isocyanates using sodium iodide
    • Nadir, U.K.; Basu, N. Regiospecific cycloaddition reaction of 2-aryl and 2-alkyl 1-arenesulfonylaziridines with isocyanates using sodium iodide. Tetrahedron Lett. 1992, 33 (51), 7949-7952.
    • (1992) Tetrahedron Lett. , vol.33 , Issue.51 , pp. 7949-7952
    • Nadir, U.K.1    Basu, N.2
  • 14
    • 0002370216 scopus 로고
    • Asymmetric cyclopropanation
    • Ojima, I., Ed.; VCH: New York; Chap. 3
    • (b) Doyle, M.P. Asymmetric cyclopropanation. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993; Chap. 3;
    • (1993) Catalytic Asymmetric Synthesis
    • Doyle, M.P.1
  • 15
    • 0024662426 scopus 로고
    • Transition-metal-catalyzed epoxidations
    • (c) Jorgensen, K.A. Transition-metal-catalyzed epoxidations. Chem. Rev. 1989, 89, 431-458.
    • (1989) Chem. Rev. , vol.89 , pp. 431-458
    • Jorgensen, K.A.1
  • 16
    • 33748236032 scopus 로고
    • Carbenoid transfer to imines: A new asymmetric catalytic synthesis of aziridines
    • (a) Hansen, K.B.; Finney, N.S.; Jacobsen, E.N. Carbenoid transfer to imines: a new asymmetric catalytic synthesis of aziridines. Angew. Chem. Int. Ed. Engl. 1995, 34 (6), 676-678;
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , Issue.6 , pp. 676-678
    • Hansen, K.B.1    Finney, N.S.2    Jacobsen, E.N.3
  • 17
    • 37049088149 scopus 로고
    • Catalytic formation of aziridines from imines and diazoacetate
    • (b) Rasmussen, K.G.; Jorgensen, K.A. Catalytic formation of aziridines from imines and diazoacetate. J. Chem. Soc. Chem. Commun. 1995, 14, 1401-1402;
    • (1995) J. Chem. Soc. Chem. Commun. , vol.14 , pp. 1401-1402
    • Rasmussen, K.G.1    Jorgensen, K.A.2
  • 18
    • 0000376738 scopus 로고
    • Reactions of diazo compounds with imines. Preliminary communication
    • (c) Moran, M.; Bernardinelli, G.; Müller, P. Reactions of diazo compounds with imines. Preliminary communication. Helv. Chim. Acta 1995, 78 (8), 2048;
    • (1995) Helv. Chim. Acta , vol.78 , Issue.8 , pp. 2048
    • Moran, M.1    Bernardinelli, G.2    Müller, P.3
  • 20
    • 0000053011 scopus 로고
    • Carbonylnitrenes
    • Lwowski, W., Ed.; Interscience: New York
    • (a) Lwowski, W. Carbonylnitrenes. In Nitrenes; Lwowski, W., Ed.; Interscience: New York, 1970; 185-247;
    • (1970) Nitrenes , pp. 185-247
    • Lwowski, W.1
  • 21
    • 0000014210 scopus 로고
    • Acylazides and nitrenes
    • Scriven, E.F.V., Ed.; Academic: New York
    • (b) Lwowski, W. Acylazides and nitrenes. In Azides and Nitrenes, Reactivity and Utility; Scriven, E.F.V., Ed.; Academic: New York, 1984; 205-246.
