메뉴 건너뛰기




Volumn 5, Issue C, 2001, Pages 89-196

The asymmetric synthesis of unnatural α-amino acids as building blocks for complex molecule synthesis

Author keywords

[No Author keywords available]

Indexed keywords


EID: 34247271645     PISSN: 1047773X     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1047-773X(01)80004-4     Document Type: Article
Times cited : (8)

References (272)
  • 1
    • 0033043246 scopus 로고    scopus 로고
    • How to Build Optically Active α-Amino Acids
    • Calmes, M., Daunis, J., How to Build Optically Active α-Amino Acids. Amino Acids 16 (1999), 215–250.
    • (1999) Amino Acids , vol.16 , pp. 215-250
    • Calmes, M.1    Daunis, J.2
  • 3
    • 0002618911 scopus 로고
    • Asymmetric Synthesis of α-Amino Acids
    • JAI Press Inc.
    • Williams, r.M., Asymmetric Synthesis of α-Amino Acids. Adv. Asym. Syn. [1], 1995, JAI Press Inc., 45–94.
    • (1995) Adv. Asym. Syn. [1] , pp. 45-94
    • Williams, R.M.1
  • 4
    • 0028355337 scopus 로고
    • Recent Developments in the Stereoselective Synthesis of α-Aminoacids
    • Duthaler, r.O., Recent Developments in the Stereoselective Synthesis of α-Aminoacids. Tetrahedron 50 (1994), 1539–1650.
    • (1994) Tetrahedron , vol.50 , pp. 1539-1650
    • Duthaler, R.O.1
  • 5
    • 0028696580 scopus 로고
    • Approaches to the Asymmetric Synthesis of Unusual Amino Acids
    • Hruby, v.J., Qian, X., Approaches to the Asymmetric Synthesis of Unusual Amino Acids. Met Mol Biol 55 (1994), 249–286.
    • (1994) Met Mol Biol , vol.55 , pp. 249-286
    • Hruby, V.J.1    Qian, X.2
  • 6
    • 0001459021 scopus 로고
    • Asymmetric Synthesis of α-Amino Acids
    • Williams, r.M., Asymmetric Synthesis of α-Amino Acids. Aldrichimica Acta 25 (1992), 11–25.
    • (1992) Aldrichimica Acta , vol.25 , pp. 11-25
    • Williams, R.M.1
  • 7
    • 0001122927 scopus 로고
    • Asymmetric Synthesis of Arylglycines
    • Williams, r.M., Hendrix, j.A., Asymmetric Synthesis of Arylglycines. Chem.Rev. 92 (1992), 889–917.
    • (1992) Chem.Rev. , vol.92 , pp. 889-917
    • Williams, R.M.1    Hendrix, J.A.2
  • 8
    • 0041910154 scopus 로고    scopus 로고
    • Asymmetric Synthesis of Fluoroalkyl Amino Compounds via Chiral Sulfoxides
    • Bravo, P., Bruche, L., Crucianelli, M., Viani, F., Zanda, M., Asymmetric Synthesis of Fluoroalkyl Amino Compounds via Chiral Sulfoxides. ACS Symp.Ser. 746 (2000), 98–116.
    • (2000) ACS Symp.Ser. , vol.746 , pp. 98-116
    • Bravo, P.1    Bruche, L.2    Crucianelli, M.3    Viani, F.4    Zanda, M.5
  • 9
    • 0030513164 scopus 로고    scopus 로고
    • Self-Regeneration of Stereocenters (SRS) - Applications, Limitations, and Abandonment of a Synthetic Principle
    • Seebach, D., Sting, a.R., Hoffmann, M., Self-Regeneration of Stereocenters (SRS) - Applications, Limitations, and Abandonment of a Synthetic Principle. Angew. Chem. Int. Ed. Engl. 35 (1996), 2708–2748.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 2708-2748
    • Seebach, D.1    Sting, A.R.2    Hoffmann, M.3
  • 10
    • 0001446941 scopus 로고    scopus 로고
    • Synthesis of Chiral Amino Acids and Amines over Solid Catalysts
    • Tungler, A., Fodor, K., Synthesis of Chiral Amino Acids and Amines over Solid Catalysts. Catal. Today 37 (1997), 191–208.
    • (1997) Catal. Today , vol.37 , pp. 191-208
    • Tungler, A.1    Fodor, K.2
  • 11
    • 0033389244 scopus 로고    scopus 로고
    • Developing a Chiral Toolbox for Asymmetric Catalytic Reactions
    • Zhang, X., Developing a Chiral Toolbox for Asymmetric Catalytic Reactions. Enantiomer 4 (1999), 541–555.
    • (1999) Enantiomer , vol.4 , pp. 541-555
    • Zhang, X.1
  • 12
    • 0000238987 scopus 로고    scopus 로고
    • Asymmetric Syntheses of Unnatural Amino Acids and Hy-droxyethylene Peptide Isosteres
    • Williams, r.M., Asymmetric Syntheses of Unnatural Amino Acids and Hy-droxyethylene Peptide Isosteres. Met. Mol. Med. 23 (1999), 339–356.
    • (1999) Met. Mol. Med. , vol.23 , pp. 339-356
    • Williams, R.M.1
  • 13
    • 0033475513 scopus 로고    scopus 로고
    • Biotechnology in the Fine-Chemicals Industry. Cyclic Amino Acids by Enantioselective Biocatalysis
    • Petersen, M., Sauter, M., Biotechnology in the Fine-Chemicals Industry. Cyclic Amino Acids by Enantioselective Biocatalysis. Chimia 53 (1999), 608–612.
    • (1999) Chimia , vol.53 , pp. 608-612
    • Petersen, M.1    Sauter, M.2
  • 14
    • 0032969622 scopus 로고    scopus 로고
    • Asymmetric Syntheses of Pipecolic Acid and Derivatives
    • Couty, F., Asymmetric Syntheses of Pipecolic Acid and Derivatives. Amino Acids 16 (1999), 297–320.
    • (1999) Amino Acids , vol.16 , pp. 297-320
    • Couty, F.1
  • 15
    • 0007951842 scopus 로고    scopus 로고
    • Synthesis of Kainoids and Kainoid Analogs
    • Wood, m.E., Fryer, a.M., Synthesis of Kainoids and Kainoid Analogs. Adv. Nitrogen Heterocycl 3 (1998), 159–218.
    • (1998) Adv. Nitrogen Heterocycl , vol.3 , pp. 159-218
    • Wood, M.E.1    Fryer, A.M.2
  • 16
    • 0029864974 scopus 로고    scopus 로고
    • Recent Developments in Kainoid Amino Acid Chemistry
    • Parsons, a.F., Recent Developments in Kainoid Amino Acid Chemistry. Tetrahedron 52 (1996), 4149–4174.
    • (1996) Tetrahedron , vol.52 , pp. 4149-4174
    • Parsons, A.F.1
  • 19
    • 84914028265 scopus 로고
    • Stereoselective Synthesis of Amino Acids from Sugars
    • Kochetkov, k.A., Sviridov, a.F., Stereoselective Synthesis of Amino Acids from Sugars. I. Bioorg. Khim. 17 (1991), 5–34.
    • (1991) I. Bioorg. Khim. , vol.17 , pp. 5-34
    • Kochetkov, K.A.1    Sviridov, A.F.2
  • 20
    • 0030605059 scopus 로고    scopus 로고
    • Trans-4-Hydroxy-L-Proline, a Useful and Versatile Chiral Starting Block
    • Remuzon, P., Trans-4-Hydroxy-L-Proline, a Useful and Versatile Chiral Starting Block. Tetrahedron 52 (1996), 13803–13835.
    • (1996) Tetrahedron , vol.52 , pp. 13803-13835
    • Remuzon, P.1
  • 21
    • 0345151817 scopus 로고    scopus 로고
    • Recent Advances in the Enantioselective Synthesis of α-Amino Acids
    • Juaristi, E., Lopez-Ruiz, H., Recent Advances in the Enantioselective Synthesis of α-Amino Acids. Curr. Med. Chem. 6 (1999), 983–1004.
    • (1999) Curr. Med. Chem. , vol.6 , pp. 983-1004
    • Juaristi, E.1    Lopez-Ruiz, H.2
  • 22
    • 0032829866 scopus 로고    scopus 로고
    • Chemical Process Synthesis of β-Amino Acids and Esters
    • Abdel-Magid, a.F., Cohen, j.H., Maryanoff, c.A., Chemical Process Synthesis of β-Amino Acids and Esters. Curr. Med. Chem. 6 (1999), 955–970.
    • (1999) Curr. Med. Chem. , vol.6 , pp. 955-970
    • Abdel-Magid, A.F.1    Cohen, J.H.2    Maryanoff, C.A.3
  • 23
    • 0003880736 scopus 로고    scopus 로고
    • Asymmetric Synthesis of β-Amino Acids and β-Lactam Derivatives via Conjugate Addition of Metal Amides
    • Yamamoto, Y., Asao, N., Tsukada, N., Asymmetric Synthesis of β-Amino Acids and β-Lactam Derivatives via Conjugate Addition of Metal Amides. Adv. Asymmetric Synth 3 (1998), 1–37.
    • (1998) Adv. Asymmetric Synth , vol.3 , pp. 1-37
    • Yamamoto, Y.1    Asao, N.2    Tsukada, N.3
  • 24
    • 0344746480 scopus 로고    scopus 로고
    • Biocatalytic Entry to Enantiomerically Pure β-Amino Acids
    • Soloshonok, v.A., Biocatalytic Entry to Enantiomerically Pure β-Amino Acids. Enantiosel. Synth. β-Amino Acids, 1997, 64–443.
    • (1997) Enantiosel. Synth. β-Amino Acids , pp. 64-443
    • Soloshonok, V.A.1
  • 25
    • 0006728594 scopus 로고    scopus 로고
    • Asymmetric Synthesis of β-Amino Acids from Catalytic Sharpless Epoxidation
    • Pericas, m.A., Riera, A., Moyano, A., Asymmetric Synthesis of β-Amino Acids from Catalytic Sharpless Epoxidation. Enantiosel. Synth. β-Amino Acids, 1997, 373–389.
    • (1997) Enantiosel. Synth. β-Amino Acids , pp. 373-389
    • Pericas, M.A.1    Riera, A.2    Moyano, A.3
  • 26
    • 85023002264 scopus 로고    scopus 로고
    • Enantioselective Synthesis of β-Amino Acids Using the Nicholas Reaction
    • Jacobi, p.A., Zheng, W., Enantioselective Synthesis of β-Amino Acids Using the Nicholas Reaction. Enantiosel. Synth. β-Amino Acids, 1997, 359–372.
    • (1997) Enantiosel. Synth. β-Amino Acids , pp. 359-372
    • Jacobi, P.A.1    Zheng, W.2
  • 27
    • 0033986387 scopus 로고    scopus 로고
    • Preparation of Achiral and of Enantiopure Geminally Disubstituted β-Amino Acids for P-Peptide Synthesis
    • Abele, S., Seebach, D., Preparation of Achiral and of Enantiopure Geminally Disubstituted β-Amino Acids for P-Peptide Synthesis. Eur. J. Org. Chem., 2000, 1–15.
    • (2000) Eur. J. Org. Chem. , pp. 1-15
    • Abele, S.1    Seebach, D.2
  • 28
    • 0002292746 scopus 로고    scopus 로고
    • Recent Developments in the Synthesis of α-Hydroxy- β-Amino Acids
    • Andruszkiewicz, R., Recent Developments in the Synthesis of α-Hydroxy- β-Amino Acids. Pol. J. Chem. 72 (1998), 1–48.
    • (1998) Pol. J. Chem. , vol.72 , pp. 1-48
    • Andruszkiewicz, R.1
  • 29
    • 0032859102 scopus 로고    scopus 로고
    • Recent Advances in the Medicinal Chemistry of Taxoids With Novel β-Amino Acid Side Chains
    • Ojima, I., Lin, S., Wang, T., Recent Advances in the Medicinal Chemistry of Taxoids With Novel β-Amino Acid Side Chains. Curr. Med. Chem. 6 (1999), 927–954.
    • (1999) Curr. Med. Chem. , vol.6 , pp. 927-954
    • Ojima, I.1    Lin, S.2    Wang, T.3
  • 30
    • 14844312173 scopus 로고    scopus 로고
    • Asymmetric Synthesis of β-Amino Acids and α-Substituted β-Amino Acids
    • Cardillo, G., Tomasini, C., Asymmetric Synthesis of β-Amino Acids and α-Substituted β-Amino Acids. Chem. Soc. Rev. 25 (1996), 117–128.
    • (1996) Chem. Soc. Rev. , vol.25 , pp. 117-128
    • Cardillo, G.1    Tomasini, C.2
  • 31
    • 0032561221 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Quaternary α-Amino Acids. Part 1: Acyclic Compounds
    • Cativiela, C, Díaz-de-Villegas, m.D., Stereoselective Synthesis of Quaternary α-Amino Acids. Part 1: Acyclic Compounds. Tetrahedron: Asymmetry 9 (1998), 3517–3599.
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 3517-3599
    • Cativiela, C.1    Díaz-de-Villegas, M.D.2
  • 32
    • 0034712270 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Quaternary α-Amino Acids. Part 2: Cyclic Compounds
    • Cativiela, C, Díaz-de-Villegas, m.D., Stereoselective Synthesis of Quaternary α-Amino Acids. Part 2: Cyclic Compounds. Tetrahedron: Asymmetry 11 (2000), 645–732.
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 645-732
    • Cativiela, C.1    Díaz-de-Villegas, M.D.2
  • 33
    • 33845185214 scopus 로고
    • The Stereoselective Synthesis of α-Amino Acids by Phase Transfer Catalysis
    • O'Donnell, m.J., Bennett, w.D., Wu, S., The Stereoselective Synthesis of α-Amino Acids by Phase Transfer Catalysis. J. Am. Chem. Soc. 111 (1989), 2353–2355.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 2353-2355
    • O'Donnell, M.J.1    Bennett, W.D.2    Wu, S.3
  • 35
    • 0001776104 scopus 로고    scopus 로고
    • Chiral Phase Transfer Catalysis
    • Chapter 14 Sasson Y. Neumann R. Blackie Academic and Professional Washington DC
    • Chapter 14 Shioiri, T., Chiral Phase Transfer Catalysis. Sasson, Y., Neumann, R., (eds.) Handbook of Phase Transfer Catalysis, 1997, Blackie Academic and Professional, Washington DC.
    • (1997) Handbook of Phase Transfer Catalysis
    • Shioiri, T.1
  • 36
    • 0000344872 scopus 로고
    • Theoretical Studies in Molecular Recognition: Asymmetric Induction of Benzophenone Imine Ester Enolates by the Benzylcinchoninium Ion
    • Lipkowitz, k.B., Cavanaugh, m.W., Baker, B., O'Donnell, m.J., Theoretical Studies in Molecular Recognition: Asymmetric Induction of Benzophenone Imine Ester Enolates by the Benzylcinchoninium Ion. J. Org. Chem. 56 (1991), 5181–5192.
    • (1991) J. Org. Chem. , vol.56 , pp. 5181-5192
    • Lipkowitz, K.B.1    Cavanaugh, M.W.2    Baker, B.3    O'Donnell, M.J.4
  • 37
    • 0000637655 scopus 로고
    • Efficient Catalytic Asymmetric Alkylations. 3. A Kinetic and Mechanistic Study of the Enantioselective Phase-Transfer Methylation of 6, 7-Dichloro-5- Methoxy
    • Hughes, d.L., Dolling, U.-H., Ryan, k.M., Schoenewaldt, e.F., Grabowski, e.J. J., Efficient Catalytic Asymmetric Alkylations. 3. A Kinetic and Mechanistic Study of the Enantioselective Phase-Transfer Methylation of 6, 7-Dichloro-5- Methoxy-. J. Org. Chem. 52 (1987), 4745–4752.
    • (1987) J. Org. Chem. , vol.52 , pp. 4745-4752
    • Hughes, D.L.1    Dolling, U.-H.2    Ryan, K.M.3    Schoenewaldt, E.F.4    Grabowski, E.J.J.5
  • 38
    • 0028300898 scopus 로고
    • A New Active Catalyst Species for Enantioselective Alkylation by Phase-Transfer Catalysis
    • O'Donnell, m.J., Wu, S., Huffman, j.C., A New Active Catalyst Species for Enantioselective Alkylation by Phase-Transfer Catalysis. Tetrahedron 50 (1994), 4507–4518.
