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1.“General Synthetic Entry to Highly-Oxygenated Angularly-Fused Polycyclic
Aromatic Compounds” S. Koo, L. S. Liebeskind,* J.
Am. Chem. Soc. 1995, 117, 3389-3404.
2.“Microbial Deoxygenation of N- with Baker'sYeast-NaOH” W. Baik,* D. I.
Kim, S. Koo, J. U. Rhee, S. H. Shin, B. H. Kim, Tetrahedron Lett. 1997, 38, 845-848.
3.“Highly Efficient Synthesis of Methyl-Substituted Conjugate Cyclohexenones” B.-D. Chong,
Y.-I. Ji, S.-S. Oh, J.-D. Yang, W. P. Baik, S. Koo,* J. Org. Chem. 1997, 62, 9323-9325.
4.“Chemoselective Reactions of Anthrone with α,β-Unsaturated Ketones” W. Baik,* C. H.
Yoon, K. C. Lee, H. J. Lee, S. Koo, J. Kim, B. Yoon, H. Kim, J. Chem. Res. 1998, 358-359.
5.“LiAlH4 Promoted Reductive Deoxygenation of Hydroxybenzyl
Alcohols via Benzoquinone Methide Intermediates” W. Baik,* H. J. Lee, S.
Koo, B. H. Kim, Tetrahedron Lett.
1998, 39, 8125-8128.
6.“Photostimulated Reductive Cyclization of o-Nitrophenylazo Dyes Using
Sodium Hydroxide in Isopropyl Alcohol. A New Synthesis of
2-Aryl-2H-benzotriazoles” W. Baik,* C. H. Yoo, S. Koo, H. Kim, Y. H. Hwang,
B. H. Kim, S. W. Lee, Heterocycles 1999, 51, 1779-1783.
7.“Diallylic Sulfides as
Key Structures for Carotenoid Syntheses” H. J. Choi, M. Ji, M. Park, I.-K.
Yun, S.-S. Oh, W. Baik, S. Koo,* J. Org.
Chem. 1999, 64, 8051-8053.
8.“NBS-Promoted
Reactions of Symmetrically Hindered Methylphenols via p-Benzoquinone Methide” W. Baik,* H. J. Lee, J. M. Jang, S. Koo, B. H. Kim, J. Org. Chem. 2000, 65, 108-115.
9.“Highly Efficient
Synthesis of Bicyclo[3.3.1]nonane Skeleton” J.-D. Yang, M.-S. Kim, M. Lee, W.
Baik, S. Koo,* Synthesis 2000, 801-804.
10. “Highly Efficient Chain-extension
Process in the Systematic Syntheses of Carotenoid Natural Products” M. Ji, H. Choi,
M. Park, M. Kee, Y. C. Jeong, S. Koo,* Angew.
Chem., Int. Ed. 2001, 40, 3627-3629.
11.“Selective Oxidation of
Allylic Sulfides by Hydrogen Peroxide with Trirutile-type Solid Oxide Catalyst
- LiNbMoO6” S. Choi, J.-D. Yang, M. Ji, H. Choi, M. Kee, K.-H.
Ahn, S.-H. Byeon, W. Baik, S. Koo,* J. Org.
Chem. 2001, 66, 8192-8198.
12. “The Reactivity and
Stability Studies of Benzoquinone Methides by Ab Initio Calculations” W. Baik,* S. J.
Kim, E.-Y. Hurh, S. Koo, B. H. Kim, Bull.
Korean Chem. Soc. 2001, 22, 1127-1130.
13. “Mn(III)-Mediated Radical
Cyclization for △1-3-Octalone Synthesis” M. Lee, J.-D. Yang, M.-S. Kim, H.-S. Jeon, W. Baik, S. Koo,* Bull.
Korean Chem. Soc. 2002, 23, 736-740.
