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https://hdl.handle.net/10356/137778
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DC Field | Value | Language |
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dc.contributor.author | Zheng, Pengcheng | en_US |
dc.contributor.author | Li, Chengcheng | en_US |
dc.contributor.author | Mou, Chengli | en_US |
dc.contributor.author | Pan, Dingwu | en_US |
dc.contributor.author | Wu, Shuquan | en_US |
dc.contributor.author | Xue, Wei | en_US |
dc.contributor.author | Jin, Zhichao | en_US |
dc.contributor.author | Chi, Robin Yonggui | en_US |
dc.date.accessioned | 2020-04-14T07:21:32Z | - |
dc.date.available | 2020-04-14T07:21:32Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Zheng, P., Li, C., Mou, C., Pan, D., Wu, S., Xue, W., … Chi, R. Y. (2019). Efficient access to 2-pyrones via carbene-catalyzed oxidative [3+3] reactions between enals and nitrogen ylides. Asian Journal of Organic Chemistry, 8(7), 1067-1070. doi:10.1002/ajoc.201900153 | en_US |
dc.identifier.issn | 2193-5807 | en_US |
dc.identifier.uri | https://hdl.handle.net/10356/137778 | - |
dc.description.abstract | Pyrones are important structural units in natural products and synthetic functional molecules. Here, we report a carbene-catalyzed oxidative [3+3] cycloaddition reaction between enals and nitrogen ylides for quick access to 2-pyrones. Inexpensive and easily prepared 2′-pyridinium acetophenone bromide salts are used as precursors of pyridinium ylides to react with enals in our catalytic reactions. | en_US |
dc.description.sponsorship | NRF (Natl Research Foundation, S’pore) | en_US |
dc.description.sponsorship | ASTAR (Agency for Sci., Tech. and Research, S’pore) | en_US |
dc.description.sponsorship | MOE (Min. of Education, S’pore) | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Asian Journal of Organic Chemistry | en_US |
dc.rights | This is the peer reviewed version of the following article: Zheng, P., Li, C., Mou, C., Pan, D., Wu, S., Xue, W., … Chi, R. Y. (2019). Efficient access to 2-pyrones via carbene-catalyzed oxidative [3+3] reactions between enals and nitrogen ylides. Asian Journal of Organic Chemistry, 8(7), 1067-1070, which has been published in final form at https://doi.org/10.1002/ajoc.201900153. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | en_US |
dc.subject | Science::Chemistry::Organic chemistry | en_US |
dc.title | Efficient access to 2-pyrones via carbene-catalyzed oxidative [3+3] reactions between enals and nitrogen ylides | en_US |
dc.type | Journal Article | en |
dc.contributor.school | School of Physical and Mathematical Sciences | en_US |
dc.identifier.doi | 10.1002/ajoc.201900153 | - |
dc.description.version | Accepted version | en_US |
dc.identifier.scopus | 2-s2.0-85065666042 | - |
dc.identifier.issue | 7 | en_US |
dc.identifier.volume | 8 | en_US |
dc.identifier.spage | 1067 | en_US |
dc.identifier.epage | 1070 | en_US |
dc.subject.keywords | NHC Catalysis | en_US |
dc.subject.keywords | Enals | en_US |
item.grantfulltext | open | - |
item.fulltext | With Fulltext | - |
Appears in Collections: | SPMS Journal Articles |
Files in This Item:
File | Description | Size | Format | |
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Efficient Access to 2-Pyrones via Carbene-Catalyzed Oxidative [3+3] Reactions between Enals and Nitrogen Ylides.pdf | 937.72 kB | Adobe PDF | View/Open |
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