Total syntheses of isodihydrofutoquinol a, futoquinol, and isofutoquinol A and B

Yoshikazu Shizuri; Kensuke Nakamura; Shosuke Yamamura; Shigeru Ohba; Hiroshi Yamashita; Yoshihiko Saito

doi:10.1016/S0040-4039(00)84085-X

Total syntheses of isodihydrofutoquinol a, futoquinol, and isofutoquinol A and B

Yoshikazu Shizuri, Kensuke Nakamura, Shosuke Yamamura, Shigeru Ohba, Hiroshi Yamashita, Yoshihiko Saito

Research output: Contribution to journal › Article › peer-review

8 Citations (Scopus)

Abstract

Isodihydrofutoquinol A has been synthesized starting from 4-benzyloxy-2-methoxy-acetophenone, wherein the 2,5-cyclohexadienone moiety has been constructed efficiently by means of electrochemical method. Isodihydrofutoquinol A has been further converted into isofutoquinol A and B through futoquinol. In addition, the stereostructure of isofutoquinol A has been unambiguously determined on the basis of an X-ray crystallographic analysis.

Original language	English
Pages (from-to)	727-730
Number of pages	4
Journal	Tetrahedron Letters
Volume	27
Issue number	6
DOIs	https://doi.org/10.1016/S0040-4039(00)84085-X
Publication status	Published - 1986
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)84085-X

Cite this

@article{19ff00ccba2b468dbbfd606581e8d31f,

title = "Total syntheses of isodihydrofutoquinol a, futoquinol, and isofutoquinol A and B",

abstract = "Isodihydrofutoquinol A has been synthesized starting from 4-benzyloxy-2-methoxy-acetophenone, wherein the 2,5-cyclohexadienone moiety has been constructed efficiently by means of electrochemical method. Isodihydrofutoquinol A has been further converted into isofutoquinol A and B through futoquinol. In addition, the stereostructure of isofutoquinol A has been unambiguously determined on the basis of an X-ray crystallographic analysis.",

author = "Yoshikazu Shizuri and Kensuke Nakamura and Shosuke Yamamura and Shigeru Ohba and Hiroshi Yamashita and Yoshihiko Saito",

year = "1986",

doi = "10.1016/S0040-4039(00)84085-X",

language = "English",

volume = "27",

pages = "727--730",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "6",

}

TY - JOUR

T1 - Total syntheses of isodihydrofutoquinol a, futoquinol, and isofutoquinol A and B

AU - Shizuri, Yoshikazu

AU - Nakamura, Kensuke

AU - Yamamura, Shosuke

AU - Ohba, Shigeru

AU - Yamashita, Hiroshi

AU - Saito, Yoshihiko

PY - 1986

Y1 - 1986

N2 - Isodihydrofutoquinol A has been synthesized starting from 4-benzyloxy-2-methoxy-acetophenone, wherein the 2,5-cyclohexadienone moiety has been constructed efficiently by means of electrochemical method. Isodihydrofutoquinol A has been further converted into isofutoquinol A and B through futoquinol. In addition, the stereostructure of isofutoquinol A has been unambiguously determined on the basis of an X-ray crystallographic analysis.

AB - Isodihydrofutoquinol A has been synthesized starting from 4-benzyloxy-2-methoxy-acetophenone, wherein the 2,5-cyclohexadienone moiety has been constructed efficiently by means of electrochemical method. Isodihydrofutoquinol A has been further converted into isofutoquinol A and B through futoquinol. In addition, the stereostructure of isofutoquinol A has been unambiguously determined on the basis of an X-ray crystallographic analysis.

UR - http://www.scopus.com/inward/record.url?scp=85004271749&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85004271749&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)84085-X

DO - 10.1016/S0040-4039(00)84085-X

M3 - Article

AN - SCOPUS:85004271749

VL - 27

SP - 727

EP - 730

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 6

ER -

Total syntheses of isodihydrofutoquinol a, futoquinol, and isofutoquinol A and B

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this