메뉴 건너뛰기




Volumn 9, Issue 5, 2012, Pages 695-726

Catalytic synthesis of optically active β-amino acid derivatives

Author keywords

Bifunctional organocatalysts; Chiral amino acids; Conjugate addition; Hydrogenation; Mannich reaction; Proline; Transition metal catalysts

Indexed keywords


EID: 84864539930     PISSN: 15701794     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017912803251783     Document Type: Review
Times cited : (14)

References (140)
  • 2
    • 0000193384 scopus 로고    scopus 로고
    • Synthesis of a β-hexapeptide from (R)-2-aminomethyl-alkanoic acids and structural investigations
    • Hintermann, T.; Seebach, D. Synthesis of a β-hexapeptide from (R)-2-aminomethyl-alkanoic acids and structural investigations. Synlett., 1997, 437-438.
    • (1997) Synlett , pp. 437-438
    • Hintermann, T.1    Seebach, D.2
  • 4
    • 0034597518 scopus 로고    scopus 로고
    • Synthesis of α-substituted β-amino acids using pseudoephedrine as a chiral auxiliary
    • Nagula, G.; Huber, V.J.; Lum, C.; Goodman, B.A. Synthesis of α-substituted β-amino acids using pseudoephedrine as a chiral auxiliary. Org. Lett., 2000, 2, 3527-3529.
    • (2000) Org. Lett , vol.2 , pp. 3527-3529
    • Nagula, G.1    Huber, V.J.2    Lum, C.3    Goodman, B.A.4
  • 5
    • 0035939196 scopus 로고    scopus 로고
    • Enantioselective synthesis of β-amino acids. Part 11: Diastereoselective alkylation of chiral derivatives of-aminopropionic acid containing the α-phenethyl group
    • Gutiérrez-García, V.M.; López-Ruiz, H.; Reyes-Rangel, G.; Juaristi, E. Enantioselective synthesis of β-amino acids. Part 11: Diastereoselective alkylation of chiral derivatives of β-aminopropionic acid containing the α-phenethyl group. Tetrahedron., 2001, 57, 6487-6496.
    • (2001) Tetrahedron , vol.57 , pp. 6487-6496
    • Gutiérrez-García, V.M.1    López-Ruiz, H.2    Reyes-Rangel, G.3    Juaristi, E.4
  • 6
    • 0032859102 scopus 로고    scopus 로고
    • Recent-advances in medicinal chemistry of taxoids with novel β-amino acid side chains
    • Ojima, I.; Lin, S.; Wang, T. Recent-advances in medicinal chemistry of taxoids with novel β-amino acid side chains. Curr. Med. Chem., 1999, 6, 927-953.
    • (1999) Curr. Med. Chem , vol.6 , pp. 927-953
    • Ojima, I.1    Lin, S.2    Wang, T.3
  • 8
    • 0028130028 scopus 로고
    • Recent stereoselective synthetic approaches to β-amino acids
    • Cole, D.C. Recent stereoselective synthetic approaches to β-amino acids. Tetrahedron., 1994, 50, 9517-9582.
    • (1994) Tetrahedron , vol.50 , pp. 9517-9582
    • Cole, D.C.1
  • 9
    • 14844312173 scopus 로고    scopus 로고
    • Asymmetric synthesis of ß-amino acids and α-substituted β-amino acids
    • Cardillo, G.; Tomasini, C. Asymmetric synthesis of ß-amino acids and α-substituted β-amino acids. Chem. Soc. Rev., 1996, 25, 117-128.
    • (1996) Chem. Soc. Rev. , vol.25 , pp. 117-128
    • Cardillo, G.1    Tomasini, C.2
  • 10
    • 0345151817 scopus 로고    scopus 로고
    • Recent advances in the enantioselective synthesis of β-amino acids
    • Juaristi, E.; López-Ruiz, H. Recent advances in the enantioselective synthesis of β-amino acids. Curr. Med. Chem., 1999, 6, 983-1004.
    • (1999) Curr. Med. Chem , vol.6 , pp. 983-1004
    • Juaristi, E.1    López-Ruiz, H.2
  • 13
    • 47749154512 scopus 로고    scopus 로고
    • Some potential chiral catalysts for preparation of asymmetric α-aminophosphonates
    • Bhadury, P.S.; Song, B.A.; Yang, S.; Zhang, Y.P.; Zhang, S. Some potential chiral catalysts for preparation of asymmetric α-aminophosphonates. Curr. Org. Synth., 2008, 5, 134-150.
    • (2008) Curr. Org. Synth , vol.5 , pp. 134-150
    • Bhadury, P.S.1    Song, B.A.2    Yang, S.3    Zhang, Y.P.4    Zhang, S.5
  • 14
    • 70349617279 scopus 로고    scopus 로고
    • Bifunctional chiral organocatalysts in organic transformations
    • Bhadury, P.S.; Song, B.A.; Yang, S.; Hu, D.Y.; Xue, W. Bifunctional chiral organocatalysts in organic transformations. Curr. Org. Synth., 2009, 6, 380-399.
    • (2009) Curr. Org. Synth , vol.6 , pp. 380-399
    • Bhadury, P.S.1    Song, B.A.2    Yang, S.3    Hu, D.Y.4    Xue, W.5
  • 15
    • 72449153409 scopus 로고    scopus 로고
    • Organocatalysis in organic synthesis
    • and references therein
    • Hegedus, L.S. Organocatalysis in organic synthesis. J. Am. Chem. Soc., 2009, 131, 17995-17997 and references therein.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 17995-17997
    • Hegedus, L.S.1
  • 17
    • 53349153675 scopus 로고    scopus 로고
    • Organocatalytic reactions with acetaldehyde
    • Alcaide, B.; Almendros, P. Organocatalytic reactions with acetaldehyde. Angew. Chem. Int. Ed., 2008, 47, 4632-4634.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4632-4634
    • Alcaide, B.1    Almendros, P.2
  • 19
    • 77957993635 scopus 로고    scopus 로고
    • Chemistry of organocatalytic asymmetric Mannich reactions
    • Bhadury, P.S.; Song, B.A. Chemistry of organocatalytic asymmetric Mannich reactions. Curr. Org. Chem., 2010, 14, 1989-2006.
    • (2010) Curr. Org. Chem , vol.14 , pp. 1989-2006
    • Bhadury, P.S.1    Song, B.A.2
  • 20
    • 0037032754 scopus 로고    scopus 로고
    • Chemistry: The simplest enzyme
    • Movassaghi, M.; Jacobsen, E.N. Chemistry: the simplest enzyme. Science., 2002, 298, 1904-1905.
    • (2002) Science , vol.298 , pp. 1904-1905
    • Movassaghi, M.1    Jacobsen, E.N.2
  • 21
    • 0037043180 scopus 로고    scopus 로고
    • Proline catalyzed asymmetric reactions
    • List, B. Proline catalyzed asymmetric reactions. Tetrahedron., 2002, 58, 5573-5590.
    • (2002) Tetrahedron , vol.58 , pp. 5573-5590
    • List, B.1
  • 22
    • 0034721440 scopus 로고    scopus 로고
    • The direct catalytic asymmetric three-component Mannich reaction
    • List, B. The direct catalytic asymmetric three-component Mannich reaction. J. Am. Chem. Soc., 2000, 122, 9336-9337.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 9336-9337
    • List, B.1
  • 24
    • 71049138987 scopus 로고    scopus 로고
    • One-pot highly enantioselective catalytic Mannich-type reactions between aldehydes and stable α-amido sulfones: Asymmetric synthesis of β-amino aldehydes and β-amino acids
    • Deiana, L.; Zhao, G.L.; Dziedzic, P.; Rios, R.; Vesely, J.; Ekstrom, J.; Cordova, A. One-pot highly enantioselective catalytic Mannich-type reactions between aldehydes and stable α-amido sulfones: asymmetric synthesis of β-amino aldehydes and β-amino acids. Tetrahedron Lett., 2010, 51, 234-237.
