Intramolecular reaction of electrogenerated phenoxy cations with an olefin bearing an electron-releasing group at the side chain

Shojiro Maki, Toshiyuki Suzuki, Seiji Kosemura, Yoshikazu Shizuri, Shosuke Yamamura

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Some phenols with an olefinic side chain have been electrolyzed under various conditions to afford both intramolecular [5 + 1]cycloaddition products and spiro compounds depending on solvent, substituents on the olefinic double bond and others. These rection products are regarded as a synthetic key intermediate of bioactive terpenoids.

Original languageEnglish
Pages (from-to)4973-4976
Number of pages4
JournalTetrahedron Letters
Volume32
Issue number37
DOIs
Publication statusPublished - 1991 Sep 9

Fingerprint

Spiro Compounds
Bearings (structural)
Cycloaddition
Phenols
Terpenes
Cycloaddition Reaction
Alkenes
Cations
Electrons

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Intramolecular reaction of electrogenerated phenoxy cations with an olefin bearing an electron-releasing group at the side chain. / Maki, Shojiro; Suzuki, Toshiyuki; Kosemura, Seiji; Shizuri, Yoshikazu; Yamamura, Shosuke.

In: Tetrahedron Letters, Vol. 32, No. 37, 09.09.1991, p. 4973-4976.

Research output: Contribution to journalArticle

Maki, Shojiro ; Suzuki, Toshiyuki ; Kosemura, Seiji ; Shizuri, Yoshikazu ; Yamamura, Shosuke. / Intramolecular reaction of electrogenerated phenoxy cations with an olefin bearing an electron-releasing group at the side chain. In: Tetrahedron Letters. 1991 ; Vol. 32, No. 37. pp. 4973-4976.
@article{8ac4788189aa456da3e522918ebf67d4,
title = "Intramolecular reaction of electrogenerated phenoxy cations with an olefin bearing an electron-releasing group at the side chain",
abstract = "Some phenols with an olefinic side chain have been electrolyzed under various conditions to afford both intramolecular [5 + 1]cycloaddition products and spiro compounds depending on solvent, substituents on the olefinic double bond and others. These rection products are regarded as a synthetic key intermediate of bioactive terpenoids.",
author = "Shojiro Maki and Toshiyuki Suzuki and Seiji Kosemura and Yoshikazu Shizuri and Shosuke Yamamura",
year = "1991",
month = "9",
day = "9",
doi = "10.1016/S0040-4039(00)93511-1",
language = "English",
volume = "32",
pages = "4973--4976",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "37",

}

TY - JOUR

T1 - Intramolecular reaction of electrogenerated phenoxy cations with an olefin bearing an electron-releasing group at the side chain

AU - Maki, Shojiro

AU - Suzuki, Toshiyuki

AU - Kosemura, Seiji

AU - Shizuri, Yoshikazu

AU - Yamamura, Shosuke

PY - 1991/9/9

Y1 - 1991/9/9

N2 - Some phenols with an olefinic side chain have been electrolyzed under various conditions to afford both intramolecular [5 + 1]cycloaddition products and spiro compounds depending on solvent, substituents on the olefinic double bond and others. These rection products are regarded as a synthetic key intermediate of bioactive terpenoids.

AB - Some phenols with an olefinic side chain have been electrolyzed under various conditions to afford both intramolecular [5 + 1]cycloaddition products and spiro compounds depending on solvent, substituents on the olefinic double bond and others. These rection products are regarded as a synthetic key intermediate of bioactive terpenoids.

UR - http://www.scopus.com/inward/record.url?scp=0025916410&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025916410&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)93511-1

DO - 10.1016/S0040-4039(00)93511-1

M3 - Article

AN - SCOPUS:0025916410

VL - 32

SP - 4973

EP - 4976

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 37

ER -