Supporting Information
| Supporting Information File 1: Coordinates and energies of quiannulatene biosynthesis. | ||
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| Supporting Information File 2: Coordinates and energies of sesterfisherol biosynthesis. | ||
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| Supporting Information File 3: Software for inherent mobility analysis. | ||
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| Supporting Information File 4: How to use in house software to calculate inherent atomic mobility. | ||
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Cite the Following Article
Inherent atomic mobility changes in carbocation intermediates during the sesterterpene cyclization cascade
Hajime Sato, Takaaki Mitsuhashi, Mami Yamazaki, Ikuro Abe and Masanobu Uchiyama
Beilstein J. Org. Chem. 2019, 15, 1890–1897.
https://doi.org/10.3762/bjoc.15.184
How to Cite
Sato, H.; Mitsuhashi, T.; Yamazaki, M.; Abe, I.; Uchiyama, M. Beilstein J. Org. Chem. 2019, 15, 1890–1897. doi:10.3762/bjoc.15.184
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Scholarly Works
- Moreira, V. M. doi:10.1002/9781119608288.ch6
- Zhang, P.; Qi, J.; Duan, Y.; Gao, J.-M.; Liu, C. Research Progress on Fungal Sesterterpenoids Biosynthesis. Journal of fungi (Basel, Switzerland) 2022, 8, 1080. doi:10.3390/jof8101080
- Sakamoto, K.; Sato, H.; Uchiyama, M. DFT Study on the Biosynthesis of Asperterpenol and Preasperterpenoid Sesterterpenoids: Exclusion of Secondary Carbocation Intermediates and Origin of Structural Diversification. The Journal of organic chemistry 2022, 87, 6432–6437. doi:10.1021/acs.joc.2c00291
- Li, K.; Gustafson, K. R. Sesterterpenoids: chemistry, biology, and biosynthesis. Natural product reports 2020, 38, 1251–1281. doi:10.1039/d0np00070a
- Kutateladze, D. A.; Strassfeld, D. A.; Jacobsen, E. N. Enantioselective Tail-to-Head Cyclizations Catalyzed by Dual-Hydrogen-Bond Donors. Journal of the American Chemical Society 2020, 142, 6951–6956. doi:10.1021/jacs.0c02665
- Mitsuhashi, T.; Abe, I. Sesterterpenoids. Progress in the chemistry of organic natural products 2020, 111, 1–79. doi:10.1007/978-3-030-37865-3_1
