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dc.contributor.authorPhung, Nhu Hoa-
dc.contributor.authorNguyen, Thi Thu Trang-
dc.contributor.authorNguyen, Tien Tuan Anh-
dc.contributor.authorPham, Van Phong-
dc.contributor.authorNguyen, Van Ky-
dc.date.accessioned2018-03-22T03:55:14Z-
dc.date.available2018-03-22T03:55:14Z-
dc.date.issued2016-
dc.identifier.issn2588-1140-
dc.identifier.urihttp://repository.vnu.edu.vn/handle/VNU_123/61455-
dc.descriptiontr. 220-227en_US
dc.description.abstractWe have developed two esterification strategies fora challenging coupling between camphoric acid and solanesol to achieve a hybrid natural product - solanesyl camphorate. Both synthetic strategies applied the classic activationmode of carboxylic acid group by anhydride formation to overcome the difficulties caused by steric hindrance and the difference in polarity of two reactants. The first method took advantages of easy prepared camphoric anhydride from camphoric acid, whereas the second one allowed direct esterification via in situanhydride formation. Moreover, no solvent is required in synthetic process. This work would provide greener approaches for syntheses of hybrid esters from similar natural products.en_US
dc.language.isootheren_US
dc.publisherH. : ĐHQGHNen_US
dc.relation.ispartofseriesTập 32;Số 4-
dc.subjectSolanesyl Camphorateen_US
dc.subjectantisepticen_US
dc.subjectwound healingen_US
dc.subjectchallenging couplingen_US
dc.subjectsolvent-freeen_US
dc.titleA Challenging Classic Coupling: Esterification of Camphoric Acid - a Steric - Hindered Polar Carboxylic Acid and Solanesol - a Long - Chain Nonpolar Alcohol.en_US
dc.typeArticleen_US
Appears in Collections:Natural Sciences and Technology


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  • Full metadata record
    DC FieldValueLanguage
    dc.contributor.authorPhung, Nhu Hoa-
    dc.contributor.authorNguyen, Thi Thu Trang-
    dc.contributor.authorNguyen, Tien Tuan Anh-
    dc.contributor.authorPham, Van Phong-
    dc.contributor.authorNguyen, Van Ky-
    dc.date.accessioned2018-03-22T03:55:14Z-
    dc.date.available2018-03-22T03:55:14Z-
    dc.date.issued2016-
    dc.identifier.issn2588-1140-
    dc.identifier.urihttp://repository.vnu.edu.vn/handle/VNU_123/61455-
    dc.descriptiontr. 220-227en_US
    dc.description.abstractWe have developed two esterification strategies fora challenging coupling between camphoric acid and solanesol to achieve a hybrid natural product - solanesyl camphorate. Both synthetic strategies applied the classic activationmode of carboxylic acid group by anhydride formation to overcome the difficulties caused by steric hindrance and the difference in polarity of two reactants. The first method took advantages of easy prepared camphoric anhydride from camphoric acid, whereas the second one allowed direct esterification via in situanhydride formation. Moreover, no solvent is required in synthetic process. This work would provide greener approaches for syntheses of hybrid esters from similar natural products.en_US
    dc.language.isootheren_US
    dc.publisherH. : ĐHQGHNen_US
    dc.relation.ispartofseriesTập 32;Số 4-
    dc.subjectSolanesyl Camphorateen_US
    dc.subjectantisepticen_US
    dc.subjectwound healingen_US
    dc.subjectchallenging couplingen_US
    dc.subjectsolvent-freeen_US
    dc.titleA Challenging Classic Coupling: Esterification of Camphoric Acid - a Steric - Hindered Polar Carboxylic Acid and Solanesol - a Long - Chain Nonpolar Alcohol.en_US
    dc.typeArticleen_US
    Appears in Collections:Natural Sciences and Technology


  • document(38).pdf
    • Size : 164,18 kB

    • Format : Adobe PDF

    • View : 
    • Download :