    • (2010) Tetrahedron Lett , vol.51 , pp. 234-237
    • Deiana, L.1    Zhao, G.L.2    Dziedzic, P.3    Rios, R.4    Vesely, J.5    Ekstrom, J.6    Cordova, A.7
  • 25
    • 33746079973 scopus 로고    scopus 로고
    • Asymmetric synthesis of (+)-polyoxamic acid via an efficient organocatalytic Mannich reaction as the key step
    • Enders, D.; Vrettou, M. Asymmetric synthesis of (+)-polyoxamic acid via an efficient organocatalytic Mannich reaction as the key step. Synthesis., 2006, 2155-2158.
    • (2006) Synthesis , pp. 2155-2158
    • Enders, D.1    Vrettou, M.2
  • 26
    • 33846550172 scopus 로고    scopus 로고
    • Proline-catalyzed Mannich reaction of aldehydes with N-Boc imines
    • Yang, J.W.; Stadler, M.; List, B. Proline-catalyzed Mannich reaction of aldehydes with N-Boc imines. Angew. Chem. Int. Ed., 2007, 46, 609-611.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 609-611
    • Yang, J.W.1    Stadler, M.2    List, B.3
  • 27
    • 41349123549 scopus 로고    scopus 로고
    • Prolinecatalyzed Mannich reactions of acetaldehyde
    • Yang, J.W.; Chandler, C.; Stadler, M.; Kampen, D.; List, B. Prolinecatalyzed Mannich reactions of acetaldehyde. Nature, 2008, 452, 453-455.
    • (2008) Nature , vol.452 , pp. 453-455
    • Yang, J.W.1    Chandler, C.2    Stadler, M.3    Kampen, D.4    List, B.5
  • 28
    • 61849109221 scopus 로고    scopus 로고
    • The proline-catalyzed double Mannich reaction of acetaldehyde with N-Boc imines
    • Chandler, C.; Galzerano, P.; Michrowska, A.; List, B. The proline-catalyzed double Mannich reaction of acetaldehyde with N-Boc imines. Angew. Chem. Int. Ed., 2009, 48, 1978-1980.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 1978-1980
    • Chandler, C.1    Galzerano, P.2    Michrowska, A.3    List, B.4
  • 29
    • 11844253794 scopus 로고    scopus 로고
    • Organocatalysis with proline derivatives: Improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions
    • Cobb, A.J.A.; Shaw, D.M.; Longbottom, D.A.; Gold, J.B.; Ley, S.V. Organocatalysis with proline derivatives: improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions. Org. Biomol. Chem., 2005, 3, 84-86.
    • (2005) Org. Biomol. Chem , vol.3 , pp. 84-86
    • Cobb, A.J.A.1    Shaw, D.M.2    Longbottom, D.A.3    Gold, J.B.4    Ley, S.V.5
  • 30
    • 38349145665 scopus 로고    scopus 로고
    • Organic solventfree, enantio-and diastereoselective, direct Mannich reaction in the presence of water
    • Hayashi, Y.; Urshima, T.; Aratake, S.; Okano, T.; Obi, K. Organic solventfree, enantio-and diastereoselective, direct Mannich reaction in the presence of water. Org. Lett., 2008, 10, 21-24.
    • (2008) Org. Lett , vol.10 , pp. 21-24
    • Hayashi, Y.1    Urshima, T.2    Aratake, S.3    Okano, T.4    Obi, K.5
  • 31
    • 51749116225 scopus 로고    scopus 로고
    • 3-Trifluoromethanesulfonamido-pyrrolidine: A general organocatalyst for antiselective Mannich reactions
    • Pouliquen, M.; Blanchet, J.; Lasne, M.C.; Rouden, J. 3-Trifluoromethanesulfonamido-pyrrolidine: a general organocatalyst for antiselective Mannich reactions. Org. Lett.; 2008, 10, 1029-1032.
    • (2008) Org. Lett. , vol.10 , pp. 1029-1032
    • Pouliquen, M.1    Blanchet, J.2    Lasne, M.C.3    Rouden, J.4
  • 32
    • 56249086830 scopus 로고    scopus 로고
    • Direct organocatalytic Mannich reaction of acetaldehyde: An improved catalyst and mechanistic insight from a computational study
    • Hayashi, Y.; Okano, T.; Itoh, T.; Urushima, T.; Ishikawa, H.; Uchimaru, T. Direct organocatalytic Mannich reaction of acetaldehyde: an improved catalyst and mechanistic insight from a computational study. Angew. Chem. Int. Ed., 2008, 47, 9053-9058.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 9053-9058
    • Hayashi, Y.1    Okano, T.2    Itoh, T.3    Urushima, T.4    Ishikawa, H.5    Uchimaru, T.6
  • 34
    • 1442286542 scopus 로고    scopus 로고
    • 5-Pyrrolidin-2-yltetrazole: A new, catalytic, more soluble alternative to proline in an organocatalytic asymmetric Mannich-type reaction
    • Cobb, A.Z.A.; Shaw, D.M.; Ley, S.V. 5-Pyrrolidin-2-yltetrazole: a new, catalytic, more soluble alternative to proline in an organocatalytic asymmetric Mannich-type reaction. Synlett., 2004, 558-560.
    • (2004) Synlett , pp. 558-560
    • Cobb, A.Z.A.1    Shaw, D.M.2    Ley, S.V.3
  • 35
    • 64249148782 scopus 로고    scopus 로고
    • Enantioselective Mannich reactions with practical proline mimetic N-(p-dodecylphenyl-sulfonyl)-2-pyrroli-dinecarboxamide
    • Yang, H.; Carter, R.G. Enantioselective Mannich reactions with practical proline mimetic N-(p-dodecylphenyl-sulfonyl)-2-pyrroli-dinecarboxamide. J. Org. Chem., 2009, 74, 2246-2249.
    • (2009) J. Org. Chem , vol.74 , pp. 2246-2249
    • Yang, H.1    Carter, R.G.2
  • 36
    • 21244473265 scopus 로고    scopus 로고
    • Dihydroxyacetone in amino acid catalyzed Mannich-type reactions
    • Westermann, B.; Neuhaus, C. Dihydroxyacetone in amino acid catalyzed Mannich-type reactions. Angew. Chem. Int. Ed., 2005, 44, 4077-4079.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 4077-4079
    • Westermann, B.1    Neuhaus, C.2
  • 37
    • 33846550172 scopus 로고    scopus 로고
    • Proline-catalyzed Mannich reaction of aldehydes with N-Boc imines
    • Yang, J.W.; Stadler, M.; List, B. Proline-catalyzed Mannich reaction of aldehydes with N-Boc imines. Angew. Chem. Int. Ed., 2007, 46, 609-611.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 609-611
    • Yang, J.W.1    Stadler, M.2    List, B.3
  • 38
    • 0142059750 scopus 로고    scopus 로고
    • Highly enantioselective synthesis of 1,2-amino alcohol derivatives via proline-catalyzed Mannich reaction
    • Pojarliev, P.; Biller, W.T.; Martin, H.J.; List, B. Highly enantioselective synthesis of 1,2-amino alcohol derivatives via proline-catalyzed Mannich reaction. Synlett., 2003, 1903-1905.
