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https://doi.org/10.1021/ja064636n
DC Field | Value | |
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dc.title | Chiral bicyclic guanidine-catalyzed enantioselective reactions of anthrones | |
dc.contributor.author | Shen, J. | |
dc.contributor.author | Nguyen, T.T. | |
dc.contributor.author | Goh, Y.-P. | |
dc.contributor.author | Ye, W. | |
dc.contributor.author | Fu, X. | |
dc.contributor.author | Xu, J. | |
dc.contributor.author | Tan, C.-H. | |
dc.date.accessioned | 2014-06-23T05:34:09Z | |
dc.date.available | 2014-06-23T05:34:09Z | |
dc.date.issued | 2006-10-25 | |
dc.identifier.citation | Shen, 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.issn | 00027863 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/75745 | |
dc.description.abstract | Chiral 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja064636n | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1021/ja064636n | |
dc.description.sourcetitle | Journal of the American Chemical Society | |
dc.description.volume | 128 | |
dc.description.issue | 42 | |
dc.description.page | 13692-13693 | |
dc.description.coden | JACSA | |
dc.identifier.isiut | 000241360100021 | |
Appears in Collections: | Staff Publications |
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