A Straightforward Synthesis of Emericellamide A Using Matteson's Homologation Approach

被引:2
|
作者
Priester, Ronja [1 ]
Kazmaier, Uli [1 ]
机构
[1] Saarland Univ, Organ Chem, D-66123 Saarbrucken, Germany
关键词
boronic esters; Matteson homologation; natural products; peptides; stereoselective synthesis; ANTI-ALDOL REACTIONS; BORONIC ESTERS; STEREOSELECTIVE-SYNTHESIS; BIOLOGICAL EVALUATION; ASYMMETRIC-SYNTHESIS; ESTERIFICATION; SELECTIVITY;
D O I
10.1055/a-2077-2113
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The Matteson homologation is the perfect approach for the synthesis of polyketide-peptide natural products such as the emericellamides. In only four steps, the polyketide fragment with three stereo genic centers can be obtained as a single stereoisomer. The peptide fragment is easily available via solid-phase peptide synthesis.
引用
收藏
页码:2159 / 2164
页数:6
相关论文
共 50 条