    • (1984) Azides and Nitrenes, Reactivity and Utility , pp. 205-246
    • Lwowski, W.1
  • 22
    • 37049095037 scopus 로고
    • Iron- and manganese-porphyrin catalyzed aziridination of alkenes by p- tolylsulfonyland acyliminoiodobenzene
    • (a) Mansuy, D.; Mahy, J.P.; Dureault, A.; Bedi, G.; Battioni, P.J. Iron- and manganese-porphyrin catalyzed aziridination of alkenes by p- tolylsulfonyland acyliminoiodobenzene. Chem. Soc. Chem. Commun. 1984 (17), 1161-1163;
    • (1984) Chem. Soc. Chem. Commun. , Issue.17 , pp. 1161-1163
    • Mansuy, D.1    Mahy, J.P.2    Dureault, A.3    Bedi, G.4    Battioni, P.J.5
  • 23
    • 0001743473 scopus 로고
    • Allylic amination of alkenes by tosyliminoiodobenzene: Manganese porphyrins as suitable catalysts
    • (b) Mahy, J.P.; Bedi, G.; Battioni, P.; Mansuy, D. Allylic amination of alkenes by tosyliminoiodobenzene: manganese porphyrins as suitable catalysts. Tetrahedron Lett. 1988, 29, 1927-1930;
    • (1988) Tetrahedron Lett. , vol.29 , pp. 1927-1930
    • Mahy, J.P.1    Bedi, G.2    Battioni, P.3    Mansuy, D.4
  • 24
    • 11644312278 scopus 로고
    • Development of the copper-catalyzed olefin aziridination reaction
    • (c) Evans, D.A.; Faul, M.M.; Bilodeau, M.T. Development of the copper-catalyzed olefin aziridination reaction. J. Am. Chem. Soc. 1994, 116, 2742-2753;
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 2742-2753
    • Evans, D.A.1    Faul, M.M.2    Bilodeau, M.T.3
  • 25
    • 0001022701 scopus 로고
    • A copper(I) catalyst for carbene and nitrene transfer to form cyclopropanes, cyclopropenes, and aziridines
    • (d) Perez, P.J.; Brookhart, M.; Templeton, J.L. A copper(I) catalyst for carbene and nitrene transfer to form cyclopropanes, cyclopropenes, and aziridines. Organometallics 1993, 12 (2), 261-262;
    • (1993) Organometallics , vol.12 , Issue.2 , pp. 261-262
    • Perez, P.J.1    Brookhart, M.2    Templeton, J.L.3
  • 26
    • 85064712108 scopus 로고
    • Synthesis of N-p-toluenesulfonyl-2-alkenylaziridines by regioselective aziridination of 1,3-dienes
    • (e) Knight, J.G.; Muldowney, M.P. Synthesis of N-p-toluenesulfonyl-2-alkenylaziridines by regioselective aziridination of 1,3-dienes. Synlett. 1995 (9), 949-951.
    • (1995) Synlett , Issue.9 , pp. 949-951
    • Knight, J.G.1    Muldowney, M.P.2
  • 27
    • 0038660113 scopus 로고    scopus 로고
    • A method for rhodium(II)-catalyzed aziridination of olefins
    • (a) Müller, P.; Baud, C.; Jacquier, Y. A method for rhodium(II)-catalyzed aziridination of olefins. Tetrahedron 1996, 53 (5), 1543-1548;
    • (1996) Tetrahedron , vol.53 , Issue.5 , pp. 1543-1548
    • Müller, P.1    Baud, C.2    Jacquier, Y.3
  • 28
    • 0038321455 scopus 로고    scopus 로고
    • Rhodium(II)-catalyzed CH insertions with {[(4-nitrophenyl)sulfonyl] imino}phenyl-λ 3-iodane
    • (b) Nägeli, I.; Baud, C.; Bernardinelli, G.; Jacquier, Y.; Moran, M.; Müller, P. Rhodium(II)-catalyzed CH insertions with {[(4-nitrophenyl)sulfonyl] imino}phenyl-λ 3-iodane. Helv. Chim. Acta 1997, 80 (4), 1087-1105;
    • (1997) Helv. Chim. Acta , vol.80 , Issue.4 , pp. 1087-1105
    • Nägeli, I.1    Baud, C.2    Bernardinelli, G.3    Jacquier, Y.4    Moran, M.5    Müller, P.6
  • 30
    • 0032518773 scopus 로고    scopus 로고
    • Solubilization of the primary nitrene sources (tosyliminoiodo)arenes (ArINTs)
    • (d) Macikenas, D.; Meprathu, B.V.; Protasiewicz, J.D. Solubilization of the primary nitrene sources (tosyliminoiodo)arenes (ArINTs). Tetrahedron Lett. 1998, 39 (3/4), 191-194.