    • (2003) Synlett , pp. 1903-1905
    • Pojarliev, P.1    Biller, W.T.2    Martin, H.J.3    List, B.4
  • 39
    • 2342431575 scopus 로고    scopus 로고
    • The direct catalytic asymmetric cross-Mannich reaction: A highly enantioselective route to 3-amino alcohols and α-amino acid derivatives
    • Cordova, A. The direct catalytic asymmetric cross-Mannich reaction: a highly enantioselective route to 3-amino alcohols and α-amino acid derivatives. Chem. Eur. J., 2004, 10, 1987-1997.
    • (2004) Chem. Eur. J , vol.10 , pp. 1987-1997
    • Cordova, A.1
  • 40
    • 27944434602 scopus 로고    scopus 로고
    • Cyclic chiral amines and amino acids as inexpensive and readily tunable catalysts for the direct asymmetric three-component Mannich reaction
    • Ibrahem, I.; Zou, W.; Engqvist, M.; Xu, Y.; Cordova, A. Cyclic chiral amines and amino acids as inexpensive and readily tunable catalysts for the direct asymmetric three-component Mannich reaction. Chem. Eur. J., 2005, 11, 7024-7029.
    • (2005) Chem. Eur. J , vol.11 , pp. 7024-7029
    • Ibrahem, I.1    Zou, W.2    Engqvist, M.3    Xu, Y.4    Cordova, A.5
  • 41
    • 38349089956 scopus 로고    scopus 로고
    • Catalysis of 3-pyrrolidine carboxylic acid and related pyrrolidine derivatives in enantioselective anti-Mannich type reactions: Importance of the 3-acid group on pyrrolidine for stereocontrol
    • Zhang, H.; Mitsumori, S.; Utsumi, N.; Imai, M.; Delgado, N.G.; Mifsud, M.; Albertshofer, K.; Cheong, P.H.Y.; Houk, K.N.; Tanaka, F.; Barbas, C.F. III. Catalysis of 3-pyrrolidine carboxylic acid and related pyrrolidine derivatives in enantioselective anti-Mannich type reactions: importance of the 3-acid group on pyrrolidine for stereocontrol. J. Am. Chem. Soc., 2008, 130, 875-886.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 875-886
    • Zhang, H.1    Mitsumori, S.2    Utsumi, N.3    Imai, M.4    Delgado, N.G.5    Mifsud, M.6    Albertshofer, K.7    Cheong, P.H.Y.8    Houk, K.N.9    Tanaka, F.10    Barbas III, C.F.11
  • 42
    • 44949251617 scopus 로고    scopus 로고
    • Primary amino acids: Privileged catalysts in enantioselective organocatalysis
    • Xu, L.W.; Lu, Y. Primary amino acids: privileged catalysts in enantioselective organocatalysis. Org. Biomol. Chem., 2008, 6, 2047-2053.
    • (2008) Org. Biomol. Chem , vol.6 , pp. 2047-2053
    • Xu, L.W.1    Lu, Y.2
  • 43
    • 55249112288 scopus 로고    scopus 로고
    • Aminocatalytic enantioselective anti-Mannich reaction of aldehydes with in situ generated N-Cbz and N-Boc imines
    • Gianelli, C.; Sambri, L.; Carlone, A.; Bartoli, G.; Melchiorre, P. Aminocatalytic enantioselective anti-Mannich reaction of aldehydes with in situ generated N-Cbz and N-Boc imines. Angew. Chem. Int. Ed., 2008, 47, 8700-8702.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 8700-8702
    • Gianelli, C.1    Sambri, L.2    Carlone, A.3    Bartoli, G.4    Melchiorre, P.5
  • 44
    • 37649001505 scopus 로고    scopus 로고
    • Anti-selective direct asymmetric Mannich reactions catalyzed by chiral pyrrolidine-based amino sulfonamides
    • Kano, T.; Hato, Y.; Yamamoto, A.; Maruoka, K. Anti-selective direct asymmetric Mannich reactions catalyzed by chiral pyrrolidine-based amino sulfonamides. Tetrahedron., 2008, 64, 1197-1203.
    • (2008) Tetrahedron , vol.64 , pp. 1197-1203
    • Kano, T.1    Hato, Y.2    Yamamoto, A.3    Maruoka, K.4
  • 45
    • 38349089956 scopus 로고    scopus 로고
    • Catalysis of 3-pyrrolidine carboxylic acid and related pyrrolidine derivatives in enantioselective anti-Mannich type reactions: Importance of the 3-acid group on pyrrolidine for stereocontrol
    • Zhang, H.; Mitsumori, S.; Utsumi, N.; Imai, M.; Delgado, N.G.; Mifsud, M.; Albertshofer, K.; Cheong, P.H.Y.; Houk, K.N.; Tanaka, F.; Barbas, C.F. III. Catalysis of 3-pyrrolidine carboxylic acid and related pyrrolidine derivatives in enantioselective anti-Mannich type reactions: importance of the 3-acid group on pyrrolidine for stereocontrol. J. Am. Chem. Soc., 2008, 130, 875-886.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 875-886
    • Zhang, H.1    Mitsumori, S.2    Utsumi, N.3    Imai, M.4    Delgado, N.G.5    Mifsud, M.6    Albertshofer, K.7    Cheong, P.H.Y.8    Houk, K.N.9    Tanaka, F.10    Barbas III, C.F.11
  • 46
    • 37649024285 scopus 로고    scopus 로고
    • Direct catalytic asymmetric threecomponent Mannich reactions with dihydroxyacetone: Enantioselective synthesis of amino sugar derivatives
    • Dziedzic, P.; Ibrahem, I.; Cordova, A. Direct catalytic asymmetric threecomponent Mannich reactions with dihydroxyacetone: enantioselective synthesis of amino sugar derivatives. Tetrahedron Lett., 2008, 49, 803-807.
    • (2008) Tetrahedron Lett , vol.49 , pp. 803-807
    • Dziedzic, P.1    Ibrahem, I.2    Cordova, A.3
  • 47
    • 34249888744 scopus 로고    scopus 로고
    • Acyclic β-amino acid catalyzed asymmetric antiselective Mannich type reactions
    • Dziedzic, P.; Cordova, A. Acyclic β-amino acid catalyzed asymmetric antiselective Mannich type reactions. Tetrahedron: Asym., 2007, 18, 1033-1037.
    • (2007) Tetrahedron: Asym , vol.18 , pp. 1033-1037
    • Dziedzic, P.1    Cordova, A.2
  • 49
    • 78049380161 scopus 로고    scopus 로고
    • Enantioselective synthesis of syn-and anti-1,3-aminoalcohols via β-aminoketones and subsequent reduction/dynamic kinetic asymmetric transformation
    • Millet, R.; Traff, A.M.; Petrus, M.L.; Backvall, Jan-E. Enantioselective synthesis of syn-and anti-1,3-aminoalcohols via β-aminoketones and subsequent reduction/dynamic kinetic asymmetric transformation. J. Am. Chem. Soc., 2010, 132, 15182-15184.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15182-15184
    • Millet, R.1    Traff, A.M.2    Petrus, M.L.3    Backvall, J.-E.4
  • 50
    • 33947545143 scopus 로고    scopus 로고
    • Direct asymmetric three-component organocatalytic anti-selective Mannich reactions in a purely aqueous system
    • Cheng, L.; Wu, X.; Lu, Y. Direct asymmetric three-component organocatalytic anti-selective Mannich reactions in a purely aqueous system. Org. Biomol. Chem., 2007, 5, 1018-1020.
    • (2007) Org. Biomol. Chem , vol.5 , pp. 1018-1020
    • Cheng, L.1    Wu, X.2    Lu, Y.3
  • 51
    • 35248872887 scopus 로고    scopus 로고
    • Highly diastereoselective and enantioselective direct organocatalytic anti-selective Mannich reactions employing N-tosylimines
    • Cheng, L.; Han, H.; Huang, H.; Wong, M.W.; Lu, Y. Highly diastereoselective and enantioselective direct organocatalytic anti-selective Mannich reactions employing N-tosylimines. Chem. Commun., 2007, 4143-4145.