    • (1994) Tetrahedron , vol.50 , pp. 4507-4518
    • O'Donnell, M.J.1    Wu, S.2    Huffman, J.C.3
  • 39
    • 0029964126 scopus 로고    scopus 로고
    • Improved Enantioselective Dihydroxylation of bis-Homoallylic Alcohol Derivatives Using a Mechanistically Inspired to-Cinchona Alkaloid Catalyst
    • Corey, e.J., Noe, m.C, Ting, a.Y., Improved Enantioselective Dihydroxylation of bis-Homoallylic Alcohol Derivatives Using a Mechanistically Inspired to-Cinchona Alkaloid Catalyst. Tetrahedron Lett 37 (1996), 1735–1738.
    • (1996) Tetrahedron Lett , vol.37 , pp. 1735-1738
    • Corey, E.J.1    Noe, M.C.2    Ting, A.Y.3
  • 40
    • 0000234063 scopus 로고    scopus 로고
    • A Rational Approach to Catalytic En- antioselective Enolate Alkylation Using a Structurally Rigidified and Defined Chiral Quaternary Ammonium Salt Under Phase
    • Corey, e.J., Xu, F., Noe, m.C., A Rational Approach to Catalytic En- antioselective Enolate Alkylation Using a Structurally Rigidified and Defined Chiral Quaternary Ammonium Salt Under Phase. J. Am. Chem. Soc. 119 (1997), 12414–12415.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 12414-12415
    • Corey, E.J.1    Xu, F.2    Noe, M.C.3
  • 41
    • 0033554053 scopus 로고    scopus 로고
    • 2-Symmetric Chiral Phase-Transfer Catalyst for Practical Asymmetric Synthesis of α-Amino Acids
    • 2-Symmetric Chiral Phase-Transfer Catalyst for Practical Asymmetric Synthesis of α-Amino Acids. J. Am. Chem. Soc. 121 (1999), 6519–6520.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6519-6520
    • Ooi, T.1    Kameda, M.2    Maruoka, K.3
  • 42
    • 0030659804 scopus 로고    scopus 로고
    • A New Class of Asymmetric Phase-Transfer Catalysis Derived from Cinchona Alkaloids - Application in the Enantioselective Synthesis of α-Amino Acids
    • Lygo, B., Wainwright, p.G., A New Class of Asymmetric Phase-Transfer Catalysis Derived from Cinchona Alkaloids - Application in the Enantioselective Synthesis of α-Amino Acids. Tetrahedron Lett., 38, 1997, 8595–8598.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 8595-8598
    • Lygo, B.1    Wainwright, P.G.2
  • 43
    • 0032560703 scopus 로고    scopus 로고
    • Highly Enantioselective Synthesis of Cyclic and Functionalized α-Amino Acids by Means of a Chiral Phase Transfer Catalyst
    • Corey, e.J., Noe, m.C, Xu, F., Highly Enantioselective Synthesis of Cyclic and Functionalized α-Amino Acids by Means of a Chiral Phase Transfer Catalyst. Tetrahedron Lett. 39 (1998), 5347–5350.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5347-5350
    • Corey, E.J.1    Noe, M.C.2    Xu, F.3
  • 45
    • 0033547930 scopus 로고    scopus 로고
    • Enantioselective Synthesis of bis-α-Amino Acid Esters via Asymmetric Phase-Transfer Catalysis
    • Lygo, B., Crosby, J., Peterson, j.A., Enantioselective Synthesis of bis-α-Amino Acid Esters via Asymmetric Phase-Transfer Catalysis. Tetrahedron Lett. 40 (1999), 1385–1388.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 1385-1388
    • Lygo, B.1    Crosby, J.2    Peterson, J.A.3
  • 46
    • 0033547985 scopus 로고    scopus 로고
    • Enantioselective Synthesis of Dityrosine and Isodityrosine via Asymmetric Phase-Transfer Catalysis
    • Lygo, B., Enantioselective Synthesis of Dityrosine and Isodityrosine via Asymmetric Phase-Transfer Catalysis. Tetrahedron Lett. 40 (1999), 1389–1392.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 1389-1392
    • Lygo, B.1
  • 47
    • 0029805757 scopus 로고    scopus 로고
    • Enantioselective Total Synthesis of Ecteinascidin 743
    • Corey, e.J., Gin, d.Y., Kaptein, B., Enantioselective Total Synthesis of Ecteinascidin 743. J. Am. Chem. Soc. 118 (1996), 9202–9203.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 9202-9203
    • Corey, E.J.1    Gin, D.Y.2    Kaptein, B.3
  • 48
    • 0033553450 scopus 로고    scopus 로고
    • Enantioselective Synthesis of P-Hydroxy-α-Amino Acid Esters by Aldol Coupling Using a Chiral Quaternary Ammonium Salt As Catalyst
    • Horikawa, M., Busch-Petersen, J., Corey, e.J., Enantioselective Synthesis of P-Hydroxy-α-Amino Acid Esters by Aldol Coupling Using a Chiral Quaternary Ammonium Salt As Catalyst. Tetrahedron Lett. 40 (1999), 3843–3846.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 3843-3846
    • Horikawa, M.1    Busch-Petersen, J.2    Corey, E.J.3
  • 49
    • 0030955088 scopus 로고    scopus 로고
    • New Strategies to α-alkylated α-amino acids Angew
    • Wirth, T., New Strategies to α-alkylated α-amino acids Angew. Chem. Int. Ed. Engl. 36 (1997), 225–227.
    • (1997) Chem. Int. Ed. Engl. , vol.36 , pp. 225-227
    • Wirth, T.1
  • 50
    • 0026652090 scopus 로고
    • A Catalytic Enantioselective Synthesis of α-Methyl Amino Acid Derivatives by Phase Transfer Catalysis
    • O'Donnell, m.J., Wu, S., A Catalytic Enantioselective Synthesis of α-Methyl Amino Acid Derivatives by Phase Transfer Catalysis. Tetrahedron: Asymmetry 3 (1992), 591–594.
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 591-594
    • O'Donnell, M.J.1    Wu, S.2
  • 51
    • 0034738068 scopus 로고    scopus 로고
    • Practical Catalytic En- antioselective Synthesis of α, α-Dialkyl-α-Amino Acids by Chiral Phase-Transfer Catalysis
    • Ooi, T., Takeuchi, M., Kameda, M., Maruoka, K., Practical Catalytic En- antioselective Synthesis of α, α-Dialkyl-α-Amino Acids by Chiral Phase-Transfer Catalysis. J. Am. Chem. Soc. 122 (2000), 5228–5229.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 5228-5229
    • Ooi, T.1    Takeuchi, M.2    Kameda, M.3    Maruoka, K.4
  • 52
    • 0022490196 scopus 로고
    • Asymmetric Glycine Enolate Aldol Reactions: Synthesis of Cyclosporin's Unusual Amino Acid, MeBmt
    • Evans, d.A., Weber, a.E., Asymmetric Glycine Enolate Aldol Reactions: Synthesis of Cyclosporin's Unusual Amino Acid, MeBmt. J. Am. Chem. Soc. 108 (1986), 6757–6761.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 6757-6761
    • Evans, D.A.1    Weber, A.E.2
  • 53
    • 0023619369 scopus 로고
    • Synthesis of the Cyclic Hexapeptide Echinocandin D. New Approaches to the Asymmetric Synthesis of β-Hydroxy α-Amino Acids
    • Evans, d.A., Weber, a.E., Synthesis of the Cyclic Hexapeptide Echinocandin D. New Approaches to the Asymmetric Synthesis of β-Hydroxy α-Amino Acids. J. Am. Chem. Soc. 109 (1987), 7151–7157.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 7151-7157
    • Evans, D.A.1    Weber, A.E.2
  • 55
    • 0032538360 scopus 로고    scopus 로고
    • Nonconventional Stereochemical Issues in the Design of the Synthesis of the Vancomycin Antibiotics: Challenges Imposed by Axial and Nonplanar Chiral Elements
    • Evans, d.A., Dinsmore, c.J., Watson, p.J., Wood, m.R., Richardson, t.I., Trotter, b.W., Katz, j.L., Nonconventional Stereochemical Issues in the Design of the Synthesis of the Vancomycin Antibiotics: Challenges Imposed by Axial and Nonplanar Chiral Elements. Angew. Chem., Int. Ed. Engl. 37 (1998), 2704–2708.
    • (1998) Angew. Chem., Int. Ed. Engl. , vol.37 , pp. 2704-2708
    • Evans, D.A.1    Dinsmore, C.J.2    Watson, P.J.3    Wood, M.R.4    Richardson, T.I.5    Trotter, B.W.6    Katz, J.L.7
  • 56
    • 0008495409 scopus 로고
    • Dichlorine Minoxide: A Powerful and Selective Chlorinating Reagent
    • March, f.D., Farnham, w.B., Sam, d.J., Smart, b.E., Dichlorine Minoxide: A Powerful and Selective Chlorinating Reagent. J. Am. Chem. Soc. 104 (1982), 4680–4682.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 4680-4682
    • March, F.D.1    Farnham, W.B.2    Sam, D.J.3    Smart, B.E.4
  • 58
    • 0030820620 scopus 로고    scopus 로고
    • Chiral Magnesium bis-(Sulfonamide) Complexes as Catalysts for the Merged Enolization and Enantioselective Animation of N-Acyloxazolidinones. A Catalytic Appro
    • Evans, d.A., Nelson, s.G., Chiral Magnesium bis-(Sulfonamide) Complexes as Catalysts for the Merged Enolization and Enantioselective Animation of N-Acyloxazolidinones. A Catalytic Appro. J. Am. Chem. Soc. 119 (1997), 6452–6453.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 6452-6453
    • Evans, D.A.1    Nelson, S.G.2
  • 59
    • 0000744779 scopus 로고
    • The Asymmetric Synthesis of α-Amino and α-Hydrazino Acid Derivatives via the Stereoselective Animation of Chiral Enolates with Azodicarboxylate
    • Evans, d.A., Britton, t.C, Dorow, r.L., Dellaria, j.F. Jr, The Asymmetric Synthesis of α-Amino and α-Hydrazino Acid Derivatives via the Stereoselective Animation of Chiral Enolates with Azodicarboxylate. Tetrahedron 44 (1988), 5525–5540.
    • (1988) Tetrahedron , vol.44 , pp. 5525-5540
    • Evans, D.A.1    Britton, T.C.2    Dorow, R.L.3    Dellaria, J.F.4
  • 60
    • 85023128479 scopus 로고    scopus 로고
    • Synthesis of a Chiral Azodi- carboxamide Containing a Bridging Binaphthyl Moiety: Electrophilic Animation Reactions of Achiral Ester Enolates
    • Harris, j.M., McDonald, R., Vederas, j.C., Synthesis of a Chiral Azodi- carboxamide Containing a Bridging Binaphthyl Moiety: Electrophilic Animation Reactions of Achiral Ester Enolates. J. Chem. Soc, Perkin Trans. 1 (1996), 2269–2674.
    • (1996) J. Chem. Soc, Perkin Trans. , vol.1 , pp. 2269-2674
    • Harris, J.M.1    McDonald, R.2    Vederas, J.C.3
  • 61
    • 0000830285 scopus 로고    scopus 로고
    • Strategies for the Stereoselective Synthesis of Molecules with Remote Stereogenic Centers Across a Double Bond of Fixed Configuration
    • Mitchell, h.J., Nelson, A., Warren, S., Strategies for the Stereoselective Synthesis of Molecules with Remote Stereogenic Centers Across a Double Bond of Fixed Configuration. J. Chem. Soc, Perkin Trans. 1 (1999), 1899–1914.
    • (1999) J. Chem. Soc, Perkin Trans. , vol.1 , pp. 1899-1914
    • Mitchell, H.J.1    Nelson, A.2    Warren, S.3
  • 63
    • 0029857692 scopus 로고    scopus 로고
    • Synthesis of Non-Proteinogenic D- or L-Amino Acids by Asymmetric Hydrogenation
    • Kreuzfeld, h.J., Döbler, C, Schmidt, U., Krause, h.W., Synthesis of Non-Proteinogenic D- or L-Amino Acids by Asymmetric Hydrogenation. Amino Acids 11 (1996), 269–282.
    • (1996) Amino Acids , vol.11 , pp. 269-282
    • Kreuzfeld, H.J.1    Döbler, C.2    Schmidt, U.3    Krause, H.W.4
  • 64
    • 0000136461 scopus 로고
    • 2-Symmetric bis-(Phospholanes) and their Use in Highly Enantioselective Hydrogenation Reactions
    • 2-Symmetric bis-(Phospholanes) and their Use in Highly Enantioselective Hydrogenation Reactions. J. Am. Chem. Soc. 113 (1991), 8518–8519.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 8518-8519
    • Burk, M.J.1
  • 65
    • 0000740766 scopus 로고
    • 2-Symmetric bis-(Phospholanes): Production of a-Amino Acid Derivatives via Highly Enantioselective Hydrogenation Reactions
    • 2-Symmetric bis-(Phospholanes): Production of a-Amino Acid Derivatives via Highly Enantioselective Hydrogenation Reactions. J. Am. Chem. Soc. 115 (1993), 10125–10138.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10125-10138
    • Burk, M.J.1    Feaster, J.E.2    Nugent, W.A.3    Harlow, R.L.4
  • 66
    • 0033918708 scopus 로고    scopus 로고
    • Modular Phospholane Ligands in Asymmetric Catalysis
    • Burk, m.J., Modular Phospholane Ligands in Asymmetric Catalysis. Acc. Chem. Res. 33 (2000), 363–372.
    • (2000) Acc. Chem. Res. , vol.33 , pp. 363-372
    • Burk, M.J.1
  • 67
    • 0001296673 scopus 로고    scopus 로고
    • Synthesis of a New Class of Functionalized Chiral Bisphospholane Ligands and the Application in Enantioselective Hydrogenations
    • Holz, J., Quirmbach, M., Schmidt, U., Heller, D., Stërmer, R., Bërner, A., Synthesis of a New Class of Functionalized Chiral Bisphospholane Ligands and the Application in Enantioselective Hydrogenations. J. Org. Chem. 63 (1998), 8031–8034.
    • (1998) J. Org. Chem. , vol.63 , pp. 8031-8034
    • Holz, J.1    Quirmbach, M.2    Schmidt, U.3    Heller, D.4    Stërmer, R.5    Bërner, A.6
  • 68
    • 0030909008 scopus 로고    scopus 로고
    • Highly Enantioselective Rh-Catalyzed Hydrogenations with a New Chiral 1, 4-Diphosphine Containing a Cyclic Backbone
    • Zhu, G., Cao, P., Jiang, Q., Zhang, X., Highly Enantioselective Rh-Catalyzed Hydrogenations with a New Chiral 1, 4-Diphosphine Containing a Cyclic Backbone. J. Am. Chem. Soc. 119 (1997), 1799–1800.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 1799-1800
    • Zhu, G.1    Cao, P.2    Jiang, Q.3    Zhang, X.4
  • 72
    • 0033617302 scopus 로고    scopus 로고
    • Methylene-Bridged P-Chiral Diphosphines in Highly Enantioselective Reactions
    • Yamanoi, Y., Imamoto, T., Methylene-Bridged P-Chiral Diphosphines in Highly Enantioselective Reactions. J. Org. Chem. 64 (1999), 2988–2989.
    • (1999) J. Org. Chem. , vol.64 , pp. 2988-2989
    • Yamanoi, Y.1    Imamoto, T.2
  • 73
    • 0032581486 scopus 로고    scopus 로고
    • Asymmetric Synthesis of a New Cylindrically Chiral and Air-Stable Ferrocenyldiphosphine and its Application to Rhodium-Catalyzed Asymmetric Hydrogenation
    • Kang, J., Lee, j.H., Ahn, s.H., Choi, j.S., Asymmetric Synthesis of a New Cylindrically Chiral and Air-Stable Ferrocenyldiphosphine and its Application to Rhodium-Catalyzed Asymmetric Hydrogenation. Tetrahedron Lett. 39 (1998), 5523–5526.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5523-5526
    • Kang, J.1    Lee, J.H.2    Ahn, S.H.3    Choi, J.S.4
  • 74
    • 0032578890 scopus 로고    scopus 로고
    • 2-Symmetrical Ferrocenyl Ligands: Highly Enantioselective Rh-Catalyzed Hydrogenation of α-Acetamidoacrylic A
    • 2-Symmetrical Ferrocenyl Ligands: Highly Enantioselective Rh-Catalyzed Hydrogenation of α-Acetamidoacrylic A. Tetrahedron Lett. 39 (1998), 8073–8076.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 8073-8076
    • Perea, J.J.A.1    Bërner, A.2    Knochel, P.3
  • 75
    • 0000672301 scopus 로고    scopus 로고
    • 2-Symmetric Diamino FERRIPHOS as Ligands for Enantioselective Rh-Catalyzed Preparation of Chiral α-Amino Acids
    • 2-Symmetric Diamino FERRIPHOS as Ligands for Enantioselective Rh-Catalyzed Preparation of Chiral α-Amino Acids. Tetrahedron: Asymmetry 10 (1999), 375–384.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 375-384
    • Perea, J.J.A.1    Lotz, M.2    Knochel, P.3
  • 76
    • 17544387855 scopus 로고    scopus 로고
    • Unusual Amino Acids. Part 8: Asymmetric Hydrogenation of some Heteroaryl-N-CBZ and IV-Boc-Aminocinnamic Acid Derivatives
    • Dobler, C., Kreuzfeld, h.J., Michalik, M., Unusual Amino Acids. Part 8: Asymmetric Hydrogenation of some Heteroaryl-N-CBZ and IV-Boc-Aminocinnamic Acid Derivatives. Amino Acids 16 (1999), 21–27.