    • (1998) Tetrahedron Lett. , vol.39 , Issue.3-4 , pp. 191-194
    • Macikenas, D.1    Meprathu, B.V.2    Protasiewicz, J.D.3
  • 31
    • 0035813420 scopus 로고    scopus 로고
    • Iron(IV) corroles are potent catalysts for aziridination of olefins by chloramine-T
    • Simkhovich, L.; Gross, Z. Iron(IV) corroles are potent catalysts for aziridination of olefins by chloramine-T. Tetrahedron Lett. 2001, 42 (45), 8089-8092.
    • (2001) Tetrahedron Lett. , vol.42 , Issue.45 , pp. 8089-8092
    • Simkhovich, L.1    Gross, Z.2
  • 32
    • 0032518652 scopus 로고    scopus 로고
    • Nitrogen atom transfer to alkenes utilizing chloramine-T as a nitrogen source
    • (a) Ando, T.; Minakata, S.; Ryu, I.; Komatsu, M. Nitrogen atom transfer to alkenes utilizing chloramine-T as a nitrogen source. Tetrahedron Lett. 1998, 39 (3/4), 309-312;
    • (1998) Tetrahedron Lett. , vol.39 , Issue.3-4 , pp. 309-312
    • Ando, T.1    Minakata, S.2    Ryu, I.3    Komatsu, M.4
  • 33
    • 0040518632 scopus 로고    scopus 로고
    • Mechanistic studies of copper-catalyzed alkene aziridination
    • (b) Brandt, P.; Sodergren, M.J.; Anderson, P.O.; Norrby, P.O. Mechanistic studies of copper-catalyzed alkene aziridination. J. Am. Chem. Soc. 2000, 122 (33), 8013-8020;
    • (2000) J. Am. Chem. Soc. , vol.122 , Issue.33 , pp. 8013-8020
    • Brandt, P.1    Sodergren, M.J.2    Anderson, P.O.3    Norrby, P.O.4
  • 34
    • 0032509247 scopus 로고    scopus 로고
    • A simple copper catalyst for both aziridination of alkenes and amination of activated hydrocarbons with chloramine-T trihydrate
    • (c) Albone, D.P.; Aujla, P.S.; Taylor, P.C.; Challenger, S.; Derrick, A.M. A simple copper catalyst for both aziridination of alkenes and amination of activated hydrocarbons with chloramine-T trihydrate. J. Org. Chem. 1998, 63 (25), 9569-9571;
    • (1998) J. Org. Chem. , vol.63 , Issue.25 , pp. 9569-9571
    • Albone, D.P.1    Aujla, P.S.2    Taylor, P.C.3    Challenger, S.4    Derrick, A.M.5
  • 35
    • 0032578675 scopus 로고    scopus 로고
    • Iodine-catalyzed aziridination of alkenes using chloramine-T as a nitrogen source
    • (d) Ando, T.; Kano, D.; Minakata, S.; Ryu, I.; Komatsu, M. Iodine-catalyzed aziridination of alkenes using chloramine-T as a nitrogen source. Tetrahedron 1998, 54, 13485-13494.
    • (1998) Tetrahedron , vol.54 , pp. 13485-13494
    • Ando, T.1    Kano, D.2    Minakata, S.3    Ryu, I.4    Komatsu, M.5
  • 36
    • 0032527724 scopus 로고    scopus 로고
    • Bromine-catalyzed aziridination of olefins. A rare example of atom-transfer redox catalysis by a main group element
    • Jeong, J.U.; Tao, B.; Sagasser, I.; Henniges, H.; Sharpless, K.B. Bromine-catalyzed aziridination of olefins. A rare example of atom-transfer redox catalysis by a main group element. J. Am. Chem. Soc. 1998, 120 (27), 6844-6845.