    • (2007) Chem. Commun , pp. 4143-4145
    • Cheng, L.1    Han, H.2    Huang, H.3    Wong, M.W.4    Lu, Y.5
  • 52
    • 33846198424 scopus 로고    scopus 로고
    • Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions
    • Ramasastry, S.S.V.; Zhang, H.L.; Tanaka, F.; Barbas, C.F. III. Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions. J. Am. Chem. Soc., 2007,129, 288-289.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 288-289
    • Ramasastry, S.S.V.1    Zhang, H.L.2    Tanaka, F.3    Barbas III, C.F.4
  • 53
    • 2342570203 scopus 로고    scopus 로고
    • Enantioselective Mannichtype reaction catalyzed by a chiral Bronsted acid
    • Akiyama, T.; Itoh, J.; Yokota, K.; Fuchibe, K. Enantioselective Mannichtype reaction catalyzed by a chiral Bronsted acid. Angew. Chem. Int. Ed., 2004, 43, 1566-1568.
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 1566-1568
    • Akiyama, T.1    Itoh, J.2    Yokota, K.3    Fuchibe, K.4
  • 54
    • 2342521907 scopus 로고    scopus 로고
    • Chiral Bronsted acid-catalyzed direct Mannich reactions via electrophilic activation
    • Uraguchi, D.; Terada, M. Chiral Bronsted acid-catalyzed direct Mannich reactions via electrophilic activation. J. Am. Chem. Soc., 2004, 126, 5356-5357.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 5356-5357
    • Uraguchi, D.1    Terada, M.2
  • 55
    • 23844490047 scopus 로고    scopus 로고
    • Asymmetric Mannich reactions of β-keto esters with acyl imines catalyzed by cinchona alkaloids
    • Lou, S.; Taoka, B.M.; Ting, A.; Schaus, S. Asymmetric Mannich reactions of β-keto esters with acyl imines catalyzed by cinchona alkaloids. J. Am. Chem. Soc., 2005, 127, 11256-11257.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 11256-11257
    • Lou, S.1    Taoka, B.M.2    Ting, A.3    Schaus, S.4
  • 56
    • 33644747543 scopus 로고    scopus 로고
    • Direct enantio-and diastereoselective Mannich reactions of malonate and β-keto esters with N-Boc and N-Cbz aldimines catalyzed by a bifunctional cinchonine derivative
    • Tillman, A.L.; Ye, J.; Dixon, D.J. Direct enantio-and diastereoselective Mannich reactions of malonate and β-keto esters with N-Boc and N-Cbz aldimines catalyzed by a bifunctional cinchonine derivative. Chem. Commun., 2006, 1191-1193.
    • (2006) Chem. Commun , pp. 1191-1193
    • Tillman, A.L.1    Ye, J.2    Dixon, D.J.3
  • 57
    • 84962407641 scopus 로고    scopus 로고
    • Chiral Brønsted acid catalyzed enantioselective Mannich-type reaction
    • Yamanaka, M.; Itoh, J.; Fuchibe, K.; Akiyama, T. Chiral Brønsted acid catalyzed enantioselective Mannich-type reaction. J. Am. Chem. Soc., 2007, 129, 6756-6764.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 6756-6764
    • Yamanaka, M.1    Itoh, J.2    Fuchibe, K.3    Akiyama, T.4
  • 58
    • 53249083582 scopus 로고    scopus 로고
    • Brønsted-acid-catalyzed activation of nitroalkanes: A direct enantioselective aza-Henry reaction
    • Rueping, M.; Antonchick, A.P. Brønsted-acid-catalyzed activation of nitroalkanes: a direct enantioselective aza-Henry reaction. Org. Lett., 2008, 10, 1731-1734.
    • (2008) Org. Lett. , vol.10 , pp. 1731-1734
    • Rueping, M.1    Antonchick, A.P.2
  • 59
    • 74849128892 scopus 로고    scopus 로고
    • Chiral lithium(I) binaphtholate salts for the enantioselective direct Mannich-type reaction with a change of syn/anti and absolute stereochemistry
    • Hatano, M.; Horibe, T.; Ishihara, K. Chiral lithium(I) binaphtholate salts for the enantioselective direct Mannich-type reaction with a change of syn/anti and absolute stereochemistry. J. Am. Chem. Soc., 2010, 132, 56-57.
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 56-57
    • Hatano, M.1    Horibe, T.2    Ishihara, K.3
  • 60
    • 33847782578 scopus 로고    scopus 로고
    • Asymmetric Mannich reactions with in situ generation of carbamate-protected imines by an organic catalyst
    • Song, J.; Shih, Hui-W.; Deng, L. Asymmetric Mannich reactions with in situ generation of carbamate-protected imines by an organic catalyst. Org. Lett., 2007, 9, 603-606.
    • (2007) Org. Lett , vol.9 , pp. 603-606
    • Song, J.1    Shih, H.-W.2    Deng, L.3
  • 61
    • 33646511310 scopus 로고    scopus 로고
    • The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: Enantioselective synthesis of β-amino acids
    • Song, J.; Wang, Y.; Deng, L. The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: enantioselective synthesis of β-amino acids. J. Am. Chem. Soc., 2006, 128, 6048-6049.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 6048-6049
    • Song, J.1    Wang, Y.2    Deng, L.3
  • 62
    • 33744733390 scopus 로고    scopus 로고
    • Highly diastereoselective asymmetric Mannich reactions of 1,3-dicarbonyls with acyl imines
    • Ting, A.; Lou, S.; Schaus, S.E. Highly diastereoselective asymmetric Mannich reactions of 1,3-dicarbonyls with acyl imines. Org. Lett., 2006, 8, 2003-2006.
    • (2006) Org. Lett , vol.8 , pp. 2003-2006
    • Ting, A.1    Lou, S.2    Schaus, S.E.3
  • 63
    • 18844456337 scopus 로고    scopus 로고
    • Direct organocatalytic and highly enantio-and diastereoselective Mannich reactions of α-substituted α-cyanoacetates
    • Poulsen, T.B.; Alemparte, C.; Saaby, S.; Bella, M.; Jørgensen, K.A. Direct organocatalytic and highly enantio-and diastereoselective Mannich reactions of α-substituted α-cyanoacetates. Angew. Chem. Int. Ed., 2005, 44, 2896-2899.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 2896-2899
    • Poulsen, T.B.1    Alemparte, C.2    Saaby, S.3    Bella, M.4    Jørgensen, K.A.5
  • 64
    • 54049122287 scopus 로고    scopus 로고
    • Organocatalytic Mannich-type reactions of trifluoroethyl thioesters
    • Utsumi, N.; Kitagaki, S.; Barbas III, C.F. Organocatalytic Mannich-type reactions of trifluoroethyl thioesters. Org. Lett., 2008, 10, 3405-3408.
    • (2008) Org. Lett , vol.10 , pp. 3405-3408
    • Utsumi, N.1    Kitagaki, S.2    Barbas III, C.F.3
  • 65
    • 77955161875 scopus 로고    scopus 로고
    • Direct carboncarbon bond formation via soft enolization: A biomimetic asymmetric Mannich reaction of phenylacetate thioesters
    • Kohler, M.C.; Yost, J.M.; Garnsey, M.R.; Coltart, D.M. Direct carboncarbon bond formation via soft enolization: a biomimetic asymmetric Mannich reaction of phenylacetate thioesters. Org. Lett., 2010, 12, 3376-3379.
