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dc.contributor.authorKaur, Navdeep-
dc.contributor.authorDhillon, Ranjit S-
dc.date.accessioned2013-10-18T06:33:31Z-
dc.date.available2013-10-18T06:33:31Z-
dc.date.issued2001-04-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/22243-
dc.description327-328en_US
dc.description.abstractMonoenes and dienes upon treatment with mercuric acetate in dry methanol, followed by demercuration with Na in methanol at 0°C, give ethers in good yields. The coagulation of mercury makes this a simple and convenient work-up process for such reactions.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.40B(04) [April 2001]en_US
dc.titleA convenient methodology for demercuration of organomercurials by Na/MeOH — Synthesis of ethersen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.40B(04) [April 2001]

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