14. “Identification of FM001 as Plant Growth-Promoting
Substance from Acremonium strictum MJN1 Culture” J.-H. Jung, D.-M. Shin, W.-C. Bae, S.-K. Hong,
J.-W. Suh, S. Koo, B.-C. Jeong,* J. Microbiol. Biotech. 2002, 12, 327-330.
15. “Allylic Triene Sulfones
as Key Synthons for Carotenoid Synthesis” M.
Ji, H. Choi, Y. C. Jung, J. Jin, W. Baik, S. Lee, J. S. Kim, M. Park, S. Koo,* Helv. Chim. Acta 2003, 86, 2620-2628.
16. “The Friedel-Crafts Allylation of a Prenyl Group Stabilized by a Sulfone
Moiety - Expeditious Syntheses of Ubiquinones and Menaquinones”J.-H. Min, J.-S. Lee, J.-D. Yang, S. Koo,* J.
Org. Chem. 2003, 68, 7925-7927.
17. “The intramolecular Baylis-Hillman reaction: easy
preparation of versatile substrates, facile reactions, and synthetic applications” J.-E. Yeo, X. Yang, H. J. Kim, S.
Koo,* Chem. Commun. 2004,
236-237.
18. “Highly Efficient and
General Synthetic Method of Various Retinyl Ethers” J. S. Lee, Y. C.
Jeong, M. Ji, W. Baik. S. Lee, S. Koo,* Synlett 2004, 1937-1940.
19. “A computational Investigation of the Stability of
Cyclopropyl Carbenes” W. Baik,* C. H. Yoon, S. Koo, B. H. Kim, Bull. Korean Chem. Soc. 2004, 25, 90-96.
20. “Preparation of the
conjugated polyene chains with the 1,4-dimethyl substitution” H.-S.
Jeon, S. Koo,* Tetrahedron Lett. 2004, 45, 7023-7026.
21. “Lewis acid-catalyzed
reactions of anthrone: Preference for cycloaddition reaction over conjugate
addition depending on the functionality of α,β-unsaturated carbonyl compounds” W. Baik,* C. H.
Yoon, S. Koo, H. Kim, J. Kim, J. Kim, S. Hong, Bull. Korean Chem. Soc. 2004, 25, 491-500.
22. “General and systematic synthetic entry
to carotenoid natural products” Y. C. Jeong, M. Ji, J. S. Lee, J.-D. Yang, J. Jin, W. Baik, S. Koo,* Tetrahedron 2004, 60, 10181-10185.
23. “Stereoselective and
Convergent Syntheses of Retinoic Acid and Its Ester Derivatives by the Sulfone
Olefination Reaction” H.-S. Jeon, J. E. Yeo, Y. C. Jeong, S. Koo,* Synthesis 2004, 2813-2820.
24. “Efficient Syntheses of Keto-carotenoid Canthaxanthin, Astaxanthin, and
Astacene” S. Choi, S. Koo,* J.
Org. Chem. 2005, 70, 3328-3331.
25. “Efficient one-pot
transformation of aminoarenes to haloarenes using halodimethylisulfonium
halides generated in situ” W. Baik,* W. Luan, H. J. Lee, C. H. Yoon, S. Koo,
B. H. Kim, Can. J. Chem. 2005, 83, 213-219.
26. “Preparation of 1,4-hydrobenzoquinones by
the PCC/SiO2-promoted double oxidation of 3-cyclohexene-1,2-diols”
H. J. Kim, S. Koo,* Org. Biomol. Chem.
2005, 3, 3479-3481.
27. “Sulfone Coupling and Double Elimination
Strategy for Carotenoid Synthesis” S. K.
Guha, S. Koo,* J. Org. Chem. 2005, 70, 9662-9665.
28. “TMS·OTf-Catalyzed α-bromination of
carbonyl compounds by N-bromosuccinimide” S. K. Guha, B. Wu, B. S. Kim, W. Baik, S. Koo,* Tetrahedron Lett. 2006, 47, 291-293.
