Year |
Citation |
Score |
2017 |
Seo B, Kim H, Kim YG, Baek Y, Um K, Lee PH. Synthesis of Bicyclic Isothiazoles through an Intramolecular Rhodium-Catalyzed Transannulation of Cyanothiadiazoles. The Journal of Organic Chemistry. PMID 28889744 DOI: 10.1021/Acs.Joc.7B02077 |
0.748 |
|
2017 |
Park S, Kim H, Son JY, Um K, Lee S, Baek Y, Seo B, Lee PH. Synthesis of Imidazopyridines via Copper-Catalyzed, Formal Aza-[3 + 2] Cycloaddition Reaction of Pyridine Derivatives with α-Diazo Oxime Ethers. The Journal of Organic Chemistry. PMID 28869378 DOI: 10.1021/Acs.Joc.7B01714 |
0.776 |
|
2017 |
Ko GH, Son J, Kim H, Maeng C, Baek Y, Seo B, Um K, Lee PH. Synthesis of Indolo-1,2-Benzothiazines from Sulfoximines and 3-Diazoindolin-2-imines Advanced Synthesis & Catalysis. 359: 3362-3370. DOI: 10.1002/Adsc.201700764 |
0.786 |
|
2017 |
Son J, Kim H, Jeon WH, Baek Y, Seo B, Um K, Lee K, Lee PH. Synthesis of Dihydrophosphaisocoumarins through a Palladium-Catalyzed Oxidative Cyclization of Arylphosphonic Acid Monoethyl Esters with 1,3-Dienes Advanced Synthesis & Catalysis. 359: 3194-3206. DOI: 10.1002/Adsc.201700742 |
0.773 |
|
2016 |
Seo B, Kim YG, Lee PH. Synthesis of Isothiazole via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Nitriles. Organic Letters. PMID 27668825 DOI: 10.1021/Acs.Orglett.6B02499 |
0.635 |
|
2016 |
Seo B, Jeon WH, Kim C, Kim S, Kim SH, Lee PH. ChemInform Abstract: Sequential Functionalization of the O-H and C(sp2)-O Bonds of Tropolones by Alkynes and N-Sulfonyl Azides. Cheminform. 47. DOI: 10.1002/CHIN.201632086 |
0.588 |
|
2015 |
Seo B, Jeon WH, Kim J, Kim S, Lee PH. Correction to Synthesis of Fluorenes via Tandem Copper-Catalyzed [3 + 2] Cycloaddition and Rhodium-Catalyzed Denitrogenative Cyclization in a 5-Exo Mode from 2-Ethynylbiaryls and N-Sulfonyl Azides in One-Pot. The Journal of Organic Chemistry. PMID 26360317 DOI: 10.1021/acs.joc.5b02070 |
0.759 |
|
2015 |
Kim CE, Son JY, Shin S, Seo B, Lee PH. Alkenylation of phosphacoumarins via aerobic oxidative Heck reactions and their synthetic application to fluorescent benzophosphacoumarins. Organic Letters. 17: 908-11. PMID 25644690 DOI: 10.1021/Acs.Orglett.5B00020 |
0.744 |
|
2015 |
Seo B, Jeon WH, Kim J, Kim S, Lee PH. Synthesis of fluorenes via tandem copper-catalyzed [3 + 2] cycloaddition and rhodium-catalyzed denitrogenative cyclization in a 5-exo mode from 2-ethynylbiaryls and N-sulfonyl azides in one pot. The Journal of Organic Chemistry. 80: 722-32. PMID 25543833 DOI: 10.1021/Jo5027113 |
0.765 |
|
2015 |
Seo B, Jeon WH, Kim C, Kim S, Kim SH, Lee PH. Front Cover Picture: Sequential Functionalization of the OH and C(sp2)O Bonds of Tropolones by Alkynes andN-Sulfonyl Azides (Adv. Synth. Catal. 7/2016) Advanced Synthesis & Catalysis. 358: 1003-1003. DOI: 10.1002/Adsc.201501042 |
0.716 |
|
2015 |
Seo B, Jeon WH, Kim CE, Kim S, Kim SH, Lee PH. Sequential Functionalization of the O-H and C(sp2)-O Bonds of Tropolones by Alkynes and N-Sulfonyl Azides Advanced Synthesis and Catalysis. DOI: 10.1002/Adsc.201500829 |
0.749 |
|
2014 |
Kim S, Kim CE, Seo B, Lee PH. In situ generation of phosphoryl alkylindiums and their synthetic application to arylalkyl phosphonates via palladium-catalyzed cross-coupling reactions. Organic Letters. 16: 5552-5. PMID 25338199 DOI: 10.1021/Ol502540Z |
0.76 |
|
2014 |
Kim CE, Park S, Eom D, Seo B, Lee PH. Synthesis of pyrroles from terminal alkynes, N-sulfonyl azides, and alkenyl alkyl ethers through 1-sulfonyl-1,2,3-triazoles. Organic Letters. 16: 1900-3. PMID 24660875 DOI: 10.1021/Ol500718S |
0.802 |
|
2013 |
Park S, Seo B, Shin S, Son JY, Lee PH. Rhodium-catalyzed oxidative coupling through C-H activation and annulation directed by phosphonamide and phosphinamide groups. Chemical Communications (Cambridge, England). 49: 8671-3. PMID 23949774 DOI: 10.1039/C3Cc44995E |
0.756 |
|
2010 |
Seo JH, Seo BB. Independent chromosomal localization of two different size 5S rDNA of Allium victorialis var. platyphyllum by sequential fluorescence in situ hybridization in accordance with sequence polymorphism Genes and Genomics. 32: 129-135. DOI: 10.1007/s13258-009-0804-0 |
0.428 |
|
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