Title of article
A practical total synthesis of both enantiomers of epoxyquinols A and B
Author/Authors
Shoji، نويسنده , , Mitsuru and Kishida، نويسنده , , Satoshi and Takeda، نويسنده , , Mitsuhiro and Kakeya، نويسنده , , Hideaki and Osada، نويسنده , , HIROYUKI and HAYASHI، نويسنده , , Yujiro، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
4
From page
9155
To page
9158
Abstract
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.
Keywords
Diels–Alder reaction , Lipase , epoxyquinols A and B , RESOLUTION
Journal title
Tetrahedron Letters
Serial Year
2002
Journal title
Tetrahedron Letters
Record number
1659489
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