□논문
1. B. T. Cho, “Recent development and improvement for boron hydride-based catalytic asymmetric reduction of unsymmetrical ketones” Chem. Soc. Rev. 2009, 38 (2), 443-452.
2. B. T. Cho; S. H. Shin, “Enantioselective Ring Opening of Meso- and Racemic Epoxides with Phenyl lithium Catalyzed by Chiral -Amino Alcohols Derived from -D-Xylose” Bull. Korean Chem. Soc. 2006, 27(9), 1283-1284.
3. B. T. Cho; S. K. Kang; M. S. Kim; S. R. Ryu; D. K. An, “Solvent-free reduction of aldehydes and ketones using solid acid-activated sodium borohydride” Tetrahedron 2006, 62(34), 8164-8168.
4. B. T. Cho, “Recent advances in the synthetic applications of the oxazaborolidine-mediated asymmetric reduction” Tetrahedron 2006, 62 (33), 7621-7643.
5. B. T. Cho; S. H. Shin, “Highly enantioselective synthesis of multifunctionalized allylic building blocks via oxazaborolidine-catalyzed borane reduction”, Tetrahedron 2005, 61 (29), 6959-6966.
6. B. T. Cho; S. K. Kang, “Synthesis of New Chiral -Amino Alcohols Derived from Isomannide And Their Application to The Catalytic Enantioselective Addition of Diethylzinc to Aldehydes”, Bull. Korean Chem. Soc. 2005, 26(7), 1101-1103.
7. B. T. Cho; S. K. Kang, “Direct and indirect reductive amination of aldehydes and ketones with solid acid-activated sodium borohydride under solvent-free conditions” Tetrahedron 2005, 61 (24), 5725-5734.
8. B. T. Cho, In Boronic acids: Preparation, Applications in Organic Synthesis and Medicine (Oxazaborolidines as asymmetric inducers for the reduction of ketones and ketimines), D. G.. Hall, Ed. Chapter 11, pp 411-439, Wiley-VCH, 2005.
9. B. T. Cho; D. J. Kim, “A Convenient Synthesis of Optically Active Unhindered Aliphatic Alcohols with High Optical Purity from Non-Racemic -Hydroxy Sulfides”, Bull. Korean Chem. Soc. 2004, 25 (9), 1385-1391.
10. B. T. Cho; S. K. Kang, “Clean and Simple Chemoselective Reduction of Imines to Amines Using Boric Acid-Activated Sodium Borohydride under Solvent-Free Conditions” Synlett 2004, (9), 1484-1488.
11. B. T. Cho; S. H. Shin, “Efficient Synthesis of Optically Active 2-N-Boc (or Cbz)-Amino-1-Arylethanols as Key Intermediates for Synthesis of Chiral Drugs via Asymmetric Reduction” Bull. Korean Chem. Soc. 2004, 25 (5), 747-750.
12. D. J. Kim; B. T. Cho “New Approach to the Synthesis of Optically Active Norephedrine, Norpseudoephedrine and Cathinone via Double Asymmetric Induction” Bull. Korean Chem. Soc. 2003, 24 (11), 1641-1648.
13. S. H. Shin; S. K. Kang; B. T. Cho “An Easy and Convenient Synthesis of Optically Active -Amino Alcohols and 1,2-Diamines. Applications in Enantioselective Deprotonation of Cyclohexene Oxide” Bull. Korean Chem. Soc. 2003, 24 (11), 1695-1698.
14. B. T. Cho.; O. K. Choi.; D. J. Kim “Facile Synthesis of Enantiopure 1,2-Diols and Terminal Epoxides from Chiral -Hydroxy Sulfides” Bull. Korean Chem. Soc. 2003, 24 (7), 1023-1025.
15. B. T. Cho.; D. J. Kim “Efficient synthesis of (R)- and (S)-3-octanol, (R)-2-dodecanol, (R)-2-methyl-4-heptanol and (R)-2-methyl-4-octanol: the pheromones of Myrmica scabrinodis, Crematogaster castanea, C. liengmei, C. auberti and Metamasius hemipterus” Tetrahedron 2003, 59 (14), 2457-2462.
16. B. T. Cho; S. K. Kang; S. H. Shin “Application of optically active 1,2-diol monotosylates for synthesis of -azido and -amino alcohols with very high optical purity. Synthesis of enantiopure (R)-octopamine, (R)-tembamide and (R)-aegeline”Tetrahedron: Asymmetry 2002, 13 (11), 1209-1217.
