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Sakakibara, Shumpei, Inukai, Noriyoshi (1965) The Trifluoroacetate Method of Peptide Synthesis. I. The Synthesis and Use of Trifluoroacetate Reagents. Bulletin of the Chemical Society of Japan, 38 (11). 1979-1984 doi:10.1246/bcsj.38.1979

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Reference TypeJournal (article/letter/editorial)
TitleThe Trifluoroacetate Method of Peptide Synthesis. I. The Synthesis and Use of Trifluoroacetate Reagents
JournalBulletin of the Chemical Society of Japan
AuthorsSakakibara, ShumpeiAuthor
Inukai, NoriyoshiAuthor
Year1965 (November)Volume38
Issue11
PublisherThe Chemical Society of Japan
DOIdoi:10.1246/bcsj.38.1979Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID4474791Long-form Identifiermindat:1:5:4474791:4
GUID0
Full ReferenceSakakibara, Shumpei, Inukai, Noriyoshi (1965) The Trifluoroacetate Method of Peptide Synthesis. I. The Synthesis and Use of Trifluoroacetate Reagents. Bulletin of the Chemical Society of Japan, 38 (11). 1979-1984 doi:10.1246/bcsj.38.1979
Plain TextSakakibara, Shumpei, Inukai, Noriyoshi (1965) The Trifluoroacetate Method of Peptide Synthesis. I. The Synthesis and Use of Trifluoroacetate Reagents. Bulletin of the Chemical Society of Japan, 38 (11). 1979-1984 doi:10.1246/bcsj.38.1979
In(1965, November) Bulletin of the Chemical Society of Japan Vol. 38 (11) The Chemical Society of Japan

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Sakakibara, Shumpei, Inukai, Noriyoshi (1966) The Trifluoroacetate Method of Peptide Synthesis. II. An Improved Synthesis of Bradykinin. Bulletin of the Chemical Society of Japan, 39 (7). 1567-1572 doi:10.1246/bcsj.39.1567
Sakakibara, Shumpei, Shin, Masaru, Fujino, Masahiko, Shimonishi, Yasutsugu, Inoue, Sumiko, Inukai, Noriyoshi (1965) t-Amyloxycarbonyl as a New Protecting Group in Peptide Synthesis. I. The Synthesis and Properties ofN-t-Amyloxycarbonylamino Acids and Related Compounds. Bulletin of the Chemical Society of Japan, 38 (9). 1522-1525 doi:10.1246/bcsj.38.1522
Inukai, Noriyoshi, Nakano, Kohzi, Murakami, Masuo (1968) The Peptide Synthesis. II. Use of the Phenol Resin for the Peptide Synthesis. Bulletin of the Chemical Society of Japan, 41 (1). 182-186 doi:10.1246/bcsj.41.182
Sakakibara, Shumpei, Inukai, Noriyoshi (1964) A New Reagent for thep-Nitrophenylation of Carboxylic Acids. Bulletin of the Chemical Society of Japan, 37 (8). 1231-1232 doi:10.1246/bcsj.37.1231
Sakakibara, Shumpei, Nobuhara, Yoshibumi, Shimonishi, Yasutsugu, Kiyoi, Reiko (1965) A Synthesis of Oxytocin. Bulletin of the Chemical Society of Japan, 38 (1). 120-123 doi:10.1246/bcsj.38.120
Sakakibara, Shumpei, Nakamizo, Nobuhiro, Kishida, Yasuo, Yoshimura, Shoko (1968) Use of Anhydrous Hydrogen Fluoride in Peptide Synthesis. III. Synthesis of Bradykinin. Bulletin of the Chemical Society of Japan, 41 (6). 1477-1479 doi:10.1246/bcsj.41.1477
Inukai, Noriyoshi, Nakano, Kohzi, Murakami, Masuo (1967) The Peptide Synthesis. I. Use of theS-Ethylmercapto Group for the Protection of the Thiol Function of Cysteine. Bulletin of the Chemical Society of Japan, 40 (12). 2913-2918 doi:10.1246/bcsj.40.2913
Sakakibara, Shumpei, Fujii, Toshiyuki (1969) Synthesis and Use ofNim-Tosyl-L-histidine. Bulletin of the Chemical Society of Japan, 42 (5). 1466 doi:10.1246/bcsj.42.1466
Honda, Ichiro, Shimonishi, Yasutsugu, Sakakibara, Shumpei (1967) t-Amyloxycarbonyl as a New Protecting Group in Peptide Synthesis. IV. Synthesis and Use oft-Amyl Azidoformate. Bulletin of the Chemical Society of Japan, 40 (10). 2415-2418 doi:10.1246/bcsj.40.2415
Akabori, Shiro, Sakakibara, Shumpei, Shiina, Sumiko (1958) Synthesis and Use of L-Histidine Benzylester. Bulletin of the Chemical Society of Japan, 31 (6). 784-785 doi:10.1246/bcsj.31.784
Akabori, Shiro, Sakakibara, Shumpei, Shimonishi, Yasutsugu, Nobuhara, Yoshifumi (1964) A New Method for the Protection of the Sulfhydryl Group during Peptide Synthesis. Bulletin of the Chemical Society of Japan, 37 (3). 433-434 doi:10.1246/bcsj.37.433
 
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