    • (1999) Amino Acids , vol.16 , pp. 21-27
    • Dobler, C.1    Kreuzfeld, H.J.2    Michalik, M.3
  • 77
    • 0003151014 scopus 로고    scopus 로고
    • Asymmetric Synthesis
    • Part 28: Novel Chiral Amino-phosphine Phosphinite Ligand and its Application in Homogeneous Catalytic Asymmetric Hydrogenation of Dehydro Amino Acid Derivativ
    • Part 28: Novel Chiral Amino-phosphine Phosphinite Ligand and its Application in Homogeneous Catalytic Asymmetric Hydrogenation of Dehydro Amino Acid DerivativMi, a.Q., Lou, r.L., Jiang, y.Z., Deng, j.G., Qin, Y., Fu, f.M., Li, Z., Hu, w.H., Chan, a.S. C., Asymmetric Synthesis. Synlett, 1998, 847–848.
    • (1998) Synlett , pp. 847-848
    • Mi, A.Q.1    Lou, R.L.2    Jiang, Y.Z.3    Deng, J.G.4    Qin, Y.5    Fu, F.M.6    Li, Z.7    Hu, W.H.8    Chan, A.S.C.9
  • 78
    • 0030831034 scopus 로고    scopus 로고
    • Novel Spirobicyclic Phosphinite Ligands and their Application in Homogeneous Catalytic Hydrogenation Reactions
    • Chan, A.S. C, Hu, W., Pai, c.C, Lau, c.P., Jiang, Y., Mi, A., Yan, M., Sun, J., Lou, R., Deng, J., Novel Spirobicyclic Phosphinite Ligands and their Application in Homogeneous Catalytic Hydrogenation Reactions. J. Am. Chem. Soc. 119 (1997), 9570–9571.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 9570-9571
    • Chan, A.S.C.1    Hu, W.2    Pai, C.C.3    Lau, C.P.4    Jiang, Y.5    Mi, A.6    Yan, M.7    Sun, J.8    Lou, R.9    Deng, J.10
  • 79
    • 0032080389 scopus 로고    scopus 로고
    • Highly Enantioselective Rhodium-Catalyzed Hydrogenation of Dehydroamino Acids with New Chiral Bisphosphinites
    • Zhu, G., Zhang, X., Highly Enantioselective Rhodium-Catalyzed Hydrogenation of Dehydroamino Acids with New Chiral Bisphosphinites. J. Org. Chem. 63 (1998), 3133–3136.
    • (1998) J. Org. Chem. , vol.63 , pp. 3133-3136
    • Zhu, G.1    Zhang, X.2
  • 80
    • 0001486820 scopus 로고    scopus 로고
    • Carbohydrate Phosphinites as Practical Ligands in Asymmetric Catalysis: Electronic Effects and Dependence of Backbone Chirality in Rh-Catalyzed Asymmetric Hyd
    • RajanBabu, t.V., Ayers, t.A., Halliday, g.A., You, k.K., Calabrese, j.C., Carbohydrate Phosphinites as Practical Ligands in Asymmetric Catalysis: Electronic Effects and Dependence of Backbone Chirality in Rh-Catalyzed Asymmetric Hyd. J. Org. Chem. 62 (1997), 6012–6028.
    • (1997) J. Org. Chem. , vol.62 , pp. 6012-6028
    • RajanBabu, T.V.1    Ayers, T.A.2    Halliday, G.A.3    You, K.K.4    Calabrese, J.C.5
  • 81
    • 0033613696 scopus 로고    scopus 로고
    • A Highly Effective Phosphinite Ligand Derived from D-Mannitol for Rh-Catalyzed Asymmetric Hydrogenation
    • Chen, Y., Li, X., Tong, s.K., Choi, m.C. K., Chan, a.S. C., A Highly Effective Phosphinite Ligand Derived from D-Mannitol for Rh-Catalyzed Asymmetric Hydrogenation. Tetrahedron Lett. 40 (1999), 957–960.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 957-960
    • Chen, Y.1    Li, X.2    Tong, S.K.3    Choi, M.C.K.4    Chan, A.S.C.5
  • 82
    • 0033597845 scopus 로고    scopus 로고
    • Novel Water-Soluble Bisphosphinite Chiral Ligands Derived from α, α- and β, β-Trehalose. Application to Asymmetric Hydrogenation of Dehydroamino Acids
    • Yonehara, K., Hashizume, T., Mori, K., Ohe, K., Uemura, S., Novel Water-Soluble Bisphosphinite Chiral Ligands Derived from α, α- and β, β-Trehalose. Application to Asymmetric Hydrogenation of Dehydroamino Acids. J. Org. Chem. 64 (1999), 5593–5598.
    • (1999) J. Org. Chem. , vol.64 , pp. 5593-5598
    • Yonehara, K.1    Hashizume, T.2    Mori, K.3    Ohe, K.4    Uemura, S.5
  • 83
    • 0031927511 scopus 로고    scopus 로고
    • Drugs for Chiral Discrimination: Non-Coded Amino Acids and Dipeptides by Asymmetric Hydrogenation
    • Kreuzfeld, h.J., Dobler, C., Schmidt, U., Krause, h.W., Drugs for Chiral Discrimination: Non-Coded Amino Acids and Dipeptides by Asymmetric Hydrogenation. Chirality 10 (1998), 535–539.
    • (1998) Chirality , vol.10 , pp. 535-539
    • Kreuzfeld, H.J.1    Dobler, C.2    Schmidt, U.3    Krause, H.W.4
  • 84
    • 0029987157 scopus 로고    scopus 로고
    • Enantioselective Hydrogenation of Dehydroamino Acid Derivatives Using PINDOPHOS-Rhodium as Chiral Catalyst
    • Kreuzfeld, h.J., Schmidt, U., Dobler, C., Krause, h.W., Enantioselective Hydrogenation of Dehydroamino Acid Derivatives Using PINDOPHOS-Rhodium as Chiral Catalyst. Tetrahedron: Asymmetry 7 (1996), 1011–1018.
    • (1996) Tetrahedron: Asymmetry , vol.7 , pp. 1011-1018
    • Kreuzfeld, H.J.1    Schmidt, U.2    Dobler, C.3    Krause, H.W.4
  • 85
    • 0029080089 scopus 로고
    • Asymmetric Catalytic Synthesis of β-Branched Amino Acids via Highly Enantioselective Hydrogenation of α-Enamides
    • Burk, m.J., Gross, m.F., Martinez, j.P., Asymmetric Catalytic Synthesis of β-Branched Amino Acids via Highly Enantioselective Hydrogenation of α-Enamides. J. Am. Chem. Soc. 111 (1995), 9375–9376.
    • (1995) J. Am. Chem. Soc. , vol.111 , pp. 9375-9376
    • Burk, M.J.1    Gross, M.F.2    Martinez, J.P.3
  • 86
    • 0000188240 scopus 로고
    • Enantioselective Hydrogenation of α-Disubstituted α-Acetamidoacrylates Catalyzed by Rhodium Complexes with TRAP Trans-Chelating Chiral Phosphine Ligands
    • Sawamura, M., Kuwano, R., Ito, Y., Enantioselective Hydrogenation of α-Disubstituted α-Acetamidoacrylates Catalyzed by Rhodium Complexes with TRAP Trans-Chelating Chiral Phosphine Ligands. J. Am. Chem. Soc. 117 (1995), 9602–9603.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 9602-9603
    • Sawamura, M.1    Kuwano, R.2    Ito, Y.3
  • 89
    • 0000429726 scopus 로고    scopus 로고
    • Catalytic Asymmetric Synthesis of P-Hydroxy-α- Amino Acids: Highly Enantioselective Hydrogenation of β-Oxy-α-Acet-amidoacrylates
    • Kuwano, R., Okuda, S., Ito, Y., Catalytic Asymmetric Synthesis of P-Hydroxy-α- Amino Acids: Highly Enantioselective Hydrogenation of β-Oxy-α-Acet-amidoacrylates. J. Org. Chem. 63 (1998), 3499–3503.
    • (1998) J. Org. Chem. , vol.63 , pp. 3499-3503
    • Kuwano, R.1    Okuda, S.2    Ito, Y.3
  • 91
    • 0025827163 scopus 로고
    • Asymmetric Synthesis. Practical Production of D and L Threonine. Dynamic Kinetic Resolution in Rhodium and Ruthenium Catalyzed Hydrogenation of 2-(Acylamino)
    • Genet, j.P., Pinel, C, Mallart, S., Juge, S., Thorimbert, S., Laffitte, j.A., Asymmetric Synthesis. Practical Production of D and L Threonine. Dynamic Kinetic Resolution in Rhodium and Ruthenium Catalyzed Hydrogenation of 2-(Acylamino)-. Tetrahedron: Asymmetry 2 (1991), 555–567.
    • (1991) Tetrahedron: Asymmetry , vol.2 , pp. 555-567
    • Genet, J.P.1    Pinel, C.2    Mallart, S.3    Juge, S.4    Thorimbert, S.5    Laffitte, J.A.6
  • 92
    • 0032481423 scopus 로고    scopus 로고
    • Highly Regio- and Enantioselective Catalytic Hydrogenation of Enamides in Conjugated Diene Systems: Synthesis and Application of γ, δ-Unsaturated Amino Ac
    • Burk, m.J., Allen, j.G., Kiesman, w.F., Highly Regio- and Enantioselective Catalytic Hydrogenation of Enamides in Conjugated Diene Systems: Synthesis and Application of γ, δ-Unsaturated Amino Ac. J. Am. Chem. Soc. 120 (1998), 657–663.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 657-663
    • Burk, M.J.1    Allen, J.G.2    Kiesman, W.F.3
  • 93
    • 0033574553 scopus 로고    scopus 로고
    • Catalytic Asymmetric Hydrogenation of α, β, δ, γ-Unsaturated Amino Acids
    • Burk, m.J., Bedingfield, k.M., Keisman, w.F., Allen, j.G., Catalytic Asymmetric Hydrogenation of α, β, δ, γ-Unsaturated Amino Acids. Tetrahedron Lett. 40 (1999), 3093–3096.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 3093-3096
    • Burk, M.J.1    Bedingfield, K.M.2    Keisman, W.F.3    Allen, J.G.4
  • 94
    • 0028596355 scopus 로고
    • Asymmetric Alkylations of a Sultam-Derived Glycine Equivalent: Practical Preparation of Enantiomerically Pure α-Amino Acids
    • Oppolzer, W., Moretti, R., Zhou, C., Asymmetric Alkylations of a Sultam-Derived Glycine Equivalent: Practical Preparation of Enantiomerically Pure α-Amino Acids. Helv. Chim. Acta 77 (1994), 2363–2380.
    • (1994) Helv. Chim. Acta , vol.77 , pp. 2363-2380
    • Oppolzer, W.1    Moretti, R.2    Zhou, C.3
  • 95
    • 0029014202 scopus 로고
    • Synthesis and Reactions of α-(Tri-fluoromethanesulfonyloxy) Enecarbamates Prepared from N-Acyllactams
    • Foti, c.J., Comins, d.L., Synthesis and Reactions of α-(Tri-fluoromethanesulfonyloxy) Enecarbamates Prepared from N-Acyllactams. J. Org. Chem. 60 (1995), 2656–2657.
    • (1995) J. Org. Chem. , vol.60 , pp. 2656-2657
    • Foti, C.J.1    Comins, D.L.2
  • 96
    • 0000436139 scopus 로고    scopus 로고
    • Synthesis of N-Heterocycles via Lactam-Derived Ketene Aminal Phosphates. Asymmetric Synthesis of Cyclic Amino Acids
    • Nicolaou, k.C, Namoto, K., Synthesis of N-Heterocycles via Lactam-Derived Ketene Aminal Phosphates. Asymmetric Synthesis of Cyclic Amino Acids. Chem. Commun. (Cambridge), 1998, 1757–1758.
    • (1998) Chem. Commun. (Cambridge) , pp. 1757-1758
    • Nicolaou, K.C.1    Namoto, K.2
  • 97
    • 0032784298 scopus 로고    scopus 로고
    • Synthesis of α- and β-Carbon-Linked Serine Analogues of the Pk Trisaccharide
    • Debenham, s.D., Cossrow, J., Toone, e.J., Synthesis of α- and β-Carbon-Linked Serine Analogues of the Pk Trisaccharide. J. Org. Chem. 64 (1999), 9153–9163.
    • (1999) J. Org. Chem. , vol.64 , pp. 9153-9163
    • Debenham, S.D.1    Cossrow, J.2    Toone, E.J.3
  • 98
    • 0027308184 scopus 로고
    • An Efficient Asymmetric Synthesis of the Four Stereoisomers of 3-Hydroxyleucine
    • Sunazuka, T., Nagamitsu, T., Tanaka, H., Omura, S., An Efficient Asymmetric Synthesis of the Four Stereoisomers of 3-Hydroxyleucine. Tetrahedron Lett. 34 (1993), 4447–4448.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 4447-4448
    • Sunazuka, T.1    Nagamitsu, T.2    Tanaka, H.3    Omura, S.4
  • 100
    • 18844410382 scopus 로고
    • Catalytic Asymmetric Epoxidation and Kinetic Resolution: Modified Procedures Including in situ Derivatization
    • Gao, Y., Hanson, R., Klunder, j.M., Ko, s.Y., Masamune, H., Sharpless, k.B., Catalytic Asymmetric Epoxidation and Kinetic Resolution: Modified Procedures Including in situ Derivatization. J. Am. Chem. Soc. 109 (1987), 5765–5780.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 5765-5780
    • Gao, Y.1    Hanson, R.2    Klunder, J.M.3    Ko, S.Y.4    Masamune, H.5    Sharpless, K.B.6
  • 101
    • 0025252275 scopus 로고
    • A Convenient Synthesis of Enantiomerically Pure (25, 35)- or (2R, 3R)-3-Hydroxyleucine
    • Caldwell, c.G., Bondy, s.S., A Convenient Synthesis of Enantiomerically Pure (25, 35)- or (2R, 3R)-3-Hydroxyleucine. Synthesis 1 (1990), 34–36.
    • (1990) Synthesis , vol.1 , pp. 34-36
    • Caldwell, C.G.1    Bondy, S.S.2
  • 102
    • 0001589756 scopus 로고
    • Directed Openings of 2, 3-Epoxy Alcohols via Reactions with Isocyanates: Synthesis of (+)-Erythro-Dihydrosphingosine
    • Roush, w.R., Adam, m.A., Directed Openings of 2, 3-Epoxy Alcohols via Reactions with Isocyanates: Synthesis of (+)-Erythro-Dihydrosphingosine. J. Org. Chem. 50 (1985), 3752–3757.
    • (1985) J. Org. Chem. , vol.50 , pp. 3752-3757
    • Roush, W.R.1    Adam, M.A.2
  • 103
    • 0028041027 scopus 로고
    • A Practical New Asymmetric Synthesis of (2S, 3S)- and (2R, 3R)3-Hydroxyleucine
    • Hale, k.J., Manaviazar, S., Delisser, v.M., A Practical New Asymmetric Synthesis of (2S, 3S)- and (2R, 3R)3-Hydroxyleucine. Tetrahedron 50 (1994), 9181–9188.
    • (1994) Tetrahedron , vol.50 , pp. 9181-9188
    • Hale, K.J.1    Manaviazar, S.2    Delisser, V.M.3
  • 104
    • 0026495324 scopus 로고
    • Azinothricin Synthetic Studies
    • 1. Efficient Asymmetric Synthesis of (3R)- and (3S)-Piperazic Acids
    • Efficient Asymmetric Synthesis of (3R)- and (3S)-Piperazic Acids Hale, k.J., Delisser, v.M., Manaviazar, S., Azinothricin Synthetic Studies. Tetrahedron Lett 33 (1992), 7613–7616.