17. B. T. Cho; S. K. Kang; S. H. Shin “A Simple and Efficient Synthesis of Near Enantiopure -hydroxy nitriles” Bull. Korean Chem. Soc. 2002, 23 (12), 1693-1694.
18. B. T. Cho.; S. K. Kang.; W. K. Yang “Convenient Synthesis of Enantiopure -Adrenergic Blockers: (R)-Nifenalol, (R)-Denopamine, (R)-Dichloroisoproterenol, and (R)-Pronethalol” Bull. Korean Chem. Soc. 2002, 23 (09), 1328-1330.
19. B. T. Cho.; O. K. Choi.; D. J. Kim “Highly efficient synthesis of chiral -hydroxy sulfides with high optical purity via CBS-oxazaborolidine-catalyzed borane reduction” Tetrahedron: Asymmetry, 2002, 13 (7), 697-703.
20. B. T. Cho “Boron-Based Reducing Agents for the Asymmetric Reduction of Functionalized Ketones and Ketimines” Aldrichimica Acta, 2002, 35 (1), 3-16.
21. B. T. Cho and O. K. Choi “Synthesis of Optically Active 1,2-Indene Oxide and Vicinal cis-Aminoindanols via Asymmetric Reduction of 2-Tolylsulfonyloxy-1-indanone with (-)-B-Chlorodiisopinocampheylborane” Bull. Korean Chem. Soc. 2001, 22 (11), 1261-1263.
22. B. T. Cho and D. J. Kim “Efficient Synthesis of Optically Active -Hydroxy p-Tolylsulfones with Very High Optical Purity via CBS-Oxazaborolidine-Catalyzed Borane Reduction” Tetrahedron: Asymmetry, 2001,12 (14), 2043-2047.
23. B. T. Cho and Y. S. Chun, “Asymmeric Reduction of -Functionalized Ketones with Organoboron-Based Chiral Reducing Agents” Organoboranes for Syntheses (ACS Symposium series 783), P. V. Ramachandran and H. C. Brown, Ed.; American Chemical Society, Washington DC, 2001, pp 122-135.
24. Byung Tae Cho, Weon Ki Yang and Ok Kyoung Choi “Convenient synthesis of optically active 1,2-diol monosulfonylates and terminal epoxides via oxazaborolidine-catalyzed asymmetric borane reduction of -sulfonyloxy ketones” J. Chm. Soc. Perkin Trans. I, 2001, (10), 1204-1211.
25. Ok Kyoung Choi and Byung Tae Cho “A convenient synthesis of optically active 1,2-indene oxide and trans-2-bromo-1-indanol via oxazaborolidine-catalyzed borane reduction” Tetrahedron: Asymmetry, 2001,12 (6), 903-907.
26. Byung Tae Cho and Ok Kyoung Choi “Facile Synthesis of Optically Active Styrene Oxide Derivatives by Asymmetric Reduction of Substituted 2-Sulfonyloxyacetophenones with (-)-B-Chlorodiisopinocampheylborane (dIpc2BCl)” Bull. Korean Chem. Soc. 2001, 22 (5), 443-444.
27. Ok Kyung Choi and Byung Tae Cho “An efficient synthesis of enantiopure 3-chlorostyrene oxide via oxazaborolidine-catalyzed reduction” Org. Prep. Proced. Int., 2000, 32(5), 493-497.
28. Weon Ki Yang and Byung Tae Cho “Facile synthesis of chiral isopropyl carbinols with high optical purity via catalytic enantioselective addition of diisopropylzinc to aldehydes” Tetrahedron: Asymmetry, 2000, 11(14), 2947-2953.
29. Byung Tae Cho,* Yu Sung Chun and Weon Ki Yang “Catalytic enantioselective reactions. Part 18. Preparation of 3-deoxy-3-N,N-dialkylamino-1,2;5,6-di-O-isopropylidene-D-altritol derivatives from D-mannitol and their applications for catalytic enantioselective addition of dialkylzinc to aldehydes” Tetrahedron: Asymmetry, 2000, 11(10), 2149-2157.
30. B. T. Cho; Y. S. Chun,”A Practical Method for Synthesis of Terminal 1,2-Diols with High Optical Purity via Oxazaborolidine-Catalyzed Asymmetric Reduction” Tetrahedron: Asymmetry, 1999, 10(10), 1843-1846.
