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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ja064636n
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dc.titleChiral bicyclic guanidine-catalyzed enantioselective reactions of anthrones
dc.contributor.authorShen, J.
dc.contributor.authorNguyen, T.T.
dc.contributor.authorGoh, Y.-P.
dc.contributor.authorYe, W.
dc.contributor.authorFu, X.
dc.contributor.authorXu, J.
dc.contributor.authorTan, C.-H.
dc.date.accessioned2014-06-23T05:34:09Z
dc.date.available2014-06-23T05:34:09Z
dc.date.issued2006-10-25
dc.identifier.citationShen, J., Nguyen, T.T., Goh, Y.-P., Ye, W., Fu, X., Xu, J., Tan, C.-H. (2006-10-25). Chiral bicyclic guanidine-catalyzed enantioselective reactions of anthrones. Journal of the American Chemical Society 128 (42) : 13692-13693. ScholarBank@NUS Repository. https://doi.org/10.1021/ja064636n
dc.identifier.issn00027863
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75745
dc.description.abstractChiral bicyclic guanidine 1 was found to be an excellent catalyst for reactions between anthrones and various dienophiles. The catalyst can tolerate a range of substituents and substitution patterns, making several anthrone derivatives suitable for this reaction. Both Diels-Alder and Michael adducts were obtained in excellent yields, high regioselectivities, and high enantioselectivities. This is the first case of a highly enantioselective base-catalyzed anthrone Diels-Alder reaction. Copyright © 2006 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja064636n
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ja064636n
dc.description.sourcetitleJournal of the American Chemical Society
dc.description.volume128
dc.description.issue42
dc.description.page13692-13693
dc.description.codenJACSA
dc.identifier.isiut000241360100021
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