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Volumn 37, Issue 8, 2004, Pages 506-517

The enantioselective synthesis of α-amino acids by phase-transfer catalysis with achiral Schiff base esters

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA AMINO ACID; CINCHONA ALKALOID; ESTER; SCHIFF BASE;

EID: 4143049107     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar0300625     Document Type: Review
Times cited : (732)

References (101)
  • 2
    • 0001851179 scopus 로고    scopus 로고
    • Asymmetric phase-transfer reactions
    • Ojima, I., Ed.; Wiley-VCH: New York; Chapter 10
    • (a) O'Donnell, M. J. Asymmetric Phase-Transfer Reactions. In Catalytic Asymmetric Synthesis, 2nd ed.; Ojima, I., Ed.; Wiley-VCH: New York, 2000; Chapter 10, pp 727-755.
    • (2000) Catalytic Asymmetric Synthesis, 2nd Ed. , pp. 727-755
    • O'Donnell, M.J.1
  • 3
    • 84903914524 scopus 로고    scopus 로고
    • Phase-transfer reactions
    • Elsevier: Oxford, U.K.
    • (b) Lygo, B. Phase-Transfer Reactions. Rodd's Chemistry of Carbon Compounds; Elsevier: Oxford, U.K., 2001; Vol. 5, pp 101-149.
    • (2001) Rodd's Chemistry of Carbon Compounds , vol.5 , pp. 101-149
    • Lygo, B.1
  • 5
    • 0037263702 scopus 로고    scopus 로고
    • Recent advances in chiral quaternary ammonium salts as phase-transfer catalysts
    • (d) Shen, Z.-X.; Kong, A.-D.; Chen, W.-Y.; Zhang, Y.-W. Recent Advances in Chiral Quaternary Ammonium Salts as Phase-Transfer Catalysts. Chin. J. Org. Chem. 2003, 23, 10-21.
    • (2003) Chin. J. Org. Chem. , vol.23 , pp. 10-21
    • Shen, Z.-X.1    Kong, A.-D.2    Chen, W.-Y.3    Zhang, Y.-W.4
  • 6
    • 0001039009 scopus 로고
    • α-amino acid synthesis. Symposium-in-print
    • Lead references concerning the synthesis of α-amino acids: (a) O'Donnell, M. J. α-Amino Acid Synthesis. Symposium-in-Print. Tetrahedron 1988, 44, 5253-5814.
    • (1988) Tetrahedron , vol.44 , pp. 5253-5814
    • O'Donnell, M.J.1
  • 7
    • 0003416748 scopus 로고
    • Baldwin, J. E., Ed.; Organic Chemistry Series; Pergamon Press: Oxford, U.K.
    • (b) Williams, R. M. In Synthesis of Optically Active α-Amino Acids; Baldwin, J. E., Ed.; Organic Chemistry Series; Pergamon Press: Oxford, U.K., 1989.
    • (1989) Synthesis of Optically Active α-Amino Acids
    • Williams, R.M.1
  • 8
    • 0028355337 scopus 로고
    • Recent developments in the stereoselective synthesis of α-amino acids
    • (c) Duthaler, R. O. Recent Developments in the Stereoselective Synthesis of α-Amino Acids. Tetrahedron 1994, 50, 1539-1650.
    • (1994) Tetrahedron , vol.50 , pp. 1539-1650
    • Duthaler, R.O.1
  • 9
    • 0038795772 scopus 로고    scopus 로고
    • Asymmetric synthesis of novel sterically constrained amino acids. Symposium-in-print
    • (d) Hruby, V. J.; Soloshonok, V. A. Asymmetric Synthesis of Novel Sterically Constrained Amino Acids. Symposium-in-Print. Tetrahedron 2001, 57, 6329-6650.
    • (2001) Tetrahedron , vol.57 , pp. 6329-6650
    • Hruby, V.J.1    Soloshonok, V.A.2
  • 10
    • 0036036249 scopus 로고    scopus 로고
    • From α-amino acids to peptides: All you need for the journey
    • (a) Nájera, C. From α-Amino Acids to Peptides: All You Need for the Journey. Synlett 2002, 1388-1403.
    • (2002) Synlett , pp. 1388-1403
    • Nájera, C.1
  • 11
    • 0141869057 scopus 로고    scopus 로고
    • Recent developments in the catalytic asymmetric synthesis of α- and β-amino acids
    • (f) Ma, J.-A. Recent Developments in the Catalytic Asymmetric Synthesis of α- and β-Amino Acids. Angew. Chem., Int. Ed. 2003, 42, 4290-4299.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 4290-4299
    • Ma, J.-A.1
  • 12
    • 0002248986 scopus 로고
    • The synthesis of amino acid derivatives by catalytic phase-transfer alkylations
    • O'Donnell, M. J.; Eckrich, T. M. The Synthesis of Amino Acid Derivatives by Catalytic Phase-Transfer Alkylations. Tetrahedron Lett. 1978, 4625-4628.
    • (1978) Tetrahedron Lett. , pp. 4625-4628
    • O'Donnell, M.J.1    Eckrich, T.M.2
  • 13
    • 0013617740 scopus 로고
    • Diethyl acetamidomalonate
    • Paquette, L. A., Ed.; John Wiley: Chichester, U.K.
    • O'Donnell, M. J. Diethyl Acetamidomalonate. In Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; John Wiley: Chichester, U.K., 1995; pp 1771-1773.
    • (1995) Encyclopedia of Reagents for Organic Synthesis , pp. 1771-1773
    • O'Donnell, M.J.1
  • 14
    • 0002076066 scopus 로고    scopus 로고
    • The preparation of optically active α-amino acids from the benzophenone imines of glycine derivatives
    • O'Donnell, M. J. The Preparation of Optically Active α-Amino Acids from the Benzophenone Imines of Glycine Derivatives. Aldrichimica Acta 2001, 34, 3-15.
    • (2001) Aldrichimica Acta , vol.34 , pp. 3-15
    • O'Donnell, M.J.1
  • 16
    • 33845555590 scopus 로고
    • A mild efficient route to schiff base derivatives of amino acids
    • O'Donnell, M. J.; Polt, R. L. A Mild and Efficient Route to Schiff Base Derivatives of Amino Acids. J. Org. Chem. 1982, 47, 2883-2666.