31. B. T. Cho; Y. S. Chun, “Catalytic Enantioselective Reactions. Part 16. Oxazaborolidine Catalyzed Asymmetric Borane Reduction of -Keto Acetals”, J. Chm. Soc. Perkin Trans. I, 1999, 2095-2100.
32. B. T. Cho; Y. S. Chun, “Catalytic Enantioselective Reactions. Part 12. Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by Zinc Complexes Modified with Chiral -Sulfonamido Alcohols”, Synth. Commun. 1999, 29(3), 521-531.
33. B. T. Cho; Y. S. Chun, “Oxazaborolidine-Catalyzed Asymmetric Reduction of -Keto Acetals with N,N-Diethylaniline-Borane (DEANB) Complex”, Bull. Korean Chem. Soc. 1999, 20(4), 397-399.
34. J. Kang; C. W. Lee; G. J. Lim; B. T. Cho, “A Concise Synthesis of Unnatural (+)-epi-norjirimycin--lactam via Asymmetric Reduction of meso-Imide”, Tetrahedron: Asymmetry, 1999, 10(4), 657-660.
35. B. T. Cho; Y. S. Chun, “Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by A New Chiral -Amino Alcohol Derived from D-Mannitol”, Tetrahedron: Asymmetry 1998, 9(9), 1489-1491.
36. B. T. Cho; Y. S. Chun, “Facile Synthesis of Terminal 1,2-Diols with High Optical Purity via Oxazaborolidine-Catalyzed Asymmetric Borane Reduction”, J. Org. Chem. 1998, 63(15), 5280-5282.
37. S. Y. Lee; B. T. Cho; N. M. Yoon, “Reductive Amination of Aldehydes and Ketones with Dimethylamine Using Borohydride Exchange Resin (BER)” Bull. Korean Chem. Soc. 1998, 19(11), 1268-1270.
38. J. Kang; J. B. Kim; K. H. Cho; B. T. Cho, “Enantioselective Catalytic Reduction of Dihydroisoquinoline Derivatives” Tetrahedron: Asymmetry, 1997, 8(5), 657-659.
39. B. T. Cho; N. Kim; J.-H. Khoo, “Catalytic Enantioselective Reactions. Part 6. A New Chiral Catalysts for Highly Enantioselective Addition of Diethylzinc to Aliphatic Aldehydes” Bull. Korean Chem. Soc., 1996, 17(1), 1-2.
40. B. T. Cho; N. Kim, “Catalytic Enantioselective Reactions. Part 7. Synthesis of New -Aminoalcohols Derived from -D-Glucose as Chiral Catalysts for the Catalytic Enantioselective Addition of Diethylzinc to Aldehydes” Synth. Commun. 1996, 26(2), 855-865.
41. B. T. Cho; N. Kim, “Catalytic Enantioselective Reactions. Part 8. Catalytic Enantioselective Addition of Diethylzinc to Aldehydes Using (2S,3S)-(-)-1,4-Diamino-2,3-Butanediol Derivatives as Chiral Catalysts” Synth. Commun. 1996, 26(12), 2273-2280.
42. B. T. Cho; N. Kim, “Catalytic Enantioselective Reactions. Part 9. 1,2-Isopropylidene-5-deoxy-5-N,N-dialkyl(or N-monoalkyl)amino--D-xylofuranose Derivatives as the highly Effective Chiral Catalysts for Enantioselective Addition of Diethylzinc to Aliphatic and Aromatic Aldehydes” J. Chem. Soc. Perkin Trans. 1., 1996, 2901-2907.
43. B. T. Cho; Y. S. Chun, “Catalytic Enantioselective Reactions. Part 10. Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by Chiral Oxazaborolidines”, Bull. Korean Chem. Soc.1996, 17(12), 1096-1098.
44. B. T. Cho; Y. S. Chun, “Catalytic Enantioselective Reactions. Part 11. Asymmetric Borane Reduction of Prochiral Ketones Catalyzed by A New Chiral Oxazaborolridine Derived from D-Mannitol”, Bull. Korean Chem. Soc.1996, 17(12), 1098-1099.
45. B. T. Cho; N. Kim, “Preparation of 1,2-Isopropylidene-5-Deoxy-5-Dialkylamino--D-Xylofuranose Derivatives as Chiral Catalysts for Enantioselective Addition of Dialkylzincs to Aldehydes” Synth. Commun. 1995, 25(2), 167-175.
