Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 6385-6386 |
| Seitenumfang | 2 |
| Fachzeitschrift | Tetrahedron letters |
| Jahrgang | 38 |
| Ausgabenummer | 36 |
| Publikationsstatus | Veröffentlicht - 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 Sachgebiete
- Biochemie, Genetik und Molekularbiologie (insg.)
- Biochemie
- Pharmakologie, Toxikologie und Pharmazie (insg.)
- Wirkstoffforschung
- Chemie (insg.)
- Organische Chemie
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in: Tetrahedron letters, Jahrgang 38, Nr. 36, 07.09.1997, S. 6385-6386.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
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 -