29. “Origin of the Diastereoselection in the
Indium-mediated Addition of Haloallylic Sulfones to Aldehydes” J.-H. Min,
S.-Y. Jung, B. Wu, J. T. Oh, M. S. Lah, S. Koo,* Org. Lett. 2006, 8, 1459-1462.
30. “Stereoselective Synthesis of Allylic
Sulfones via the Oxonia-Cope Rearrangement of Homoallylic Alcohols Containing a
Homoallylic Sulfone Moiety” S.-Y. Jung, J.-H. Min, J. T. Oh, S. Koo,* J. Org. Chem. 2006, 71, 4823-4828.
31. “Expeditious and Practical Synthesis of
Lycopene” E. Choi, J. E. Yeo, S. Koo,* Adv. Synth. Catal. 2008,
350, 365-369.
32. “General Preparation and Controlled
Cyclization of Acyclic Terpenoids” J. Kuk, B. S. Kim, H. Jung, S. Choi,
J.-Y. Park, S. Koo,* J. Org. Chem. 2008, 73, 1991-1994.
33. “Ring-Expansion Protocol: Preparation of
Synthetically Versatile Dihydrotropones” Y.-S. Do, R. Sun, H. J. Kim, J.
E. Yeo, S.-H. Bae, S. Koo,* J. Org. Chem.
2009, 74, 917-920.
34. “Synthesis of highly conductive
poly(3,4-ethylenedioxythiophene) fiber by simple chemical polymerization” W. Baik, W. Luan,
R. H. Zhao, S. Koo, K.-S. Kim, Synth. Metals 2009, 159, 1244-1246.
35. “Conductance Control in the Stabilized
Carotenoid Wires” J. Maeng, S. B. Kim, N. J. Lee, E. Choi, S.-Y. Jung,
I. Hong, S.-H. Bae, J. T. Oh, B. Lim, J. W. Kim, C. J. Kang, S. Koo,* Chem. Eur. J. 2010, 16, 7395-7399.
36. “Convergent synthesis of new types of
stabilized carotenoid compounds” S. B. Kim, H.
Kim, B. Lim, J. Maeng, S.-H. Bae, E. Choi, J. T. Oh, I. Hong, S.-Y. Jung, J. E.
Yeo, S. Koo,* Pure Appl. Chem. 2011, 83, 613-620.
37. “Ultrafast excited state dynamics and
spectroscopy of 13,13'-diphenyl-β-carotene” K. Golibrzuch, F. Ehlers, M.
Scholz, R. Oswald, T. Lenzer, K. Oum,* H. Kwon, S. Koo,* Phys. Chem. Chem. Phys. 2011,
13, 6340-6351.
38. “Selective Deoxygenation of Allylic
Alcohol; Stereo-controlled Synthesis of Lavandulol” H. J. Kim, L. Su, H. Jung, S. Koo,* Org.
Lett. 2011, 13, 2682-2685.
39. “Mn(III)-Promoted Tandem Oxidation and
Cyclization of β-Ketoester Derivatives of Terpenoids” Z.
Li, H. Jung, M. Park, M. Lah, S. Koo,* Adv. Synth. Catal. 2011,
353, 1913-1917.
40. “Synthesis of Coenzyme Q-10” E.-T. Oh, H. J. Kim, J. T. Oh, L. Su, I. Yun, K. Nam, J.-H. Min, J. W.
Kim, S. Koo,* Eur. J. Org. Chem. 2012, 4954-4962.
41. “Bis-sulfonic Acid Ionic Liquids for the
Conversion of Fructose to 5-Hydroxymethyl-2-furfural” S.
E. Sim, S. Kwon, S. Koo,* Molecules 2012, 17, 12804-12811.
42. “Mechanism and Scope of the
Mn(III)-Initiated Oxidation of beta-Ketocarbonyl Compounds; the Furan Synthesis” C. Wang, Z. Li, Y. Ju, S. Koo,* Eur. J. Org. Chem. 2012,
6976-6985.