46. B. T. Cho; M. H. Ryu; Y. S. Chun; Ch. Dauelsberg; S. Wallbaum; J. Martens, “Direct Comparison Study of Asymmetric Borane Reduction of C=N Bond Mediated by Chiral Oxazaborolidines” Bull. Korean Chem. Soc., 1994, 15(10, 53-57.
47. B. T. Cho; Y. S. Chun; Ch. Dauelsberg; S. Wallbaum; J. Martens, “Catalytic Enantioselective Reaction. Part 2. A Comparison Study of Asymmetric Borane Reduction of Prochiral Ketones Catalyzed by Chiral Oxazaborolidines” Bull. Korean Chem. Soc., 1994, 15(2), 101-103.
48. B. T. Cho; M. H. Ryu, “Asymmetric Borane Reduction Ketoxime O-Trimethylsilyl Ethers Mediated by A Chiral 1,3,2-Oxazaborolidine Derived from (-)-Ephedrine” Bull. Korean Chem. Soc., 1994, 15(3), 191-192.
49. B. T. Cho; N. Kim, “Chiral Enantioselective Addition of Diethylzinc to Aldehydes by Chiral Secondary -Amionalcohol” Bull. Korean Chem. Soc., 1994, 15(11), 931-932.
50. B. T. Cho; M. H. Ryu, “Influence of Different Classes of Boranes and Solvents on Asymmetric Induction in Enantioselective Borane Reduction of Prochiral Ketones Catalyzed by A Chiral Oxazaborolidines” Bull. Korean Chem. Soc., 1994, 15(12), 1027-1029.
51. B. T. Cho; Y.S. Chun, “Asymmetric Reduction of -Keto Acetals with Potassium 9-O-(1,2-Isopropylidene-5-deoxy--D-xylofuranosyl)-9-boratabi-cyclo[3.3.1]nonane. Enantioselective Synthesis of -Hydroxy Acetals with High Optical Purities” Tetrahedron: Asymmetry, 1994, 5(5), 1147-1150.
52. B. T. Cho; N. Kim, “Enantioselective Addition of Diethylzinc to Aldehydes Using -Aminoalcohols Derived from -D-Xylose as New Chiral Catalysts” Tetrahedron Lett. 1994, 34(24), 4115-4118.
53. B. T. Cho; M. H. Ryu, “Asymmetric Inducing Effect of Substituents in Chiral Oxazaborolidines on Enantioselective Borane Reduction of Ketones” Bull. Korean Chem. Soc., 1994, 15(12), 1080-1084.
54. B. T. Cho; Y.S. Chun, “New Chiral Borohydrides. 3. Preparation and Asymmetric Reducing Properties of Potassium 9-O-(1,2-Isopropylidene-5-deoxy--D-xylofuranosyl)-9-boratabicyclo[3.3.1]nonane” Tetrahedron: Asy-mmetry, 1992, 3(1) 73-82.
55. B. T. Cho; Y. S. Chun, “Enantioselective Synthesis of Optically Active Metolachlor via Asymmetric Reduction” Tetrahedron: Asymmetry, 1992, 3(3), 337-340.
56. B. T. Cho; Y. S. Chun, “Enantioselective Synthesis of Optically Active -Aminoalcohols via Asymmetric Reduction” Tetrahedron: Asymmetry, 1992, 3(3), 341-342.
57. B. T. Cho; Y. S. Chun, “Asymmetric Borane Reduction of Achiral Ketones Mediated by A Chiral Oxazaborolidine Derived from (-)-Ephedrine” Tetrahedron: Asymmetry, 1992, 3(12), 1539-1542.
58. B. T. Cho; Y. S. Chun, “Enantioselective Synthesis of Optically Active Secondary Amines via Asymmetric Reduction” Tetrahedron: Asymmetry, 1992, 3(12), 1583-1590.
59. B. T. Cho; C. K. Han, “Enantioselective Synthesis of 1-Substituted 1,2,3,4-Tetra-hydroisoquinoline Alkaloids via Asymmetric Reduction” Bull. Korean Chem. Soc., 1991, 12(5), 565-570.
60. B. T. Cho, “New Chiral Borohydrides. 2. Preparation of Potassium B-Methoxy-diisopinocampheylborohydride and Its Asymmetric Reducing Properties” Bull. Korean Chem. Soc., 1991, 12(6), 662-665.
