Publication

33. Selective Depletion of ABO-Responsive B Cells by T-Cell-Engaging Bispecific Antibody Conjugates for ABOi Transplantation.Choi, H. R.; Piao, H.; Atriardi, S. R.; Kang, I.; Chang, T. K.; Kim, S.; Jang, J. Y.; Lee, G.; Jung, K. C.; Mardhiyah, H.; Machmud, F. I.; Park, J.; Woo, S. K.*; Yang, J.*; Kim, C. H.* Blood 2026, 147 (17), 1928

32. Visible-Light Photoredox-Catalyzed Synthesis of β-Aminosulfides and β-Aminosulfoxides via Radical Addition to Imines. Gontala, A., Mardhiyah, H.; Woo, S. K.* Asian J. Org. Chem. 2026, 15 (1), e00630

31. Batch and flow synthesis of sulfides and sulfoxides using green solvents and oxidant through visible-light photocatalysis. Park, J.; Kim, S. H.; Cho, J.-Y.; Atriardi, S. R.; Kim, J.-Y.; Mardhiyah, H.; Park, B. Y.*; Woo, S. K.* Green Chem. 2025, 27, 3284-3292

Selected for “A selection of articles on sustainable process intensification in Green Chemistry."

30. Harnessing Photoredox and Weak Brønsted Base Dual Catalysis for Selective C(sp3)–H Bond Activation. Atriardi, S. R.; Anita, Y.; Woo, S. K.* Synthesis 2025, 57 (05), 953-964

Invited to a Special issue on "Dual Catalysis"

29. Visible-Light-Photocatalyzed Pinacol Coupling in Water. Huh, H. H.; Lee, Y. J.; Anita, Y.; Woo, S. K.* Asian J. Org. Chem. 2024, 13 (2), e202300591

28. Single-Electron Oxidation-Induced Chemical Transformations: Carbon-Carbon Bond Formation and Selective Oxaziridine Rearrangement. Atriardi. S. R., Woo, S. K.*, Aldrichimica Acta, 2023, 56 (1), 25-33

Invited to a Special issue on “Chemistry in Korea Special Issue”

27. Visible-Light Photoredox-Catalysed Giese Reaction of α-Silyl Ether with Various Michael Acceptor . Kang. Y. W., Kim. R. H., Atriardi. S. R., Woo, S. K.*, J. Org. Chem. 2023, 88 (6), 3555-3566.

26. Photoredox-Catalyzed Synthesis of β-Amino Alcohols: Hydroxymethylation of Imines with α-Silyl Ether as Hydroxymethyl Radical Precursor. Gontala, A., Huh, H., Woo, S. K.*, Org. Lett. 2023, 25, 21-26

25. Synthesis of gem-difluoroalkenes via photoredox-catalyzed defluoroaryloxymethylation of α-trifluoromethyl alkenes. Atriardi, S. R., Kim, J. Y., Anita, Y., Woo, S. K.*, Bull. Korean Chem. Soc. 2023, 40, 50-54

Invited to a Special issue on “Emerging Investigators”

24. KOtBu-promoted C3-homocoupling of quinoxalinones through single electron transfer from an sp2 carbanion intermediate. Kwon, N. Y.; Mishra, N. K.; Park, J. S.; Woo, S. K.; Ghosh, P.*; Kim, I. S.* ,Chem. Commun. 2022, 58 (50), 7078-7081

23. 1.12 - Oxaziridines and Oxazirines. In Comprehensive Heterocyclic Chemistry IV. Woo, S.K.*; Elsevier, 2022; pp 582-611.

22. Weak Base-Promoted Selective Rearrangement of Oxaziridines to Amides via Visible-Light Photoredox Catalysis. Park, J., Park, S., Jang, G. S., Kim, R. H., Jung, J.* and Woo, S.K.*, Chem. Comm. 2021, 57, 9995-9998

Invited to a Special issue on “Green Synthesis”

21. Visible‐Light Photoredox‐Catalyzed α‐Allylation of α‐Bromocarbonyl Compounds Using Allyltrimethylsilane. Gontala, A., Jang, G. S. and Woo, S.K.*, Bull. Korean Chem. Soc. 2021, 42: 506-509.

Invited to a Special issue on “Chemical Synthesis & Reaction Development”

20. 가시광선 광촉매 화학에서 라디칼 전구체를 이용한 알킬 라디칼의 생성 및 활용. 우상국*, 화학세계, 읽기쉬운 총설, 2020, 10, 18-25

19. Visible‐Light Photoredox‐Catalyzed α‐Regioselective Conjugate Addition of Allyl Groups to Activated Alkenes. Gontala, A.; Woo, S. K.*, Adv. Synth. Catal. 2020, 362, 3223.

https://onlinelibrary.wiley.com/doi/10.1002/adsc.202000445

18. Controllable One-Pot Synthesis for Scaffold Diversity via Visible-Light Photoredox-Catalyzed Giese Reaction and Further Transformation. Nam, S. B.; Khatun, N.; Kang, Y. W.; Park, B. Y.*; Woo, S. K*., Chem. Commun. 2020, 56, 2873.

https://pubs.rsc.org/en/Content/ArticleLanding/2020/CC/C9CC08781H#!divAbstract

17. Oxidative Deprotection of p-Methoxybenzyl Ethers via Metal-Free Photoredox Catalysis. Ahn, D. K.; Kang, Y. W; Woo, S. K.*, J. Org. Chem. 2019, 84, 3612.