43. “Combined Effect of Polar Substituents on
the Electronic Flows in the Carotenoid Molecular Wires” Y. Zhao, S.
Lindsay,* S. Jeon, H.-J. Kim, L. Su, B. Lim, S. Koo,* Chem. Eur. J. 2013, 19, 10832-10835.
44. “Sulfone-Mediated Syntheses of Crocetin
Derivatives: Regioselectivity of Highly Functionalized Building Blocks” E.-T.
Oh, Y.-H. Kim, J. Jin, L. Su, J.-A. Seo, S. Koo,* J. Org. Chem. 2014, 79, 4712-4715.
45. “Catalytic Oxidation of beta-Ketoester by
Mn(III)/Co(II) and Consecutive Cyclization to Heterocycles” Y. Ju, D.
Miao, J. G. Seo, S. Koo,* Adv. Synth.
Catal. 2014, 356, 3059-3066.
46. “Resonance Raman Spectra of Carotenoid Molecules:
Influence of Methyl Substitutions” M. Macernis,* D. Galzerano, J. Sulskus, E. Kish, Y.-H.
Kim, S. Koo, L. Valkunas, B. Robert, J. Phys. Chem. A 2015, 119, 56-66.
47.
“Regioselective Synthesis of
1,3- and 1,2-Tocopheryl Glyceride Ethers of Carboxylic Acids” B. S. Choi, J.
Choi, S. Bak, S. Koo,* Eur. J. Org. Chem. 2015,
514-524.
48. “Synthesis and characterization of
multi-walled carbon nanotubes-supported dibenzo-14-crown ether with proton ionizable
carboxyl sidearm as Li+ adsorbents” R. E. C. Torrejos, G. M. Nisola, M. J. Park,
H. K. Shon, J. G. Seo, S. Koo, W.-J. Chung, Chem. Engineer. J.
2015, 264, 89-98.
49. “Tandem Catalytic Oxidative Deacetylation of Acetoacetic Esters and
Hetero Aromatic Cyclizations” Y. Ju, D. Miao, R. Yu, S. Koo,* Org. Biomol. Chem. 2015, 13, 2588-2599.
50. “A Chain Extension Method for Apocarotenoids; Lycopene and Lycophyll
Syntheses” J. Choi, E.-T. Oh, S. Koo,* Arch. Biochem.
Biophys. 2015, 572, 142-150.
51. “Enhanced biological
activity of carotenoids stabilized by phenyl groups” J. S. You, S. Jeon, Y. J. Byun, S. Koo,* S.
S. Choi,* Food Chem. 2015,
177, 339-345.
52. “Esterification of carboxylic acids with alkyl halides using imidazolium
based dicationic ionic liquids containing bis-?trifluoromethane
sulfonimide anions at room temperature” A. H. Jadhav, K. Lee, S. Koo, J. G. Seo,* RSC
Advances 2015, 5, 26197-26208.
53. “Fine-tuning of single-molecule
conductance by tweaking both electronic structure and conformation of side
substituents” A. Aragones, N. Darwish, J.O. Im, B. Lim, J. Choi, S. Koo,* I. Diez-Perez,* Chem. Eur. J. 2015, 21, 7716-7720.
54. “One-Pot Conversion of Carbohydrates into
Pyrrole-2-Carbaldehydes as Sustainable Platform Chemicals” A. Nirmal Das, S. Kwon, W.-J. Chung, S. Koo,* J. Org. Chem. 2015, 80, 7693-7701.
55. “Synthesis of Tribenzotropone by Ring
Expansion of Phenanthren-9,10-dione” J. Choi, H. Jung, J. E. Yeo, S. Koo,* Synthesis
2015, 47, 2971-2975.
