Synthesis of microcolin analogs using trimethylsilylated lactams
摘要:
The synthesis of microcolin analogs is described using an approach that could be of considerable practical interest for structure-activity studies on microcolin and related peptides. This synthetic pathway is more efficient than the methods reported to date, and allows the variation of the Xaa-pyrrolin-2-one unit of these molecules, which has been shown to be crucial for the biological activity. (C) 1997 Elsevier Science Ltd.
Synthesis of microcolin analogs using trimethylsilylated lactams
摘要:
The synthesis of microcolin analogs is described using an approach that could be of considerable practical interest for structure-activity studies on microcolin and related peptides. This synthetic pathway is more efficient than the methods reported to date, and allows the variation of the Xaa-pyrrolin-2-one unit of these molecules, which has been shown to be crucial for the biological activity. (C) 1997 Elsevier Science Ltd.
Synthesis of microcolin analogs using trimethylsilylated lactams
作者:Ralph-Heiko Mattern、Sarath P. Gunasekera、Oliver J. McConnell
DOI:10.1016/s0040-4039(97)00336-5
日期:1997.3
The synthesis of microcolin analogs is described using an approach that could be of considerable practical interest for structure-activity studies on microcolin and related peptides. This synthetic pathway is more efficient than the methods reported to date, and allows the variation of the Xaa-pyrrolin-2-one unit of these molecules, which has been shown to be crucial for the biological activity. (C) 1997 Elsevier Science Ltd.