참고문헌 (35)

1. For reviews on chiral recognition see: 

2. Pu, Lin. Enantioselective Fluorescent Recognition of Free Amino Acids: Challenges and Opportunities. Angewandte Chemie. international edition, vol.59, no.49, 21814-21828.

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3. Herrera, Brenden T., Pilicer, Samantha L., Anslyn, Eric V., Joyce, Leo A., Wolf, Christian. Optical Analysis of Reaction Yield and Enantiomeric Excess: A New Paradigm Ready for Prime Time. Journal of the American Chemical Society, vol.140, no.33, 10385-10401.

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4. Pu, Lin. Simultaneous Determination of Concentration and Enantiomeric Composition in Fluorescent Sensing. Accounts of chemical research, vol.50, no.4, 1032-1040.

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5. Werner, Helmut. Alfred Werner: A Forerunner to Modern Inorganic Chemistry. Angewandte Chemie. international edition, vol.52, no.24, 6146-6153.

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6. Werner, Helmut. Alfred Werner: ein Wegbereiter der modernen anorganischen Chemie. Angewandte Chemie, vol.125, no.24, 6262-6269.

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7. Werner, A.. Zur Kenntnis des asymmetrischen Kobaltatoms. I. Berichte der Deutschen Chemischen Gesellschaft zu Berlin, vol.44, no.2, 1887-1898.

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8. For reviews on chiral-at-metal complexes see: 

9. Cruchter, Thomas, Larionov, Vladimir A.. Asymmetric catalysis with octahedral stereogenic-at-metal complexes featuring chiral ligands. Coordination chemistry reviews, vol.376, 95-113.

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10. Zhang, Lilu, Meggers, Eric. Steering Asymmetric Lewis Acid Catalysis Exclusively with Octahedral Metal-Centered Chirality. Accounts of chemical research, vol.50, no.2, 320-330.

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11. 10.1002/(SICI)1521-3773(19990503)38:9<1194::AID-ANIE1194>3.0.CO;2-X 

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12. 10.1002/(SICI)1521-3757(19990503)111:9<1248::AID-ANGE1248>3.0.CO;2-K 

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13. Gladysz, J. A., Boone, Brian J.. Chiral Recognition in π Complexes of Alkenes, Aldehydes, and Ketones with Transition Metal Lewis Acids; Development of a General Model for Enantioface Binding Selectivities. Angewandte Chemie. International edition in English, vol.36, no.6, 550-583.

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14. For reviews on Ru(bpy)3 2+ and Ir(ppy)3 see: 

15. Romero, Nathan A., Nicewicz, David A.. Organic Photoredox Catalysis. Chemical reviews, vol.116, no.17, 10075-10166.

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16. Skubi, Kazimer L., Blum, Travis R., Yoon, Tehshik P.. Dual Catalysis Strategies in Photochemical Synthesis. Chemical reviews, vol.116, no.17, 10035-10074.

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17. Shaw, Megan H., Twilton, Jack, MacMillan, David W. C.. Photoredox Catalysis in Organic Chemistry. Journal of organic chemistry, vol.81, no.16, 6898-6926.

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18. Huo, Haohua, Fu, Chen, Harms, Klaus, Meggers, Eric. Asymmetric Catalysis with Substitutionally Labile yet Stereochemically Stable Chiral-at-Metal Iridium(III) Complex. Journal of the American Chemical Society, vol.136, no.8, 2990-2993.

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19. Huo, Haohua, Shen, Xiaodong, Wang, Chuanyong, Zhang, Lilu, Röse, Philipp, Chen, Liang-An, Harms, Klaus, Marsch, Michael, Hilt, Gerhard, Meggers, Eric. Asymmetric photoredox transition-metal catalysis activated by visible light. Nature, vol.515, no.7525, 100-103.

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20. Tan, Yuqi, Yuan, Wei, Gong, Lei, Meggers, Eric. Aerobic Asymmetric Dehydrogenative Cross‐Coupling between Two C_sp³H Groups Catalyzed by a Chiral‐at‐Metal Rhodium Complex. Angewandte Chemie. international edition, vol.54, no.44, 13045-13048.

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21. Tan, Yuqi, Yuan, Wei, Gong, Lei, Meggers, Eric. Aerobic Asymmetric Dehydrogenative Cross‐Coupling between Two C_sp³H Groups Catalyzed by a Chiral‐at‐Metal Rhodium Complex. Angewandte Chemie, vol.127, no.44, 13237-13240.

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22. Wang, Chuanyong, Chen, Liang-An, Huo, Haohua, Shen, Xiaodong, Harms, Klaus, Gong, Lei, Meggers, Eric. Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality. Chemical science, vol.6, no.2, 1094-1100.

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23. Hong, Yubiao, Jarrige, Lucie, Harms, Klaus, Meggers, Eric. Chiral-at-Iron Catalyst: Expanding the Chemical Space for Asymmetric Earth-Abundant Metal Catalysis. Journal of the American Chemical Society, vol.141, no.11, 4569-4572.

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24. Kumar, Anil, Ghosh, Subrata K., Gladysz, John A.. Tris(1,2-diphenylethylenediamine)cobalt(III) Complexes: Chiral Hydrogen Bond Donor Catalysts for Enantioselective α-Aminations of 1,3-Dicarbonyl Compounds. Organic letters, vol.18, no.4, 760-763.

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25. Lewis, Kyle G., Ghosh, Subrata K., Bhuvanesh, Nattamai, Gladysz, John A.. Cobalt(III) Werner Complexes with 1,2-Diphenylethylenediamine Ligands: Readily Available, Inexpensive, and Modular Chiral Hydrogen Bond Donor Catalysts for Enantioselective Organic Synthesis. ACS central science, vol.1, no.1, 50-56.

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26. Alimohammadi, Motahareh, Hasaninejad, Alireza, Luu, Quang H., Gladysz, John A.. Λ-[Co((S,S)-dpen)₃]³⁺ 2I^-B(C₆F₅)₄^-: A Second Generation Air- and Water-Stable Chiral Solvating Agent for Chirality Sensing (dpen = NH₂CHPhCHPhNH₂). Journal of organic chemistry, vol.85, no.17, 11250-11257.

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27. Luu, Quang H., Lewis, Kyle G., Banerjee, Anik, Bhuvanesh, Nattamai, Gladysz, John A.. The robust, readily available cobalt( III ) trication [Co(NH ₂ CHPhCHPhNH ₂ ) ₃ ] ³⁺ is a progenitor of broadly applicable chirality and prochirality sensing agents. Chemical science, vol.9, no.22, 5087-5099.

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28. Seo, Min-Seob, Kim, Hyunwoo. ¹H NMR Chiral Analysis of Charged Molecules via Ion Pairing with Aluminum Complexes. Journal of the American Chemical Society, vol.137, no.44, 14190-14195.

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29. Jang, Sumin, Kim, Hyunwoo. A Gallium-based Chiral Solvating Agent Enables the Use of 1H NMR Spectroscopy to Differentiate Chiral Alcohols. iscience, vol.19, 425-435.

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30. Jang, Sumin, Kim, Hyunwoo. Chiral ¹H NMR Analysis of Carbonyl Compounds Enabled by Cationic Cobalt Complex. Organic letters, vol.22, no.11, 4185-4189.

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