56. “Liquid-liquid
extraction of lithium using lipophilic dibenzo-14-crown-4 ether carboxylic acid
in hydrophobic room temperature ionic liquid” R. E. C. Torrejos, G. M. Nisola, H. S. Song, J. W. Han, C. P. Lawagon, J.
S. Seo, S. Koo, H. Kim, W.-J. Chung, Hydrometallurgy
2016, 164, 362-371.
57. “Efficient preparation
method of 4-hydroxybenzoic esters – Oxidation of substituted Hagemman’s ester” S. Kang, D. Kim, I. J. In, S. Koo* Tetrahedron Lett. 2017, 58, 2264-2266.
58. “Design of lithium
selective crown ethers: Synthesis, extraction and theoretical binding studies” R. E. C. Torrejos, G. M. Nisola, H. S. Song, L. A.
Limjuco, C. P. Lawagon, K. J. Parohinog, S. Koo, J. W. Han, W.-J. Chung,
Chem. Engineer. J. 2017, 326, 921-933.
59. “Aethusifolins A–D:
Four new components from a traditional Mongolian medicinal herb Clematis
aethusifolia Turcz” Y. Chang, P. Zhang, J. Jurhiin, X. Zhang,
W. Borgihiin, H. Zhao, S. Koo, W.-D. Rausch, B. Agula, B. Bao, Phytochem. Lett. 2017, 22, 87-91.
60. “Systematic synthesis
of diphenyl-substituted carotenoids as molecular wires” B. Lim, E.-T. Oh, J.O. Im, K. S. Lee, H. Jung, M. Kim, D. Kim, J. T. Oh,
S.-H. Bae, W.-J. Chung, K.-H. Ahn, S. Koo* Eur.
J. Org. Chem. 2017, 6390-6400.
61. “Aerosol Cross-Linked
Crown Ether Diols Melded with Poly(vinyl alcohol) as Specialized Microfibrous
Li+ Adsorbents” L. A. Limjuco, G. M. Nisola, R. E. C.
Torrejos, J. W. Han, H. S. Song, K. J. Parohinog, S. Koo, S.-P. Lee,
W.-J. Chung, ACS Appl. Mater. Interfaces
2017, 9, 42862-42874.
62. “Deprotection of
durable benzenesulfonyl protection for phenols – efficient synthesis of
polyphenols” M. S. Alam, S. Koo* Synth. Commun. 2018 ,
48, 247-254.
63. “Role of Ring Ortho Substituents
on the Configuration of Carotenoid Polyene Chains” M. Kim, H. Jung, A. C. Aragones, I. Diez-Perez, K.-H. Ahn, W.-J. Chung,
D. Kim, S. Koo* Org. Lett. 2018, 20, 493-496.
64. “Lycorin Displays Potent Antitumor Efficacy in Colon Carcinoma by
Targeting STAT3” S. Wu, Y. Qiu, Y. Shao, S. Yin, R. Wang, X. Pang, J. Ma, C.
Zhang, B. Wu, S. Koo, L. Han, Y. Zhang, X. Gao, T. Wang, H. Yu,* frontiers in Pharmacology, 2018, 9, 881/1-881/11.
65. “Fast Assembly and High-Throughput Screening of Structure and Antioxidant
Relationship of Carotenoids” D. Kim, G. Shi, Y. Kim, S. Koo* Org. Lett. 2019, 21, 714-718.
66. “Aqueous Synthesis of 14-15-Membered Crown Ethers with
Mixed O, N, and S Heteroatoms: Experimental and Theoretical Binding Studies
with Platinum-Group Metals” R. E. C. Torrejos,
G. M. Nisola, S. H. Min, J. W. Han, S. Koo, K. J. Parohinog, S. Lee, H.
Kim, W.-J. Chung,* ChemPlusChem 2019, 84, 210-221.
