Enantioselective Synthesis of the C(1)-C(11) Fragment of Tedanolide C

[摘要]：A convergent synthesis of the protected C(1)-C(11) fragment 6 of the targeted enantiomer of tedanolide C is described. The key step of the synthesis is the Felkin-Ahn addition of vinyl iodide 7 to aldehyde 8 that proceeds in 80% yield with 4:1 diastereoselectivity.

[全文传递流程]：

一般上传文献全文的时限在1个工作日内