    • (1992) Tetrahedron Lett , vol.33 , pp. 7613-7616
    • Hale, K.J.1    Delisser, V.M.2    Manaviazar, S.3
  • 105
    • 0027293498 scopus 로고
    • Synthetic Studies on the Azinothricin Family of Antibiotics
    • 2. Asymmetric Synthesis of the C(28)-C(47)Subunit of A83586C
    • Asymmetric Synthesis of the C(28)-C(47)Subunit of A83586C Hale, k.J., Bhatia, g.S., Peak, s.A., Manaviazar, S., Synthetic Studies on the Azinothricin Family of Antibiotics. Tetrahedron Lett. 34 (1993), 5343–5346.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 5343-5346
    • Hale, K.J.1    Bhatia, G.S.2    Peak, S.A.3    Manaviazar, S.4
  • 108
    • 33748233248 scopus 로고    scopus 로고
    • Catalytic Asymmetric Aminohydroxylation (AA) of Olefins
    • Li, G., Chang, H.-T., Sharpless, k.B., Catalytic Asymmetric Aminohydroxylation (AA) of Olefins. Angew. Chem., Int. Ed. Engl. 35 (1996), 451–454.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 451-454
    • Li, G.1    Chang, H.-T.2    Sharpless, K.B.3
  • 109
    • 33847085200 scopus 로고
    • Asymmetric Induction in the Reaction of Osmium Tetroxide with Olefins
    • Hentges, S., Sharpless, k.B., Asymmetric Induction in the Reaction of Osmium Tetroxide with Olefins. J. Am. Chem. Soc. 102 (1980), 4263–4265.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 4263-4265
    • Hentges, S.1    Sharpless, K.B.2
  • 110
    • 85023122291 scopus 로고    scopus 로고
    • The Sharpless Asymmetric Aminohydroxylation of Olefins
    • Reiser, O., The Sharpless Asymmetric Aminohydroxylation of Olefins. Chem. Rev. 55 (1996), 1308–1309.
    • (1996) Chem. Rev. , vol.55 , pp. 1308-1309
    • Reiser, O.1
  • 111
    • 0001030240 scopus 로고    scopus 로고
    • Asymmetric aminohydroxylation. Transition Met
    • Kolb, h.C, Sharpless, k.B., Asymmetric aminohydroxylation. Transition Met. Org. Synth 2 (1998), 243–260.
    • (1998) Org. Synth , vol.2 , pp. 243-260
    • Kolb, H.C.1    Sharpless, K.B.2
  • 112
    • 0033083525 scopus 로고    scopus 로고
    • Sharpless Asymmetric Aminohydroxylation: Scope, Limitations, and Use in Synthesis
    • O'Brien, P., Sharpless Asymmetric Aminohydroxylation: Scope, Limitations, and Use in Synthesis. Angew. Chem., Int. Ed. Engl. 38 (1999), 326–329.
    • (1999) Angew. Chem., Int. Ed. Engl. , vol.38 , pp. 326-329
    • O'Brien, P.1
  • 114
    • 0030484915 scopus 로고    scopus 로고
    • N-Halocarbamate Salts Lead to More Efficient Catalytic Asymmetric Aminohydroxylation
    • Li, G., Angert, h.H., Sharpless, k.B., N-Halocarbamate Salts Lead to More Efficient Catalytic Asymmetric Aminohydroxylation. Angew. Chem., Int. Ed. Engl. 35 (1996), 2813–2817.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 2813-2817
    • Li, G.1    Angert, H.H.2    Sharpless, K.B.3
  • 115
    • 0030484752 scopus 로고    scopus 로고
    • Smaller Substituents on Nitrogen Facilitate the Osmium-Catalyzed Asymmetric Aminohydroxylation
    • Rudolph, J., Sennhenn, p.C, Vlaar, c.P., Sharpless, k.B., Smaller Substituents on Nitrogen Facilitate the Osmium-Catalyzed Asymmetric Aminohydroxylation. Angew. Chem., Int. Ed. Engl. 35 (1996), 2810–2813.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 2810-2813
    • Rudolph, J.1    Sennhenn, P.C.2    Vlaar, C.P.3    Sharpless, K.B.4
  • 116
    • 0002858266 scopus 로고    scopus 로고
    • From Styrenes to Enantiopure α-Arylglycines in Two Steps
    • Reddy, k.L., Sharpless, k.B., From Styrenes to Enantiopure α-Arylglycines in Two Steps. J. Am. Chem. Soc. 120 (1998), 1207–1217.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 1207-1217
    • Reddy, K.L.1    Sharpless, K.B.2
  • 119
    • 0032575177 scopus 로고    scopus 로고
    • B. N-Chloro-N-Sodio-2-Trimethylsilyl Ethyl Carbamate: A New Nitrogen Source for the Catalytic Asymmetric Aminohydroxylation
    • Reddy, k.L., Dress, k.R., Sharpless, K., B. N-Chloro-N-Sodio-2-Trimethylsilyl Ethyl Carbamate: A New Nitrogen Source for the Catalytic Asymmetric Aminohydroxylation. Tetrahedron Lett. 39 (1998), 3667–3670.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 3667-3670
    • Reddy, K.L.1    Dress, K.R.2    Sharpless, K.3
  • 120
    • 0030215491 scopus 로고    scopus 로고
    • Catalytic Asymmetric Aminohydroxylation Provides a Short Taxol Side-Chain Synthesis. Acta
    • Li, G., Sharpless, k.B., Catalytic Asymmetric Aminohydroxylation Provides a Short Taxol Side-Chain Synthesis. Acta. Chemica Scandinavica 50 (1996), 649–651.
    • (1996) Chemica Scandinavica , vol.50 , pp. 649-651
    • Li, G.1    Sharpless, K.B.2
  • 121
    • 0030799342 scopus 로고    scopus 로고
    • B. N-Bromoacetamide - A New Nitrogen Source for the Catalytic Asymmetric Aminohydroxylation of Olefins
    • Bruncko, M., Schlingloff, G., Sharpless, K., B. N-Bromoacetamide - A New Nitrogen Source for the Catalytic Asymmetric Aminohydroxylation of Olefins. Angew. Chem., Int. Ed. Engl 36 (1997), 1483–1486.
    • (1997) Angew. Chem., Int. Ed. Engl , vol.36 , pp. 1483-1486
    • Bruncko, M.1    Schlingloff, G.2    Sharpless, K.3
  • 122
    • 0031737498 scopus 로고    scopus 로고
    • Synthesis of (3R)- Amino-(2S)-Hydroxy Amino Acids for Inhibition of Methionine Aminopeptidase-1
    • Keding, s.J., Dales, n.A., Lim, S., Beaulieu, D., Rich, d.H., Synthesis of (3R)- Amino-(2S)-Hydroxy Amino Acids for Inhibition of Methionine Aminopeptidase-1. Synth. Commun. 28 (1998), 4463–4470.
    • (1998) Synth. Commun. , vol.28 , pp. 4463-4470
    • Keding, S.J.1    Dales, N.A.2    Lim, S.3    Beaulieu, D.4    Rich, D.H.5
  • 123
    • 0032560012 scopus 로고    scopus 로고
    • Reversal of Regioselection in the Asymmetric Aminohydroxylation of Cinnamates
    • Tao, B., Schlingloff, G., Sharpless, k.B., Reversal of Regioselection in the Asymmetric Aminohydroxylation of Cinnamates. Tetrahedron Lett. 39 (1998), 2507–2510.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2507-2510
    • Tao, B.1    Schlingloff, G.2    Sharpless, K.B.3
  • 124
    • 0032912625 scopus 로고    scopus 로고
    • A Substrate-Based Methodology That Allows the Regioselective Control of the Catalytic Aminohydroxylation Reaction
    • Han, H., Cho, C.-W., Janda, k.D., A Substrate-Based Methodology That Allows the Regioselective Control of the Catalytic Aminohydroxylation Reaction. Chem. Eur. J. 5 (1999), 1565–1569.
    • (1999) Chem. Eur. J. , vol.5 , pp. 1565-1569
    • Han, H.1    Cho, C.-W.2    Janda, K.D.3
  • 125
    • 0000458209 scopus 로고
    • Substrate-Directable Chemical Reactions
    • Hoveyda, a.H., Evans, d.A., Fu, g.C., Substrate-Directable Chemical Reactions. Chem. Rev. 93 (1993), 1307–1370.
    • (1993) Chem. Rev. , vol.93 , pp. 1307-1370
    • Hoveyda, A.H.1    Evans, D.A.2    Fu, G.C.3
  • 126
    • 0033576420 scopus 로고    scopus 로고
    • Reversal of Regioselection in the Sharpless Asymmetric Aminohydroxylation of Aryl Ester Substrates
    • Morgan, a.J., Masse, c.E., Panek, j.S., Reversal of Regioselection in the Sharpless Asymmetric Aminohydroxylation of Aryl Ester Substrates. Org. Lett. 1 (1999), 1949–1952.
    • (1999) Org. Lett. , vol.1 , pp. 1949-1952
    • Morgan, A.J.1    Masse, C.E.2    Panek, J.S.3
  • 128
    • 0034709563 scopus 로고    scopus 로고
    • Regioselective Asymmetric Aminohydroxylation of Precursors to 2, 3, 6-Trideoxy-3-Aminohexoses
    • Davey, r.M., Brimble, m.A., McLeod, m.D., Regioselective Asymmetric Aminohydroxylation of Precursors to 2, 3, 6-Trideoxy-3-Aminohexoses. Tetrahedron Lett. 41 (2000), 5141–5145.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 5141-5145
    • Davey, R.M.1    Brimble, M.A.2    McLeod, M.D.3
  • 130
    • 0029959145 scopus 로고    scopus 로고
    • A Critical Analysis of the Mechanistic Basis of En- antioselectivity in the bis-Cinchona Alkaloid Catalyzed Dihydroxylation of Olefins
    • Corey, e.J., Noe, m.C., A Critical Analysis of the Mechanistic Basis of En- antioselectivity in the bis-Cinchona Alkaloid Catalyzed Dihydroxylation of Olefins. J. Am. Chem. Soc. 118 (1996), 11038–11053.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 11038-11053
    • Corey, E.J.1    Noe, M.C.2
  • 131
    • 0000711829 scopus 로고
    • The Application of a Mechanistic Model Leads to the Extension of the Sharpless Asymmetric Dihydroxylation to Allylic 4-Methoxybenzoates and Conformationally R
    • Corey, e.J., Guzman-Perez, A., Noe, m.C., The Application of a Mechanistic Model Leads to the Extension of the Sharpless Asymmetric Dihydroxylation to Allylic 4-Methoxybenzoates and Conformationally R. J. Am. Chem. Soc. 117 (1995), 10805–10816.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 10805-10816
    • Corey, E.J.1    Guzman-Perez, A.2    Noe, M.C.3
  • 132
    • 0032732493 scopus 로고    scopus 로고
    • Asymmetric Aminohydroxylation of Heteroaromatic Acrylates
    • Raatz, D., Innertsberger, C, Reiser, O., Asymmetric Aminohydroxylation of Heteroaromatic Acrylates. Synlett 12 (1999), 1907–1910.
    • (1999) Synlett , vol.12 , pp. 1907-1910
    • Raatz, D.1    Innertsberger, C.2    Reiser, O.3
  • 133
    • 4243924840 scopus 로고
    • Studies Directed Toward the Synthesis of Vancomycin and Related Cyclic Peptides
    • Rao, a.V. R., Gurjar, m.K., Reddy, L., Rao, a.S., Studies Directed Toward the Synthesis of Vancomycin and Related Cyclic Peptides. Chem. Rev. 95 (1995), 2135–2167.
    • (1995) Chem. Rev. , vol.95 , pp. 2135-2167
    • Rao, A.V.R.1    Gurjar, M.K.2    Reddy, L.3    Rao, A.S.4
  • 137
    • 0029950618 scopus 로고    scopus 로고
    • Synthesis of (R)-(4-Methoxy-3, 5- Dihydroxyphenyl)Glycine Derivatives: The Central Amino Acid of Vancomycin and Related Agents
    • Boger, d.L., Borzilleri, r.M., Nukui, S., Synthesis of (R)-(4-Methoxy-3, 5- Dihydroxyphenyl)Glycine Derivatives: The Central Amino Acid of Vancomycin and Related Agents. J. Org. Chem. 61 (1996), 3561–3565.
    • (1996) J. Org. Chem. , vol.61 , pp. 3561-3565
    • Boger, D.L.1    Borzilleri, R.M.2    Nukui, S.3
  • 138
    • 0033520774 scopus 로고    scopus 로고
    • Diastereoselective Total Synthesis of the Vancomycin Aglycon with Ordered Atropisomer Equilibrations
    • Boger, d.L., Miyazaki, S., Kim, s.H., Wu, j.H., Loiseleur, O., Castle, s.L., Diastereoselective Total Synthesis of the Vancomycin Aglycon with Ordered Atropisomer Equilibrations. J. Am. Chem. Soc. 121 (1999), 3226–3227.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 3226-3227
    • Boger, D.L.1    Miyazaki, S.2    Kim, S.H.3    Wu, J.H.4    Loiseleur, O.5    Castle, S.L.6
  • 139
    • 0032956642 scopus 로고    scopus 로고
    • Asymmetric Synthesis of ConformationaHy Restricted L-Arginine Analogues as Active Site Probes of Nitric Oxide
    • Atkinson, r.N., Moore, L., Tobin, J., King, s.B., Asymmetric Synthesis of ConformationaHy Restricted L-Arginine Analogues as Active Site Probes of Nitric Oxide. J. Org. Chem. 64 (1999), 3467–3475.
    • (1999) J. Org. Chem. , vol.64 , pp. 3467-3475
    • Atkinson, R.N.1    Moore, L.2    Tobin, J.3    King, S.B.4
  • 140
    • 0000733768 scopus 로고
    • The Bimolecular Aliphatic Mannich and Related Reactions
    • Chapter 4.1 Trost b.M. Fleming I. Pergamon Press New York
    • Chapter 4.1 Kleinman, e.F., The Bimolecular Aliphatic Mannich and Related Reactions. Trost, b.M., Fleming, I., (eds.) Comprehensive Organic Synthesis, 1991, Pergamon Press, New York.
    • (1991) Comprehensive Organic Synthesis
    • Kleinman, E.F.1
  • 141
    • 0001803662 scopus 로고
    • Reduction of C=N to CHNH by Metal Hydrides
    • Chapter 1.2 Trost b.M. Fleming I. Pergamon Press Oxford
    • Chapter 1.2 Hutchins, r.O., Reduction of C=N to CHNH by Metal Hydrides. Trost, b.M., Fleming, I., (eds.) Comprehensive Organic Synthesis, 1991, Pergamon Press, Oxford.
    • (1991) Comprehensive Organic Synthesis
    • Hutchins, R.O.1
  • 142
    • 0000862669 scopus 로고    scopus 로고
    • Catalytic Enantioselective Addition to Imines
    • Kobayashi, S., Ishitani, H., Catalytic Enantioselective Addition to Imines. Chem. Rev. 99 (1999), 1069–1094.
    • (1999) Chem. Rev. , vol.99 , pp. 1069-1094
    • Kobayashi, S.1    Ishitani, H.2
  • 143
    • 0033523708 scopus 로고    scopus 로고
    • Asymmetric Catalytic Aminoalkylations: New Powerful Methods for the Enantioselective Synthesis of Amino Acid Derivatives, Mannich Bases, and Homoallilic Amine
    • Arend, M., Asymmetric Catalytic Aminoalkylations: New Powerful Methods for the Enantioselective Synthesis of Amino Acid Derivatives, Mannich Bases, and Homoallilic Amine. Angew. Chem., Int. Ed. Engl. 38 (1999), 2873–2874.
    • (1999) Angew. Chem., Int. Ed. Engl. , vol.38 , pp. 2873-2874
    • Arend, M.1
  • 144
    • 0032542749 scopus 로고    scopus 로고
    • Enantioselective Addition of Enol Silyl Ethers to Imines Catalyzed by Palladium Complexes: A Novel Way to Optically Active Acylalanine Derivatives
    • Hagiwara, E., Fujii, A., Sodeoka, M., Enantioselective Addition of Enol Silyl Ethers to Imines Catalyzed by Palladium Complexes: A Novel Way to Optically Active Acylalanine Derivatives. J. Am. Chem. Soc. 120 (1998), 2474–2475.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 2474-2475
    • Hagiwara, E.1    Fujii, A.2    Sodeoka, M.3
  • 145
    • 0000263137 scopus 로고
    • Catalytic Asymmetric Aldol Reaction via Chiral Pd(II) Enolate in Wet DMF
    • Sodeoka, M., Ohrai, K., Shibasaki, M., Catalytic Asymmetric Aldol Reaction via Chiral Pd(II) Enolate in Wet DMF. J. Org. Chem. 60 (1995), 2648–2649.
