Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/22549
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dc.contributor.authorSudini, Ravinder R-
dc.contributor.authorKhire, Uday R-
dc.contributor.authorPandey, Rajesh K-
dc.contributor.authorKumar, Pradeep-
dc.date.accessioned2013-10-23T08:39:05Z-
dc.date.available2013-10-23T08:39:05Z-
dc.date.issued2000-10-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/22549-
dc.description738-745en_US
dc.description.abstractThe synthesis of a variety of spirodiones 7,12 related to fredericamycin A 1 has been reported. The preparation of DielsA-lder adducts employing the nonfunctionalised and functionalised isobenzofurans 13, 14 as dienes and spirodiones 7, 12 as dienophiles has been described. The subsequent acid induced rearrangement of Diels-Alder adducts 15, 17, 19, 21 leads to the formation of spiro compounds 16, 18, 20, 22 related to fredericamycin A.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.39B(10) [October 2000]en_US
dc.titleDiels-Alder approach for the synthesis of spiro compounds related to Fredericamycin Aen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.39B(10) [October 2000]

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