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For recent example: (a) Magnus N.A., Confalone P.N., Storace L. Tetrahedron Lett. 41:2000;3015 (b) Kauffman G.S., Harris G.D., Dorow R.L., Stone B.R.P., Parsons R.L. Jr., Pesti J.A., Magnus N.A., Fortunak J.M., Confalone P.N., Nugent W.A. Org. Lett. 2:2000;3119 (c) Corbett J.W., Kresge K.J., Pan S., Cordova B.C., Klabe R.M., Rodgers J.D., Erickson-Viitanen S.K. Bioorg. Med. Chem. Lett. 11:2001;309 (d) Tan L., Chen C., Tillyer R.D., Grabowski E.J.J., Reider P.J. Angew. Chem., Int. Ed. 38:1999;711.
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For recent example: (a) Magnus N.A., Confalone P.N., Storace L. Tetrahedron Lett. 41:2000;3015 (b) Kauffman G.S., Harris G.D., Dorow R.L., Stone B.R.P., Parsons R.L. Jr., Pesti J.A., Magnus N.A., Fortunak J.M., Confalone P.N., Nugent W.A. Org. Lett. 2:2000;3119 (c) Corbett J.W., Kresge K.J., Pan S., Cordova B.C., Klabe R.M., Rodgers J.D., Erickson-Viitanen S.K. Bioorg. Med. Chem. Lett. 11:2001;309 (d) Tan L., Chen C., Tillyer R.D., Grabowski E.J.J., Reider P.J. Angew. Chem., Int. Ed. 38:1999;711.
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Kauffman, G.S.1
Harris, G.D.2
Dorow, R.L.3
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Parsons Jr., R.L.5
Pesti, J.A.6
Magnus, N.A.7
Fortunak, J.M.8
Confalone, P.N.9
Nugent, W.A.10
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For recent example: (a) Magnus N.A., Confalone P.N., Storace L. Tetrahedron Lett. 41:2000;3015 (b) Kauffman G.S., Harris G.D., Dorow R.L., Stone B.R.P., Parsons R.L. Jr., Pesti J.A., Magnus N.A., Fortunak J.M., Confalone P.N., Nugent W.A. Org. Lett. 2:2000;3119 (c) Corbett J.W., Kresge K.J., Pan S., Cordova B.C., Klabe R.M., Rodgers J.D., Erickson-Viitanen S.K. Bioorg. Med. Chem. Lett. 11:2001;309 (d) Tan L., Chen C., Tillyer R.D., Grabowski E.J.J., Reider P.J. Angew. Chem., Int. Ed. 38:1999;711.
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Corbett, J.W.1
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Pan, S.3
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Klabe, R.M.5
Rodgers, J.D.6
Erickson-Viitanen, S.K.7
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For recent example: (a) Magnus N.A., Confalone P.N., Storace L. Tetrahedron Lett. 41:2000;3015 (b) Kauffman G.S., Harris G.D., Dorow R.L., Stone B.R.P., Parsons R.L. Jr., Pesti J.A., Magnus N.A., Fortunak J.M., Confalone P.N., Nugent W.A. Org. Lett. 2:2000;3119 (c) Corbett J.W., Kresge K.J., Pan S., Cordova B.C., Klabe R.M., Rodgers J.D., Erickson-Viitanen S.K. Bioorg. Med. Chem. Lett. 11:2001;309 (d) Tan L., Chen C., Tillyer R.D., Grabowski E.J.J., Reider P.J. Angew. Chem., Int. Ed. 38:1999;711.
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Tan, L.1
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Tillyer, R.D.3
Grabowski, E.J.J.4
Reider, P.J.5
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(f) Bravo P., Capelli S., Meille S.V., Seresini P., Volonterio A., Zanda M. Tetrahedron: Asymmetry. 7:1996;2321
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Zanda, M.6
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(h) Assensio A., Bravo P., Crucianelli M., Farina A., Fustero S., Soler J.G., Meille S.V., Panzeri W., Viani F., Volonterio A., Zanda M. Eur. J. Org. Chem. 2001;1449
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(i) Volonterio A., Bravo P., Panzeri W., Pesenti C., Zanda M. Eur. J. Org. Chem. 2002;3336
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(j) Bravo P., Soloshonok V., Farina A., Frigerio M., Meille S.V., Viani F. Tetrahedron: Asymm. 5:1994;987
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(l) Bravo P., Fustero S., Guidetti M., Volonterio A., Zanda M. J. Org. Chem. 64:1999;8731.
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For review on construction of α-amino acids with α-quaternary carbon, see: (a) Ctiviela C., Diaz-de-Villegas M.D. Tetrahedron: Asymmetry. 9:1998;3517 (b) Ctiviela C., Diaz-de-Villegas M.D. Tetrahedron: Asymmetry. 11:2000;645.
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Diaz-De-Villegas, M.D.2
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0034712270
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For review on construction of α-amino acids with α-quaternary carbon, see: (a) Ctiviela C., Diaz-de-Villegas M.D. Tetrahedron: Asymmetry. 9:1998;3517 (b) Ctiviela C., Diaz-de-Villegas M.D. Tetrahedron: Asymmetry. 11:2000;645.
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Ctiviela, C.1
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For review on this epoxide see: (a) Katagiri T. Soloshonok V.A. Enantiocontrolled Synthesis of Fluoro-Organic Compounds: Stereochemical Challenges and Biomedicinal Targets. 1999;161 Wiley, Chichester, (b) Katagiri T., Uneyama K. J. Fluorine Chem. 105:2000;285 (c) Furuhashi K. Collins A.N., Sheldrake G.N., Crosby J. Chirality in Industry. 1992;Wiley, New York.
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For review on this epoxide see: (a) Katagiri T. Soloshonok V.A. Enantiocontrolled Synthesis of Fluoro-Organic Compounds: Stereochemical Challenges and Biomedicinal Targets. 1999;161 Wiley, Chichester, (b) Katagiri T., Uneyama K. J. Fluorine Chem. 105:2000;285 (c) Furuhashi K. Collins A.N., Sheldrake G.N., Crosby J. Chirality in Industry. 1992;Wiley, New York.
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The strategy for preparation of non-fluorinated amino acids, see: (a) Shao H., Zhu Q., Goodman M. J. Org. Chem. 60:1995;790 (b) Dodd R.H. Molecules. 5:2000;293.
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The strategy for preparation of non-fluorinated amino acids, see: (a) Shao H., Zhu Q., Goodman M. J. Org. Chem. 60:1995;790 (b) Dodd R.H. Molecules. 5:2000;293.
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Molecules
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A stronger base, sec-BuLi with TMEDA had been used for generation of aziridinyl and oxiranyl anions: see Ref. 17c and d, also see Luisi R., Capriati V., Florio S., Ranaldo R. Tetrahedron. Lett. 44:2003;2677.
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