Publication

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 

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.

http://dx.doi.org/10.1002/bkcs.11219

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
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