    • (2010) Org. Lett , vol.12 , pp. 3376-3379
    • Kohler, M.C.1    Yost, J.M.2    Garnsey, M.R.3    Coltart, D.M.4
  • 66
    • 34447136276 scopus 로고    scopus 로고
    • Organocatalysis in conjugate amine additions. synthesis of β-amino acid derivatives
    • Sibi, M.P.; Itho, K. Organocatalysis in conjugate amine additions. synthesis of β-amino acid derivatives. J. Am. Chem. Soc., 2007, 129, 8064-8065.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 8064-8065
    • Sibi, M.P.1    Itho, K.2
  • 67
    • 27144522622 scopus 로고    scopus 로고
    • Organocatalytic asymmetric Michael addition of 2,4-pentandione to nitroolefins
    • Wang, J.; Li, H.; Duan, W.; Zu, L.; Wang, W. Organocatalytic asymmetric Michael addition of 2,4-pentandione to nitroolefins. Org. Lett., 2005, 7, 4713-4716.
    • (2005) Org. Lett , vol.7 , pp. 4713-4716
    • Wang, J.1    Li, H.2    Duan, W.3    Zu, L.4    Wang, W.5
  • 69
    • 0025895518 scopus 로고
    • Enantioselective synthesis of β-amino acids based on BINAP-ruthenium(II) catalyzed hydrogenation
    • Lubell, W.D.; Kitamura, M.; Noyori, R. Enantioselective synthesis of β-amino acids based on BINAP-ruthenium(II) catalyzed hydrogenation. Tetrahedron: Asym., 1991, 2, 543-554.
    • (1991) Tetrahedron: Asym , vol.2 , pp. 543-554
    • Lubell, W.D.1    Kitamura, M.2    Noyori, R.3
  • 70
    • 39649117987 scopus 로고    scopus 로고
    • Synthesis of β--aminoacid derivatives via enantioselective hydrogenation of β-substituted-β-(acylamino) acrylates
    • Bruneau, C.; Renaud, J.L.; Jerphagnon, T. Synthesis of β--aminoacid derivatives via enantioselective hydrogenation of β-substituted-β-(acylamino) acrylates. Coord. Chem. Rev., 2008, 252, 532-544.
    • (2008) Coord. Chem. Rev. , vol.252 , pp. 532-544
    • Bruneau, C.1    Renaud, J.L.2    Jerphagnon, T.3
  • 71
    • 38049077372 scopus 로고    scopus 로고
    • Developing chiral ligands for asymmetric hydrogenation
    • Zhang, W.; Chi, Y.; Zhang, X. Developing chiral ligands for asymmetric hydrogenation. Acc. Chem. Res., 2007, 40, 1278-1290.
    • (2007) Acc. Chem. Res , vol.40 , pp. 1278-1290
    • Zhang, W.1    Chi, Y.2    Zhang, X.3
  • 72
    • 38049004864 scopus 로고    scopus 로고
    • Developments in asymmetric hydrogenation from an industrial perspective
    • Shimizu, H.; Nagasaki, I.; Matsumura, K.; Sayo, N.; Saito, T. Developments in asymmetric hydrogenation from an industrial perspective. Acc. Chem. Res., 2007, 40, 1385-1393.
    • (2007) Acc. Chem. Res , vol.40 , pp. 1385-1393
    • Shimizu, H.1    Nagasaki, I.2    Matsumura, K.3    Sayo, N.4    Saito, T.5
  • 73
    • 0043240879 scopus 로고    scopus 로고
    • New chiral phosphorus ligands for enantioselective hydrogenation
    • Tang, W.; Zhang, X. New chiral phosphorus ligands for enantioselective hydrogenation. Chem. Rev., 2003, 103, 3029-3070.
    • (2003) Chem. Rev , vol.103 , pp. 3029-3070
    • Tang, W.1    Zhang, X.2
  • 77
    • 28244456285 scopus 로고    scopus 로고
    • Efficient rhodium-catalyzed asymmetric hydrogenation for the synthesis of a new class of N-aryl β-amino acid derivatives
    • Dai, Q.; Yang, W.; Zhang, X. Efficient rhodium-catalyzed asymmetric hydrogenation for the synthesis of a new class of N-aryl β-amino acid derivatives. Org. Lett., 2005, 7, 5343-5345.
    • (2005) Org. Lett , vol.7 , pp. 5343-5345
    • Dai, Q.1    Yang, W.2    Zhang, X.3
  • 78
    • 0037062870 scopus 로고    scopus 로고
    • Rh(I)-Catalyzed enantioselective hydro-genation of (E)-and (Z)-β-(acylamino)acrylates using 1,4-bispho-sphine ligands under mild conditions
    • Lee, S.G.; Zhang, Y.J. Rh(I)-Catalyzed enantioselective hydro-genation of (E)-and (Z)-β-(acylamino)acrylates using 1,4-bispho-sphine ligands under mild conditions. Org. Lett., 2002, 4, 2429-2431.
    • (2002) Org. Lett , vol.4 , pp. 2429-2431
    • Lee, S.G.1    Zhang, Y.J.2
  • 79
    • 1642374172 scopus 로고    scopus 로고
    • Economic preparation of 1,3-diphenyl-1,3-bis(diphenylphosphino) propane: A versatile chiral diphosphine ligand for enantioselective hydrogenations
    • Dubrovina, N.V.; Tararov, V.I.; Monsees, A.; Kadyrov, R.; Fischer, C.; Börner, A. Economic preparation of 1,3-diphenyl-1,3-bis(diphenylphosphino) propane: a versatile chiral diphosphine ligand for enantioselective hydrogenations. Tetrahedron: Asym., 2003, 14, 2739-2745.
    • (2003) Tetrahedron: Asym , vol.14 , pp. 2739-2745
    • Dubrovina, N.V.1    Tararov, V.I.2    Monsees, A.3    Kadyrov, R.4    Fischer, C.5    Börner, A.6
  • 80
    • 28044454135 scopus 로고    scopus 로고
    • New chiral 1,3-diphosphine ligands for Rh-catalyzed enantioselective hydrogenation: A search for electronic effects. Tetrahedron
    • Dubrovina, N.V.; Tararov, V.I.; Monsees, A.; Spannenberg, A.; Kostas, I.D.; Börner, A. New chiral 1,3-diphosphine ligands for Rh-catalyzed enantioselective hydrogenation: a search for electronic effects. Tetrahedron: Asym., 2005, 16, 3640-3649.
    • (2005) Asym , vol.16 , pp. 3640-3649
    • Dubrovina, N.V.1    Tararov, V.I.2    Monsees, A.3    Spannenberg, A.4    Kostas, I.D.5    Börner, A.6
  • 81
    • 0345314096 scopus 로고    scopus 로고
    • Synthesis of a new chiral bisphospholane ligand for the Rh(I)-catalyzed enantioselective hydrogenation of isomeric β-acylamido acrylates
    • Holz, J.; Monsees, A.; Jiao, H.; You, J.; Komarov, I.V.; Fischer, C.; Drauz, K.; Börner, A. Synthesis of a new chiral bisphospholane ligand for the Rh(I)-catalyzed enantioselective hydrogenation of isomeric β-acylamido acrylates. J. Org. Chem., 2002, 68, 1701-1707.
