dc.contributor.author |
Vijay Nair, G |
|
dc.contributor.author |
Ani Deepthi |
|
dc.contributor.author |
Manojkumar, P |
|
dc.contributor.author |
Bindu, S |
|
dc.contributor.author |
Sreekumar, V |
|
dc.contributor.author |
Beneesh, P B |
|
dc.contributor.author |
Resmi Mohan |
|
dc.contributor.author |
Suresh, E |
|
dc.date.accessioned |
2014-06-17T05:24:17Z |
|
dc.date.available |
2014-06-17T05:24:17Z |
|
dc.date.issued |
2006 |
|
dc.identifier.citation |
Journal of Organic Chemistry 71(6):2313-2319;17 Mar 2006 |
en_US |
dc.identifier.issn |
0022-3263 |
|
dc.identifier.uri |
http://ir.niist.res.in:8080/jspui/handle/123456789/1532 |
|
dc.description.abstract |
The zwitterion formed by the reaction of dimethoxycarbene and DMAD adds efficiently to one of the carbonyl groups of 1,2-dicarbonyl compounds and anhydrides to generate dihydrofurans and spirodihydrofurans in good yields. In many cases, the carbene inserts into the C-C bond of the dione to yield masked vicinal tricarbonyl systems. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
American Chemical Society |
en_US |
dc.subject |
Multicomponent reaction |
en_US |
dc.subject |
Nucleophilic carbenes |
en_US |
dc.subject |
Dimethyl butynedioate |
en_US |
dc.subject |
Facile synthesis |
en_US |
dc.subject |
Electrophilic styrenes |
en_US |
dc.subject |
Vinyl isocyanates |
en_US |
dc.subject |
4+1 Cycloaddition |
en_US |
dc.subject |
Derivatives construction |
en_US |
dc.subject |
Bis(alkylthio)carbenes |
en_US |
dc.title |
Reaction of dimethoxycarbene-DMAD zwitterion with 1,2-diones and anhydrides: A novel synthesis of highly substituted dihydrofurans and spirodihydrofurans |
en_US |
dc.type |
Article |
en_US |