    • (1982) J. Org. Chem. , vol.47 , pp. 2883-2666
    • O'Donnell, M.J.1    Polt, R.L.2
  • 17
  • 19
    • 4143126718 scopus 로고    scopus 로고
    • Imination process for the preparation of substituted N-methyleneglycinate esters from imines and leaving group-substituted acetate esters
    • Eur. Pat. Appl. 1207151, 2002
    • (c) Eils, S.; Rossen, K.; Jahn, W.; Klement, I. Imination Process for the Preparation of Substituted N-Methyleneglycinate Esters from Imines and Leaving Group-Substituted Acetate Esters. Eur. Pat. Appl. 1207151, 2002; Chem. Abstr. 2002, 136, 386395.
    • (2002) Chem. Abstr. , vol.136 , pp. 386395
    • Eils, S.1    Rossen, K.2    Jahn, W.3    Klement, I.4
  • 20
    • 0013487648 scopus 로고
    • α-methyl amino acids by catalytic phase-transfer alkylations
    • O'Donnell, M. J.; LeClef, B.; Rusterholz, D. B. α-Methyl Amino Acids by Catalytic Phase-Transfer Alkylations. Tetrahedron Lett. 1982, 23, 4259-4262.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 4259-4262
    • O'Donnell, M.J.1    LeClef, B.2    Rusterholz, D.B.3
  • 21
    • 21844500968 scopus 로고
    • Selective alkylation of protected peptide derivatives by phase-transfer catalysis
    • O'Donnell, M. J.; Burkholder, T. P.; Khau, V. V.; Roeske, R. W.; Tian, Z. Selective Alkylation of Protected Peptide Derivatives by Phase-Transfer Catalysis. Pol. J. Chem. 1994, 68, 2477-2488.
    • (1994) Pol. J. Chem. , vol.68 , pp. 2477-2488
    • O'Donnell, M.J.1    Burkholder, T.P.2    Khau, V.V.3    Roeske, R.W.4    Tian, Z.5
  • 22
    • 0030057825 scopus 로고    scopus 로고
    • Solid-phase unnatural peptide synthesis (UPS)
    • (a) O'Donnell, M. J.; Zhou, C.; Scott, W. L. Solid-Phase Unnatural Peptide Synthesis (UPS). J. Am. Chem. Soc. 1996, 118, 6070-6071.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 6070-6071
    • O'Donnell, M.J.1    Zhou, C.2    Scott, W.L.3
  • 23
    • 0141795447 scopus 로고    scopus 로고
    • The Manual and automated solid-phase synthesis of α-substituted prolines and homologues
    • (b) Scott, W. L.; Alsina, J.; O'Donnell, M. J. The Manual and Automated Solid-Phase Synthesis of α-Substituted Prolines and Homologues. J. Comb. Chem. 2003, 5, 684-692.
    • (2003) J. Comb. Chem. , vol.5 , pp. 684-692
    • Scott, W.L.1    Alsina, J.2    O'Donnell, M.J.3
  • 24
    • 0008936383 scopus 로고    scopus 로고
    • Unnatural amino acid and peptide synthesis (UPS)
    • Martinez, J., Fehrentz, J.-A., Eds., EDK: Paris
    • (c) Short review: O'Donnell, M. J.; Scott, W. L. Unnatural Amino Acid and Peptide Synthesis (UPS). In Peptides 2000; Martinez, J., Fehrentz, J.-A., Eds., EDK: Paris, 2001, pp 31-36.
    • (2001) Peptides 2000 , pp. 31-36
    • O'Donnell, M.J.1    Scott, W.L.2
  • 25
    • 84888587878 scopus 로고
    • Novel, very strong, uncharged auxiliary bases; design and synthesis of monomeric and polymer-bound triaminoiminophosphorane bases of broadly varied steric demand
    • Schwesinger, R.; Willaredt, J.; Schlemper, H.; Keller, M.; Schmitt, D.; Fritz, H. Novel, Very Strong, Uncharged Auxiliary Bases; Design and Synthesis of Monomeric and Polymer-Bound Triaminoiminophosphorane Bases of Broadly Varied Steric Demand. Chem. Ber. 1994, 127, 2435-2454.
    • (1994) Chem. Ber. , vol.127 , pp. 2435-2454
    • Schwesinger, R.1    Willaredt, J.2    Schlemper, H.3    Keller, M.4    Schmitt, D.5    Fritz, H.6
  • 26
    • 0000903898 scopus 로고
    • Preparation of an electrophilic glycine cation equivalent and its reaction with heteroatom nucleophiles
    • (a) O'Donnell, M. J.; Bennett, W. D.; Polt, R. L. Preparation of an Electrophilic Glycine Cation Equivalent and its Reaction with Heteroatom Nucleophiles. Tetrahedron Lett. 1985, 26, 695-698.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 695-698
    • O'Donnell, M.J.1    Bennett, W.D.2    Polt, R.L.3
  • 27
    • 2342627043 scopus 로고
    • The synthesis of amino acids by reaction of an electrophilic glycine cation equivalent with carbon nucleophiles
    • (b) O'Donnell, M. J.; Falmagne, J.-B. The Synthesis of Amino Acids by Reaction of an Electrophilic Glycine Cation Equivalent with Carbon Nucleophiles. Tetrahedron Lett. 1985, 26, 699-702.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 699-702
    • O'Donnell, M.J.1    Falmagne, J.-B.2
  • 28
    • 0033529833 scopus 로고    scopus 로고
    • Solid-phase synthesis of unnatural α-amino acid derivatives using a resin-bound glycine cation equivalent
    • (a) O'Donnell, M. J.; Delgado, F.; Drew, M. D.; Pottorf, R. S.; Zhou, C.; Scott, W. L. Solid-Phase Synthesis of Unnatural α-Amino Acid Derivatives Using a Resin-Bound Glycine Cation Equivalent. Tetrahedron Lett. 1999, 40, 5831-5835.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 5831-5835
    • O'Donnell, M.J.1    Delgado, F.2    Drew, M.D.3    Pottorf, R.S.4    Zhou, C.5    Scott, W.L.6
  • 29
    • 37049100275 scopus 로고
    • The synthesis of amino acids via organoboranes
    • (b) For early solution-phase studies, see: O'Donnell, M. J.; Falmagne, J. B. The Synthesis of Amino Acids via Organoboranes, Chem. Commun. 1985, 1168-1169.
