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28. A Deconstruction-Reconstruction Strategy to Access 1-Naphthol Derivatives: Application to the Synthesis of Aristolactam Scaffolds

 

 Bak, J. M.; Song, M.; Shin, I.*​; Lim, H. N.​*


  




27. Synthesis of 2,5-Difunctionalized Pyridines via Sequential Chemoselective Amination and Suzuki-Miyaura Reactions


 https://doi.org/10.1016/j.tet.2023.133468


  



 

26. Recent Progress and Perspectives in Photo-Induced Organic Reactions of Acylsilanes



  




25. Regioselective Ortho-Arylation of Polyhalo-Substituted (Hetero)Aryl Tosylates Using an Integrated Continuous Flow/Batch Protocol



  




24. Reversed-Polarity Synthesis of N-Sulfonyl Ketimines with Imidoylsilanes and Diaryliodoniym Salts via Palladium-Catalyzed Reactions



  




23. 1,4-Azaborines: Origin, Modern Synthesis, and Applications as Optoelectronic Materials



  




22. Corrosion Inhibition of Mild Steel and 304 Stainless Steel in 1 M Hydrochloric Acid Solution by Tea Tree Extract and Its Main Constituents



  

 



21. Recent Advances in One-Pot Modular Synthesis of 2-Quinolones


Lim, H. N.*


  




20. Development and Structure-Activity Relationship Study of SHP2 Inhibitor Containing 3,4,6-Trihydroxy-5-oxo-5H-benzo[7]annulene






19. Chan-Lam Coupling Reaction of Sulfamoyl Azides with Arylboronic Acids for Synthesis of Unsymmetrical N-Arylsulfamides



  



Description unavailable

18. Allosteric Inhibitor TREA-0236 Containing Non-hydrolysable Quinazoline-3-one for EGFR T790M/C797S Mutants Inhibition





 


 


17. 3-Hydroxy-2-(Trialkylsilyl)phenyl Triflate: A Benzyen Precursor Triggered via 1,3-C-sp2-O Silyl Migration








Details are in the caption following the image


16. Structure-Activity Relationship Study of 2,4-Dianilinopyrimidine Containing Methanesulfonamide (TRE- 069) as Potent and Selestive Epidermal GroWth Factor Receptor T790M/C797S Mutant Inhibitor for Anticancer Treatment


Bull. Korean Chem. Soc. 2017, 38, 1353-1357.





Figure 1


15. Total Synthesis of Swinholide A: An Exposition in Hydrogen-Mediated C-C Bond Formation 


J. Am. Chem. Soc. 2016, 138, 14246-14249.






14. Asymmetric Iridium-Catalyzed C-C Coupling of Chiral Diols via Site-Selective Redox-Triggered Carbonyl Addition


2016, 372, 85-101.






13. Formal Synthesis of Premisakinolide A and C(19)-C(32) of Swinholide A via Site-Selective C-H Allylation and Crotylation of Unprotected Diols


2015, 17, 4686-4689.






12. Reductive Cyclizaion of Halo-Ketones to Form 3-Hydroxy-2-Oxindoles via Palladium Catalyzed Hydrogenation: A Hydrogen-Mediated Grignard Addition


2015, 71, 5776-5780.





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11. Catalytic C-C Bond Formation and the Hendricksonian Ideal: Atom- and Redox-Economy, Stereo- and Site-Selectivity


2015, 48, 15-19.

 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517613/






Description unavailable


10. Catalyst-Directed Diastereo- and Site-Selectivity in Succesive Nucleophilic and Electrophilic Allylation of Chiral 1,3-Diols: Protecting-Group Free Synthesis of Substituted Pyrans 


2014, 20, 13382-13389.





Description unavailable


9. Catalytic Enantioselective C-H Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon


2014, 53, 9142-9150.






Figure 1


8. Pd-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions between Sulfamates and Potassium Boc-Protected Aminomethyltrifluoroborates







Figure 1


7. Potassium Boc-Protected Secondary Aminomethyltrifluoroborates: Synthesis and Suzuki-Miyaura Cross-Coupling Reactions 







Figure 1


6. Suzuki-Miyaura Cross-Coupling of Potassium Boc-Protected Aminomethyltrifluoroborate with Aryl and HetarylMesylates







Figure 1


5. Synthesis and Suzuki-Miyaura Cross-Coupling Reactions of Potassium Boc-Protected Aminomethyltrifluoroborate with Aryl and Hetaryl Halides








Figure 1


4. Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions of Enantiomerically Enriched Potassium β-Trifluoroboratoamides with Various Aryl- and Hetaryl Chlorides


Gérard, L.; Molander, G. A.;*






Description unavailable


3. Total Synthesis of trans-Difydronarciclasine through a Highly endo-Selective Diels-Alder Cycloaddition of 3,5-Dibromo-2-pyrone








2. Synthesis of Medium Sized Rings from the Cycloadducts of 3,5-Dibromo-2-pyrone via a Radical Mediated Fragmentation Reaction

  

 http://10.5012/bkcs.2006.27.12.2091





Figure 1


1. Regioselective [5+5]-Sigmatropic Rearrangement Reactions of Aryl Hydrazides

  

Org. Lett. 2006, 8, 2047-2050.