https://pubs.acs.org/doi/abs/10.1021/acs.joc.8b02951

16. Catalytic Enantioselective Carbonyl Propargylation Beyond Preformed Carbanions: Reductive Coupling and Hydrogen Auto‐Transfer. Ambler, B. R.; Woo, S. K.*; Krische, M. J.*, ChemCatChem 2019,11, 324.

https://onlinelibrary.wiley.com/doi/10.1002/cctc.201801121

15. Visible-Light Photoredox-Catalyzed Hydroalkoxymethylation of Activated Alkenes Using α-Silyl Ethers as Alkoxymethyl Radical Equivalents. Khatun, N.; Kim, M. J.; Woo, S. K.*, Org. Lett. 2018, 20, 6239.

https://pubs.acs.org/doi/10.1021/acs.orglett.8b02721

14. Synthesis of 4-Isoxazolines via Visible-Light Photoredox-Catalyzed [3 + 2] Cycloaddition of Oxaziridines with Alkynes. Jang, G. S.; Lee, J.; Seo, J.; Woo, S. K.*, Org. Lett. 2017, 19, 6448.

https://pubs.acs.org/doi/10.1021/acs.orglett.7b03369

13. Efficient Synthesis and Characterization of Solvatochromic Fluorophore. Adnan, M.; Kim, H. S.; Jeong, H.; Ko, H. M.*; Woo, S. K.*; Lee, J. K.*, Bull. Korean Chem. Soc. 2017, 38, 1052.

12. Efficient synthesis of aryl-substituted carbazoles via tandem double or triple suzuki coupling and cadogan cyclization. Kim, H. S.; Goo, D.-y.; Woo, S. K.*, Tetrahedron 2017, 73, 1413.

http://dx.doi.org/10.1016/j.tet.2017.01.038

11. C-Propargylation Overrides O-Propargylation in Reactions of Propargyl Chloride with Primary Alcohols: Rhodium-Catalyzed Transfer Hydrogenation. Liang, T.; Woo, S. K.; Krische, M. J., Angew. Chem. Int. Ed. 2016, 55, 9207.

http://onlinelibrary.wiley.com/doi/10.1002/anie.201603575/abstract;jsessionid=BE7FA610C677FA944BC6A77F360C8C40.f04t02

10. One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination. Goo, D.-Y.; Woo, S. K.*, Org. Biomol. Chem. 2016, 14, 122.

http://pubs.rsc.org/en/content/articlelanding/2016/ob/c5ob01952d#!divAbstract

Publication as Post Doc. Fellow and Graduate Student

9. Total Synthesis of 6-Deoxyerythronolide B via C-C Bond-Forming Transfer Hydrogenation. Gao, X.; Woo, S. K.; Krische, M. J. J. Am. Chem. Soc. 2013, 135, 4223.

https://pubs.acs.org/doi/abs/10.1021/ja4008722

8. Enantioselective Carbonyl Propargylation by Iridium-Catalyzed Transfer Hydrogenative Coupling of Alcohols and Propargyl Chlorides. Woo, S. K.; Geary, L. M.; . Krische, M. J. Angew. Chem. Int. Ed. 2012, 51, 7830.

http://onlinelibrary.wiley.com/doi/10.1002/anie.201203334/abstract;jsessionid=02C5C16C00826614C5027974F25B2411.f04t02

7. Diastereo- and Enantioselective Iridium Catalyzed Carbonyl Propargylation from the Alcohol or Aldehyde Oxidation Level: 1,3-Enynes as Allenylmetal Equivalents. Geary, L. M.; Woo, S. K.; Leung, J. C. Krische, M. J. Angew. Chem. Int. Ed. 2012, 51, 2972.

http://dx.doi.org/10.1002/anie.201200239

6. Total Synthesis of Bryostatin 7 via C-C Bond Forming Hydrogenation. Lu, Y.; Woo, S. K.; Krische, M. J. J. Am. Chem. Soc. 2011, 133, 13876.

https://pubs.acs.org/doi/abs/10.1021/ja205673e

5. Polycavernoside A: The Prins Macrocyclization Approach. Woo, S. K.; Lee, E. J. Am. Chem. Soc. 2010, 132, 4564.

https://pubs.acs.org/doi/full/10.1021/ja1009579

4. Stereoselective Synthesis of (−)-Amphidinolide E. 1. Kim, C. H.; An, H. J.; Shin, W. K.; Yu, W.; Woo, S. K.; Jung, S. K.; Lee, E., Chem. Asian J. 2008, 3, 1523.

http://pubs.acs.org/doi/abs/10.1021/ja1009579

3. Total Synthesis of (+)-Neopeltolide by a Prins Macrocyclization. Woo, S. K.; Kwon, M. S.; Lee, E., Angew. Chem. Int. Ed. 2008, 47, 3242.

http://onlinelibrary.wiley.com/doi/10.1002/anie.200800386/abstract

2. Total Synthesis of (+)-Exiguolide. Kwon, M. S.; Woo, S. K.; Na, S. W.; Lee, E., Angew. Chem. Int. Ed. 2008, 47, 1733.

http://onlinelibrary.wiley.com/doi/10.1002/anie.200705018/abstract

1. Total Synthesis of (−)-Amphidinolide E. 1. Kim, C. H.; An, H. J.; Shin, W. K.; Yu, W.; Woo, S. K.; Jung, S. K.; Lee, E., Angew. Chem. Int. Ed. 2006, 45, 8019.

http://onlinelibrary.wiley.com/doi/10.1002/anie.200603363/abstract

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