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Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2010.09.123
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dc.titleSustainability from agricultural waste: Chiral ligands from oligomeric proanthocyanidins via acid-mediated depolymerization
dc.contributor.authorFu, C.
dc.contributor.authorChen, W.
dc.contributor.authorQuek, Y.L.
dc.contributor.authorNi, R.
dc.contributor.authorGhani, A.B.A.
dc.contributor.authorLeong, W.W.Y.
dc.contributor.authorZeng, H.
dc.contributor.authorHuang, D.
dc.date.accessioned2014-10-16T08:42:34Z
dc.date.available2014-10-16T08:42:34Z
dc.date.issued2010-12-01
dc.identifier.citationFu, C., Chen, W., Quek, Y.L., Ni, R., Ghani, A.B.A., Leong, W.W.Y., Zeng, H., Huang, D. (2010-12-01). Sustainability from agricultural waste: Chiral ligands from oligomeric proanthocyanidins via acid-mediated depolymerization. Tetrahedron Letters 51 (48) : 6322-6324. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2010.09.123
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94992
dc.description.abstractOligomeric proanthocyanidins (OPCs, Ar′ = 3,4-(HO)2(C 6H3) are abundant natural products found in agricultural and forestry waste such as pine bark, grape seeds, and the peels of mangosteen. We have demonstrated that the OPCs can be converted into small molecule chiral ligands by using proper nucleophiles for acid depolymerization of the OPCs. The chiral ligands may have potential for sustainable asymmetric catalysis. © 2010 Elsevier Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tetlet.2010.09.123
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.tetlet.2010.09.123
dc.description.sourcetitleTetrahedron Letters
dc.description.volume51
dc.description.issue48
dc.description.page6322-6324
dc.description.codenTELEA
dc.identifier.isiut000284303200031
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