期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 68, 期 21, 页码 8193-8198出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo0346407
关键词
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Two diastereomeric analogues of ring C of nisin incorporating a novel norlanthionine residue have been synthesized via a triply orthogonal protecting group strategy. A full structural study was carried out by NMR, which elucidated the conformational properties of the two peptides and enabled the identity of each diastereoisomer to be proposed.
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