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1
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84945031690
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Springer-Verlag, has been dedicated to the subject since
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In addition to a substantial number of monographs, a periodical journal, Amino Acids, Springer-Verlag, has been dedicated to the subject since 1994.
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Amino Acids
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2
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0001039009
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α-Amino acid synthesis
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Tetrahedron Symposium-in-Print
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(a) O'Donnell, M. J., Ed. α-Amino Acid Synthesis (Tetrahedron Symposium-in-Print) Tetrahedron 1988, 44, 5253-5614.
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O'Donnell, M.J.1
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(b) Juaristi, E.; Quintana, D.; Escalante, J. Aldrichim. Acta 1994, 27, 3-11.
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Aldrichim. Acta
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0028130028
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(c) Cole, D. C. Tetrahedron 1994, 50, 9517-9582.
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Tetrahedron
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Cole, D.C.1
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See, for example: (a) Schoellkopf, U. Tetrahedron 1983, 39, 2085-2091.
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Schoellkopf, U.1
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(b) Seebach, D.; Juaristi, E.; Miller, D. D.; Schickli, C.; Weber, T. Helv. Chim. Acta 1987, 70, 237-261.
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Weber, T.5
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11
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33845278130
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(c) Williams, R. M.; Sinclair, P. J.; Zhai, D.; Chen, D. J. Am. Chem. Soc. 1988, 110, 1547-1557.
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0001125476
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(d) Belokon, Y. N.; Sagyan, A. S.; Djamgaryan, S. M.; Bakhmutov, V. I.; Belikov, V. M. Tetrahedron 1988, 44, 5507-5514.
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(e) Orena, M.; Porzi, G.; Sandri, S. J. Org. Chem. 1992, 57, 6532-6536.
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14
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0028844193
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(f) Juaristi, E.; Anzorena, J. L.; Boog, A.; Madrigal, D.; Seebach, D.; García-Baez, E. V.; García-Barradas, O.; Gordillo, B.; Kramer, A.; Steiner, I.; Zurcher, S. J. Org. Chem. 1995, 60, 6408-6415.
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Juaristi, E.1
Anzorena, J.L.2
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Seebach, D.5
García-Baez, E.V.6
García-Barradas, O.7
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(g) Chinchilla, R.; Falvello, L. R.; Galindo, N.; Nájera, C. Angew. Chem., Int. Ed. Engl. 1997, 36, 995-997.
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0032513257
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Juaristi, E.; Escalante, J.; León-Romo, J. L.; Reyes, A. Tetrahedron: Asymmetry 1998, 9, 715-740.
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Tetrahedron: Asymmetry
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84985171172
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Decorte, E.; Toso, R.; Sega, A.; Sunjic, V.; Ruzic-Toroz, Z.; Kojic-Prodic, B.; Bresciani-Pahor, N.; Nardin, G.; Randaccio, L. Helv. Chim. Acta 1981, 64, 1145-1149.
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Decorte, E.1
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Randaccio, L.9
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18
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0345482720
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note
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Atomic coordinates for all the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Centre, 12 Union Road, Cambridge CB2 IEZ, U.K.
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19
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0040723849
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(a) Gilli, G.; Bertolasi, V.; Sacerdoti, M.; Borea, P. A. Acta Crystallogr. B 1977, 33, 2644-2667.
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(b) Sunjic, V.; Sega, A.; Lisini, A.; Kovac, T.; Kajfez, F.; Ruscic, B. J. Heterocycl. Chem. 1979, 16, 757-761.
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21
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Cardillo, G.; Orena, M.; Sandri, S.; Tomasini, C. Tetrahedron 1987, 43, 2505-2512.
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0008036505
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Juaristi, E., Ed.; Wiley-VCH: New York
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(b) Cardillo, G.; Tomasini, C. In Enantioselective Synthesis of β-Amino Acids; Juaristi, E., Ed.; Wiley-VCH: New York, 1997; pp 219-221.
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Enantioselective Synthesis of β-Amino Acids
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(a) Johnson, F. Chem. Rev. 1968, 68, 375-413.
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(b) Seebach, D.; Beck, K. A.; Studer, A. Modern Synthetic Methods, 1995; VCH Publishers: Basel, 1995; pp 1-178.
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(c) Anaya de Parrodi, C.; Juaristi, E.; Quintero-Cortés, L.; Amador, P. Tetrahedron: Asymmetry 1996, 7, 1915-1918.