    • (1985) Chem. Commun. , pp. 1168-1169
    • O'Donnell, M.J.1    Falmagne, J.B.2
  • 30
    • 85122201594 scopus 로고    scopus 로고
    • Cinchona alkaloids and their derivatives: Versatile catalysts and ligands in asymmetric synthesis
    • (a) Kacprzak, K.; Gawronski, J. Cinchona Alkaloids and Their Derivatives: Versatile Catalysts and Ligands in Asymmetric Synthesis. Synthesis 2001, 961-998.
    • (2001) Synthesis , pp. 961-998
    • Kacprzak, K.1    Gawronski, J.2
  • 31
    • 0037244819 scopus 로고    scopus 로고
    • α-imino esters: Versatile substrates for the catalytic, asymmetric synthesis of α- and β-amino acids and β-lactams
    • (b) Cinchona alkaloid derivatives that play multiple roles in a single reaction: Taggi, A. E.; Hafez, A. M.; Lectka, T. α-Imino Esters: Versatile Substrates for the Catalytic, Asymmetric Synthesis of α- and β-Amino Acids and β-Lactams. Acc. Chem. Res. 2003, 36, 10-19.
    • (2003) Acc. Chem. Res. , vol.36 , pp. 10-19
    • Taggi, A.E.1    Hafez, A.M.2    Lectka, T.3
  • 32
  • 34
    • 4143111382 scopus 로고    scopus 로고
    • note
    • (b) Images are from the Wellcome Library (London).
  • 36
    • 33845185214 scopus 로고
    • The stereoselective synthesis of α-amino acids by phase transfer catalysis
    • (a) O'Donnell, M. J.; Bennett, W. D.; Wu, S. The Stereoselective Synthesis of α-Amino Acids by Phase Transfer Catalysis. J. Am. Chem. Soc. 1989, 111, 2353-2355.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 2353-2355
    • O'Donnell, M.J.1    Bennett, W.D.2    Wu, S.3
  • 37
    • 0000344872 scopus 로고
    • Theoretical studies in molecular recognition: Asymmetric induction of benzophenone imine ester enolates by the benzylcinchonimum ion
    • (b) 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 Benzylcinchonimum Ion. J. Org. Chem. 1991, 56, 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
  • 38
    • 0035939151 scopus 로고    scopus 로고
    • Enantiomeric enrichment of α-amino acid derivatives: Recrystallization of N-Fmoc α-amino acid tert-butyl esters
    • (c) O'Donnell, M. J.; Delgado, F. Enantiomeric Enrichment of α-Amino Acid Derivatives: Recrystallization of N-Fmoc α-Amino Acid tert-Butyl Esters. Tetrahedron 2001, 57, 6641-6650.
    • (2001) Tetrahedron , vol.57 , pp. 6641-6650
    • O'Donnell, M.J.1    Delgado, F.2
  • 39
    • 0028300898 scopus 로고
    • A new active catalyst species for enantioselective alkylation by phase-transfer catalysis
    • (a) O'Donnell, M. J.; Wu, S.; Huffman, J. C. A New Active Catalyst Species for Enantioselective Alkylation by Phase-Transfer Catalysis. Tetrahedron 1994, 50, 4507-4518.
    • (1994) Tetrahedron , vol.50 , pp. 4507-4518
    • O'Donnell, M.J.1    Wu, S.2    Huffman, J.C.3
  • 40
    • 4143126717 scopus 로고    scopus 로고
    • Catalytic Enantioselective Synthesis of alpha-Amino Acid Derivatives by Phase-Transfer Catalysis, U.S. Patent 5,554,753, September 10, 1996
    • (b) O'Donnell, M. J.; Wu, S.; Esikova, I.; Mi, A. Catalytic Enantioselective Synthesis of alpha-Amino Acid Derivatives by Phase-Transfer Catalysis, U.S. Patent 5,554,753, September 10, 1996.
    • O'Donnell, M.J.1    Wu, S.2    Esikova, I.3    Mi, A.4
  • 41
    • 0001084339 scopus 로고    scopus 로고
    • A new interfacial mechanism for asymmetric alkylation by phase-transfer catalysis
    • Halpern, M. E., Ed.; ACS Symposium Series 659; American Chemical Society: Washington, DC; Chapter 7
    • Esikova, I. A.; Nahreini, T. S.; O'Donnell, M. J. A New Interfacial Mechanism for Asymmetric Alkylation by Phase-Transfer Catalysis. In Phase-Transfer Catalysis; Halpern, M. E., Ed.; ACS Symposium Series 659; American Chemical Society: Washington, DC, 1997; Chapter 7, pp 89-96.
    • (1997) Phase-Transfer Catalysis , pp. 89-96
    • Esikova, I.A.1    Nahreini, T.S.2    O'Donnell, M.J.3
  • 42
    • 0030659804 scopus 로고    scopus 로고
    • A new class of asymmetric phase-transfer catalysts 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 Catalysts Derived from Cinchona Alkaloids - Application in the Enantioselective Synthesis of α-Amino Acids. Tetrahedron Lett. 1997, 38, 8595-8598.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 8595-8598
    • Lygo, B.1    Wainwright, P.G.2
  • 43
    • 0000234063 scopus 로고    scopus 로고
    • A rational approach to catalytic enantioselective enolate alkylation using a structurally rigidified and defined chiral quaternary ammonium salt under phase transfer conditions
    • Corey, E. J.; Xu, F.; Noe, M. C. A Rational Approach to Catalytic Enantioselective Enolate Alkylation Using a Structurally Rigidified and Defined Chiral Quaternary Ammonium Salt under Phase Transfer Conditions, J. Am. Chem. Soc. 1997, 119, 12414-12415.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 12414-12415
    • Corey, E.J.1    Xu, F.2    Noe, M.C.3
  • 44
    • 0032569863 scopus 로고    scopus 로고
    • An efficient homogeneous catalytic enantioselective synthesis of α-amino acid derivatives
    • O'Donnell, M. J.; Delgado, F.; Hostettler, C.; Schwesinger, R. An Efficient Homogeneous Catalytic Enantioselective Synthesis of α-Amino Acid Derivatives. Tetrahedron Lett. 1998, 39, 8775-8778.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 8775-8778
    • O'Donnell, M.J.1    Delgado, F.2    Hostettler, C.3    Schwesinger, R.4
  • 45
    • 0033553459 scopus 로고    scopus 로고
    • Enantioselective solid-phase synthesis of α-amino acid derivatives
    • O'Donnell, M. J.; Delgado, F.; Pottorf, R. S. Enantioselective Solid-Phase Synthesis of α-Amino Acid Derivatives. Tetrahedron 1999, 55, 6347-6362,
    • (1999) Tetrahedron , vol.55 , pp. 6347-6362
    • O'Donnell, M.J.1    Delgado, F.2    Pottorf, R.S.3
  • 46
    • 85026864774 scopus 로고    scopus 로고
    • Preparation of O-allyl-N-(9-anthracenyl-methyl)cinchonidinium bromide as a phase transfer catalyst for the enantioselective alkylation of glycine benzophenone imine tert-butyl ester: (4S)-2-(Benzhydrylidenamino)pentanedioic acid, 1-tert-butyl ester-5-methyl ester
    • Corey, E. J.; Noe, M. C. Preparation of O-Allyl-N-(9-Anthracenyl-methyl) cinchonidinium Bromide as a Phase Transfer Catalyst for the Enantioselective Alkylation of Glycine Benzophenone Imine tert-Butyl Ester: (4S)-2- (Benzhydrylidenamino)pentanedioic Acid, 1-tert-Butyl Ester-5-Methyl Ester. Org. Synth. 2003, 80, 38-45.
