Stereocontrolled Synthesis of the C1-C10 Fragments of Monensin B and Laidlomycin

  • Kang, Sungkyoung
  • Lee, Wonchul
  • Jung, Byunghyuck
  • Lee, Hee-Seung
  • Kang, Sung Ho
Citations

WEB OF SCIENCE

4
Citations

SCOPUS

5

초록

An efficient synthetic route to the C1-C10 fragments of laidlomycin and monensin B has been developed toward their total synthesis. The asymmetric carbons have been elaborated by a syn-aldol reaction using the oxazolidinone chiral auxiliary for C6 and C7, an anti-aldol reaction for C3 and C4, the Tishchenko-Evans reaction for C5, and a chiral building block for C2.

키워드

aldol reactionlaidlomycinmonensin BTishchenko-Evans reactiontotal synthesisPOLYETHER IONOPHORE ANTIBIOTICSMEDIATED GROWTH-INHIBITIONCELL-CYCLE ARRESTCONVERGENT SYNTHESISCLAISEN REARRANGEMENTMOLECULAR-STRUCTUREESTER ENOLATECOMPLEXBIS(TETRAHYDROFURAN)CONVERSION
제목
Stereocontrolled Synthesis of the C1-C10 Fragments of Monensin B and Laidlomycin
저자
Kang, SungkyoungLee, WonchulJung, ByunghyuckLee, Hee-SeungKang, Sung Ho
DOI
10.1002/ajoc.201500078
발행일
2015-06
유형
Article
저널명
Asian Journal of Organic Chemistry
4
6
페이지
567 ~ 572