The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Asymmetric Synthesis of Spiropyrazolones through Phosphine‐Catalyzed [4+1] Annulation
Abstract
An enantioselective synthesis of spiropyrazolones from allenoate‐derived MBH acetates and pyrazolones through a phosphine‐mediated [4+1] annulation process has been developed. Spiropyrazolones were readily prepared in good chemical yields and good to high enantioselectivities. This is the first asymmetric example in which α‐substituted allenoates were utilized as a C 4 synthon for phosphine‐catalyzed [4+1] annulation.
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Ghrelin is a growth-hormone-releasing acylated peptide from stomach
Kojima, M., Hosoda, H., Date, Y., Nakazato, M., Matsuo, H., & Kangawa, K. (1999) · Nature · doi:10.1038/45230 · Cited by 8,479
Cited by
Catalytic Enantioselective Construction of Spiro Quaternary Carbon Stereocenters
Xu, P.-W., Yu, J.-S., Chen, C., Cao, Z.-Y., Zhou, F., & Zhou, J. (2019) · ACS Catalysis · doi:10.1021/acscatal.8b03694 · Cited by 325
All-carbon quaternary centers in natural products and medicinal chemistry: recent advances
Ling, T., & Rivas, F. (2016) · Tetrahedron · doi:10.1016/j.tet.2016.09.002 · Cited by 312
Metadata
- Authors
- Han, X., Yao, W., Wang, T., Tan, Y. R., Yan, Z., Kwiatkowski, J., & Lu, Y.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2014-04-15
- Volume
- 53
- Issue
- 22
- Pages
- 5643-5647
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2075138214
- Cited by
- 261
- References
- 1
- FWCI
- 17.49
- Type
- journal article
- Language
- en
- Open access
- closed
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- Han, X., Yao, W., Wang, T., Tan, Y. R., Yan, Z., Kwiatkowski, J., & Lu, Y. (2014). Asymmetric Synthesis of Spiropyrazolones through Phosphine‐Catalyzed [4+1] Annulation. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201311214
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