    • (2003) Org. Synth. , vol.80 , pp. 38-45
    • Corey, E.J.1    Noe, M.C.2
  • 47
    • 0037425527 scopus 로고    scopus 로고
    • Free radical-mediated aryl amination and its use in a convergent [3 + 2] strategy for enantioselective indoline α-amino acid synthesis
    • Chromatography of catalyst and indoline synthesis: Viswanathan, R.; Prabhakaran, E. N.; Plotkin, M. A.; Johnston, J. N. Free Radical-Mediated Aryl Amination and Its Use in a Convergent [3 + 2] Strategy for Enantioselective Indoline α-Amino Acid Synthesis. J. Am. Chem. Soc. 2003, 125, 163-168.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 163-168
    • Viswanathan, R.1    Prabhakaran, E.N.2    Plotkin, M.A.3    Johnston, J.N.4
  • 48
    • 0037020579 scopus 로고    scopus 로고
    • Asymmetric alkylation of glycine imines using in situ generated phase-transfer catalysts
    • (a) Lygo, B.; Andrews, B. I.; Crosby, J.; Peterson, J. A. Asymmetric Alkylation of Glycine Imines Using In Situ Generated Phase-Transfer Catalysts. Tetrahedron Lett. 2002, 43, 8015-8018.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 8015-8018
    • Lygo, B.1    Andrews, B.I.2    Crosby, J.3    Peterson, J.A.4
  • 49
    • 0037829738 scopus 로고    scopus 로고
    • Identification of a highly effective asymmetric phase-transfer catalyst derived from α-methylnaphthylamine
    • (b) Lygo, B.; Allbutt, B.; James, S. R. Identification of a Highly Effective Asymmetric Phase-Transfer Catalyst Derived from α- Methylnaphthylamine. Tetrahedron Lett. 2003, 44, 5629-5632.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 5629-5632
    • Lygo, B.1    Allbutt, B.2    James, S.R.3
  • 50
    • 0035928478 scopus 로고    scopus 로고
    • Synthesis and application of dimeric cinchona alkaloid phase-transfer catalysts: α,α′-Bis[O(9)-allylcinchonidinium]-o, m, or p-xylene dibromide
    • (a) Jew, S.-s.; Jeong, B.-S.; Yoo, M.-S.; Huh, H.; Park, H.-g. Synthesis and Application of Dimeric Cinchona Alkaloid Phase-Transfer Catalysts: α,α′-Bis[O(9)-allylcinchonidinium]-o, m, or p-xylene Dibromide. Chem. Commun. 2001,1244-1245.
    • (2001) Chem. Commun. , pp. 1244-1245
    • Jew, S.S.1    Jeong, B.-S.2    Yoo, M.-S.3    Huh, H.4    Park, H.-G.5
  • 52
    • 0037191623 scopus 로고    scopus 로고
    • An unusual electronic effect of an aromatic-F in phase-transfer catalysts derived from cinchona-alkaloid
    • (c) Jew, S.-s.; Yoo, M.-S.; Jeong, B.-S,; Park, I. Y.; Park, H.-g. An Unusual Electronic Effect of an Aromatic-F in Phase-Transfer Catalysts Derived from Cinchona-Alkaloid. Org. Lett. 2002, 4, 4245-4248.
    • (2002) Org. Lett. , vol.4 , pp. 4245-4248
    • Jew, S.S.1    Yoo, M.-S.2    Jeong, B.-S.3    Park, I.Y.4    Park, H.-G.5
  • 53
    • 0037166726 scopus 로고    scopus 로고
    • New dimeric anthracenyl-derived cinchona quaternary ammonium salts as phase-transfer catalysts for the asymmetric synthesis of α-amino acids
    • (a) Chinchilla, R.; Mazón, P.; Nájera, C. New Dimeric Anthracenyl-Derived Cinchona Quaternary Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of α-Amino Acids. Tetrahedron: Asymmetry 2002, 13, 927-931.
    • (2002) Tetrahedron: Asymmetry , vol.13 , pp. 927-931
    • Chinchilla, R.1    Mazón, P.2    Nájera, C.3
  • 54
    • 0037131665 scopus 로고    scopus 로고
    • Unexpected metal base-dependent inversion of the enantioselectivity in the asymmetric synthesis of α-amino acids using phase-transfer catalysts derived from cinchonidine
    • (b) Mazón, P.; Chinchilla, R.; Nájera, C.; Guillena, G.; Kreiter, R.; Gebbink, R. J. M. K.; van Koten, G. Unexpected Metal Base-Dependent Inversion of the Enantioselectivity in the Asymmetric Synthesis of α-Amino Acids Using Phase-Transfer Catalysts Derived from Cinchonidine. Tetrahedron: Asymmetry 2002, 13, 2181-2185.
