Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/19174
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dc.contributor.authorBUTLER, ANTHONY R.-
dc.contributor.authorHUSSAIN, ISHTIAQ-
dc.date.accessioned2023-03-14T06:37:04Z-
dc.date.available2023-03-14T06:37:04Z-
dc.date.issued1988-09-20-
dc.identifier.citationHUSSAIN, I., & BUTLER, A. (2011). NITRATION OF HECTORS BASE. Journal of The Chemical Society of Pakistan, 10(4), 311.en_US
dc.identifier.issn0253-5106-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/19174-
dc.description.abstractNi tration of Hector's Base gives both mno and dinitro products. in each case, only one out of two phenyl rings involves in the nitration process and that ring is the 3-anilino portion of the kkctor's Base. The protonation of the exocyclic nitrogen of Hector's base seems to deactivate the phenyl ring attached to nitrogen at position 4, which in turn, does not react with nitronium ion. Fi nam I y, acetyl at ion of nitrocompounds of Hector's Base and nitration of Hector's Base in acetylating mixture have also been discusseden_US
dc.language.isoenen_US
dc.publisherHEJ Research Institute of Chemistry, University of Karachi, Karachi.en_US
dc.titleNitration of Hector's Baseen_US
dc.typeArticleen_US
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