    • (1998) J. Am. Chem. Soc. , vol.120 , Issue.27 , pp. 6844-6845
    • Jeong, J.U.1    Tao, B.2    Sagasser, I.3    Henniges, H.4    Sharpless, K.B.5
  • 37
    • 1842604219 scopus 로고
    • (a) I.C.I. Ltd., B.P 1968, 1, 970;
    • (1968) B.P. , vol.1 , pp. 970
  • 38
    • 85022455748 scopus 로고
    • Phenyl-1-[p-tolyl(and phenyl)sulfonyl]aziridines
    • (b) 2-Phenyl-1-[p-tolyl(and phenyl)sulfonyl]aziridines. Chem. Abs. 1970, 72, 12545f;
    • (1970) Chem. Abs. , vol.72
  • 39
    • 37049136213 scopus 로고
    • The reaction of styrene and related compounds with N,N-dichlorosulfonamides
    • (c) Seden, T.P.; Turner, R.W. The reaction of styrene and related compounds with N,N-dichlorosulfonamides. J. Chem. Soc. (C) 1968, 876-878.
    • (1968) J. Chem. Soc. (C) , pp. 876-878
    • Seden, T.P.1    Turner, R.W.2
  • 41
    • 0001071513 scopus 로고    scopus 로고
    • Transition metal-catalyzed regioselective and stereoselective aminochlorination of cinnamic esters
    • Li, G.; Wei, H.-X.; Kim, S.H.; Neighbors, M. Transition metal-catalyzed regioselective and stereoselective aminochlorination of cinnamic esters. Org. Letters 1999, 1 (3), 395-397.
    • (1999) Org. Letters , vol.1 , Issue.3 , pp. 395-397
    • Li, G.1    Wei, H.-X.2    Kim, S.H.3    Neighbors, M.4
  • 42
    • 0000870450 scopus 로고
    • The addition of N,N-dichlorosulfonamides to unsaturates
    • (a) Daniher, F.A.; Butler, P.E. The addition of N,N-dichlorosulfonamides to unsaturates. J. Org. Chem. 1968, 33 (12), 4336-4340;
    • (1968) J. Org. Chem. , vol.33 , Issue.12 , pp. 4336-4340
    • Daniher, F.A.1    Butler, P.E.2
  • 43
    • 0000668913 scopus 로고
    • The addition of N,N-dichloro carbamates to conjugated dienes
    • (b) Daniher, F.A.; Butler, P.E. The addition of N,N-dichloro carbamates to conjugated dienes. J. Org. Chem. 1968, 33 (7), 2637-2642;
    • (1968) J. Org. Chem. , vol.33 , Issue.7 , pp. 2637-2642
    • Daniher, F.A.1    Butler, P.E.2
  • 44
    • 33746051891 scopus 로고
    • Evidence for nucleophilicity of N,N-dihalosulfonamide oxygen atoms in addition of N,N-dichlorobenzenesulfonamide to cis- and trans-but-2-ene
    • (c) Daniher, F.A.; Melchior, M.T.; Butler, P.E. Evidence for nucleophilicity of N,N-dihalosulfonamide oxygen atoms in addition of N,N-dichlorobenzenesulfonamide to cis- and trans-but-2-ene. J. Chem. Soc. Chem. Commun. 1968, 16, 931-932.
