A cheap metal for a “noble” task: preparative and mechanistic aspects of cycloisomerization and cycloaddition reactions catalyzed by low-valent iron complexes A Fürstner, K Majima, R Martin, H Krause, E Kattnig, R Goddard, ... Journal of the American Chemical Society 130 (6), 1992-2004, 2008 | 297 | 2008 |
Synthesis of a terbium fluorescent chelate and its application to time-resolved fluoroimmunoassay J Yuan, G Wang, K Majima, K Matsumoto Analytical chemistry 73 (8), 1869-1876, 2001 | 268 | 2001 |
Catalytic asymmetric michael reaction of β-keto esters: Effects of the linker heteroatom in linked-BINOL K Majima, R Takita, A Okada, T Ohshima, M Shibasaki Journal of the American Chemical Society 125 (51), 15837-15845, 2003 | 125 | 2003 |
Cycloisomerization of enynes catalyzed by iron (0)− ate complexes A Fürstner, R Martin, K Majima Journal of the American Chemical Society 127 (35), 12236-12237, 2005 | 103 | 2005 |
Quantitative measurement of 17β-estradiol and estriol in river water by time-resolved fluoroimmunoassay K Majima, T Fukui, J Yuan, G Wang, K Matsumoto Analytical sciences 18 (8), 869-874, 2002 | 50 | 2002 |
Enantio-and diastereoselective construction of vicinal quaternary and tertiary carbon centers by catalytic Michael reaction of α-substituted β-keto esters to cyclic enones K Majima, S Tosaki, T Ohshima, M Shibasaki Tetrahedron letters 46 (32), 5377-5381, 2005 | 22 | 2005 |
Fluorescent lanthanide chelates for biological systems K Matsumoto, T Nojima, H Sano, K Majima Macromolecular Symposia 186 (1), 117-121, 2002 | 18 | 2002 |
Convenient and Eco-Friendly Method for the Conversion of Benzylic Alcohols into Aldehydes, Ketones, and Carboxylic Acids Using NaOCl without any Additives in 1, 2-Dimethoxyethane N Fukuda, T Kajiwara, T Katou, K Majima, T Ikemoto Synlett 24 (11), 1438-1442, 2013 | 11 | 2013 |
Diastereoselective Synthesis of a cis-1,3-Disubstituted Cyclobutane Carboxylic Acid Scaffold for TAK-828F, a Potent Retinoic Acid Receptor-Related Orphan … K Majima, M Yamano The Journal of Organic Chemistry 86 (17), 11464-11471, 2021 | 7 | 2021 |
Method for producing sulfonyl chloride compound K Majima US Patent 9,487,485, 2016 | 6 | 2016 |
Method for producing sulfonyl chloride compound K Majima US Patent 9,932,322, 2018 | 3 | 2018 |
Fluorescent lanthanoid labels for time-resolved fluoremetry in biological trace analysis K Matsumoto, K Majima, T Fukui, S Sueda, J Yuan RIKEN REVIEW, 105-106, 2001 | 2 | 2001 |
Method for producing sulfonyl chloride compound K Majima US Patent 10,370,357, 2019 | | 2019 |
Fluorescent lanthanide chelates as labels for bio-and chip-technology K Matsumoto, T Nojima, H Sano, K Majima JOURNAL OF INORGANIC BIOCHEMISTRY 86 (1), 71-71, 2001 | | 2001 |