    • (2002) J. Org. Chem , vol.68 , pp. 1701-1707
    • Holz, J.1    Monsees, A.2    Jiao, H.3    You, J.4    Komarov, I.V.5    Fischer, C.6    Drauz, K.7    Börner, A.8
  • 82
    • 0042531839 scopus 로고    scopus 로고
    • A bisphosphepine ligand with stereogenic phosphorus centers for the practical synthesis of β-aryl-β-amino acids by asymmetric hydrogenation
    • Tang, W.; Wang, W.; Chi, Y.; Zhang, X. A bisphosphepine ligand with stereogenic phosphorus centers for the practical synthesis of β-aryl-β-amino acids by asymmetric hydrogenation. Angew. Chem. Int. Ed., 2003, 42, 3509-3511.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 3509-3511
    • Tang, W.1    Wang, W.2    Chi, Y.3    Zhang, X.4
  • 83
    • 0042626473 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of tetrasubstituted olefins of cyclic β-(acylamino)acrylates
    • Tang, W.; Wu, S.; Zhang, X. Enantioselective hydrogenation of tetrasubstituted olefins of cyclic β-(acylamino)acrylates. J. Am. Chem. Soc., 2003, 125, 9570-9571.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 9570-9571
    • Tang, W.1    Wu, S.2    Zhang, X.3
  • 84
    • 0035794970 scopus 로고    scopus 로고
    • Highly enantioselective or not?-chiral monodentate monophosphorus ligands in the asymmetric hydrogenation
    • Komarov, I.V.; Börner, A. Highly enantioselective or not?-chiral monodentate monophosphorus ligands in the asymmetric hydrogenation. Angew. Chem. Int. Ed., 2001, 40, 1197-1200.
    • (2001) Angew. Chem. Int. Ed , vol.40 , pp. 1197-1200
    • Komarov, I.V.1    Börner, A.2
  • 86
    • 3142651346 scopus 로고    scopus 로고
    • Carbohydrate-derived monophosphite ligands for Rh-catalyzed enantioselective hydrogenation of β-and β-dehydroamino acid esters. Tetrahedron
    • Huang, H.; Liu, X.; Chen, S.; Chen, H.; Zheng, Z. Carbohydrate-derived monophosphite ligands for Rh-catalyzed enantioselective hydrogenation of β-and β-dehydroamino acid esters. Tetrahedron: Asym., 2004, 15, 2011-2019.
    • (2004) Asym , vol.15 , pp. 2011-2019
    • Huang, H.1    Liu, X.2    Chen, S.3    Chen, H.4    Zheng, Z.5
  • 92
    • 79953205260 scopus 로고    scopus 로고
    • Synthesis of β-amino acid derivatives via copper-catalyzed asymmetric 1,4-reduction of β-(acylamino)acrylates
    • Wu, Y.; Qi, S.B.; Wu, F.F.; Zhang, X.C.; Li, M.; Wu, J.; Chan, A.S.C. Synthesis of β-amino acid derivatives via copper-catalyzed asymmetric 1,4-reduction of β-(acylamino)acrylates. Org. Lett., 2011, 13, 1754-1757.
    • (2011) Org. Lett , vol.13 , pp. 1754-1757
    • Wu, Y.1    Qi, S.B.2    Wu, F.F.3    Zhang, X.C.4    Li, M.5    Wu, J.6    Chan, A.S.C.7
  • 93
    • 1642415515 scopus 로고    scopus 로고
    • The direct catalytic asymmetric Mannich reaction
    • Córdova, A. The direct catalytic asymmetric Mannich reaction. Acc. Chem. Res., 2004, 37, 102-112.
    • (2004) Acc. Chem. Res , vol.37 , pp. 102-112
    • Córdova, A.1
  • 94
    • 0037244819 scopus 로고    scopus 로고
    • α-Imino esters: Versatile substrates for the catalytic, asymmetric synthesis of α-and β-amino acids and β-lactams
    • 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
  • 95
    • 0000862669 scopus 로고    scopus 로고
    • Catalytic enantioselective addition to imines
    • Kobayashi, S.; Ishitani, H. Catalytic enantioselective addition to imines. Chem Rev., 1999, 99, 1069-1094.
    • (1999) Chem Rev , vol.99 , pp. 1069-1094
    • Kobayashi, S.1    Ishitani, H.2
  • 96
    • 16244364063 scopus 로고    scopus 로고
    • Catalytic asymmetric addition of β-ketoesters to various Imines by using chiral palladium complexes
    • Hamashina, Y.; Sasamoto, N.; Hotta, D.; Somei, H.; Umebayashi, N.; Sodeoka, M. Catalytic asymmetric addition of β-ketoesters to various Imines by using chiral palladium complexes. Angew. Chem. Int. Ed., 2005, 44, 1525-1529.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 1525-1529
    • Hamashina, Y.1    Sasamoto, N.2    Hotta, D.3    Somei, H.4    Umebayashi, N.5    Sodeoka, M.6
  • 97
    • 0037462104 scopus 로고    scopus 로고
    • anti-Selective direct catalytic asymmetric Mannich-type reaction of hydroxyketone providing β-amino alcohols
    • Matsunaga, S.; Kumagai, N.; Harada, S.; Shibasaki, M. anti-Selective direct catalytic asymmetric Mannich-type reaction of hydroxyketone providing β-amino alcohols. J. Am. Chem. Soc., 2003, 125, 4712-4713.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 4712-4713
    • Matsunaga, S.1    Kumagai, N.2    Harada, S.3    Shibasaki, M.4
  • 98
    • 33646089871 scopus 로고    scopus 로고
    • Metal/linked-BINOL complexes: Applications in direct catalytic asymmetric Mannich-type reactions
    • Shibasaki, M.; Matsunuga, S. Metal/linked-BINOL complexes: applications in direct catalytic asymmetric Mannich-type reactions. J. Organomet. Chem., 2006, 691, 2089-2100.
    • (2006) J. Organomet. Chem , vol.691 , pp. 2089-2100
    • Shibasaki, M.1    Matsunuga, S.2
  • 99
    • 22744453251 scopus 로고    scopus 로고
    • Direct catalytic asymmetric Mannich-type reactions of N-(2-hydroxyacetyl)pyrrole as an ester-equivalent donor
    • Harada, S.; Handa, S.; Matsunaga, S.; Shibasaki, M. Direct catalytic asymmetric Mannich-type reactions of N-(2-hydroxyacetyl)pyrrole as an ester-equivalent donor. Angew. Chem. Int. Ed., 2005, 44, 4365-4368.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 4365-4368
    • Harada, S.1    Handa, S.2    Matsunaga, S.3    Shibasaki, M.4
  • 100
    • 34547803869 scopus 로고    scopus 로고
    • Lanthanum aryloxide/pybox-catalyzed direct asymmetric Mannich-type reactions using a trichloromethyl ketone as a propionate equivalent donor
    • Morimoto, H.; Lu, G.; Aoyama, N.; Matsunaga, S.; Shibasaki, M. Lanthanum aryloxide/pybox-catalyzed direct asymmetric Mannich-type reactions using a trichloromethyl ketone as a propionate equivalent donor. J. Am. Chem. Soc., 2007, 129, 9588-9589.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 9588-9589
    • Morimoto, H.1    Lu, G.2    Aoyama, N.3    Matsunaga, S.4    Shibasaki, M.5
  • 101
    • 39549091935 scopus 로고    scopus 로고
    • 2-Schiff base complex for catalytic asymmetric synthesis of α-tetrasubstituted anti-β,β-diamino acid surrogates
    • 2-Schiff base complex for catalytic asymmetric synthesis of α-tetrasubstituted anti-β,β-diamino acid surrogates. J. Am. Chem. Soc., 2008, 130, 2170-2171.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 2170-2171
    • Chen, Z.1    Morimoto, H.2    Matsunaga, S.3    Shibasaki, M.4
  • 102
    • 0037419152 scopus 로고    scopus 로고
    • Catalytic asymmetric Mannich reactions of glycine derivatives with imines. A new approach to optically active α,β-diamino acid derivatives
    • Bernardi, L.; Gothelf, A.S.; Hazell, R.G.; Jørgensen, K.A. Catalytic asymmetric Mannich reactions of glycine derivatives with imines. A new approach to optically active α,β-diamino acid derivatives. J. Org. Chem., 2003, 68, 2583-2591.