    • (2002) Tetrahedron: Asymmetry , vol.13 , pp. 2181-2185
    • Mazón, P.1    Chinchilla, R.2    Nájera, C.3    Guillena, G.4    Kreiter, R.5    Gebbink, R.J.M.K.6    Van Koten, G.7
  • 55
    • 0042880949 scopus 로고    scopus 로고
    • Enantioselective amino acid synthesis by chiral phase-transfer catalysis
    • (a) Review: Maruoka, K.; Ooi, T. Enantioselective Amino Acid Synthesis by Chiral Phase-Transfer Catalysis. Chem. Rev. 2003, 103, 3013-3028.
    • (2003) Chem. Rev. , vol.103 , pp. 3013-3028
    • Maruoka, K.1    Ooi, T.2
  • 56
    • 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. 1999, 121, 6519-6520.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6519-6520
    • Ooi, T.1    Kameda, M.2    Maruoka, K.3
  • 57
    • 0033820180 scopus 로고    scopus 로고
    • Dramatic rate enhancement by ultrasonic irradiation in liquid-liquid phase-transfer catalytic reactions
    • (c) Ooi, T.; Tayama, E.; Doda, K.; Takeuchi, M.; Maruoka, K. Dramatic Rate Enhancement by Ultrasonic Irradiation in Liquid-Liquid Phase-Transfer Catalytic Reactions. Synlett 2000, 1500-1502.
    • (2000) Synlett , pp. 1500-1502
    • Ooi, T.1    Tayama, E.2    Doda, K.3    Takeuchi, M.4    Maruoka, K.5
  • 58
    • 0037012716 scopus 로고    scopus 로고
    • Conformationally flexible, chiral quaternary ammonium bromides for asymmetric phase-transfer catalysis
    • (d) Ooi, T.; Uematsu, Y.; Kameda, M.; Maruoka, K. Conformationally Flexible, Chiral Quaternary Ammonium Bromides for Asymmetric Phase-Transfer Catalysis. Angew. Chem., Int. Ed. 2002, 41, 1551-1554.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 1551-1554
    • Ooi, T.1    Uematsu, Y.2    Kameda, M.3    Maruoka, K.4
  • 59
    • 0037473547 scopus 로고    scopus 로고
    • 2-symmetric chiral quaternary ammonium bromides as novel chiral phase-transfer catalysts: Synthesis and application to practical asymmetric synthesis of α-amino acids
    • 2-Symmetric Chiral Quaternary Ammonium Bromides as Novel Chiral Phase-Transfer Catalysts: Synthesis and Application to Practical Asymmetric Synthesis of α-Amino Acids. J. Am. Chem. Soc. 2003, 125, 5139-5151.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 5139-5151
    • Ooi, T.1    Kameda, M.2    Maruoka, K.3
  • 60
    • 0037415764 scopus 로고    scopus 로고
    • Highly stereoselective N-terminal functionalization of small peptices by chiral phase-transfer catalysis
    • (f) Ooi, T.; Tayama, E.; Maruoka, K. Highly Stereoselective N-Terminal Functionalization of Small Peptices by Chiral Phase-Transfer Catalysis. Angew. Chem., Int. Ed. 2003, 42, 579-582.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 579-582
    • Ooi, T.1    Tayama, E.2    Maruoka, K.3
  • 61
    • 0037011290 scopus 로고    scopus 로고
    • Direct asymmetric aldol reactions of glycine schiff base with aldehydes catalyzed by chiral quaternary ammonium salts
    • (g) Ooi, T.; Taniguchi, M.; Kameda, M.; Maruoka, K. Direct Asymmetric Aldol Reactions of Glycine Schiff Base with Aldehydes Catalyzed by Chiral Quaternary Ammonium Salts. Angew. Chem., Int. Ed. 2002, 41, 4542-4544.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 4542-4544
    • Ooi, T.1    Taniguchi, M.2    Kameda, M.3    Maruoka, K.4
  • 63
    • 0043194288 scopus 로고    scopus 로고
    • Enantioselective syntheses of aeruginosin 298-A and its analogues using a catalytic asymmetric phase-transfer reaction and epoxidation
    • (b) Ohshima, T.; Gnanadesikan, V.; Shibuguchi, T.; Fukuta, Y.; Nemoto, T.; Shibasaki, M. Enantioselective Syntheses of Aeruginosin 298-A and its Analogues Using a Catalytic Asymmetric Phase-Transfer Reaction and Epoxidation. J. Am. Chem. Soc. 2003, 125, 11206-11207,
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 11206-11207
    • Ohshima, T.1    Gnanadesikan, V.2    Shibuguchi, T.3    Fukuta, Y.4    Nemoto, T.5    Shibasaki, M.6
  • 65
    • 0037008633 scopus 로고    scopus 로고
    • 2-symmetric chiral pentacyclic guanidine: A phase-transfer catalyst for the asymmetric alkylation of tert-butyl glycinate schiff base
    • 2-Symmetric Chiral Pentacyclic Guanidine: A Phase-Transfer Catalyst for the Asymmetric Alkylation of tert-Butyl Glycinate Schiff Base. Angew. Chem., Int. Ed. 2002, 41, 2832-2834.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 2832-2834
    • Kita, T.1    Georgieva, A.2    Hashimoto, Y.3    Nakata, T.4    Nagasawa, K.5
  • 66
    • 0034714152 scopus 로고    scopus 로고
    • Asymmetric synthesis of α-amino acids using polymer-supported cinchona alkaloid-derived ammonium salts as chiral phase-transfer catalysts
    • Chinchilla, R.; Mazón, P.; Nájera, C. Asymmetric Synthesis of α-Amino Acids Using Polymer-Supported Cinchona Alkaloid-Derived Ammonium Salts as Chiral Phase-Transfer Catalysts. Tetrahedron: Asymmetry 2000, 11, 3277-3281.
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 3277-3281
    • Chinchilla, R.1    Mazón, P.2    Nájera, C.3
  • 67
    • 0038205367 scopus 로고    scopus 로고
    • Poly(ethylene glycol) supported cinchona alkaloids as phase transfer catalysts: Application to the enantioselective synthesis of α-amino acids
    • Thierry, B.; Plaquevent, J.-C.; Cahard, D. Poly(ethylene glycol) Supported Cinchona Alkaloids as Phase Transfer Catalysts: Application to the Enantioselective Synthesis of α-Amino Acids. Tetrahedron: Asymmetry 2003, 14, 1671-1677.
