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https://hdl.handle.net/10356/148229
Title: | Carbene-catalyzed N,N-nucleophilic activation of thioureas for access to pyrimidinthione derivatives | Authors: | Cao, Liya Li, Tingting Chi, Robin Yonggui Jin, Zhichao |
Keywords: | Science::Chemistry | Issue Date: | 2021 | Source: | Cao, L., Li, T., Chi, R. Y. & Jin, Z. (2021). Carbene-catalyzed N,N-nucleophilic activation of thioureas for access to pyrimidinthione derivatives. Asian Journal of Organic Chemistry, 10(5), 1090-1093. https://dx.doi.org/10.1002/ajoc.202100113 | Journal: | Asian Journal of Organic Chemistry | Abstract: | An N-heterocyclic carbene-catalyzed [3+3] cycloaddition reaction of acylthioureas with ynals is reported. Both N atoms in the thiourea substrate are activated as nucleophiles and incorporated inside the ring system of the product. Pyrimidinthione derivatives bearing various substituents and substitution patterns are afforded as the products in moderate to good yields. | URI: | https://hdl.handle.net/10356/148229 | ISSN: | 2193-5815 | DOI: | 10.1002/ajoc.202100113 | Rights: | This is the peer reviewed version of the following article: Cao, L., Li, T., Chi, R. Y. & Jin, Z. (2021). Carbene-catalyzed N,N-nucleophilic activation of thioureas for access to pyrimidinthione derivatives. Asian Journal of Organic Chemistry, 10(5), 1090-1093. https://dx.doi.org/10.1002/ajoc.202100113, which has been published in final form at https://doi.org/10.1002/ajoc.202100113. 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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