    • (2003) J. Org. Chem , vol.68 , pp. 2583-2591
    • Bernardi, L.1    Gothelf, A.S.2    Hazell, R.G.3    Jørgensen, K.A.4
  • 103
    • 33747212844 scopus 로고    scopus 로고
    • Direct-type catalytic three-component Mannich reactions leading to an efficient synthesis of α,β-diamino acid derivatives
    • Salter, M.M.; Kobayashi, J.; Shimizu, Y.; Kobayashi, S. Direct-type catalytic three-component Mannich reactions leading to an efficient synthesis of α,β-diamino acid derivatives. Org. Lett., 2006, 8, 3533-3536.
    • (2006) Org. Lett , vol.8 , pp. 3533-3536
    • Salter, M.M.1    Kobayashi, J.2    Shimizu, Y.3    Kobayashi, S.4
  • 104
    • 0037420331 scopus 로고    scopus 로고
    • Catalytic, asymmetric Mannich-type reactions of N-acylimino esters: Reactivity, diastereo-and enantioselectivity, and application to synthesis of N-acylated amino acid derivatives
    • Kobayashi, S.; Matsubara, R.; Nakamura, Y.; Kitagawa, H.; Sugiura, M. Catalytic, asymmetric Mannich-type reactions of N-acylimino esters: reactivity, diastereo-and enantioselectivity, and application to synthesis of N-acylated amino acid derivatives. J. Am. Chem. Soc., 2003, 125, 2507-2515.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 2507-2515
    • Kobayashi, S.1    Matsubara, R.2    Nakamura, Y.3    Kitagawa, H.4    Sugiura, M.5
  • 105
    • 0038340608 scopus 로고    scopus 로고
    • Catalytic asymmetric Mannich-type reactions using a novel chiral iron complex
    • Yamashita, Y.; Ueno, M.; Kuriyama, Y.; Kobayashi, S. Catalytic asymmetric Mannich-type reactions using a novel chiral iron complex. Adv. Synth. Catal., 2002, 344, 929-931.
    • (2002) Adv. Synth. Catal , vol.344 , pp. 929-931
    • Yamashita, Y.1    Ueno, M.2    Kuriyama, Y.3    Kobayashi, S.4
  • 106
    • 0037120156 scopus 로고    scopus 로고
    • Catalytic enantioselective addition of propionate units to imines: An efficient synthesis of anti-α-methyl-β-amino acid derivatives
    • Kobayashi, S.; Kobayashi, J.; Ishiani, H.; Ueno, M. Catalytic enantioselective addition of propionate units to imines: an efficient synthesis of anti-α-methyl-β-amino acid derivatives. Chem Eur. J., 2002, 8, 4185-4190.
    • (2002) Chem Eur. J , vol.8 , pp. 4185-4190
    • Kobayashi, S.1    Kobayashi, J.2    Ishiani, H.3    Ueno, M.4
  • 107
    • 0041461885 scopus 로고    scopus 로고
    • Air-stable, storable, and highly selective chiral Lewis acid catalyst
    • Ueno, M.; Ishitani, H.; Kobayashi, S. Air-stable, storable, and highly selective chiral Lewis acid catalyst. Org. Lett., 2002, 4, 3395-3397.
    • (2002) Org. Lett , vol.4 , pp. 3395-3397
    • Ueno, M.1    Ishitani, H.2    Kobayashi, S.3
  • 108
    • 27644506699 scopus 로고    scopus 로고
    • Chiral zirconium catalysts using multidentate BINOL derivatives for catalytic enantioselective Mannich-type reactions; ligand optimization and approaches to elucidation of the catalyst structure
    • Ihori, Y.; Yamashita, Y.; Ishitani, H.; Kobayashi, S. Chiral zirconium catalysts using multidentate BINOL derivatives for catalytic enantioselective Mannich-type reactions; ligand optimization and approaches to elucidation of the catalyst structure. J. Am. Chem. Soc., 2005, 127, 15528-15535.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 15528-15535
    • Ihori, Y.1    Yamashita, Y.2    Ishitani, H.3    Kobayashi, S.4
  • 110
    • 68949170991 scopus 로고    scopus 로고
    • Recent progress in asymmetric bifunctional catalysis using multimetallic systems
    • Shibasaki, M.; Kanai, M.; Matsunaga, S.; Kumagai, N. Recent progress in asymmetric bifunctional catalysis using multimetallic systems. Acc. Chem. Res., 2009, 42, 1117-1127.
    • (2009) Acc. Chem. Res , vol.42 , pp. 1117-1127
    • Shibasaki, M.1    Kanai, M.2    Matsunaga, S.3    Kumagai, N.4
  • 112
    • 84891323653 scopus 로고    scopus 로고
    • In,; Juaristi, E.; Soloshnok, V. Eds.; John Wiley & Sons, Inc., Hoboken
    • Liu, M.; Sibi, M.P. In: Enantioselective Synthesis of β-Amino Acids; Juaristi, E.; Soloshnok, V. Eds.; John Wiley & Sons, Inc., Hoboken, 2005; 377.
    • (2005) Enantioselective Synthesis of β-Amino Acids , pp. 377
    • Liu, M.1    Sibi, M.P.2
  • 117
    • 0000679263 scopus 로고    scopus 로고
    • Conjugate Addition of Organometallic Reagents
    • In,; Jacobsen, E.N.; Pfaltz, A.; Yamamoto, H. Eds.; Springer Verlag, Berlin
    • Tomioka, K.; Nagaoka, H. Conjugate Addition of Organometallic Reagents, In: Comprehensive AsymmetricCatalysis; Jacobsen, E.N.; Pfaltz, A.; Yamamoto, H. Eds.; Springer Verlag, Berlin, 1999; 833.
    • (1999) Comprehensive AsymmetricCatalysis , pp. 833
    • Tomioka, K.1    Nagaoka, H.2
  • 119
    • 0038813824 scopus 로고    scopus 로고
    • 2-homoamino acid by enantioselective catalysis
    • 2-homoamino acid by enantioselective catalysis. Org. Lett., 2003, 5, 79-80.
    • (2003) Org. Lett , vol.5 , pp. 79-80
    • Rimkus, A.1    Sewald, N.2
  • 120
    • 0037449670 scopus 로고    scopus 로고
    • 2-amino acids by Michael addition of diorgano zinc reagents to nitro acrylates. Tetrahedron
    • 2-amino acids by Michael addition of diorgano zinc reagents to nitro acrylates. Tetrahedron: Asym., 2003, 14, 189-191.
    • (2003) Asym , vol.14 , pp. 189-191
    • Eilitz, U.1    Leßmann, F.2    Seidelmann, O.3    Wendisch, V.4
  • 121
    • 1642352712 scopus 로고    scopus 로고
    • Stereoselective Michael addition of trimethyl aluminium to nitro acrylates: A route to 2-methyl-3-amino propionic acid
    • Eilitz, U.; Leßmann, F.; Seidelmann, O.; Wendisch, V. Stereoselective Michael addition of trimethyl aluminium to nitro acrylates: a route to 2-methyl-3-amino propionic acid. Tetrahedron: Asym., 2003, 14, 3095-3097.
    • (2003) Tetrahedron: Asym , vol.14 , pp. 3095-3097
    • Eilitz, U.1    Leßmann, F.2    Seidelmann, O.3    Wendisch, V.4
  • 123
    • 51649119846 scopus 로고    scopus 로고
    • Asymmetric synthesis of carboxylic acid derivatives having an all-carbon α-quaternary center through Cu-catalyzed 1,4-addition of dialkylzinc reagents to 2-aryl acetate derivatives
    • Wilsily, A.; Fillion, E. Asymmetric synthesis of carboxylic acid derivatives having an all-carbon α-quaternary center through Cu-catalyzed 1,4-addition of dialkylzinc reagents to 2-aryl acetate derivatives. Org. Lett., 2008, 10, 2801-2804.