61. B. T. Cho; C. K. Han, “Enantioselective Synthesis of Cryptostylines I, II and III via Asymmetric Reduction” Bull. Korean Chem. Soc., 1990, 11(1), 81-82.
62. B. T. Cho, “New Chiral Borohydride Reagent. Preparation and Asymmetric Reducing Properties of Potassium 9-O-(1,2:5,6-Di-O-cyclohexylidene--D-glucofuranosyl)-9- boratabicyclo[3.3.1]nonane” J. Korean Chem. Soc., 1990, 34(3), 313-315.
63. B. T. Cho; Y. S. Chun, “Asymmetric Reduction of N-Substituted Ketimines with the Reagent prepared from Borane and (S)-(-)-2-Amino-3-methyl-1,1-diphenylbutan-1-ol (Itsuno's Reagent) : Enantiosselective Synthesis of Optically Active Secondary Amines” J. Chem. Soc. Perkin Trans. 1, 1990, 3200.
64. B. T. Cho; W. S. Park, “Kinetic Resolution of Racemic Ketones with K Glucoride” Bull. Korean Chem. Soc., 1989, 10(6), 618-619.
65. B. T. Cho, “Asymmetric Reduction of -Diketone with Potassium 9-O-(1,2:5,6-Di-O-Isopropylidene--D-glucofuranosyl)-9-boratabicyclo[3.3.1]-nonane.(K glucoride)” 한림대학 논문집 (J. Hallym Univ.), 1988, 6, 23.
66. H. C. Brown; B. T. Cho; W. S. Park, “Chiral Synthesis via Organoboranes. Selective Reductions. 42. Asymmetric Reduction of Representative Prochiral Ketones with Potassium 9-O-(1,2:5,6-Di-O-Isopropylidene-a-D-glucofuranosyl)-9-boratabicyclo[3.3.1]nonane” J. Org. Chem., 1988, 53(6), 1231-1238.
67. B. T. Cho; S. Y. Seong, “Selective Reduction of Oximes to N-Monosubstituted Hydroxylamines with Lithium Borohydride” Bull. Korean Chem. Soc., 1988, 9(5), 322-324.
68. B. T. Cho; W. S. Park, “Asymmetric Reduction of -Acetylenic Ketones with Potassium 9-O-(1,2:5,6-Di-O-Isopropylidene--D-glucofuranosyl)-9-boratabi-cyclo[3.3.1]nonane” Bull. Korean Chem. Soc., 1987, 8(4), 257-260.
69. H. C. Brown; W. S. Park; B. T. Cho, “Addition Compounds of Alkali Metal Hydrides. 32. A Comparison Study of Chiral Trialkylborohydrides and Chiral Dialkylmonoalkoxyborohydrides for the Asymmetric Reduction of Prochiral Ketones : The Effect of Comparable Chiral Alkyl and Alkoxy Groups on Asymmetric Induction” Bull. Korean Chem. Soc., 1987, 8(5), 276-280.
70. H. C. Brown; B. T. Cho; W. S. Park, “Addition Compounds of Alkali Metal Hydrides. 31. Preparation and Properties of Chiral Dialkoxymonoalkylboro-hydrides. A New Class of Asymmetric Reducing Agents” J. Org. Chem., 1987, 52(18), 4020-4024.
71. H. C. Brown; W. S. Park; B. T. Cho; P. V. Ramachandran, “Selective Reductions. 40. A Critical Examination of the Relative Effectiveness of Reducing Agents for the Asymmetric Reduction of Different Classes of Ketones” J. Org. Chem., 1987, 52(24), 5406-5412.
72. W. S. Park; B. T. Cho; J. S. Cha, “Asymmetric Reduction of Prochiral Ketones with Potassium 9-O-Isopinocampheyloxy-9-boratabicyclo[3.3.1]nonane” Bull. Korean Chem. Soc., 1987, 8(3), 211-214.
73. B. T. Cho; W. S. Park, “ Exploratory Studies on the Synthesis of Lithium 9-O-(1,2:5,6-Di-O-Isopropylidene--D-glucofuranosyl)-9-boratabicyclo[3.3.1]-nonane” 한림대학 논문집 (J. Hallym Univ.), 1987, 5, 23.
