Perkin communications. 5-Substituted bicyclo[3.2.0]hept-2-en-6-ones: Synthesis and ring-opening reactions

Research output: Contribution to journalArticleResearchpeer review

External Research Organisations

  • Max-Planck-Institut für Kohlenforschung
View graph of relations

Details

Original languageEnglish
Pages (from-to)483-484
Number of pages2
JournalJournal of the Chemical Society, Perkin Transactions 1
Issue number2
Publication statusPublished - 1 Dec 1991
Externally publishedYes

Abstract

5-Methoxy- and 5-dialkylamino-bicyclo[3.2.0]hept-2-en-6-one derivatives 2 and 3 are formed in high yield by cine substitution at the fused exo-chlorocyclobutanone 1, subsequent reactions yielding 2-phenyltropone 6 and a cycloheptadienone enamine 8.

ASJC Scopus subject areas

Cite this

Perkin communications. 5-Substituted bicyclo[3.2.0]hept-2-en-6-ones: Synthesis and ring-opening reactions. / Butenschön, Holger.
In: Journal of the Chemical Society, Perkin Transactions 1, No. 2, 01.12.1991, p. 483-484.

Research output: Contribution to journalArticleResearchpeer review

Butenschön H. Perkin communications. 5-Substituted bicyclo[3.2.0]hept-2-en-6-ones: Synthesis and ring-opening reactions. Journal of the Chemical Society, Perkin Transactions 1. 1991 Dec 1;(2):483-484. doi: https://doi.org/10.1039/P19910000483
Butenschön, Holger. / Perkin communications. 5-Substituted bicyclo[3.2.0]hept-2-en-6-ones : Synthesis and ring-opening reactions. In: Journal of the Chemical Society, Perkin Transactions 1. 1991 ; No. 2. pp. 483-484.
Download
@article{5717707a352940268e9bea6a0b1ada68,
title = "Perkin communications. 5-Substituted bicyclo[3.2.0]hept-2-en-6-ones: Synthesis and ring-opening reactions",
abstract = "5-Methoxy- and 5-dialkylamino-bicyclo[3.2.0]hept-2-en-6-one derivatives 2 and 3 are formed in high yield by cine substitution at the fused exo-chlorocyclobutanone 1, subsequent reactions yielding 2-phenyltropone 6 and a cycloheptadienone enamine 8.",
author = "Holger Butensch{\"o}n",
year = "1991",
month = dec,
day = "1",
doi = "https://doi.org/10.1039/P19910000483",
language = "English",
pages = "483--484",
number = "2",

}

Download

TY - JOUR

T1 - Perkin communications. 5-Substituted bicyclo[3.2.0]hept-2-en-6-ones

T2 - Synthesis and ring-opening reactions

AU - Butenschön, Holger

PY - 1991/12/1

Y1 - 1991/12/1

N2 - 5-Methoxy- and 5-dialkylamino-bicyclo[3.2.0]hept-2-en-6-one derivatives 2 and 3 are formed in high yield by cine substitution at the fused exo-chlorocyclobutanone 1, subsequent reactions yielding 2-phenyltropone 6 and a cycloheptadienone enamine 8.

AB - 5-Methoxy- and 5-dialkylamino-bicyclo[3.2.0]hept-2-en-6-one derivatives 2 and 3 are formed in high yield by cine substitution at the fused exo-chlorocyclobutanone 1, subsequent reactions yielding 2-phenyltropone 6 and a cycloheptadienone enamine 8.

UR - http://www.scopus.com/inward/record.url?scp=0006012629&partnerID=8YFLogxK

U2 - https://doi.org/10.1039/P19910000483

DO - https://doi.org/10.1039/P19910000483

M3 - Article

AN - SCOPUS:0006012629

SP - 483

EP - 484

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

SN - 1472-7781

IS - 2

ER -