N‐Sulfanylethylanilide Peptide as a Crypto‐Thioester Peptide K Sato, A Shigenaga, K Tsuji, S Tsuda, Y Sumikawa, K Sakamoto, ... ChemBioChem 12 (12), 1840-1844, 2011 | 143 | 2011 |
Dual kinetically controlled native chemical ligation using a combination of sulfanylproline and sulfanylethylanilide peptide H Ding, A Shigenaga, K Sato, K Morishita, A Otaka Organic Letters 13 (20), 5588-5591, 2011 | 82 | 2011 |
Chemical synthesis of biologically active monoglycosylated GM2-activator protein analogue using N-sulfanylethylanilide peptide. K Sato, A Shigenaga, K Kitakaze, K Sakamoto, D Tsuji, K Itoh, A Otaka Angewandte Chemie 125 (30), 2013 | 72 | 2013 |
Characteristic fluctuations in glycosidically bound volatiles during tea processing and identification of their unstable derivatives J Cui, T Katsuno, K Totsuka, T Ohnishi, H Takemoto, N Mase, M Toda, ... Journal of Agricultural and Food Chemistry 64 (5), 1151-1157, 2016 | 64 | 2016 |
One‐Pot/Sequential Native Chemical Ligation Using N‐Sulfanylethylanilide Peptide A Otaka, K Sato, H Ding, A Shigenaga The Chemical Record 12 (5), 479-490, 2012 | 57 | 2012 |
Examination of native chemical ligation using peptidyl prolyl thioesters T Nakamura, A Shigenaga, K Sato, Y Tsuda, K Sakamoto, A Otaka Chemical Communications 50 (1), 58-60, 2014 | 43 | 2014 |
Protease-resistant modified human β-hexosaminidase B ameliorates symptoms in GM2 gangliosidosis model K Kitakaze, Y Mizutani, E Sugiyama, C Tasaki, D Tsuji, N Maita, ... The Journal of clinical investigation 126 (5), 1691-1703, 2016 | 41 | 2016 |
Synthetic Procedure for N-Fmoc Amino Acyl-N-Sulfanylethylaniline Linker as Crypto-Peptide Thioester Precursor with Application to Native Chemical Ligation K Sakamoto, K Sato, A Shigenaga, K Tsuji, S Tsuda, H Hibino, ... The Journal of Organic Chemistry 77 (16), 6948-6958, 2012 | 41 | 2012 |
Sequential native chemical ligation utilizing peptide thioacids derived from newly developed Fmoc-based synthetic method A Shigenaga, Y Sumikawa, S Tsuda, K Sato, A Otaka Tetrahedron 66 (18), 3290-3296, 2010 | 36 | 2010 |
Rapid optimization of reaction conditions based on comprehensive reaction analysis using a continuous flow microwave reactor P Vámosi, K Matsuo, T Masuda, K Sato, T Narumi, K Takeda, N Mase The Chemical Record 19 (1), 77-84, 2019 | 33 | 2019 |
Application of N–C-or C–N-directed sequential native chemical ligation to the preparation of CXCL14 analogs and their biological evaluation K Tsuji, A Shigenaga, Y Sumikawa, K Tanegashima, K Sato, K Aihara, ... Bioorganic & medicinal chemistry 19 (13), 4014-4020, 2011 | 32 | 2011 |
The total chemical synthesis of the monoglycosylated GM2 ganglioside activator using a novel cysteine surrogate K Sato, K Kitakaze, T Nakamura, N Naruse, K Aihara, A Shigenaga, ... Chemical Communications 51 (49), 9946-9948, 2015 | 31 | 2015 |
Photo-triggered fluorescent labelling of recombinant proteins in live cells D Jung, K Sato, K Min, A Shigenaga, J Jung, A Otaka, Y Kwon Chemical Communications 51 (47), 9670-9673, 2015 | 31 | 2015 |
Method for direct mass-spectrometry-based identification of monomethylated RNA nucleoside positional isomers and its application to the analysis of Leishmania rRNA H Nakayama, Y Yamauchi, Y Nobe, K Sato, N Takahashi, ... Analytical chemistry 91 (24), 15634-15643, 2019 | 29 | 2019 |
Chemical Synthesis of Proteins Using N-Sulfanylethylanilide Peptides, Based on N−S Acyl Transfer Chemistry A Otaka, K Sato, A Shigenaga Protein Ligation and Total Synthesis II, 33-56, 2015 | 29 | 2015 |
Direct synthesis of N-terminal thiazolidine-containing peptide thioesters from peptide hydrazides K Sato, S Tanaka, K Yamamoto, Y Tashiro, T Narumi, N Mase Chemical Communications 54 (66), 9127-9130, 2018 | 28 | 2018 |
Tuning the Catalyst Reactivity of Imidazolylidene Catalysts through Substituent Effects on the N-Aryl Groups R Kyan, K Sato, N Mase, N Watanabe, T Narumi Organic letters 19 (10), 2750-2753, 2017 | 26 | 2017 |
Development of an Anilide-Type Scaffold for the Thioester Precursor N-Sulfanylethylcoumarinyl Amide M Eto, N Naruse, K Morimoto, K Yamaoka, K Sato, K Tsuji, T Inokuma, ... Organic Letters 18 (17), 4416-4419, 2016 | 26 | 2016 |
Fine-bubble-based strategy for the palladium-catalyzed hydrogenation of nitro groups: measurement of ultrafine bubbles in organic solvents N Mase, Y Nishina, S Isomura, K Sato, T Narumi, N Watanabe Synlett 28 (16), 2184-2188, 2017 | 25 | 2017 |
Labelling of endogenous target protein via N–S acyl transfer-mediated activation of N-sulfanylethylanilide M Denda, T Morisaki, T Kohiki, J Yamamoto, K Sato, I Sagawa, T Inokuma, ... Organic & Biomolecular Chemistry 14 (26), 6244-6251, 2016 | 23 | 2016 |