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dc.contributor.authorPal, Mahesh-
dc.contributor.authorSingh, Meenakshi-
dc.contributor.authorSharma, R P-
dc.date.accessioned2013-10-15T09:19:53Z-
dc.date.available2013-10-15T09:19:53Z-
dc.date.issued2002-09-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/22045-
dc.description1915-1918en_US
dc.description.abstractTosylation of andrographolide 1, with p-TsCl pyridine furnishes compounds 3 and 4. The reaction of 1 with in situ generated nickel boride yields compounds 6 and 8. Monotosylation of 6 followed by reaction with NaI refluxing in acetone furnishes the iodide 13. But all attempts to generate an oxetane moiety in 13 corresponding to compund 2 failed.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.41B(09) [September 2002]en_US
dc.titleChemical transformation of andrographolideen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.41B(09) [September 2002]

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