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 1671-1677
    • Thierry, B.1    Plaquevent, J.-C.2    Cahard, D.3
  • 68
  • 69
    • 0001186173 scopus 로고    scopus 로고
    • Asymmetric alkylation of tert-butyl glycinate schiff base with chiral quaternary ammonium salt under micellar conditions
    • Okino, T.; Takemoto, Y. Asymmetric Alkylation of tert-Butyl Glycinate Schiff Base with Chiral Quaternary Ammonium Salt under Micellar Conditions. Org. Lett. 2001, 3, 1515-1517.
    • (2001) Org. Lett. , vol.3 , pp. 1515-1517
    • Okino, T.1    Takemoto, Y.2
  • 70
    • 0041830967 scopus 로고    scopus 로고
    • Phase transfer catalyzed asymmetric alkylations of imine glycinamides
    • Kumar, S.; Ramachandran, U. Phase Transfer Catalyzed Asymmetric Alkylations of Imine Glycinamides. Tetrahedron: Asymmetry 2003, 14, 2539-2545.
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 2539-2545
    • Kumar, S.1    Ramachandran, U.2
  • 71
    • 0032473509 scopus 로고    scopus 로고
    • The catalytic enantioselective construction of molecules with quaternary carbon stereocenters
    • Corey, E. J.; Guzman-Perez, A. The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters. Angew. Chem., Int. Ed. 1998, 37, 388-401.
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 388-401
    • Corey, E.J.1    Guzman-Perez, A.2
  • 72
    • 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 1992, 3, 591-594,
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 591-594
    • O'Donnell, M.J.1    Wu, S.2
  • 73
    • 0033520975 scopus 로고    scopus 로고
    • Enantioselective alkylation of alanine-derived imines using quaternary ammonium catalysts
    • Lygo, B.; Crosby, J.; Peterson, J. A. Enantioselective Alkylation of Alanine-Derived Imines Using Quaternary Ammonium Catalysts. Tetrahedron Lett, 1999, 40, 8671-8674.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 8671-8674
    • Lygo, B.1    Crosby, J.2    Peterson, J.A.3
  • 74
    • 0037764776 scopus 로고    scopus 로고
    • Highly enantioselective synthesis of α-alkyl-alanines via the catalytic phase-transfer alkylation of 2-naphthyl aldimine tert-butyl ester by using O(9)-Allyl-N(1)-2′,3′,4′- trifluorobenzylhydrocinchonidinium bromide
    • Jew, S.-s.; Jeong, B.-S.; Lee, J.-H.; Yoo, M.-S.; Lee, Y.-J.; Park, B.-s.; Kim, M. G.; Park, H.-g. Highly Enantioselective Synthesis of α-Alkyl-alanines via the Catalytic Phase-Transfer Alkylation of 2-Naphthyl Aldimine tert-Butyl Ester by Using O(9)-Allyl-N(1)-2′,3′,4′- trifluorobenzylhydrocinchonidinium Bromide. J. Org. Chem. 2003, 68, 4514-4516.
    • (2003) J. Org. Chem. , vol.68 , pp. 4514-4516
    • Jew, S.S.1    Jeong, B.-S.2    Lee, J.-H.3    Yoo, M.-S.4    Lee, Y.-J.5    Park, B.-S.6    Kim, M.G.7    Park, H.-G.8
  • 75
    • 0033532363 scopus 로고    scopus 로고
    • Enantiomerically enriched (R)- and (S)-α-methylphenylalanine via asymmetric PTC C-alkylation catalysed by NOBIN
    • Belokon', Y. N.; Kochetkov, K. A.; Churkina, T. D.; Ikonnikov, N. S.; Vyskocil, S.; Kagan, H. B. Enantiomerically Enriched (R)- and (S)-α-Methylphenylalanine via Asymmetric PTC C-Alkylation Catalysed by NOBIN. Tetrahedron: Asymmetry 1999, 10, 1723-1728,
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 1723-1728
    • Belokon', Y.N.1    Kochetkov, K.A.2    Churkina, T.D.3    Ikonnikov, N.S.4    Vyskocil, S.5    Kagan, H.B.6
  • 76
    • 0034738068 scopus 로고    scopus 로고
    • Practical catalytic enantioselective synthesis of α,α- dialkyl-α-amino acids by chiral phase-transfer catalysis
    • (a) Ooi, T.; Takeuchi, M.; Kameda, M.; Maruoka, K. Practical Catalytic Enantioselective Synthesis of α,α-Dialkyl-α-Amino Acids by Chiral Phase-Transfer Catalysis. J. Am. Chem. Soc. 2000, 122, 5228-5229.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 5228-5229
    • Ooi, T.1    Takeuchi, M.2    Kameda, M.3    Maruoka, K.4
  • 77
    • 0034930295 scopus 로고    scopus 로고
    • Advantages of anaerobic conditions in the highly enantioselective synthesis of α,α-dialkyl-α-amino acids by chiral phase-transfer catalysis
    • (b) Ooi, T.; Takeuchi, M.; Ohara, D.; Maruoka, K. Advantages of Anaerobic Conditions in the Highly Enantioselective Synthesis of α,α-Dialkyl- α-Amino Acids by Chiral Phase-Transfer Catalysis. Synlett 2001, 1185-1187.
    • (2001) Synlett , pp. 1185-1187
    • Ooi, T.1    Takeuchi, M.2    Ohara, D.3    Maruoka, K.4
  • 78
    • 0842322178 scopus 로고    scopus 로고
    • Catalytic, enantioselective Michael Addition reactions
    • Review: Jha, S. C.; Joshi, N. N. Catalytic, Enantioselective Michael Addition Reactions. Arkivoc 2002, 167-196
    • (2002) Arkivoc , pp. 167-196
    • Jha, S.C.1    Joshi, N.N.2
  • 79
    • 0035902407 scopus 로고    scopus 로고
    • Enantioselective solution- and solid-phase synthesis of glutamic acid derivatives via Michael Addition reactions
    • O'Donnell, M. J.; Delgado, F.; Dominguez, E.; de Blas, J.; Scott, W. L. Enantioselective Solution- and Solid-Phase Synthesis of Glutamic Acid Derivatives via Michael Addition Reactions. Tetrahedron: Asymmetry 2001, 12, 821-828.
