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23. Jeon, BH; Dempsey, BA; Burgos, WD; Royer, RA
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26. Finch, GR; Belosevic, M
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53. Heil, M; Podebrad, F; Prado, E; Beck, T; Mosandl, A; Sewell, AC; Bohles, H; Lehnert, W
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54. Ishihara, K; Yamaguchi, H; Hamada, H; Nakamura, K; Nakajima, N
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57. Li, T; Rosazza, JP
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58. Myers, CR; Carstens, BP; Antholine, WE; Myers, JM
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59. Beydilli, MI; Pavlostathis, SG; Tincher, WC
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60. Wei, ZL; Li, ZY; Lin, GQ; Tang, MH; Xia, LJ
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61. Stewart, JD
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62. Hioki, H; Hashimoto, T; Kodama, M
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63. Dehli, JR; Gotor, V
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64. Iwamoto, K; Kuramoto, T; Izumi, M; Kirihata, M; Dohmaru, T; Yoshizako, F
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65. Dollhopf, ME; Nealson, KH; Simon, DM; Luther, GW
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66. Gotor, V; Dehli, JR; Rebolledo, F
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67. Christensen, TH; Bjerg, PL; Banwart, SA; Jakobsen, R; Heron, G; Albrechtsen, HJ
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68. Ratering, S; Schnell, S
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69. Marsh, TL; Leon, NM; McInerney, MJ
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70. Bridge, TAM; Johnson, DB
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71. Fredrickson, JK; Kostandarithes, HM; Li, SW; Plymale, AE; Daly, MJ
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72. Kashefi, K; Lovley, DR
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    APPLIED AND ENVIRONMENTAL MICROBIOLOGY
    
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73. Roden, EE; Urrutia, MM; Mann, CJ
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74. Francis, CA; Obraztsova, AY; Tebo, BM
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75. Li, T; Rosazza, JPN
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76. Markwiese, JT; Colberg, PJS
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77. Buisson, D; Baucherel, X; Levoirier, E; Juge, S
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78. Matsuda, T; Harada, T; Nakajima, N; Nakamura, K
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79. Wei, ZL; Li, ZY; Lin, GQ
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80. Peine, A; Tritschler, A; Kusel, K; Peiffer, S
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81. Rodriguez, S; Schroeder, KT; Kayser, MM; Stewart, JD
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82. Fuhshuku, K; Funa, N; Akeboshi, T; Ohta, H; Hosomi, H; Ohba, S; Sugai, T
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83. Zachara, JM; Smith, SC; Fredrickson, JK
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84. Maurice, PA; Lee, YJ; Hersman, LE
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85. Oremland, RS; Dowdle, PR; Hoeft, S; Sharp, JO; Schaefer, JK; Miller, LG; Blum, JS; Smith, RL; Bloom, NS; Wallschlaeger, D
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    GEOCHIMICA ET COSMOCHIMICA ACTA
    
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86. Fredrickson, JK; Zachara, JM; Kennedy, DW; Duff, MC; Gorby, YA; Li, SMW; Krupka, KM
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87. Gerlach, R; Cunningham, AB; Caccavo, F
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    ENVIRONMENTAL SCIENCE & TECHNOLOGY
    
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88. Nevin, KP; Lovley, DR
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    ENVIRONMENTAL SCIENCE & TECHNOLOGY
    
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89. Wielinga, B; Bostick, B; Hansel, CM; Rosenzweig, RF; Fendorf, S
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90. Bertau, M; Burli, M
    Enantioselective microbial reduction with baker's yeast on an industrial scale
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91. Miyadera, A; Satoh, K; Imura, A
    Efficient synthesis of a key intermediate of DV-7751 via optical resolution or microbial reduction
    CHEMICAL & PHARMACEUTICAL BULLETIN
    
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92. Rodriguez, S; Kayser, M; Stewart, JD
    Improving the stereoselectivity of bakers' yeast reductions by genetic engineering
    ORGANIC LETTERS
    
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93. Forzato, C; Nitti, P; Pitacco, G; Valentin, E
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94. Quiros, M; Rebolledo, F; Gotor, V
    Bioreduction of 2-oxocyclopentanecarboxamides: syntheses of optically active 2-aminomethyl- and 2-aminocyclopentanols
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95. Dahl, AC; Fjeldberg, M; Madsen, JO
    Baker's yeast: improving the D-stereoselectivity in reduction of 3-oxo esters
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96. Balint, J; Egri, G; Kolbert, A; Dianoczky, C; Fogassy, E; Novak, L; Poppe, L
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97. Buisson, D; Azerad, R
    Preparation and use of (S)-O-acetyllactyl chloride (Mosandl's reagent) as a chiral derivatizing agent
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98. Drioli, S; Nitti, P; Pitacco, G; Tossut, L; Valentin, E
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99. Besse, P; Ciblat, S; Canet, JL; Troin, Y; Veschambre, H
    Stereoselective chemoenzymatic synthesis of both enantiomers of protected 4-amino-2-pentanone
    TETRAHEDRON-ASYMMETRY
    
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100. Hayakawa, R; Shimizu, M
     The baker's yeast reduction of the beta-keto aldehydes in the presence of a sulfur compound
     SYNLETT
     
     R. Hayakawa e M. Shimizu, "The baker's yeast reduction of the beta-keto aldehydes in the presence of a sulfur compound", SYNLETT, (8), 1999, pp. 1298-1300