A new convergent approach to biphenomycin antibiotics

被引：17

作者：

Paintner, FF

Görler, K

Voelter, W

机构：

[1] Univ Munich, Dept Pharm, Zentrum Pharmaforsch, D-81377 Munich, Germany

[2] Univ Tubingen, Inst Physiol Chem, Phys Biochem Abt, D-72076 Tubingen, Germany

来源：

SYNLETT | 2003年 / 04期

关键词：

biphenomycins; antibiotics; cyclopeptides; asymmetric synthesis; Stille coupling;

D O I：

10.1055/s-2003-37506

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A new, convergent approach to the biaryl key intermediate of Schmidt's biphenomycin B total synthesis has been accomplished via a palladacycle complex catalyzed Stille cross-coupling of two o-tyrosine building blocks.

引用

页码：522 / 526

页数：5

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