    • (2001) Tetrahedron: Asymmetry , vol.12 , pp. 821-828
    • O'Donnell, M.J.1    Delgado, F.2    Dominguez, E.3    De Blas, J.4    Scott, W.L.5
  • 80
    • 0037963684 scopus 로고    scopus 로고
    • Synthesis of a novel crown ether derived from chiro-inositol and its catalytic activity on the asymmetric Michael Addition
    • Akiyama, T.; Hara, M.; Fuchibe, K.; Sakamoto, S.; Yamaguchi, K. Synthesis of a Novel Crown Ether Derived from chiro-inositol and Its Catalytic Activity on the Asymmetric Michael Addition. Chem. Commun. 2003, 1734-1735.
    • (2003) Chem. Commun. , pp. 1734-1735
    • Akiyama, T.1    Hara, M.2    Fuchibe, K.3    Sakamoto, S.4    Yamaguchi, K.5
  • 81
    • 0037164617 scopus 로고    scopus 로고
    • Phase-transfer-catalyzed asymmetric Michael Reaction using newly-prepared chiral quaternary ammonium salts derived from L-tartrate
    • Arai, S.; Tsuji, R.; Nishida, A. Phase-Transfer-Catalyzed Asymmetric Michael Reaction Using Newly-Prepared Chiral Quaternary Ammonium Salts Derived from L-Tartrate. Tetrahedron Lett. 2002, 43, 9535-9537.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 9535-9537
    • Arai, S.1    Tsuji, R.2    Nishida, A.3
  • 82
    • 0141853177 scopus 로고    scopus 로고
    • Stereocontrolled synthesis of 3-(trans-2-aminocyclopropyl)alanine, a key component of belactosin A
    • Armstrong, A.; Scutt, J. N. Stereocontrolled Synthesis of 3-(trans-2-Aminocyclopropyl)alanine, a Key Component of Belactosin A. Org. Lett. 2003, 5, 2331-2334.
    • (2003) Org. Lett. , vol.5 , pp. 2331-2334
    • Armstrong, A.1    Scutt, J.N.2
  • 83
    • 0037198776 scopus 로고    scopus 로고
    • Lobocyclamide B from Lyngbya confervoides. Configuration and asymmetric synthesis of β-hydroxy-α-amino acids by (-)-sparteine-mediated aldol addition
    • MacMillan, J. B.; Molinski, T. F. Lobocyclamide B from Lyngbya confervoides. Configuration and Asymmetric Synthesis of β-Hydroxy-α- Amino Acids by (-)-Sparteine-Mediated Aldol Addition. Org. Lett. 2002, 4, 1883-1886.
    • (2002) Org. Lett. , vol.4 , pp. 1883-1886
    • MacMillan, J.B.1    Molinski, T.F.2
  • 84
    • 0037423971 scopus 로고    scopus 로고
    • Asymmetric protonation of lithium enolates of α-amino acid derivatives with α-amino acid-based bronsted acids
    • Futatsugi, K.; Yanagisawa, A.; Yamamoto, H. Asymmetric Protonation of Lithium Enolates of α-Amino Acid Derivatives with α-Amino Acid-Based Bronsted Acids. Chem. Commun. 2003, 566-567.
    • (2003) Chem. Commun. , pp. 566-567
    • Futatsugi, K.1    Yanagisawa, A.2    Yamamoto, H.3
  • 85
    • 0001722663 scopus 로고    scopus 로고
    • Efficient catalytic enantioselective reaction of a glycine cation equivalent with malonate anions via palladium catalysis
    • O'Donnell, M. J.; Chen, N.; Zhou, C.; Murray, A.; Kubiak, C. P.; Yang, F.; Stanley, G. G. Efficient Catalytic Enantioselective Reaction of a Glycine Cation Equivalent with Malonate Anions via Palladium Catalysis. J. Org. Chem. 1997, 62, 3962-3975.
    • (1997) J. Org. Chem. , vol.62 , pp. 3962-3975
    • O'Donnell, M.J.1    Chen, N.2    Zhou, C.3    Murray, A.4    Kubiak, C.P.5    Yang, F.6    Stanley, G.G.7
  • 86
    • 0037077616 scopus 로고    scopus 로고
    • The enantioselective synthesis of α-amino acid derivatives via organoboranes
    • O'Donnell, M. J.; Drew, M. D.; Cooper, J. T.; Delgado, F.; Zhou, C. The Enantioselective Synthesis of α-Amino Acid Derivatives via Organoboranes. J. Am. Chem. Soc. 2002, 124, 9348-9349.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 9348-9349
    • O'Donnell, M.J.1    Drew, M.D.2    Cooper, J.T.3    Delgado, F.4    Zhou, C.5
  • 87
    • 0037420357 scopus 로고    scopus 로고
    • Acyclic stereoselective boron alkylation reactions for the asymmetric synthesis of β-substituted α-amino acid derivatives
    • O'Donnell, M. J.; Cooper, J. T.; Mader, M. M. Acyclic Stereoselective Boron Alkylation Reactions for the Asymmetric Synthesis of β-Substituted α-Amino Acid Derivatives. J. Am. Chem. Soc. 2003, 125, 2370-2371.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2370-2371
    • O'Donnell, M.J.1    Cooper, J.T.2    Mader, M.M.3
  • 88
    • 4143071507 scopus 로고    scopus 로고
    • Nucleophilic Approach for Preparing Radiolabeled Imaging Agents and Associated Compounds, U. S. Provisional Patent Application 60/250,111 filed November 30, 2000, converted to utility application on November 29, 2001
    • Mulholland, G. K.; O'Donnell, M. J.; Chin, F. T.; Delgado, F. Nucleophilic Approach for Preparing Radiolabeled Imaging Agents and Associated Compounds, U. S. Provisional Patent Application 60/250,111 filed November 30, 2000, converted to utility application on November 29, 2001 (Chem. Abstr. 2002, 137, 20599).
    • Mulholland, G.K.1    O'Donnell, M.J.2    Chin, F.T.3    Delgado, F.4
  • 89
    • 37949021610 scopus 로고    scopus 로고
    • Mulholland, G. K.; O'Donnell, M. J.; Chin, F. T.; Delgado, F. Nucleophilic Approach for Preparing Radiolabeled Imaging Agents and Associated Compounds, U. S. Provisional Patent Application 60/250,111 filed November 30, 2000, converted to utility application on November 29, 2001 (Chem. Abstr. 2002, 137, 20599).
