A practical total synthesis of both enantiomers of epoxyquinols A and B

Mitsuru Shoji, Satoshi Kishida, Mitsuhiro Takeda, Hideaki Kakeya, Hiroyuki Osada, Yujiro Hayashi

研究成果: Article

37 引用 (Scopus)

抜粋

A practical total synthesis of both enantiomers of epoxyquinols A and B has been developed. Key reactions are the chromatography-free preparation of an iodolactone by using acryloyl chloride as dienophile in the Diels-Alder reaction of furan, the lipase-mediated kinetic resolution of a cyclohexenol derivative, and a modified procedure for α-iodonation of a cyclohexenone.

元の言語English
ページ(範囲)9155-9158
ページ数4
ジャーナルTetrahedron Letters
43
発行部数50
DOI
出版物ステータスPublished - 2002 12 9

    フィンガープリント

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

これを引用

Shoji, M., Kishida, S., Takeda, M., Kakeya, H., Osada, H., & Hayashi, Y. (2002). A practical total synthesis of both enantiomers of epoxyquinols A and B. Tetrahedron Letters, 43(50), 9155-9158. https://doi.org/10.1016/S0040-4039(02)02271-2