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Chemical & Pharmaceutical Bulletin|January 1, 1997
A reductive acidolysis final deprotection strategy in solid phase peptide synthesis based on safety-catch protectionT Kimura, T Fukui, S Tanaka, et al.
Chemical & Pharmaceutical Bulletin|November 1, 1991
New hydroxyl protecting groups of a safety-catch type removable by reductive acidolysisY Kiso, S Tanaka, T Kimura, et al.
Chemical & Pharmaceutical Bulletin|May 1, 1990
Solution-phase synthesis of porcine brain natriuretic peptide (pBNP) using S-trimethylacetamidomethylcysteineY Kiso, M Yoshida, T Kimura, et al.
Chemical & Pharmaceutical Bulletin|December 1, 1989
Tetrafluoroboric acid, a useful deprotecting reagent in peptide synthesisY Kiso, M Yoshida, T Tatsumi, et al.
Bioorganic & Medicinal Chemistry Letters|April 17, 1999
A new class of anti-HIV agents: synthesis and activity of conjugates of HIV protease inhibitors with a reverse transcriptase inhibitorT Kimura, H Matsumoto, T Matsuda, et al.
Chemical & Pharmaceutical Bulletin|March 1, 1994
Racemization-free synthesis of C-terminal cysteine-peptide using 2-chlorotrityl resinY Fujiwara, K Akaji, Y Kiso
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