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https://hdl.handle.net/10356/137778
Title: | Efficient access to 2-pyrones via carbene-catalyzed oxidative [3+3] reactions between enals and nitrogen ylides | Authors: | Zheng, Pengcheng Li, Chengcheng Mou, Chengli Pan, Dingwu Wu, Shuquan Xue, Wei Jin, Zhichao Chi, Robin Yonggui |
Keywords: | Science::Chemistry::Organic chemistry | Issue Date: | 2019 | Source: | 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 | Journal: | Asian Journal of Organic Chemistry | 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. | URI: | https://hdl.handle.net/10356/137778 | ISSN: | 2193-5807 | DOI: | 10.1002/ajoc.201900153 | Schools: | School of Physical and Mathematical Sciences | 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. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SPMS Journal Articles |
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