    • (1995) J. Org. Chem. , vol.60 , pp. 2648-2649
    • Sodeoka, M.1    Ohrai, K.2    Shibasaki, M.3
  • 146
    • 0033575073 scopus 로고    scopus 로고
    • Mechanism of Palladium Complex-Catalyzed Enantioselective Mannich-Type Reaction: Characterization of a Novel Binuclear Palladium Enolate Complex
    • Fujii, A., Hagiwara, E., Sodeoka, M., Mechanism of Palladium Complex-Catalyzed Enantioselective Mannich-Type Reaction: Characterization of a Novel Binuclear Palladium Enolate Complex. J. Am. Chem. Soc. 121 (1999), 5450–5458.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 5450-5458
    • Fujii, A.1    Hagiwara, E.2    Sodeoka, M.3
  • 147
    • 0003914496 scopus 로고    scopus 로고
    • Stable Diaqua Palladium(II) Complexes of BINAP and Tol-BINAP As Highly Efficient Catalysts for Asymmetric Aldol Reactions
    • Sodeoka, M, Tokunoh, R., Miyazaki, F., Hagiwara, E., Shibasaki, M., Stable Diaqua Palladium(II) Complexes of BINAP and Tol-BINAP As Highly Efficient Catalysts for Asymmetric Aldol Reactions. Synlett 5 (1997), 463–466.
    • (1997) Synlett , vol.5 , pp. 463-466
    • Sodeoka, M.1    Tokunoh, R.2    Miyazaki, F.3    Hagiwara, E.4    Shibasaki, M.5
  • 148
    • 0002867663 scopus 로고    scopus 로고
    • Asymmetric Synthesis Using Palladium Catalysts
    • Sodeoka, M, Shibasaki, M., Asymmetric Synthesis Using Palladium Catalysts. Pure Appl. Chem. 70 (1998), 411–414.
    • (1998) Pure Appl. Chem. , vol.70 , pp. 411-414
    • Sodeoka, M.1    Shibasaki, M.2
  • 149
    • 0001209391 scopus 로고    scopus 로고
    • Catalytic, Enantioselective Alkylation of α-Imino Esters Using Late Transition Metal Phosphine Complexes As Catalysts
    • Ferraris, D., Young, B., Dudding, T., Lectka, T., Catalytic, Enantioselective Alkylation of α-Imino Esters Using Late Transition Metal Phosphine Complexes As Catalysts. J. Am. Chem. Soc. 120 (1998), 4548–4549.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 4548-4549
    • Ferraris, D.1    Young, B.2    Dudding, T.3    Lectka, T.4
  • 151
  • 152
    • 0033575447 scopus 로고    scopus 로고
    • Catalytic, Enantioselective Alkylations of N, O- and N, N-Acetals and Hemiacetals
    • Ferraris, D., Young, B., Dudding, T., Drury, w.J. III, Lectka, T., Catalytic, Enantioselective Alkylations of N, O- and N, N-Acetals and Hemiacetals. Tetrahedron 55 (1999), 8869–8882.
    • (1999) Tetrahedron , vol.55 , pp. 8869-8882
    • Ferraris, D.1    Young, B.2    Dudding, T.3    Drury, W.J.4    Lectka, T.5
  • 153
    • 0001249937 scopus 로고
    • Chiral Acetals in Asymmetric Synthesis
    • Alexakis, A., Mangeney, P., Chiral Acetals in Asymmetric Synthesis. Tetrahedron: Asymmetry 1 (1990), 477–511.
    • (1990) Tetrahedron: Asymmetry , vol.1 , pp. 477-511
    • Alexakis, A.1    Mangeney, P.2
  • 154
    • 84989487284 scopus 로고
    • Cross-Coupling Reactions Based on Acetals
    • Mukaiyama, T., Murakami, M., Cross-Coupling Reactions Based on Acetals. Synthesis, 1987, 1043–1054.
    • (1987) Synthesis , pp. 1043-1054
    • Mukaiyama, T.1    Murakami, M.2
  • 155
    • 0032486806 scopus 로고    scopus 로고
    • Ni-Catalyzed Asymmetric Addition of Grignard Reagents to Unsaturated Cyclic Acetals. The Influence of Added Phosphine on Enantioselectivity
    • Gomez-Bengoa, E., Heron, n.M., Didiuk, m.T., Luchaco, c.A., Hoveyda, a.H., Ni-Catalyzed Asymmetric Addition of Grignard Reagents to Unsaturated Cyclic Acetals. The Influence of Added Phosphine on Enantioselectivity. J. Am. Chem. Soc. 120 (1998), 7649–7650.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 7649-7650
    • Gomez-Bengoa, E.1    Heron, N.M.2    Didiuk, M.T.3    Luchaco, C.A.4    Hoveyda, A.H.5
  • 156
    • 0025239638 scopus 로고
    • N. Preparation of y-oxo a-Amino Acids from Silyl Enol Ethers and Glycine Cation Equivalents; a Facile Synthesis of (±)-5-Hydroxy-4-oxonorvaline (HON)
    • Mooiweer, h.H., Ettema, k.W. A., Hiemstra, H., Spekamp, W., N. Preparation of y-oxo a-Amino Acids from Silyl Enol Ethers and Glycine Cation Equivalents; a Facile Synthesis of (±)-5-Hydroxy-4-oxonorvaline (HON). Tetrahedron 46 (1990), 2991–2998.
    • (1990) Tetrahedron , vol.46 , pp. 2991-2998
    • Mooiweer, H.H.1    Ettema, K.W.A.2    Hiemstra, H.3    Spekamp, W.4
  • 157
    • 0032576117 scopus 로고    scopus 로고
    • A Novel Synthesis of α-Amino Acid Derivatives Through Catalytic, Enantioselective Ene Reactions of a-Imino Acids
    • Drury, w.J. III, Ferraris, D., Cox, C, Young, B., Lectka, T., A Novel Synthesis of α-Amino Acid Derivatives Through Catalytic, Enantioselective Ene Reactions of a-Imino Acids. J. Am. Chem. Soc. 120 (1998), 11006–11007.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 11006-11007
    • Drury, W.J.1    Ferraris, D.2    Cox, C.3    Young, B.4    Lectka, T.5
  • 158
    • 0032556461 scopus 로고    scopus 로고
    • A. Catalytic Enantioselective Ene Reaction of Imines: A Simple Approach for the Formation of Optically Active α-Amino Acids
    • Yao, S., Fang, X., Jørgensen, K., A. Catalytic Enantioselective Ene Reaction of Imines: A Simple Approach for the Formation of Optically Active α-Amino Acids. Chem. Commun., 1998, 2547–2548.
    • (1998) Chem. Commun. , pp. 2547-2548
    • Yao, S.1    Fang, X.2    Jørgensen, K.3
  • 159
    • 0033603563 scopus 로고    scopus 로고
    • A. Catalytic Approach for the Formation of Optically Active Allyl a-Amino Acids by Addition of Allylic Metal Compounds to oc-Imino Esters
    • Fang, X., Johannsen, M., Yao, S., Gathergood, N., Hazell, r.G., Jorgensen, K., A. Catalytic Approach for the Formation of Optically Active Allyl a-Amino Acids by Addition of Allylic Metal Compounds to oc-Imino Esters. J. Org. Chem 64 (1999), 4844–4849.
    • (1999) J. Org. Chem , vol.64 , pp. 4844-4849
    • Fang, X.1    Johannsen, M.2    Yao, S.3    Gathergood, N.4    Hazell, R.G.5    Jorgensen, K.6
  • 160
    • 84918022463 scopus 로고
    • Über Die Kunstlische Bildung Der Milchsaure Und Einen Neuen, Dem Glycocoll Homologen Korper
    • Strecker, A., Über Die Kunstlische Bildung Der Milchsaure Und Einen Neuen, Dem Glycocoll Homologen Korper. Liebigs Ann. Chem. 75 (1850), 27–51.
    • (1850) Liebigs Ann. Chem. , vol.75 , pp. 27-51
    • Strecker, A.1
  • 161
    • 0000491795 scopus 로고
    • Asymmetric Synthesis of α-Amino-Acids by the Strecker Synthesis
    • Harada, K., Asymmetric Synthesis of α-Amino-Acids by the Strecker Synthesis. Nature, 200, 1963, 1201.
    • (1963) Nature , vol.200 , pp. 1201
    • Harada, K.1
  • 162
    • 0000234486 scopus 로고
    • Asymmetric Synthesis of Optically Active α-Amino Acids by Hydrocyanic Acid Addition to the Optically Active Schiff Base
    • Patel, m.S., Worsley, M., Asymmetric Synthesis of Optically Active α-Amino Acids by Hydrocyanic Acid Addition to the Optically Active Schiff Base. Can. J. Chem. 48 (1969), 1881–1884.
    • (1969) Can. J. Chem. , vol.48 , pp. 1881-1884
    • Patel, M.S.1    Worsley, M.2
  • 163
    • 0013563855 scopus 로고
    • T. Asymmetric Synthesis of α-Amino Acids
    • Phadtare, s.K., Kamat, s.K., Panse, G., T. Asymmetric Synthesis of α-Amino Acids. Ind. J. Chem. 24B (1985), 811–814.
    • (1985) Ind. J. Chem. , vol.24B , pp. 811-814
    • Phadtare, S.K.1    Kamat, S.K.2    Panse, G.3
  • 164
    • 84982059219 scopus 로고
    • Herstellung Optisch Aktiver Aminonitrile
    • Weinges, K., Blackholm, H., Herstellung Optisch Aktiver Aminonitrile. Chem. Ber. 113 (1980), 3098–3102.
    • (1980) Chem. Ber. , vol.113 , pp. 3098-3102
    • Weinges, K.1    Blackholm, H.2
  • 165
    • 84986714223 scopus 로고
    • Carbohydrates as Chiral Templates: Stereoselective Strecker Synthesis of D-α-Amino Nitriles and Acids Using O-Pivaloylated D-Galactosylamine as the Auxiliar
    • Kunz, H., Sager, W., Schanzenbach, D., Decker, M., Carbohydrates as Chiral Templates: Stereoselective Strecker Synthesis of D-α-Amino Nitriles and Acids Using O-Pivaloylated D-Galactosylamine as the Auxiliar. Liebigs Ann. Chem, 1991, 645–654.
    • (1991) Liebigs Ann. Chem , pp. 645-654
    • Kunz, H.1    Sager, W.2    Schanzenbach, D.3    Decker, M.4
  • 166
    • 0000297984 scopus 로고
    • An Efficient and Practical Synthesis f L-α-Amino Acids Using (R)-Phenylglycinol as a Chiral Auxiliary
    • Inaba, T., Kzono, I., Fujita, M., Ogura, K., An Efficient and Practical Synthesis f L-α-Amino Acids Using (R)-Phenylglycinol as a Chiral Auxiliary. Bull. Chem. Soc. Jpn. 65 (1992), 2359–2365.
    • (1992) Bull. Chem. Soc. Jpn. , vol.65 , pp. 2359-2365
    • Inaba, T.1    Kzono, I.2    Fujita, M.3    Ogura, K.4
  • 167
    • 0026317432 scopus 로고
    • A. Diastereoselective Strecker Synthesis Using α-Phenylglycinol as Chiral Auxiliary
    • Chakraborty, t.K., Reddy, g.V., Hussain, K., A. Diastereoselective Strecker Synthesis Using α-Phenylglycinol as Chiral Auxiliary. Tetrahedron Lett. 32 (1991), 7597–7600.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 7597-7600
    • Chakraborty, T.K.1    Reddy, G.V.2    Hussain, K.3
  • 168
    • 0029164282 scopus 로고
    • a-Phenylglycinol as Chiral Auxiliary in Diastereoselective Strecker Synthesis of α-Amino Acids
    • Chakraborty, t.K., Hussain, k.A., Reddy, g.V., a-Phenylglycinol as Chiral Auxiliary in Diastereoselective Strecker Synthesis of α-Amino Acids. Tetrahedron 57 (1995), 9179–9190.
    • (1995) Tetrahedron , vol.57 , pp. 9179-9190
    • Chakraborty, T.K.1    Hussain, K.A.2    Reddy, G.V.3
  • 169
    • 0032358630 scopus 로고    scopus 로고
    • Asymmetric Synthesis of Amino Acids Using Sulfinimines
    • (Thiooxime S-Oxides)
    • (Thiooxime S-Oxides)Davis, f.A., Zhou, P., Chen, B.-C., Asymmetric Synthesis of Amino Acids Using Sulfinimines. Chem. Soc. Rev. 27 (1998), 13–18.
    • (1998) Chem. Soc. Rev. , vol.27 , pp. 13-18
    • Davis, F.A.1    Zhou, P.2    Chen, B.-C.3
  • 170
    • 0032924621 scopus 로고    scopus 로고
    • Concise Asymmetric Synthesis of a-Amino Acid Derivatives from N-Sulfinylimino Esters
    • Davis, f.A., McCoull, W., Concise Asymmetric Synthesis of a-Amino Acid Derivatives from N-Sulfinylimino Esters. J. Org. Chem. 64 (1999), 3396–3397.
    • (1999) J. Org. Chem. , vol.64 , pp. 3396-3397
    • Davis, F.A.1    McCoull, W.2
  • 171
    • 0028147247 scopus 로고    scopus 로고
    • Asymmetric Strecker Synthesis Using Enantiopure Sulfinimines: A Convenient Synthesis of a-Amino Acids
    • Davis, f.A., Reddy, r.E., Portonovo, p.S., Asymmetric Strecker Synthesis Using Enantiopure Sulfinimines: A Convenient Synthesis of a-Amino Acids. Tetrahedron Lett. 35 (1998), 9351–9354.
    • (1998) Tetrahedron Lett. , vol.35 , pp. 9351-9354
    • Davis, F.A.1    Reddy, R.E.2    Portonovo, P.S.3
  • 172
    • 0032549501 scopus 로고    scopus 로고
    • Sulfinimine-Mediated Asymmetric Synthesis of (R)- (4-Methoxy-3, 5-Dihydroxyphenyl)Glycine: The Central Amino Acid of Vancomycin and Related Agents
    • Davis, f.A., Fanelli, d.A., Sulfinimine-Mediated Asymmetric Synthesis of (R)- (4-Methoxy-3, 5-Dihydroxyphenyl)Glycine: The Central Amino Acid of Vancomycin and Related Agents. J. Org. Chem. 63 (1998), 1981–1985.
    • (1998) J. Org. Chem. , vol.63 , pp. 1981-1985
    • Davis, F.A.1    Fanelli, D.A.2
  • 173
    • 0032694974 scopus 로고    scopus 로고
    • Use of Acylhydrazones as Stable Surrogates of Unstable Imines in Allylation, Mannich-Type, and Cyanide Addition Reactions
    • Manabe, K., Oyamada, H., Sugita, K., Kobayashi, S., Use of Acylhydrazones as Stable Surrogates of Unstable Imines in Allylation, Mannich-Type, and Cyanide Addition Reactions. J. Org. Chem. 64 (1999), 8054–8057.
    • (1999) J. Org. Chem. , vol.64 , pp. 8054-8057
    • Manabe, K.1    Oyamada, H.2    Sugita, K.3    Kobayashi, S.4
  • 174
    • 0029990874 scopus 로고    scopus 로고
    • Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide
    • Iyer, m.S., Gigstad, k.M., Namdev, n.D., Lipton, M., Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide. Amino Acids 11 (1996), 259–268.
    • (1996) Amino Acids , vol.11 , pp. 259-268
    • Iyer, M.S.1    Gigstad, K.M.2    Namdev, N.D.3    Lipton, M.4
  • 175
    • 0029990764 scopus 로고    scopus 로고
    • Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide
    • Iyer, m.S., Gigstad, k.M, Namdev, n.D., Lipton, M., Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide. J. Am. Chem. Soc. 775 (1996), 4910–4911.
    • (1996) J. Am. Chem. Soc. , vol.775 , pp. 4910-4911
    • Iyer, M.S.1    Gigstad, K.M.2    Namdev, N.D.3    Lipton, M.4
  • 177
    • 0003554758 scopus 로고    scopus 로고
    • Schiff Base Catalysts for the Asymmetric Strecker Reaction Identified and Optimized from Parallel Synthetic Libraries
    • Sigman, m.S., Jacobsen, e.N., Schiff Base Catalysts for the Asymmetric Strecker Reaction Identified and Optimized from Parallel Synthetic Libraries. J. Am. Chem. Soc. 120 (1998), 4901–4902.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 4901-4902
    • Sigman, M.S.1    Jacobsen, E.N.2
  • 178
    • 0034704642 scopus 로고    scopus 로고
    • Enantioselective Catalytic Addition of HCN to Ketoimines. Catalytic Synthesis of Quaternary Amino Acids
    • Vachal, P., Jacobsen, e.N., Enantioselective Catalytic Addition of HCN to Ketoimines. Catalytic Synthesis of Quaternary Amino Acids. Org. Lett. 2 (2000), 867–870.