    • (2008) Org. Lett , vol.10 , pp. 2801-2804
    • Wilsily, A.1    Fillion, E.2
  • 124
    • 33846171975 scopus 로고    scopus 로고
    • Hisaindee, S. A Heterodinuclear asymmetric catalyst for conjugate additions of α-hydroxyketones to β-substituted nitroalkenes
    • Trost, B.M.; Hisaindee, S. A Heterodinuclear asymmetric catalyst for conjugate additions of α-hydroxyketones to β-substituted nitroalkenes. Org. Lett., 2006, 8, 6003-6005.
    • (2006) Org. Lett. , vol.8 , pp. 6003-6005
    • Trost, B.M.1
  • 126
    • 0037448902 scopus 로고    scopus 로고
    • Highly enantioselective, catalytic conjugate addition of cyanide to α,β-unsaturated imides
    • Sammis, G.M.; Jacobsen, E.N. Highly enantioselective, catalytic conjugate addition of cyanide to α,β-unsaturated imides. J. Am. Chem. Soc., 2003, 125, 4442-4443.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 4442-4443
    • Sammis, G.M.1    Jacobsen, E.N.2
  • 127
    • 74949130956 scopus 로고    scopus 로고
    • Rhodium-catalyzed asymmetric addition of arylboronic acids to β-phthaliminoacrylate esters toward the synthesis of β-amino acids
    • Nishimura, T.; Wang, J.; Nagaosa, M.; Okamoto, K.; Shintani, R.; Kwong, F.Y.; Yu, W.Y.; Chan, A.S.C.; Hayashi, T. Rhodium-catalyzed asymmetric addition of arylboronic acids to β-phthaliminoacrylate esters toward the synthesis of β-amino acids. J. Am. Chem. Soc., 2010, 132, 464-465.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 464-465
    • Nishimura, T.1    Wang, J.2    Nagaosa, M.3    Okamoto, K.4    Shintani, R.5    Kwong, F.Y.6    Yu, W.Y.7    Chan, A.S.C.8    Hayashi, T.9
  • 129
    • 14944358971 scopus 로고    scopus 로고
    • A catalytic enantioselective Aza-Michael reaction: Novel protocols for asymmetric synthesis of β-amino carbonyl compounds
    • Xu, L.-W.; Xia, C.G. A catalytic enantioselective Aza-Michael reaction: novel protocols for asymmetric synthesis of β-amino carbonyl compounds. Eur. J. Org. Chem., 2005, 633-639.
    • (2005) Eur. J. Org. Chem , pp. 633-639
    • Xu, L.-W.1    Xia, C.G.2
  • 130
    • 2942594935 scopus 로고    scopus 로고
    • Asymmetric synthesis of β-amino acid and amide derivatives by catalytic conjugate addition of aromatic amines to Nalkenoylcarbamates
    • Li, K.; Cheng, X.; Hii, K.K.M. Asymmetric synthesis of β-amino acid and amide derivatives by catalytic conjugate addition of aromatic amines to Nalkenoylcarbamates. Eur. J. Org. Chem., 2004, 959-964.
    • (2004) Eur. J. Org. Chem , pp. 959-964
    • Li, K.1    Cheng, X.2    Hii, K.K.M.3
  • 131
    • 2942629592 scopus 로고    scopus 로고
    • Aminesalt-controlled, catalytic asymmetric conjugate addition of various amines and asymmetric protonation
    • Hamashima, Y.; Somei, H.; Shimura, Y.; Tamura, T.; Sodeoka, M. Aminesalt-controlled, catalytic asymmetric conjugate addition of various amines and asymmetric protonation. Org. Lett., 2004, 6, 1861-1864.
    • (2004) Org. Lett , vol.6 , pp. 1861-1864
    • Hamashima, Y.1    Somei, H.2    Shimura, Y.3    Tamura, T.4    Sodeoka, M.5
  • 132
    • 0035928479 scopus 로고    scopus 로고
    • Catalytic enantio-selective addition of aromatic amines to enones: Synthesis of optically active β-amino acid derivatives
    • Zhuang, W.; Hazell, R.G.; Jørgensen, K.A. Catalytic enantio-selective addition of aromatic amines to enones: synthesis of optically active β-amino acid derivatives. Chem. Commun., 2001, 1240-1241
    • (2001) Chem. Commun , pp. 1240-1241
    • Zhuang, W.1    Hazell, R.G.2    Jørgensen, K.A.3
  • 133
    • 38849206255 scopus 로고    scopus 로고
    • Enantioselective conjugate addition of aromatic amines to N-alkenoyloxazolidinones catalyzed by iodido(binaphtholato)samarium
    • Reboule, I.; Gil, R.; Collin, J. Enantioselective conjugate addition of aromatic amines to N-alkenoyloxazolidinones catalyzed by iodido(binaphtholato)samarium. Eur. J. Org. Chem., 2008, 532-539.
    • (2008) Eur. J. Org. Chem , pp. 532-539
    • Reboule, I.1    Gil, R.2    Collin, J.3
  • 134
    • 0037037983 scopus 로고    scopus 로고
    • Temperature dependent reversal of stereochemistry in enantioselective conjugate amine additions
    • Sibi, M.P.; Gorikunti, U.; Liu, M. Temperature dependent reversal of stereochemistry in enantioselective conjugate amine additions. Tetrahedron., 2002, 58, 8357-8363.
    • (2002) Tetrahedron , vol.58 , pp. 8357-8363
    • Sibi, M.P.1    Gorikunti, U.2    Liu, M.3
  • 135
    • 0141732263 scopus 로고    scopus 로고
    • Enantioselective synthesis of α,β-disubstituted-β-amino acids
    • Sibi, M.P.; Prabagaran, N.; Ghorpade, S.G.; Jasperse, C.P. Enantioselective synthesis of α,β-disubstituted-β-amino acids. J. Am. Chem. Soc., 2003, 125, 11796-11797.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 11796-11797
    • Sibi, M.P.1    Prabagaran, N.2    Ghorpade, S.G.3    Jasperse, C.P.4
  • 136
    • 25444512653 scopus 로고    scopus 로고
    • Lewis acid-Lewis acid heterobimetallic cooperative catalysis: Mechanistic studies and application in enantioselective aza-Michael Reaction
    • Yamagiva, N.; Qin, H.; Matsunaga, S.; Shibasaki, M. Lewis acid-Lewis acid heterobimetallic cooperative catalysis: mechanistic studies and application in enantioselective aza-Michael Reaction. J. Am. Chem. Soc., 2005, 127, 13419-13427.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 13419-13427
    • Yamagiva, N.1    Qin, H.2    Matsunaga, S.3    Shibasaki, M.4
  • 140
    • 79955469175 scopus 로고    scopus 로고
    • Asymmetric Mannich reactions catalyzed by cinchona alkaloid thiourea: Enantioselective one-pot synthesis of novel β-amino ester derivatives
    • Bai, S.; Liang, X.; Song, B.A.; Bhadury, P.S.; Hu, D.Y.; Yang, S. Asymmetric Mannich reactions catalyzed by cinchona alkaloid thiourea: enantioselective one-pot synthesis of novel β-amino ester derivatives. Tetrahedron: Asym., 2011, 22, 518-523.
    • (2011) Tetrahedron: Asym , vol.22 , pp. 518-523
    • Bai, S.1    Liang, X.2    Song, B.A.3    Bhadury, P.S.4    Hu, D.Y.5    Yang, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.