74. H. C. Brown; W. S. Park; J. S. Cha; B. T. Cho; C. A. Brown, “Addition Compounds of Alkali Metal Hydrides. 28. Preparation of Potassium Dialkoxymonoalkylborohydrides from Cyclic Boronic Esters. A New Class of Reducing Agents” J. Org. Chem., 1986, 51(3), 337-342.
75. H. C. Brown; W. S. Park; B. T. Cho, “Potassium 9-O-(1,2:5,6-Di-O-isopropylidene--D-glucofuranosyl)-9-boratabicyclo[3.3.1]nonane. A New, Effective Chiral Borohydride Reagent” J. Org. Chem., 1986, 51(10), 1934-1936.
76. H. C. Brown; W. S. Park; B. T. Cho, “Addition Compounds of Alkali Metal Hydrides. 29. Preparation and Properties of Chiral Dialkylmonoalkoxy-borohydrides. A New Class of Asymmetric Reducing Agents” J. Org. Chem., 1986, 51(17), 3278-3282.
77. H. C. Brown; B. T. Cho; W. S. Park, “Asymmetric Reduction of -Keto Esters with Potassium 9-O-(1,2:5,6-Di-O-isopropylidene--D-glucofuranosyl)-9-bora-tabicyclo[3.3.1]nonane. Chiral Synthesis of -Hydroxy Esters with Optical Purity Approaching 100 % ee” J. Org. Chem., 1986, 51(17), 3396-3398.
78. B. T. Cho; N. M. Yoon, "Selective Reduction among Carboxylic Acids with Sodium Borohydride” Synth. Commun., 1985, 15(10), 917-924.
79. 조병태, “Chemoselective Reduction of Carbonyl Compounds with Acyloxy-borohydrides” 한림 대학 논문집 (J. Hallym. Univ.), 1985, 3, 33.
80. 조병태, "붕소 화합물을 이용한 유기 화학 반응 (Recent Progress of Reactions via Organoboranes)" 화학과 공업의 진보지 (Progr. Chem. and Chem. Ind.), 1984, 24(7), 441-450.
81. B. T. Cho; N. M. Yoon, "Selective Reduction of Halides with Lithium Borohydride in the Presence of Multifunctional Compounds" J. Korean Chem. Soc., 1983, 27(1), 46-52.
82. 조병태, "금속 수소화물을 이용한 선택 환원 반응 (Selective Reduction with Metal Hydrides)" 한림 대학 논문집 (J. Hallym. Univ.), 1983, 1, 103.
83. N. M. Yoon; H. M. Park; B. T. Cho; I. W. Oh, "A Facile Reaction of Esters with Lithium Borohydride in the Presence of Triethylborane" Bull. Korean Chem. Soc., 1983, 4(6), 287-288.
84. N. M. Yoon; B. T. Cho; J. U. Yoo; G. P. Kim, "Reduction of Some Representative Organic Compounds with NaBH4-(C6H5O)3 System" J. Korean Chem. Soc., 1983, 27(6), 434-440.
85. B. T. Cho; N. M. Yoon, "Convenient Procedure for the Reduction of Carboxylic Acids via Acyloxyborohydrides" Bull. Korean Chem. Soc., 1982, 3(4), 149-152.
86. B. T. Cho; N. M. Yoon, "Fast Deoxygenation of Sulfoxides with Borane-Triethylborate (1 : 0.1) System" J. Korean Chem. Soc., 1982, 26(5), 340-348.
87. N. M. Yoon; B. T. Cho, "Rapid Reduction of Carboxylic Acid Salts with Borane in Tetrahydrofuran" Tetrahedron Lett., 1982, 23(24), 2475-2478.
□저서
1. 유기화학 제2판 (Organic Chemistry, 2nd edition), 2017, 자유아카데미
2. 비대칭환원반응: 방법과 응용(Asymmetric Reduction: Methods and Applications), 2016, 자유아카데미
3. 유기합성화학 (Synthetic Organic Chemistry), 2014, 자유아카데미
4. 유기화학 제1판 (Organic Chemistry, 1st edition), 2011, 자유아카데미
5. Boronic acids: Preparation, Applications in Organic Synthesis and Medicine (Oxazaborolidines as asymmetric inducers for the reduction of ketones and ketimines), D. G.. Hall, Ed. Chapter 11, pp 411-439, Wiley-VCH, 2005.
6. Organoboranes for Syntheses (ACS Symposium series 783), P. V. Ramachandran and H. C. Brown, Ed.; pp125-132, American Chemical Society, Washington DC, 2001
