Synthetic Study on Peptide Antibiotic Nisin. III. Synthesis of Ring C
K Fukase, M Kitazawa, T Wakamiya…
Index: Fukase; Kitazawa; Wakamiya; Shiba Bulletin of the Chemical Society of Japan, 1990 , vol. 63, # 6 p. 1838 - 1840
Full Text: HTML
Citation Number: 7
Abstract
A cyclic sulfide moiety corresponding to ring C in peptide antibiotic nisin was successfully synthesized from a disulfide compound prepared from a heptapeptide involving L-cysteine and threo-3-methyl-D-cysteine through desulfurization reaction with hexaethylphosphorus triamide.
Related Articles:
[Zhang, Jian; Li, Xiaoyang; Jiang, Yuqi; Feng, Jinhong; Li, Xiaoguang; Zhang, Yingjie; Xu, Wenfang Bioorganic and Medicinal Chemistry, 2014 , vol. 22, # 11 p. 3055 - 3064]
[Sakina; Kawazura; Morihara; Yajima Chemical and Pharmaceutical Bulletin, 1988 , vol. 36, # 10 p. 3915 - 3919]
[Zhang, Jian; Li, Xiaoyang; Jiang, Yuqi; Feng, Jinhong; Li, Xiaoguang; Zhang, Yingjie; Xu, Wenfang Bioorganic and Medicinal Chemistry, 2014 , vol. 22, # 11 p. 3055 - 3064]
[Lyons, Anthony Q.; Pettit, Leslie D. Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1984 , p. 2305 - 2308]