67. “7-?Deoxynarciclasine shows promising antitumor efficacy by targeting Akt
against hepatocellular carcinoma” S. Yin,* Y. Qiu,* C. Jin,* R. Wang, S. Wu, H.
Liu, S. Koo, L. Han, Y. Zhang, X. Gao, X. Pang, T. Wang and H. Yu International Journal of Cancer 2019, DOI:10.1002/ijc.32395.
68. “Synthesis of Phenyl-2,2?-bichalcophenes and Their Aza-analogues by
Catalytic Oxidative Deacetylation” X. Jiang, H. Jin, T. Wang, H. Yoo, S. Koo* Synthesis 2019, 51(17), 3259-3268. DOI:10.1055/s-0037-1611564.
69. “Bromoacetate Olefination Protocol for Norbixin and Julia-Kocienski
Olefination for Its Ester Syntheses” D. Kim, M. Alam, W.-J. Chung, S. Koo* ACS Omega 2019, 4(6), 10019-10024
(2019.06.07.).
70. “Synthesis and application of novel hydroxylated
thia-crown ethers as composite ionophores for selective recovery of Ag+ from
aqueous sources” H. T. Fissaha, G. M. Nisola, F. K. Burnea, J. Y. Lee, S.
Koo, S.-P. Lee, H. Kim, W.-J. Chung* Journal of Industrial and
Engineering Chemistry 2020, 81, 415-426 (2020.01.25.).
71. “Synthetic strategy
for tetraphenyl-substituted all-E-carotenoids with improved molecular
properties” B. Lim, H. Jung, H. Yoo, M. Park, H. Yang, W.-J. Chung, S. Koo* European
Journal of Organic Chemistry 2020, (11), 1769-1777 (2020.03.16.).
72. “Crown ethers
"clicked" on fibrous polyglycidyl methacrylate for selective Li+
retrieval from aqueous sources” G. M.
Nisola, K. J. Parohinoga, R. E. C. Torrejos, S. Koo, S.-P. Lee,* H. Kim,*
W.-J. Chung,* Colloids and Surfaces A 2020, 595, 124709 (2020.04).
73. “Concise and
practical synthesis of (+)-Abscisic acid” D. Kim and S. Koo* ACS
Omega 2020, 5(22), 13296-13302. (2020.05).
74. “Syntheses of
Chalcone-Derived Heteroaromatics with Anti-bacterial Activities” H. Jin, X.
Jiang, H. Yoo, T. Wang, C.l G. Sung, U. Choi, C.-R. Lee,* H. Yu, S. Koo* ChemistrySelect
2020, 5(40), 12421-12424. (online Oct. 29, 2020).
75. “Tuning
Single-Molecule Conductance by Controlled Electric Field-Induced trans-to-cis
Isomerisation” C.S. Quintans, D. Andrienko, K.F. Domke, D. Aravena, S. Koo,
I. Díez-Pérez, A.C. Aragonès, Applied Sciences 2021, 11(8),
3317. (online Apr. 7, 2021).
76.
“Apocarotenals of phenolic carotenoids for superior antioxidant
activities” Gaosheng Shi, Lina Gu, Hyunuk Jung, Wook-Jin Chung, Sangho
Koo,* ACS Omega 2021, 6, 25096-25108 (2021.9.16.). DOI:org/10.1021/acsomega.1c04432.
77. “Furan
Oxidation by Mn(III)/Co(II) catalysts–Application to Benzofuran
Synthesis” Tingshu Wang, Miao Zhang, Yifan Zheng, Junmo Seong, Myoung
Soo Lah, Sangho Koo,* RSC Advances 2021, 11, 31395-31399 (2021.09.22). DOI:10.1039/d1ra05305a.
78. “Ribose
conversion with amino acids into pyrraline platform chemicals -
expeditious synthesis of diverse pyrrole-fused alkaloid compounds”
Soohyeon Cho, Lina Gu, Ik Joon In, Bo Wu, Taehoon Lee, Hakwoon Kim,
Sangho Koo,* RSC Advances 2021, 11, 31511-31525 (2021.09.23). DOI: 10.1039/d1ra06110k.
