Studies on peptides. CLII. Hard acid deprotecting procedure for peptide synthesis.

…, A OKAMACHI, S FUNAKOSHI, M SAKURAI…

Index: Fujii; Otaka; Ikemura; Hatano; Okamachi; Funakoshi; Sakurai; Shioiri; Yajima Chemical and pharmaceutical bulletin, 1987 , vol. 35, # 8 p. 3447 - 3452

Full Text: HTML

Citation Number: 29

Abstract

NOBUTAK A FUJII,a AKIRA OTAKA,a OSAMU IKEMURA,a MIKA HATANO,a AKIRA OKAMACHI,a SUSUMU FUNAKOSHI,a MITSUYA SAKURAI,a TAKAYUKI SHIOIRI,b and HARUAKI YAJIMA*,a ... Faculty of Pharmaceutical Sciences, Kyoto University,a Kyoto 606, Japan and Faculty of Pharmaceutical Sciences, Nagoya City University,b Mizuho-ku, Nagoya 467, Japan ... The use of trimethylsilyl trifluoromethanesulfonate as a peptide deprotecting reagent was

~99%

~91%

~83%

~99%

~99%

~99%

~99%

~98%

~99%

~97%

~99%

~99%

~99%

~99%

~99%

~99%

Resolution of underivatized amino acids by reversed-phase ch...

[Journal of the American Chemical Society, , vol. 102, # 15 p. 5115 - 5117]

A mild removal of Fmoc group using sodium azide

[Chen, Chun-Chi; Rajagopal, Basker; Liu, Xuan Yu; Chen, Kuan Lin; Tyan, Yu-Chang; Lin, Fui; Lin, Po-Chiao Amino Acids, 2014 , vol. 46, # 2 p. 367 - 374]

Identification of new peptide amides as selective cathepsin ...

[Bioorganic and Medicinal Chemistry Letters, , vol. 23, # 10 p. 2968 - 2973]

New strategy for the chemical synthesis of proteins

[Yajima; Fujii; Funakoshi; Watanabe; Murayama; Otaka Tetrahedron, 1988 , vol. 44, # 3 p. 805 - 819]