    • (1968) J. Chem. Soc. Chem. Commun. , vol.16 , pp. 931-932
    • Daniher, F.A.1    Melchior, M.T.2    Butler, P.E.3
  • 45
    • 0036254438 scopus 로고    scopus 로고
    • Axially dissymmetric (R)-(+)- 5,5′,6,6′,7,7′,8, 8′ octahydro-[1,1′]binaphthyldiimine chiral salen type-ligands for copper-catalyzed asymmetric aziridination
    • (a) Shi, M.; Wang, C.-J. Axially dissymmetric (R)-(+)- 5,5′,6,6′,7,7′,8,8′ octahydro-[1,1′ ]binaphthyldiimine chiral salen type-ligands for copper-catalyzed asymmetric aziridination. Chirality 2002, 14 (5), 412-416;
    • (2002) Chirality , vol.14 , Issue.5 , pp. 412-416
    • Shi, M.1    Wang, C.-J.2
  • 46
    • 0035842869 scopus 로고    scopus 로고
    • Axially dissymmetric binaphthyldiimine chiral salen-type ligands for copper-catalyzed asymmetric aziridination
    • (b) Shi, M.; Wang, C.-J.; Chan, A.S.C. Axially dissymmetric binaphthyldiimine chiral salen-type ligands for copper-catalyzed asymmetric aziridination. Tetrahedron Asymmetr. 2001, 12 (22), 3105-3111.
    • (2001) Tetrahedron Asymmetr. , vol.12 , Issue.22 , pp. 3105-3111
    • Shi, M.1    Wang, C.-J.2    Chan, A.S.C.3
  • 47
    • 0030818780 scopus 로고    scopus 로고
    • Reduction of 2-acylaziridines by samarium(II) iodide. An efficient and regioselective route to β-amino carbonyl compounds
    • Molander, G.A.; Stengel, P.J. Reduction of 2-acylaziridines by samarium(II) iodide. An efficient and regioselective route to β-amino carbonyl compounds. Tetrahedron 1997, 53, 8887-8912.
    • (1997) Tetrahedron , vol.53 , pp. 8887-8912
    • Molander, G.A.1    Stengel, P.J.2
  • 48
    • 0001324192 scopus 로고
    • 3-Substituted 2-acyl-1-sulfonylaziridines from the reaction of triphenylbismuthonium 2-oxoalkylides and N-sulfonylaldimines. Reversal of the cis/trans-isomer ratios depending on base and additive
    • Matano, Y.; Yoshimune, M.; Suzuki, H. 3-Substituted 2-acyl-1-sulfonylaziridines from the reaction of triphenylbismuthonium 2-oxoalkylides and N-sulfonylaldimines. Reversal of the cis/trans-isomer ratios depending on base and additive. J. Org. Chem. 1995, 60, 4663-4665.
    • (1995) J. Org. Chem. , vol.60 , pp. 4663-4665
    • Matano, Y.1    Yoshimune, M.2    Suzuki, H.3
  • 49
    • 0000332463 scopus 로고    scopus 로고
    • Regiospecific reductive cleavage of the C(2)-N bond of aziridines substituted with an electron acceptor mediated by Mg/MeOH
    • Pak, C.S.; Kim, T.H.; Ha, S.J. Regiospecific reductive cleavage of the C(2)-N bond of aziridines substituted with an electron acceptor mediated by Mg/MeOH. J. Org. Chem. 1998, 63 (26), 10,006-10,010.
    • (1998) J. Org. Chem. , vol.63 , Issue.26 , pp. 10006-10010
    • Pak, C.S.1    Kim, T.H.2    Ha, S.J.3
  • 50
    • 0029943815 scopus 로고    scopus 로고
    • Influence of the kind of the alcoholic modifier on chiral separation on a Chiralpak AD column
    • Kunath, A.; Theil, F.; Jaehnisch, K.J. Influence of the kind of the alcoholic modifier on chiral separation on a Chiralpak AD column. Chromatography A 1996, 728 (1 + 2), 249-257.
    • (1996) Chromatography A , vol.728 , Issue.1-2 , pp. 249-257
    • Kunath, A.1    Theil, F.2    Jaehnisch, K.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.