79. “Multidentate
thia-crown ethers as hyper-crosslinked macroporous adsorbent resins for
the efficient Pd/Pt recovery and separation from highly acidic spent
automotive catalyst leachate” R. E. C. Torrejos, E. C. Escobar, J. W.
Han, S. H. Min, H. Yook, K. J. Parohinog, S. Koo, H. Kim, G. M. Nisola, W.-J. Chung, Chemical Engineering Journal 2021, 424, 130379 (2021.11.15).
80. “Cyclin-dependent
kinase 1 as a potential target for lycorine against hepatocellular
carcinoma,” Shuangshuang Yin,
Shenshen Yang, Yanming Luo, Jia Lu, Gaoyong Hu, Kailong Wang, Yingying
Shao, Shiyue Zhou, Sangho Koo, Yuling Qiu, Tao Wang, Haiyang Yu Biochemical Pharmacology, 2021, 193, 114806 (2021.11).
81. “13,13′‐Diphenalkyl β‐carotenes as pi‐stacking models of chlorophylls and carotenoids in photosynthesis“ Boram Lim, Young‐Hun Kim, Hyein Kim, Myeongnam Park, Huisu Yeo, Sangho Koo Bulletin of the Korean Chemical Society, 2022 43(8), 1037-1039 https://doi.org/10.1002/bkcs.12579
82. “Oxo-Carotenoids as Efficient Superoxide Radical Scavengers“ Gaosheng Shi, Hyein Kim, Sangho Koo, Antioxidants, 2022, 11, 1525 https://doi.org/10.3390/antiox11081525
83. “Expeditious Synthesis of Fluorescent Bis (phenylfuryl) benzenes“ Miao Zhang, Tingshu Wang, Chanyoung Boo and Sangho Koo, Synthesis, 2023, 55)(01), 111-120. https://doi.org/10.1055/a-1941-1535
84. “Photoinduced Dynamics of 13, 13′-Diphenylpropyl-β-carotene” Sangho Koo, Yeong Hun Kim, Oliver Flender, Mirko Scholz, Kawon Oum, Thomas Lenzer, Molecules, 2023, 28. 3505. (published online 04-16-2023), DOI: 10.3390/molecules28083505.
85.
“Rapid Assembly of Pyrrole-Ligated 1, 3, 4-Oxadiazoles and Excellent
Antibacterial Activity of Iodophenol Substituents“ Hyein Kim, Lina Gu,
Huisu Yeo, Umji Choi, Chang-Ro Lee, Haiyang Yu, Sangho Koo, Molecules, 2023, 28(8), 3638. (published online 04-21-2023), DOI: 10.3390/molecules28083639.
86.
"Preparation of Divergent Intermediates and Convergent Synthesis of
Phytofluene" Chanyoung Boo, Hyein Kim, Huijeong Yang, Seunghyo Han,
Huisu Yeo, Chibeom Seo, Sangho Koo, Synthesis 2023, 55(16), 2517-2525.
Books
1. Encyclopedia of
Reagents for Organic Synthesis, Wiley, 1995:
「Allyl Trifluoromethanesulfonate
Vol. 1, pp 130;
Bis(N-propylsalicylideneaminato)cobalt(II) Vol. 1, pp 552;
3-Nitro-9-nitrosocarbazole
Vol. 6, pp 3747;
N-Phenylcampholylhydroxamic
Acid Vol. 6, pp 3965; Thallium(I) Acetate Vol. 7, pp 4832.」
2. Science of
Synthesis, Thieme, 2009: Vol. 45.30 Conjugated Polyenes.
3. e- Encyclopedia
of Reagents for Organic Synthesis, Wiley, 2011: 4-Bromo-1-chloro-2-methyl-2-butene.
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