    • (2000) Org. Lett. , vol.2 , pp. 867-870
    • Vachal, P.1    Jacobsen, E.N.2
  • 179
    • 0033564990 scopus 로고    scopus 로고
    • Enantioselective Synthesis of a-Amino Nitriles from N-Benzhydryl Imines and HCN with a Chiral Bicyclic Guanidine as Catalyst
    • Corey, e.J., Grogan, m.J., Enantioselective Synthesis of a-Amino Nitriles from N-Benzhydryl Imines and HCN with a Chiral Bicyclic Guanidine as Catalyst. Org. Lett. 1 (1999), 157–160.
    • (1999) Org. Lett. , vol.1 , pp. 157-160
    • Corey, E.J.1    Grogan, M.J.2
  • 180
    • 0032479019 scopus 로고    scopus 로고
    • Enantioselective Addition of Hydrogen Cyanide to Imines Catalyzed by a Chiral (Salen)Al(III) Complex
    • Sigman, m.S., Jacobsen, e.N., Enantioselective Addition of Hydrogen Cyanide to Imines Catalyzed by a Chiral (Salen)Al(III) Complex. J. Am. Chem. Soc. 120 (1998), 5315–5316.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5315-5316
    • Sigman, M.S.1    Jacobsen, E.N.2
  • 181
    • 0033526392 scopus 로고    scopus 로고
    • Ti-Catalyzed Enantioselective Addition of Cyanide to Imines. A Practical Synthesis of Optically Pure a-Amino Acids
    • Krueger, c.A., Kuntz, k.W., Dzierba, c.D., Wirschun, w.G., Gleason, j.D., Snapper, m.L., Hoveyda, a.H., Ti-Catalyzed Enantioselective Addition of Cyanide to Imines. A Practical Synthesis of Optically Pure a-Amino Acids. J. Am. Chem. Soc. 121 (1999), 4284–4285.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 4284-4285
    • Krueger, C.A.1    Kuntz, K.W.2    Dzierba, C.D.3    Wirschun, W.G.4    Gleason, J.D.5    Snapper, M.L.6    Hoveyda, A.H.7
  • 182
    • 0032484050 scopus 로고    scopus 로고
    • Catalytic, of α-Aminonitriles with a Novel Zirconium Catalyst. Enantioselective Synthesis Angew
    • Ishitani, H., Komiyama, S., Kobayashi, S., Catalytic, of α-Aminonitriles with a Novel Zirconium Catalyst. Enantioselective Synthesis Angew. Chem. Int. Ed. Engl. 122 (1998), 3186–3188.
    • (1998) Chem. Int. Ed. Engl. , vol.122 , pp. 3186-3188
    • Ishitani, H.1    Komiyama, S.2    Kobayashi, S.3
  • 183
    • 0034624418 scopus 로고    scopus 로고
    • Catalytic Asymmetric trecker Synthesis. Preparation of Enantiomerically Pure a-Amino Acid Derivatives from Aldimines and Tributyltin Cyanide or Achiral Aldehy
    • Ishitani, H., Komiyama, S., Hasegawa, Y., Kobayashi, S., Catalytic Asymmetric trecker Synthesis. Preparation of Enantiomerically Pure a-Amino Acid Derivatives from Aldimines and Tributyltin Cyanide or Achiral Aldehy. J. Am. Chem. Soc 122 (2000), 762–766.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 762-766
    • Ishitani, H.1    Komiyama, S.2    Hasegawa, Y.3    Kobayashi, S.4
  • 184
    • 0031980938 scopus 로고    scopus 로고
    • The First Enantioselective Aza-Diels - Alder Reactions of Imino Dienophiles on Use of a Chiral Zirconium Catalyst
    • Kobayashi, S., Komiyama, S., Ishitani, H., The First Enantioselective Aza-Diels - Alder Reactions of Imino Dienophiles on Use of a Chiral Zirconium Catalyst. Angew. Chem., Int. Ed. Engl., 37, 1998, 1998.
    • (1998) Angew. Chem., Int. Ed. Engl. , vol.37 , pp. 1998
    • Kobayashi, S.1    Komiyama, S.2    Ishitani, H.3
  • 185
    • 0030788354 scopus 로고    scopus 로고
    • Catalytic, Enantioselective Mannich-Type Reactions Using a Novel Chiral Zirconium Catalyst
    • Ishitani, H., Ueno, M., Kobayishi, S., Catalytic, Enantioselective Mannich-Type Reactions Using a Novel Chiral Zirconium Catalyst. J. Am. Chem. Soc. 119 (1997), 7153–7154.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 7153-7154
    • Ishitani, H.1    Ueno, M.2    Kobayishi, S.3
  • 186
    • 0032554058 scopus 로고    scopus 로고
    • Catalytic Asymmetric Synthesis of Both Syn- and Anti-(3-Amino Alcohols
    • Kobayashi, S., Ishitani, H., Ueno, M., Catalytic Asymmetric Synthesis of Both Syn- and Anti-(3-Amino Alcohols. J. Am. Chem. Soc. 120 (1998), 431–432.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 431-432
    • Kobayashi, S.1    Ishitani, H.2    Ueno, M.3
  • 187
    • 0034038496 scopus 로고    scopus 로고
    • Novel Binuclear Chiral Zirconium Catalysts Used in Enantioselective Strecker Reactions
    • Kobayashi, S., Ishitani, H., Novel Binuclear Chiral Zirconium Catalysts Used in Enantioselective Strecker Reactions. Chirality 12 (2000), 540–543.
    • (2000) Chirality , vol.12 , pp. 540-543
    • Kobayashi, S.1    Ishitani, H.2
  • 188
    • 0000293860 scopus 로고    scopus 로고
    • Asymmetric Synthesis of α, α-Disubstituted α-Amino Acids
    • Ohfune, Y., Moon, S.-H., Horikawa, M., Asymmetric Synthesis of α, α-Disubstituted α-Amino Acids. Pure Appl. Chem. 68 (1996), 645–648.
    • (1996) Pure Appl. Chem. , vol.68 , pp. 645-648
    • Ohfune, Y.1    Moon, S.-H.2    Horikawa, M.3
  • 189
    • 0032837567 scopus 로고    scopus 로고
    • Heteroatom Radical Addition-Cyclization and Its Synthetic Application
    • Naito, T., Heteroatom Radical Addition-Cyclization and Its Synthetic Application. Heterocycles 50 (1999), 505–541.
    • (1999) Heterocycles , vol.50 , pp. 505-541
    • Naito, T.1
  • 190
    • 0030666083 scopus 로고    scopus 로고
    • Free Radical Cyclizations Involving Nitrogen
    • Fallis, a.G., Brinza, i.M., Free Radical Cyclizations Involving Nitrogen. Tetrahedron 53 (1997), 17543–17594.
    • (1997) Tetrahedron , vol.53 , pp. 17543-17594
    • Fallis, A.G.1    Brinza, I.M.2
  • 191
    • 0032572888 scopus 로고    scopus 로고
    • Initiation of Tin-Mediated Radical Reactions by Diethylzinc-Air
    • Ryu, I., Araki, F., Minakata, S., Komatsu, M., Initiation of Tin-Mediated Radical Reactions by Diethylzinc-Air. Tetrahedron Lett. 39 (1998), 6335–6336.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 6335-6336
    • Ryu, I.1    Araki, F.2    Minakata, S.3    Komatsu, M.4
  • 192
    • 0032509938 scopus 로고    scopus 로고
    • Carbon-Carbon Bond Formation via Intermolecular Carbon Radical Addition to Aldoxime Ethers
    • Miyabe, H., Shibata, R., Ushiro, C, Naito, T., Carbon-Carbon Bond Formation via Intermolecular Carbon Radical Addition to Aldoxime Ethers. Tetrahedron Lett. 39 (1998), 631–634.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 631-634
    • Miyabe, H.1    Shibata, R.2    Ushiro, C.3    Naito, T.4
  • 193
    • 0028198198 scopus 로고
    • Zinc Chloride as a Radical Initiator as well as a Chelating Agent
    • Yamamoto, Y., Onuki, S., Yumoto, M., Asao, N., Zinc Chloride as a Radical Initiator as well as a Chelating Agent. J. Am. Chem. Soc. 116 (1994), 421–422.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 421-422
    • Yamamoto, Y.1    Onuki, S.2    Yumoto, M.3    Asao, N.4
  • 194
    • 0032894908 scopus 로고    scopus 로고
    • Carbon Radical Addition to Glyoxylic Oxime Ether via Iodine Atom-Transfer Process
    • Miyabe, H., Ueda, M., Yoshioka, N., Naito, T., Carbon Radical Addition to Glyoxylic Oxime Ether via Iodine Atom-Transfer Process. Synlett, 1999, 465–467.
    • (1999) Synlett , pp. 465-467
    • Miyabe, H.1    Ueda, M.2    Yoshioka, N.3    Naito, T.4
  • 195
    • 0033515460 scopus 로고    scopus 로고
    • Novel Synthesis of α-Amino Acid Derivatives Through Triethylborane-Induced Solid-Phase Radical Reactions
    • Miyabe, H., Fujishima, Y., Naito, T., Novel Synthesis of α-Amino Acid Derivatives Through Triethylborane-Induced Solid-Phase Radical Reactions. J. Org. Chem. 64 (1999), 2174–2175.
    • (1999) J. Org. Chem. , vol.64 , pp. 2174-2175
    • Miyabe, H.1    Fujishima, Y.2    Naito, T.3
  • 196
    • 0032784299 scopus 로고    scopus 로고
    • Diethylzinc: A Chain- Transfer Agent in Intermolecular Radical Additions. A Parallel with Triethyl- borane
    • Bertrand, m.P., Feray, L., Nouguier, R., Perfetti, P., Diethylzinc: A Chain- Transfer Agent in Intermolecular Radical Additions. A Parallel with Triethyl- borane. J. Org. Chem. 64 (1999), 9189–9193.
    • (1999) J. Org. Chem. , vol.64 , pp. 9189-9193
    • Bertrand, M.P.1    Feray, L.2    Nouguier, R.3    Perfetti, P.4
  • 197
    • 0032796594 scopus 로고    scopus 로고
    • Diethyl Zinc-Mediated Radical Additions to Glyoxylate Imines
    • Bertrand, m.P., Feray, L., Nouguier, R., Perfetti, P., Diethyl Zinc-Mediated Radical Additions to Glyoxylate Imines. Synlett, 1999, 1148–1150.
    • (1999) Synlett , pp. 1148-1150
    • Bertrand, M.P.1    Feray, L.2    Nouguier, R.3    Perfetti, P.4
  • 198
    • 33748731177 scopus 로고    scopus 로고
    • One-Pot Synthesis of a-Amino Acids Based on Free Radical-Mediated Carbon-Carbon Bond Formation
    • Miyabe, H., Yoshioka, N., Ueda, M., Naito, T., One-Pot Synthesis of a-Amino Acids Based on Free Radical-Mediated Carbon-Carbon Bond Formation. J. Chem. Soc, Perkin Trans. 1 (1998), 3659–3660.
    • (1998) J. Chem. Soc, Perkin Trans. , vol.1 , pp. 3659-3660
    • Miyabe, H.1    Yoshioka, N.2    Ueda, M.3    Naito, T.4
  • 199
    • 0033607738 scopus 로고    scopus 로고
    • Triethylborane-Induced Solid-Phase Radical Cyclization of Oxime Ethers
    • Miyabe, H., Tanaka, H., Naito, T., Triethylborane-Induced Solid-Phase Radical Cyclization of Oxime Ethers. Tetrahedron Lett. 40 (1999), 3887–3890.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 3887-3890
    • Miyabe, H.1    Tanaka, H.2    Naito, T.3
  • 200
    • 0034646774 scopus 로고    scopus 로고
    • Reactions of Alkyl Radicals with Oxime Ether: One-Pot Synthesis of α-Amino Acids
    • Miyabe, H., Ueda, M., Yoshioka, N., Yamakawa, K., Naito, T., Reactions of Alkyl Radicals with Oxime Ether: One-Pot Synthesis of α-Amino Acids. Tetrahedron 56 (2000), 2413–2420.
    • (2000) Tetrahedron , vol.56 , pp. 2413-2420
    • Miyabe, H.1    Ueda, M.2    Yoshioka, N.3    Yamakawa, K.4    Naito, T.5
  • 201
    • 0001342149 scopus 로고    scopus 로고
    • 1, 3-Stereoinduction in Radical Additions to Glyoxylate Imines
    • Bertrand, m.P., Feray, L., Nouguier, R., Stella, L., 1, 3-Stereoinduction in Radical Additions to Glyoxylate Imines. Synlett, 1998, 780–782.
    • (1998) Synlett , pp. 780-782
    • Bertrand, M.P.1    Feray, L.2    Nouguier, R.3    Stella, L.4
  • 202
    • 0032796594 scopus 로고    scopus 로고
    • Diethylzinc Mediated Radical Additions to Glyoxylate Imines
    • Bertrand, m.P., Feray, L., Nouguier, R., Perfetti, P., Diethylzinc Mediated Radical Additions to Glyoxylate Imines. Synlett 7 (1999), 1148–1150.
    • (1999) Synlett , vol.7 , pp. 1148-1150
    • Bertrand, M.P.1    Feray, L.2    Nouguier, R.3    Perfetti, P.4
  • 203
    • 0002047232 scopus 로고    scopus 로고
    • Highly Diastereoselective Radical Addition to Glyoxylic Oxime Ether: Asymmetric Synthesis of a-Amino Acids
    • Miyabe, H., Ushiro, C, Naito, T., Highly Diastereoselective Radical Addition to Glyoxylic Oxime Ether: Asymmetric Synthesis of a-Amino Acids. Chem. Commun. (Cambridge), 1997, 1789–1790.
    • (1997) Chem. Commun. (Cambridge) , pp. 1789-1790
    • Miyabe, H.1    Ushiro, C.2    Naito, T.3
  • 204
    • 0030598086 scopus 로고    scopus 로고
    • The Asymmetric Synthesis of Allylglycine and Other Unnatural a-Amino Acids via Zinc Mediated Allylation of Oximes iun Aqueous Media
    • Hanessian, S., Yang, R.-Y., The Asymmetric Synthesis of Allylglycine and Other Unnatural a-Amino Acids via Zinc Mediated Allylation of Oximes iun Aqueous Media. Tetrahedron Lett. 37 (1996), 5273–5376.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 5273-5376
    • Hanessian, S.1    Yang, R.-Y.2
  • 205
    • 0033515460 scopus 로고    scopus 로고
    • Novel Synthesis of a-Amino Acid Derivatives through Triethylborane-Induced Solid-Phase Radical Reactions
    • Miyabe, H., Fujishima, Y., Naito, T., Novel Synthesis of a-Amino Acid Derivatives through Triethylborane-Induced Solid-Phase Radical Reactions. J. Org. Chem. 64 (1999), 2174–2175.
    • (1999) J. Org. Chem. , vol.64 , pp. 2174-2175
    • Miyabe, H.1    Fujishima, Y.2    Naito, T.3
  • 206
    • 0033607738 scopus 로고    scopus 로고
    • Triethylborane-Induced Solid-Phase Radical Cyclization of Oxime Ethers
    • Miyabe, H., Tanaka, H., Naito, T., Triethylborane-Induced Solid-Phase Radical Cyclization of Oxime Ethers. Tetrahedron Lett. 40 (1999), 8387–8390.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 8387-8390
    • Miyabe, H.1    Tanaka, H.2    Naito, T.3
  • 207
    • 0000500365 scopus 로고    scopus 로고
    • Stereocontrol in Solid-Phase Radical Reactions: Radical Addition to Oxime Ether Anchored to Polymer Support
    • Miyabe, H., Konishi, C, Naito, T., Stereocontrol in Solid-Phase Radical Reactions: Radical Addition to Oxime Ether Anchored to Polymer Support. Org. Lett. 2 (2000), 1443–1445.
