Eiichi Ensatsu

α-Chymotrypsin-catalysed peptide synthesis via the kinetically controlled approach using activated esters as acyl donors in organic solvents with low water content: incorporation of non-protein amino acids into peptides

Toshifumi Miyazawa, Shin’ichi Nakajo, Miyako Nishikawa et al. · Journal of the Chemical Society Perkin Transactions 1 · 2001 · 24 citations

Natural Sciences, Biochemistry, Catalysis +8

Broadening of the substrate tolerance of α-chymotrypsin by using the carbamoylmethyl ester as an acyl donor in kinetically controlled peptide synthesis

Toshifumi Miyazawa, Kayoko Tanaka, Eiichi Ensatsu et al. · Journal of the Chemical Society Perkin Transactions 1 · 2001 · 24 citations

Life Sciences, Biochemistry, Molecular Biology +15

Superiority of the carbamoylmethyl ester as an acyl donor for the kinetically controlled amide-bond formation mediated by α-chymotrypsinElectronic supplementary information (ESI) available: elemental analyses and HPLC separation data. See http://www.rsc.org/suppdata/p1/b1/b108735p/

Toshifumi Miyazawa, Eiichi Ensatsu, Nobuhiro Yabuuchi et al. · Journal of the Chemical Society Perkin Transactions 1 · 2002 · 18 citations

Life Sciences, Biochemistry, Chemistry +17

Remarkable effects of donor esters on the α-chymotrypsin-catalyzed couplings of inherently poor amino acid substrates

Toshifumi Miyazawa, Kayoko Tanaka, Eiichi Ensatsu et al. · Tetrahedron Letters · 1998 · 16 citations

Life Sciences, Biochemistry, Catalysis +11

α-Chymotrypsin-catalysed segment condensations via the kinetically controlled approach using carbamoylmethyl esters as acyl donors in organic mediaElectronic supplementary information (ESI) available: elemental analyses and HPLC separation data. See http://www.rsc.org/suppdata/p1/b1/b108738j/

Toshifumi Miyazawa, Eiichi Ensatsu, Makoto Hiramatsu et al. · Journal of the Chemical Society Perkin Transactions 1 · 2002 · 14 citations

Natural Sciences, Biochemistry, Chemistry +7