A new and convenient synthesis of 1,2-dioxobenzocyclobutene via photodecarbonylation

Research output: Contribution to journalArticleResearchpeer review

Authors

Research Organisations

View graph of relations

Details

Original languageEnglish
Pages (from-to)6385-6386
Number of pages2
JournalTetrahedron letters
Volume38
Issue number36
Publication statusPublished - 7 Sept 1997

Abstract

The new preparation of 1,2-dioxobenzocyclobutene (4) via a short and efficient three-step route starting from the commercially available ninhydrin represents a superior procedure to all hitherto known syntheses of this valuable compound. The photo-extrusion of carbon monoxide from 1,3-bis(ethylendioxy)indan-3-one (2) is one of the rare examples using a decarbonylation of a five-membered cyclic ketone to prepare a highly strained and functionalized cyclobutane derivative.

ASJC Scopus subject areas

Cite this

A new and convenient synthesis of 1,2-dioxobenzocyclobutene via photodecarbonylation. / Leinweber, Dirk; Butenschön, Holger.
In: Tetrahedron letters, Vol. 38, No. 36, 07.09.1997, p. 6385-6386.

Research output: Contribution to journalArticleResearchpeer review

Leinweber D, Butenschön H. A new and convenient synthesis of 1,2-dioxobenzocyclobutene via photodecarbonylation. Tetrahedron letters. 1997 Sept 7;38(36):6385-6386. doi: 10.1016/S0040-4039(97)01447-0
Download
@article{c2d57063c10947de94fbec1c731cf041,
title = "A new and convenient synthesis of 1,2-dioxobenzocyclobutene via photodecarbonylation",
abstract = "The new preparation of 1,2-dioxobenzocyclobutene (4) via a short and efficient three-step route starting from the commercially available ninhydrin represents a superior procedure to all hitherto known syntheses of this valuable compound. The photo-extrusion of carbon monoxide from 1,3-bis(ethylendioxy)indan-3-one (2) is one of the rare examples using a decarbonylation of a five-membered cyclic ketone to prepare a highly strained and functionalized cyclobutane derivative.",
author = "Dirk Leinweber and Holger Butensch{\"o}n",
year = "1997",
month = sep,
day = "7",
doi = "10.1016/S0040-4039(97)01447-0",
language = "English",
volume = "38",
pages = "6385--6386",
journal = "Tetrahedron letters",
issn = "0040-4039",
publisher = "Elsevier Ltd.",
number = "36",

}

Download

TY - JOUR

T1 - A new and convenient synthesis of 1,2-dioxobenzocyclobutene via photodecarbonylation

AU - Leinweber, Dirk

AU - Butenschön, Holger

PY - 1997/9/7

Y1 - 1997/9/7

N2 - The new preparation of 1,2-dioxobenzocyclobutene (4) via a short and efficient three-step route starting from the commercially available ninhydrin represents a superior procedure to all hitherto known syntheses of this valuable compound. The photo-extrusion of carbon monoxide from 1,3-bis(ethylendioxy)indan-3-one (2) is one of the rare examples using a decarbonylation of a five-membered cyclic ketone to prepare a highly strained and functionalized cyclobutane derivative.

AB - The new preparation of 1,2-dioxobenzocyclobutene (4) via a short and efficient three-step route starting from the commercially available ninhydrin represents a superior procedure to all hitherto known syntheses of this valuable compound. The photo-extrusion of carbon monoxide from 1,3-bis(ethylendioxy)indan-3-one (2) is one of the rare examples using a decarbonylation of a five-membered cyclic ketone to prepare a highly strained and functionalized cyclobutane derivative.

UR - http://www.scopus.com/inward/record.url?scp=0030863672&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(97)01447-0

DO - 10.1016/S0040-4039(97)01447-0

M3 - Article

AN - SCOPUS:0030863672

VL - 38

SP - 6385

EP - 6386

JO - Tetrahedron letters

JF - Tetrahedron letters

SN - 0040-4039

IS - 36

ER -

By the same author(s)