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and references therein
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Juaristi, E.; Beck, A. K.; Hansen, J.; Matt, T.; Mukhopadhyay, T.; Simson, M.; Seebach, D. Synthesis 1993, 1271-1290 and references therein.
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Synthesis
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Seebach, D.7
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35
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0000254037
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The idea behind the use of 6 equiv of the cosolvent is that this will lead to tetrasolvated lithium cation and an essentially free anion instead of a contact ion pair or aggregate thereof: (a) Reich, H. J.; Borst, J. P. J. Am. Chem. Soc. 1991, 113, 1835-1837.
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For a discussion on the like/unlike stereochemical descriptors, see: (a) Seebach, D.; Prelog, V. Angew. Chem., Int. Ed. Engl. 1982, 21, 654-660.
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39
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0344188837
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note
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The major isomer was separated prior to hydrolysis, so that enantiopure amino acids may be obtained.
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40
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0004133516
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Gaussian: Pittsburgh
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Frisch, M. J.; Trucks G. W.; Schelegel, H. B.; Gill, P. M. W.; Johnson, B. G.; Robb, M. A.; Cheeseman, J. R.; Keith, T. A.; Peterson, G. A.; Montgomery, J. A.; Raghavachai, K.; Al-Laham, M. A.; Zarrzewski, V. G.; Ortiz, J. V.; Foresman, J. B.; Cioslowski, J.; Stefanov, B. R.; Nanayakkara, A.; Challacombe, M.; Peng, C. Y.; Ayala, P. Y.; Chen, W.; Wong, M. W.; Andres, J. L.; Replogle, E. S.; Gomperts, R.; Martin, R. L.; Fox, D. J.; Binkley, J. S.; Defreess, D. J.; Baker, J.; Stewart, J. P.; Head-Gordon, M.; Gonzales, C.; Pople, J. A. GAUSSIAN 94 (revision C.2); Gaussian: Pittsburgh, 1995.
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GAUSSIAN 94 (Revision C.2)
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Frisch, M.J.1
Trucks, G.W.2
Schelegel, H.B.3
Gill, P.M.W.4
Johnson, B.G.5
Robb, M.A.6
Cheeseman, J.R.7
Keith, T.A.8
Peterson, G.A.9
Montgomery, J.A.10
Raghavachai, K.11
Al-Laham, M.A.12
Zarrzewski, V.G.13
Ortiz, J.V.14
Foresman, J.B.15
Cioslowski, J.16
Stefanov, B.R.17
Nanayakkara, A.18
Challacombe, M.19
Peng, C.Y.20
Ayala, P.Y.21
Chen, W.22
Wong, M.W.23
Andres, J.L.24
Replogle, E.S.25
Gomperts, R.26
Martin, R.L.27
Fox, D.J.28
Binkley, J.S.29
Defreess, D.J.30
Baker, J.31
Stewart, J.P.32
Head-Gordon, M.33
Gonzales, C.34
Pople, J.A.35
more..
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41
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0344620439
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Sapse, A.-M., Schleyer, P. v. R., Eds.; Wiley: New York, Chapter 1
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(a) Streitwieser, A.; Bachrach, S. M.; Dorigo, A.; Schleyer, P. v. R. In Lithium Chemistry; Sapse, A.-M., Schleyer, P. v. R., Eds.; Wiley: New York, 1995; Chapter 1.
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Lithium Chemistry
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Streitwieser, A.1
Bachrach, S.M.2
Dorigo, A.3
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(c) See also: Ghera, E.; Kleiman, V.; Hassner, A. J. Org. Chem. 1999, 64, 8.
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Ghera, E.1
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45
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0000680481
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(a) For general experimental procedures, see: Juaristi, E.; López-Ruiz, H.; Madrigal, D.; Ramírez-Quirós, Y.; Escalante, J. J. Org. Chem. 1998, 63, 4706.
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Escalante, J.5
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(b) For a detailed description of the computational method, see: Cuevas, G.; Juaristi, E. J. Am. Chem. Soc. 1997, 119, 7545.
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J. Am. Chem. Soc.
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0040723847
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Aldrich: Milwaukee
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Aldrich Chemical Catalogue, 1994-1995; Aldrich: Milwaukee, 1994; (a) p 37; (b) p 61; (c) p 1064; (d) p 1115; (e) p 1102.
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(1994)
Aldrich Chemical Catalogue, 1994-1995
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