    • (2000) Org. Lett. , vol.2 , pp. 1443-1445
    • Miyabe, H.1    Konishi, C.2    Naito, T.3
  • 208
    • 0033966817 scopus 로고    scopus 로고
    • Asymmetric Synthesis of a-Amino Acids Based on Carbon Radical Addition to Glyoxylic Oxime Ether
    • Miyabe, H., Ushiro, C, Ueda, M., Yamakawa, K., Naito, T., Asymmetric Synthesis of a-Amino Acids Based on Carbon Radical Addition to Glyoxylic Oxime Ether. J. Org. Chem. 65 (2000), 176–185.
    • (2000) J. Org. Chem. , vol.65 , pp. 176-185
    • Miyabe, H.1    Ushiro, C.2    Ueda, M.3    Yamakawa, K.4    Naito, T.5
  • 209
    • 85022996313 scopus 로고
    • Carbon-Carbon Bonding of Carboxylic Acids with Allyl Alcohols Using 2-Phenylglycine as Vehicle
    • Engel, N., Kübel, B., Steglich, W., Carbon-Carbon Bonding of Carboxylic Acids with Allyl Alcohols Using 2-Phenylglycine as Vehicle. Angew. Chem., Int. Ed. Engl 27 (1911), 848–850.
    • (1911) Angew. Chem., Int. Ed. Engl , vol.27 , pp. 848-850
    • Engel, N.1    Kübel, B.2    Steglich, W.3
  • 210
    • 84982349429 scopus 로고
    • Hetero Cope Rearrangement in the Cyclization of N-Acymino Acid Allyl and Propargyl Esters in 5-Oxazolinones
    • Kübel, B., Höfle, G., Steglich, W., Hetero Cope Rearrangement in the Cyclization of N-Acymino Acid Allyl and Propargyl Esters in 5-Oxazolinones. Angew. Chem., Int. Ed. Engl. 14 (1975), 58–60.
    • (1975) Angew. Chem., Int. Ed. Engl. , vol.14 , pp. 58-60
    • Kübel, B.1    Höfle, G.2    Steglich, W.3
  • 211
    • 33751500165 scopus 로고
    • Stereoselective Synthesis of C-Glycosyl α-Amino Acids
    • Colombo, L., Casiraghi, G., Pittalis, A., Rassu, G., Stereoselective Synthesis of C-Glycosyl α-Amino Acids. J. Org. Chem. 56 (1991), 3897–3900.
    • (1991) J. Org. Chem. , vol.56 , pp. 3897-3900
    • Colombo, L.1    Casiraghi, G.2    Pittalis, A.3    Rassu, G.4
  • 212
    • 0000718669 scopus 로고
    • Ester-Enolate Claisen Rearrangement of a-Amino Acid Derivatives
    • Bartlett, p.A., Barstow, j.F., Ester-Enolate Claisen Rearrangement of a-Amino Acid Derivatives. J. Org. Chem. 47 (1982), 3933–3941.
    • (1982) J. Org. Chem. , vol.47 , pp. 3933-3941
    • Bartlett, P.A.1    Barstow, J.F.2
  • 213
    • 0001799508 scopus 로고
    • A Stereoselective Method for the Generation of Aldol-Type Systems
    • Ireland, r.E., Wilcox, c.S., A Stereoselective Method for the Generation of Aldol-Type Systems. Tetrahedron Lett. 33 (1977), 2839–2842.
    • (1977) Tetrahedron Lett. , vol.33 , pp. 2839-2842
    • Ireland, R.E.1    Wilcox, C.S.2
  • 214
    • 33847799798 scopus 로고
    • The Ester Enolate Claisen Re-arrangement. Stereochemical Control Through Stereoselective Enolate Formation
    • Ireland, r.E., Müller, r.H., Willard, a.K., The Ester Enolate Claisen Re-arrangement. Stereochemical Control Through Stereoselective Enolate Formation. J. Am. Chem. Soc. 98 (1976), 2868–2877.
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 2868-2877
    • Ireland, R.E.1    Müller, R.H.2    Willard, A.K.3
  • 215
    • 85023125839 scopus 로고
    • Kinetics and Stereochemical Course of the Thermal Rearrangement of the Four Stereoisomers of But-2′-Enyl Ether
    • Vittorelli, P., Hansen, H.-J., Schmid, H., Kinetics and Stereochemical Course of the Thermal Rearrangement of the Four Stereoisomers of But-2′-Enyl Ether. Helv. Chim. Acta 58 (1915), 1293–1309.
    • (1915) Helv. Chim. Acta , vol.58 , pp. 1293-1309
    • Vittorelli, P.1    Hansen, H.-J.2    Schmid, H.3
  • 217
    • 0000055357 scopus 로고
    • Stereoselective Synthesis of 2-(2′-Cycloalkenyl)Glycinates via Ester-Enolate Claisen Rearrangement
    • Bartlett, p.A., Barstow, j.F., Stereoselective Synthesis of 2-(2′-Cycloalkenyl)Glycinates via Ester-Enolate Claisen Rearrangement. Tetrahedron Lett. 23 (1982), 623–626.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 623-626
    • Bartlett, P.A.1    Barstow, J.F.2
  • 218
    • 33748826144 scopus 로고
    • Synthesis of Unsaturated Amino Acids by [3, 3]-Sigmatropic Rearrangement of Chelate-Bridged Glycine Ester Enolates
    • Kazmaier, U., Synthesis of Unsaturated Amino Acids by [3, 3]-Sigmatropic Rearrangement of Chelate-Bridged Glycine Ester Enolates. Angew. Chem., Int. Ed. Engl. 33 (1994), 998–999.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 998-999
    • Kazmaier, U.1
  • 219
    • 21044443170 scopus 로고    scopus 로고
    • Asymmetric Synthesis of Unsaturated Amino Acids and Peptides via Chelate-Enolate Claisen Rearrangements
    • Kazmaier, U., Asymmetric Synthesis of Unsaturated Amino Acids and Peptides via Chelate-Enolate Claisen Rearrangements. J. Ind. Chem. Soc. 76 (1999), 631–639.
    • (1999) J. Ind. Chem. Soc. , vol.76 , pp. 631-639
    • Kazmaier, U.1
  • 220
    • 33748837205 scopus 로고    scopus 로고
    • Application of the Chelate-Enolate Claisen Rearrangement to the Synthesis of γ, δ-Unsaturated Amino Acids
    • Kazmaier, U., Application of the Chelate-Enolate Claisen Rearrangement to the Synthesis of γ, δ-Unsaturated Amino Acids. Liebigs Ann. Recl., 1997, 285–295.
    • (1997) Liebigs Ann. Recl. , pp. 285-295
    • Kazmaier, U.1
  • 221
    • 0029857855 scopus 로고    scopus 로고
    • Synthesis of χ, δ-Unsaturated Amino Acids via Ester Enolate Claisen Rearrangement of Chelated Allylic Esters
    • Kazmaier, U., Synthesis of χ, δ-Unsaturated Amino Acids via Ester Enolate Claisen Rearrangement of Chelated Allylic Esters. Amino Acids 11 (1996), 283–299.
    • (1996) Amino Acids , vol.11 , pp. 283-299
    • Kazmaier, U.1
  • 222
    • 0002325951 scopus 로고
    • Amino Acids and Peptides, XLIII
    • Dehydroamino Acids, XVIII. Synthesis of Dehydroamino Acids and Amino Acids from N-Acyl-2-(Dialkyloxyphosphinyl)Glycine Esters, II
    • Dehydroamino Acids, XVIII. Synthesis of Dehydroamino Acids and Amino Acids from N-Acyl-2-(Dialkyloxyphosphinyl)Glycine Esters, IISchmidt, U., Lieberknecht, A., Wild, J., Amino Acids and Peptides, XLIII. Synthesis 1 (1984), 53–60.
    • (1984) Synthesis , vol.1 , pp. 53-60
    • Schmidt, U.1    Lieberknecht, A.2    Wild, J.3
  • 223
    • 37049067667 scopus 로고
    • Stereoselective Synthesis of α-Alkylated γ, δ-Unsaturated Amino Acids via Claisen Rearrangement of Chelated Enolates
    • Kazmaier, U., Maier, S., Stereoselective Synthesis of α-Alkylated γ, δ-Unsaturated Amino Acids via Claisen Rearrangement of Chelated Enolates. J. Chem. Soc, Chem. Commun., 1995, 1991–1992.
    • (1995) J. Chem. Soc, Chem. Commun. , pp. 1991-1992
    • Kazmaier, U.1    Maier, S.2
  • 224
    • 0002683860 scopus 로고
    • Diastereoselective Synthesis of Amino Acids Containing β-Quaternary Carbon Centers via Ester Enolate Claisen Rearrangement
    • Kazmaier, U., Diastereoselective Synthesis of Amino Acids Containing β-Quaternary Carbon Centers via Ester Enolate Claisen Rearrangement. Synlett, 1995, 1138–1140.
    • (1995) Synlett , pp. 1138-1140
    • Kazmaier, U.1
  • 225
    • 0030598033 scopus 로고    scopus 로고
    • Synthesis of Quaternary Amino Acids Containing β, γ- as well as γ, 5-Unsaturated Side Chains via Chelate-Enolate Claisen Rearrangement
    • Kazmaier, U., Synthesis of Quaternary Amino Acids Containing β, γ- as well as γ, 5-Unsaturated Side Chains via Chelate-Enolate Claisen Rearrangement. Tetrahedron Lett. 37 (1996), 5351–5354.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 5351-5354
    • Kazmaier, U.1
  • 226
    • 0030457755 scopus 로고    scopus 로고
    • Synthesis of Allenic Amino Acids via Chelate-Controlled Ester Enolate Claisen Rearrangement
    • Kazmaier, U., Gorbitz, c.H., Synthesis of Allenic Amino Acids via Chelate-Controlled Ester Enolate Claisen Rearrangement. Synthesis 12 (1996), 1489–1493.
    • (1996) Synthesis , vol.12 , pp. 1489-1493
    • Kazmaier, U.1    Gorbitz, C.H.2
  • 227
    • 21044451417 scopus 로고    scopus 로고
    • Chemoselective Claisen Rearrangement of Amino Acid Esters of Enynols
    • Zumpe, f.L., Kazmaier, U., Chemoselective Claisen Rearrangement of Amino Acid Esters of Enynols. Synlett 4 (1998), 434–436.
    • (1998) Synlett , vol.4 , pp. 434-436
    • Zumpe, F.L.1    Kazmaier, U.2
  • 228
    • 0030200756 scopus 로고    scopus 로고
    • Asymmetric [3, 3]-Sigmatropic Rearrangements in Organic Synthesis
    • Enders, D., Knopp, M., Schiffers, R., Asymmetric [3, 3]-Sigmatropic Rearrangements in Organic Synthesis. Tetrahedron: Asymmetry 7 (1996), 1847–1882.
    • (1996) Tetrahedron: Asymmetry , vol.7 , pp. 1847-1882
    • Enders, D.1    Knopp, M.2    Schiffers, R.3
  • 229
    • 0002172075 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Unsaturated Poly-hydroxylated Amino Acids via Ester Enolate Claisen Rearrangement
    • Kazmaier, U., Schneider, C., Stereoselective Synthesis of Unsaturated Poly-hydroxylated Amino Acids via Ester Enolate Claisen Rearrangement. Synlett 10 (1996), 975–977.
    • (1996) Synlett , vol.10 , pp. 975-977
    • Kazmaier, U.1    Schneider, C.2
  • 230
    • 0031706012 scopus 로고    scopus 로고
    • Application of the Asymmetric Chelate Enolate Claisen Rearrangement to the Synthesis of Unsaturated Polyhydroxylated Amino Acids
    • Kazmaier, U., Schneider, C., Application of the Asymmetric Chelate Enolate Claisen Rearrangement to the Synthesis of Unsaturated Polyhydroxylated Amino Acids. Synthesis 9 (1998), 1321–1326.
    • (1998) Synthesis , vol.9 , pp. 1321-1326
    • Kazmaier, U.1    Schneider, C.2
  • 231
    • 0032546143 scopus 로고    scopus 로고
    • Application of the Asymmetric Chelate-Enolate Claisen Rearrangement to the Synthesis of 5-Epi-Isofagomine
    • Kazmaier, U., Schneider, C., Application of the Asymmetric Chelate-Enolate Claisen Rearrangement to the Synthesis of 5-Epi-Isofagomine. Tetrahedron Lett. 39 (1998), 817–818.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 817-818
    • Kazmaier, U.1    Schneider, C.2
  • 232
    • 0003122728 scopus 로고    scopus 로고
    • Synthesis of 5-Epi-Isofagomine via Asymmetric Chelate-Enolate Claisen Rearrangement
    • Schneider, C, Kazmaier, U., Synthesis of 5-Epi-Isofagomine via Asymmetric Chelate-Enolate Claisen Rearrangement. Eur. J. Org. Chem., 1998, 1159.
    • (1998) Eur. J. Org. Chem. , pp. 1159
    • Schneider, C.1    Kazmaier, U.2
  • 234
    • 0030889520 scopus 로고    scopus 로고
    • Chemoenzymic Synthesis of Unnatural Amino Acids via Modified Claisen Rearrangement of Glycine Enolates. Approach to Morphine Synthesis
    • González, D., Schapiro, V., Seoane, G., Hudlicky, T., Abboud, K., Chemoenzymic Synthesis of Unnatural Amino Acids via Modified Claisen Rearrangement of Glycine Enolates. Approach to Morphine Synthesis. J. Org. Chem. 62 (1997), 1194–1195.
    • (1997) J. Org. Chem. , vol.62 , pp. 1194-1195
    • González, D.1    Schapiro, V.2    Seoane, G.3    Hudlicky, T.4    Abboud, K.5
  • 235
    • 0001846314 scopus 로고    scopus 로고
    • Enzymatic Dihydroxylation of Aromatics in Enantioselective Synthesis: Expanding Asymmetric Methodology
    • Hudlicky, T., González, D., Gibson, d.T., Enzymatic Dihydroxylation of Aromatics in Enantioselective Synthesis: Expanding Asymmetric Methodology. Aldrichimica Acta 32 (1999), 35–62.
    • (1999) Aldrichimica Acta , vol.32 , pp. 35-62
    • Hudlicky, T.1    González, D.2    Gibson, D.T.3
  • 236
    • 0035848410 scopus 로고    scopus 로고
    • Chemoenzymatic Synthesis of Functionalized Cyclohexyl-Glycines and - Alanines via Kazmeier-Claisen Rearrangement
    • Hudlicky, T., Oppong, K., Duan, C, Stanton, C, Natchus, m.G., Laufersweiler, m.J., Chemoenzymatic Synthesis of Functionalized Cyclohexyl-Glycines and - Alanines via Kazmeier-Claisen Rearrangement. Bioorg. Med. Chem. Lett., 11, 2001, 627.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 627
    • Hudlicky, T.1    Oppong, K.2    Duan, C.3    Stanton, C.4    Natchus, M.G.5    Laufersweiler, M.J.6
  • 237
    • 0032556448 scopus 로고    scopus 로고
    • Application of the Chelate Enolate Claisen Rearrangement to the Modification of Dipeptides
    • Kazmaier, U., Maier, S., Application of the Chelate Enolate Claisen Rearrangement to the Modification of Dipeptides. J. Chem. Soc, Chem. Commun., 1998, 2535–2536.
    • (1998) J. Chem. Soc, Chem. Commun. , pp. 2535-2536
    • Kazmaier, U.1    Maier, S.2
  • 238
    • 0034051951 scopus 로고    scopus 로고
    • Modifications of Peptides by Chelate Claisen Rearrangements of Manganese Enolates
    • Maier, S., Kazmaier, U., Modifications of Peptides by Chelate Claisen Rearrangements of Manganese Enolates. Eur. J. Org. Chem., 2000, 1241–1251.
    • (2000) Eur. J. Org. Chem. , pp. 1241-1251
    • Maier, S.1    Kazmaier, U.2
  • 239
    • 0033603455 scopus 로고    scopus 로고
    • Stereoselective Backbone Modifications of Peptides via Chelate Enolate Claisen Rearrangement
    • Kazmaier, U., Maier, S., Stereoselective Backbone Modifications of Peptides via Chelate Enolate Claisen Rearrangement. J. Org. Chem. 64 (1999), 4574–4575.
    • (1999) J. Org. Chem. , vol.64 , pp. 4574-4575
    • Kazmaier, U.1    Maier, S.2
  • 240
    • 0032479389 scopus 로고    scopus 로고
    • Metal Complexes With Biologically Important Ligands, Part 100: Bioorganometallic Chemistry-Transition Metal Complexes With α-Amino Acids and Peptides
    • Severin, K., Bergs, R., Beck, W., Metal Complexes With Biologically Important Ligands, Part 100: Bioorganometallic Chemistry-Transition Metal Complexes With α-Amino Acids and Peptides. Angew. Chem. Int. Ed. Engl. 37 (1998), 1634–1654.