    • (2002) Chem. Abstr. , vol.137 , pp. 20599
  • 90
    • 0037048512 scopus 로고    scopus 로고
    • Enantioselective synthesis of α-carbon deuterium-labeled L-α-amino acids
    • Lygo, B.; Humphreys, L. D. Enantioselective Synthesis of α-Carbon Deuterium-Labeled L-α-Amino Acids. Tetrahedron Lett. 2002, 43, 6677-6679.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 6677-6679
    • Lygo, B.1    Humphreys, L.D.2
  • 91
    • 0037727924 scopus 로고    scopus 로고
    • Enantioselective synthesis of aroylalanine derivatives
    • Lygo, B.; Andrews, B. I. Enantioselective Synthesis of Aroylalanine Derivatives. Tetrahedron Lett. 2003, 44, 4499-4502.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 4499-4502
    • Lygo, B.1    Andrews, B.I.2
  • 92
    • 0036972164 scopus 로고    scopus 로고
    • Enantioselective synthesis and application of the highly fluorescent and environment-sensitive amino acid 6-(2-dimethylaminonaphthoyl) alanine (DANA)
    • Nitz, M.; Mezo, A. R.; Ali, M. H.; Imperiali, B. Enantioselective Synthesis and Application of the Highly Fluorescent and Environment-Sensitive Amino Acid 6-(2-Dimethylaminonaphthoyl) alanine (DANA). Chem. Commun. 2002, 1912-1913.
    • (2002) Chem. Commun. , pp. 1912-1913
    • Nitz, M.1    Mezo, A.R.2    Ali, M.H.3    Imperiali, B.4
  • 93
    • 0042355634 scopus 로고    scopus 로고
    • Modular and tunable chemosensor scaffold for divalent zinc
    • Shults, M. D.; Pearce, D. A.; Imperiali, B. Modular and Tunable Chemosensor Scaffold for Divalent Zinc. J. Am. Chem. Soc. 2003, 125, 10591-10597.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 10591-10597
    • Shults, M.D.1    Pearce, D.A.2    Imperiali, B.3
  • 94
    • 0037185047 scopus 로고    scopus 로고
    • A ruthenium(II) tris(bipyridyl) amino acid: Synthesis and direct incorporation into an α-helical peptide by solid-phase synthesis
    • Kise, K. J., Jr.; Bowler, B. E. A Ruthenium(II) Tris(bipyridyl) Amino Acid: Synthesis and Direct Incorporation into an α-Helical Peptide by Solid-Phase Synthesis. Inorg. Chem. 2002, 41, 379-386.
    • (2002) Inorg. Chem. , vol.41 , pp. 379-386
    • Kise Jr., K.J.1    Bowler, B.E.2
  • 95
    • 0142011139 scopus 로고    scopus 로고
    • Catalytic asymmetric synthesis of the central tryptophan residue of celogentin C
    • Castle, S. L.; Srikanth, G. S. C. Catalytic Asymmetric Synthesis of the Central Tryptophan Residue of Celogentin C. Org. Lett. 2003, 5, 3611-3614.
    • (2003) Org. Lett. , vol.5 , pp. 3611-3614
    • Castle, S.L.1    Srikanth, G.S.C.2
  • 96
    • 0034847347 scopus 로고    scopus 로고
    • Concise, catalytic asymmetric synthesis of tetrahydroisoquinoline and dihydroisoquinoline-3-carboxylic acid derivatives
    • Ooi, T.; Takeuchi, M.; Maruoka, K. Concise, Catalytic Asymmetric Synthesis of Tetrahydroisoquinoline and Dihydroisoquinoline-3-carboxylic Acid Derivatives. Synthesis 2001, 1716-1718.
    • (2001) Synthesis , pp. 1716-1718
    • Ooi, T.1    Takeuchi, M.2    Maruoka, K.3
  • 97
    • 0141631522 scopus 로고    scopus 로고
    • First asymmetric total synthesis of (-)-antofine by using an enantioselective catalytic phase transfer alkylation
    • Kim, S.; Lee, J.; Lee, T.; Park, H.-g.; Kim, D. First Asymmetric Total Synthesis of (-)-Antofine by Using an Enantioselective Catalytic Phase Transfer Alkylation. Org. Lett. 2003, 5, 2703-2706.
    • (2003) Org. Lett. , vol.5 , pp. 2703-2706
    • Kim, S.1    Lee, J.2    Lee, T.3    Park, H.G.4    Kim, D.5
  • 98
    • 0035963664 scopus 로고    scopus 로고
    • Studies on the total synthesis of RP 66453: Synthesis of fully functionalized 15-membered biaryl-containing macrocycle
    • Boisnard, S.; Carbonnelle, A.-C.; Zhu, J. Studies on the Total Synthesis of RP 66453: Synthesis of Fully Functionalized 15-Membered Biaryl-Containing Macrocycle. Org. Lett. 2001, 3, 2061-2064.
    • (2001) Org. Lett. , vol.3 , pp. 2061-2064
    • Boisnard, S.1    Carbonnelle, A.-C.2    Zhu, J.3
  • 100
    • 0037071927 scopus 로고    scopus 로고
    • A practical enantioselective total synthesis of the bengamides B, E, and Z
    • Boeckman, R. K., Jr.; Clark, T. J.; Shook, B. C. A Practical Enantioselective Total Synthesis of the Bengamides B, E, and Z. Org. Lett. 2002, 4, 2109-2112.
    • (2002) Org. Lett. , vol.4 , pp. 2109-2112
    • Boeckman Jr., R.K.1    Clark, T.J.2    Shook, B.C.3
  • 101
    • 0035939202 scopus 로고    scopus 로고
    • An enantioselective approach to bis-α-amino acids
    • Lygo, B.; Crosby, J.; Peterson, J. A. An Enantioselective Approach to bis-α-Amino Acids. Tetrahedron 2001, 57, 6447-6453.
    • (2001) Tetrahedron , vol.57 , pp. 6447-6453
    • Lygo, B.1    Crosby, J.2    Peterson, J.A.3


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