Convenient peptide synthesis without protection of C-terminals
T Noguchi, N Tehara, Y Uesugi, S Jung, N Imai
Index: Noguchi, Takuya; Tehara, Naoka; Uesugi, Yuki; Jung, Seunghee; Imai, Nobuyuki Chemistry Letters, 2012 , vol. 41, # 1 p. 42 - 43
Full Text: HTML
Citation Number: 7
Abstract
Condensation of carboxylic acids 1 and 5 with unprotected α-amino acids 2 via activation by ethyl chloroformate and triethylamine proceeded effectively to afford the corresponding amides in 50–99% yields. Tripeptide 7c was obtained in 42% yield from the dipeptide 6c in a similar manner.
Related Articles:
[Katritzky, Alan R.; Suzuki, Kazuyuki; Singh, Sandeep K. Synthesis, 2004 , # 16 p. 2645 - 2652]
[Kanosue, Yoshifumi; Kojima, Satoshi; Hiraga, Yoshikazu; Ohkata, Katsuo Bulletin of the Chemical Society of Japan, 2004 , vol. 77, # 6 p. 1187 - 1193]
[Katritzky, Alan R.; Suzuki, Kazuyuki; Singh, Sandeep K. Synthesis, 2004 , # 16 p. 2645 - 2652]
[Gagnon, Paul; Huang, Xicai; Therrien, Eric; Keillor, Jeffrey W. Tetrahedron Letters, 2002 , vol. 43, # 43 p. 7717 - 7719]
[Ueoka, Ryuichi; Matsumoto, Yoko; Harada, Katsuhiko; Akahoshi, Hirohiko; Ihara, Yasuji; Kato, Yasuo Journal of the American Chemical Society, 1992 , vol. 114, # 21 p. 8339 - 8340]