    • (1998) Angew. Chem. Int. Ed. Engl. , vol.37 , pp. 1634-1654
    • Severin, K.1    Bergs, R.2    Beck, W.3
  • 241
    • 0001477716 scopus 로고    scopus 로고
    • Application of the Peptide Claisen Rearrangement Toward the Synthesis of Cyclic Peptides
    • Kazmaier, U., Maier, S., Application of the Peptide Claisen Rearrangement Toward the Synthesis of Cyclic Peptides. Org. Lett. 1 (1999), 1763–1766.
    • (1999) Org. Lett. , vol.1 , pp. 1763-1766
    • Kazmaier, U.1    Maier, S.2
  • 242
    • 0242392462 scopus 로고
    • Asymmetric Claisen Rearrangement Catalyzed by Chiral Organoaluminum Reagent
    • Maruoka, K., Banno, H., Yamamoto, H., Asymmetric Claisen Rearrangement Catalyzed by Chiral Organoaluminum Reagent. J. Am. Chem. Soc. 112 (1990), 7791–7793.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 7791-7793
    • Maruoka, K.1    Banno, H.2    Yamamoto, H.3
  • 243
    • 0001681743 scopus 로고
    • Molecular Design of a Chiral Lewis Acid or the Asymmetric Claisen Rearrangement
    • Maruoka, K., Saito, S., Yamamoto, H., Molecular Design of a Chiral Lewis Acid or the Asymmetric Claisen Rearrangement. J. Am. Chem. Soc. 117 (1995), 1165–1166.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 1165-1166
    • Maruoka, K.1    Saito, S.2    Yamamoto, H.3
  • 244
    • 0001206985 scopus 로고
    • Highly Enantioselective and Diastereoselective Ireland- Claisen Rearrangement of Achiral Allylic Esters
    • Corey, e.J., Lee, d.H., Highly Enantioselective and Diastereoselective Ireland- Claisen Rearrangement of Achiral Allylic Esters. J. Am. Chem. Soc. 113 (1991), 4026–4028.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4026-4028
    • Corey, E.J.1    Lee, D.H.2
  • 245
    • 33748845721 scopus 로고
    • Synthesis of Chiral γ, δ-Unsaturated Amino Acids by Asymmetric Ester Enolate Claisen Rearrangement
    • Kazmaier, U., Krebs, A., Synthesis of Chiral γ, δ-Unsaturated Amino Acids by Asymmetric Ester Enolate Claisen Rearrangement. Angew. Chem., Int. Ed. Engl. 34 (1995), 2012–2014.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2012-2014
    • Kazmaier, U.1    Krebs, A.2
  • 246
    • 0033556135 scopus 로고    scopus 로고
    • A Straightforward Synthesis of Protected Isostatine from Achiral Precursors Using the Asymmetric Chelate Claisen Rearrangement
    • Kazmaier, U., Krebs, A., A Straightforward Synthesis of Protected Isostatine from Achiral Precursors Using the Asymmetric Chelate Claisen Rearrangement. Tetrahedron Lett. 40 (1999), 479–482.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 479-482
    • Kazmaier, U.1    Krebs, A.2
  • 247
    • 0030605051 scopus 로고    scopus 로고
    • The Asymmetric Ester Enolate Claisen Rearrangement as a Suitable Method for the Synthesis of Highly Sterically Demanding Amino Acids
    • Krebs, A., Kazmaier, U., The Asymmetric Ester Enolate Claisen Rearrangement as a Suitable Method for the Synthesis of Highly Sterically Demanding Amino Acids. Tetrahedron Lett. 37 (1996), 7945–7946.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7945-7946
    • Krebs, A.1    Kazmaier, U.2
  • 248
    • 33847798567 scopus 로고
    • A General Method for the Synthesis of Amines by the Rearrangement of Allylic Trichloroacetimidates. 1, 3-Transposition of Alcohol and Amine Functions
    • Overman, l.E., A General Method for the Synthesis of Amines by the Rearrangement of Allylic Trichloroacetimidates. 1, 3-Transposition of Alcohol and Amine Functions. J. Am. Chem. Soc. 98 (1976), 2901–2910.
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 2901-2910
    • Overman, L.E.1
  • 249
    • 84985634168 scopus 로고
    • New Synthetic Methods. (46). Mercury(II)- and Palladium(II)- Catalyzed [3.3]-Sigmatropic Rearrangements
    • Overman, l.E., New Synthetic Methods. (46). Mercury(II)- and Palladium(II)- Catalyzed [3.3]-Sigmatropic Rearrangements. Angew. Chem., Int. Ed. Engl. 23 (1984), 579–587.
    • (1984) Angew. Chem., Int. Ed. Engl. , vol.23 , pp. 579-587
    • Overman, L.E.1
  • 250
    • 0001244429 scopus 로고
    • Homogeneous Catalysis. Transition-Metal-Catalyzed Claisen Rearrangements
    • Schenck, t.G., Bosnich, B., Homogeneous Catalysis. Transition-Metal-Catalyzed Claisen Rearrangements. J. Am. Chem. Soc. 107 (1985), 2058–2066.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 2058-2066
    • Schenck, T.G.1    Bosnich, B.2
  • 251
    • 0026515878 scopus 로고
    • On the Palladium(II)-Catalyzed Rearrangement of Allyl Imidates
    • Metz, P., Mues, C, Schoop, A., On the Palladium(II)-Catalyzed Rearrangement of Allyl Imidates. Tetrahedron 48 (1992), 1071–1080.
    • (1992) Tetrahedron , vol.48 , pp. 1071-1080
    • Metz, P.1    Mues, C.2    Schoop, A.3
  • 252
    • 0027260325 scopus 로고
    • Diastereoselective Synthesis of 1, 2-Diamines by Palladium-Catalyzed Aza-Claisen Rearrangement
    • Gonda, J., Helland, a.C, Ernst, B., Bellus, D., Diastereoselective Synthesis of 1, 2-Diamines by Palladium-Catalyzed Aza-Claisen Rearrangement. Synthesis, 1993, 729–733.
    • (1993) Synthesis , pp. 729-733
    • Gonda, J.1    Helland, A.C.2    Ernst, B.3    Bellus, D.4
  • 254
    • 33845554466 scopus 로고
    • Synthesis of D- Biotin from L-Cystine via Intramolecular [3+2] Cycloaddition
    • Baggiolini, e.G., Lee, h.L., Pizzolato, G., Uskokovic, m.R., Synthesis of D- Biotin from L-Cystine via Intramolecular [3+2] Cycloaddition. J. Am. Chem. Soc. 104 (1982), 6460–6462.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 6460-6462
    • Baggiolini, E.G.1    Lee, H.L.2    Pizzolato, G.3    Uskokovic, M.R.4
  • 255
    • 0001424487 scopus 로고
    • Palladium(II)-Catalyzed Exchange and isomerization Reactions. III. Allylic Esters Isomerization in Acetic Acid Catalyzed by Palladium(II) Chloride
    • Henry, p.M., Palladium(II)-Catalyzed Exchange and isomerization Reactions. III. Allylic Esters Isomerization in Acetic Acid Catalyzed by Palladium(II) Chloride. J. Am. Chem. Soc. 94 (1972), 5200–5206.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 5200-5206
    • Henry, P.M.1
  • 256
    • 0000528944 scopus 로고
    • Self-Immolative Asymmetric Synthesis. III. Allylic Rearrangement of Optically Active Trichloroacetimidate
    • Yamamoto, Y., Shimoda, H., Oda, J., Inouye, Y., Self-Immolative Asymmetric Synthesis. III. Allylic Rearrangement of Optically Active Trichloroacetimidate. Bull. Chem. Soc. Jpn. 49 (1976), 3247–3249.
    • (1976) Bull. Chem. Soc. Jpn. , vol.49 , pp. 3247-3249
    • Yamamoto, Y.1    Shimoda, H.2    Oda, J.3    Inouye, Y.4
  • 257
    • 0026773290 scopus 로고
    • Synthesis of (E)-β, γ -Unsaturated α-Amino Acids by Rearrangement of Allyltrichloracetimidates
    • Mehmandoust, M., Petit, Y., Larcheveque, M., Synthesis of (E)-β, γ -Unsaturated α-Amino Acids by Rearrangement of Allyltrichloracetimidates. Tetrahedron Lett. 33 (1992), 4313–4316.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 4313-4316
    • Mehmandoust, M.1    Petit, Y.2    Larcheveque, M.3
  • 258
    • 0001923963 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Allylic Amines by Rearrangement of Allylic Trifluoroacetimidates: Stereoselective Synthesis of Polyoxamic Acid and Derivatives of
    • Savage, I., Thomas, e.J., Wilson, p.D., Stereoselective Synthesis of Allylic Amines by Rearrangement of Allylic Trifluoroacetimidates: Stereoselective Synthesis of Polyoxamic Acid and Derivatives of. J. Chem. Soc, Perkin Trans. 1 (1999), 3291–3303.
    • (1999) J. Chem. Soc, Perkin Trans. , vol.1 , pp. 3291-3303
    • Savage, I.1    Thomas, E.J.2    Wilson, P.D.3
  • 259
    • 0014682610 scopus 로고
    • Polyoxins, Antifungal Antibiotics. XIII. Structure of Polyoxins
    • Isono, K., Asahi, K., Suzuki, S., Polyoxins, Antifungal Antibiotics. XIII. Structure of Polyoxins. J. Am. Chem. Soc 91 (1969), 7490–7505.
    • (1969) J. Am. Chem. Soc , vol.91 , pp. 7490-7505
    • Isono, K.1    Asahi, K.2    Suzuki, S.3
  • 260
    • 0018694297 scopus 로고
    • The Polyoxins: Pyrimidine Nucleoside Peptide Antibiotics Inhibiting Fungal Cell Wall Biosynthesis
    • Isono, K., Suzuki, S., The Polyoxins: Pyrimidine Nucleoside Peptide Antibiotics Inhibiting Fungal Cell Wall Biosynthesis. Heterocycles 13 (1979), 333–351.
    • (1979) Heterocycles , vol.13 , pp. 333-351
    • Isono, K.1    Suzuki, S.2
  • 261
    • 0000587893 scopus 로고
    • Allylic Epoxide Rearrangement. A Stereospecific Approach to Chiral Epoxide Pheromones
    • Bell, t.W., Ciaccio, j.A., Allylic Epoxide Rearrangement. A Stereospecific Approach to Chiral Epoxide Pheromones. J. Org. Chem. 58 (1993), 5153–5162.
    • (1993) J. Org. Chem. , vol.58 , pp. 5153-5162
    • Bell, T.W.1    Ciaccio, J.A.2
  • 262
    • 0001943536 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Thymine Polyoxin C Using an Allylic Trifluoroacetimidate-Trifluoroacetamide Rearrangement
    • Chen, A., Thomas, e.J., Wilson, p.D., Stereoselective Synthesis of Thymine Polyoxin C Using an Allylic Trifluoroacetimidate-Trifluoroacetamide Rearrangement. J. Chem. Soc, Perkin Trans. 1 (1999), 3305–3310.
    • (1999) J. Chem. Soc, Perkin Trans. , vol.1 , pp. 3305-3310
    • Chen, A.1    Thomas, E.J.2    Wilson, P.D.3
  • 263
    • 0027371470 scopus 로고
    • Asymmetric α-Aminoacid Synthesis Using [3, 3] Rearrangement of Allylic Trifluoroacetimidates: Synthesis of Thymine Polyoxin C
    • Chen, A., Savage, I., Thomas, e.J., Wilson, p.D., Asymmetric α-Aminoacid Synthesis Using [3, 3] Rearrangement of Allylic Trifluoroacetimidates: Synthesis of Thymine Polyoxin C. Tetrahedron Lett. 34 (1993), 6769–6772.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 6769-6772
    • Chen, A.1    Savage, I.2    Thomas, E.J.3    Wilson, P.D.4
  • 264
    • 0030788964 scopus 로고    scopus 로고
    • Aza-Claisen Rearrangement. Synthesis of 5′-Branched 5′-Aminothymidines
    • Ammenn, J., Altmann, k.H., Bellus, D., Aza-Claisen Rearrangement. Synthesis of 5′-Branched 5′-Aminothymidines. Helv. Chim. Acta 80 (1997), 1589–1606.
    • (1997) Helv. Chim. Acta , vol.80 , pp. 1589-1606
    • Ammenn, J.1    Altmann, K.H.2    Bellus, D.3
  • 265
    • 0034700884 scopus 로고    scopus 로고
    • Stereo- controlled Introduction of an Amino Group at C-6 of D-Galactose via (3, 3)- Sigmatropic Rearrangements - Novel Synthesis of Lincosamine and 1-Epi.- Li
    • Gonda, J., Zavacká, E., Budesinsky, M., Cisarova, I., Podlaha, J., Stereo- controlled Introduction of an Amino Group at C-6 of D-Galactose via (3, 3)- Sigmatropic Rearrangements - Novel Synthesis of Lincosamine and 1-Epi.- Li. Tetrahedron Lett. 41 (2000), 525–529.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 525-529
    • Gonda, J.1    Zavacká, E.2    Budesinsky, M.3    Cisarova, I.4    Podlaha, J.5
  • 266
    • 0028930106 scopus 로고
    • Thermally Induced and Transition Metal Catalyzed Aza-Claisen Rearrangement of 2-Cyclopropylideneethyl Imidates: a New Entry to 1-Aminocyclopropanecarboxylic A
    • Estieu, K., Ollivier, J., Salaun, J., Thermally Induced and Transition Metal Catalyzed Aza-Claisen Rearrangement of 2-Cyclopropylideneethyl Imidates: a New Entry to 1-Aminocyclopropanecarboxylic A. Tetrahedron Lett. 36 (1995), 2974–2978.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 2974-2978
    • Estieu, K.1    Ollivier, J.2    Salaun, J.3
  • 267
    • 0029926328 scopus 로고    scopus 로고
    • Stereocontrolled Synthesis of α, α-Disubstituted α-Amino Aldehydes and α-Amino Acids Using a [3, 3] Allylic Tri- chloroacetimidate Rearrangement
    • Imogai, H., Petit, Y., Larcheveque, M., Stereocontrolled Synthesis of α, α-Disubstituted α-Amino Aldehydes and α-Amino Acids Using a [3, 3] Allylic Tri- chloroacetimidate Rearrangement. Tetrahedron Lett. 37 (1996), 2573–2576.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 2573-2576
    • Imogai, H.1    Petit, Y.2    Larcheveque, M.3
  • 268
    • 0001269223 scopus 로고
    • Bimetallic Catalytic Systems Containing Titanium, Zirconium, Nickel and Palladium. Their Applications to Selective Organic Syntheses
    • Negishi, E., Bimetallic Catalytic Systems Containing Titanium, Zirconium, Nickel and Palladium. Their Applications to Selective Organic Syntheses. Pure Appl. Chem. 55 (1981), 2333–2356.
    • (1981) Pure Appl. Chem. , vol.55 , pp. 2333-2356
    • Negishi, E.1
  • 269
    • 85066897792 scopus 로고
    • Stereospecific Syntheses of Alke- nyllithium Reagents from Alkenyl Iodides
    • Cahiez, G., Bernard, D., Normant, j.F., Stereospecific Syntheses of Alke- nyllithium Reagents from Alkenyl Iodides. Synthesis, 1976, 245–248.
    • (1976) Synthesis , pp. 245-248
    • Cahiez, G.1    Bernard, D.2    Normant, J.F.3
  • 270
    • 0000094788 scopus 로고
    • Vinyl Organo Copper. II. Deuterolysis, Iodolysis, Coupling, and Stereospecific Allkylation of Vinyl Copper
    • Normant, j.F., Cahiez, G., Chuit, C, Villieras, J., Vinyl Organo Copper. II. Deuterolysis, Iodolysis, Coupling, and Stereospecific Allkylation of Vinyl Copper. J. Organomet. Chem. 77 (1974), 269–279.
    • (1974) J. Organomet. Chem. , vol.77 , pp. 269-279
    • Normant, J.F.1    Cahiez, G.2    Chuit, C.3    Villieras, J.4
  • 272
    • 33947334412 scopus 로고
    • Novel Method for the Synthesis of Isomerically Pure Vinyl Halides from Alkynes via the Hydroalumination Reaction
    • Zweifel, G., Whitney, c.C., Novel Method for the Synthesis of Isomerically Pure Vinyl Halides from Alkynes via the Hydroalumination Reaction. J. Am. Chem. Soc. 89 (1967), 2753–2754.
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 2753-2754
    • Zweifel, G.1    Whitney, C.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.