Enantioselective route to an AE-ring intermediate in the total synthesis of talatisamine
Author:
Funder
Japan Science and Technology Agency
Japan Society for the Promotion of Science
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference45 articles.
1. (a) Y. Shen, W.-J. Liang, Y.-N. Shi, E. J. Kennelly, D.-K. Zhao, Structural diversity, bioactivities, and biosynthesis of natural diterpenoid alkaloids. Nat. Prod. Rep. 37 (2020) 763−796
2. Elsevier, New York, 2022, 87, pp. 1−360.
3. (a) Y. Shen, W.-J. Liang, Y.-N. Shi, E. J. Kennelly, D.-K. Zhao, Structural diversity, bioactivities, and biosynthesis of natural diterpenoid alkaloids. Nat. Prod. Rep. 37 (2020) 763−796;
4. (b) X.-Y. Liu, B.-W. Ke, Y. Qin, F.-P. Wang, The Diterpenoid Alkaloids. In The Alkaloids: Chemistry and Biology; Knölker, H.-J., Eds.; Elsevier, New York, 2022, 87, pp. 1−360.
5. (a) M. A. Khaimova, M. D. Palamareva, N. M. Mollov, V. P. Krestev, The Structures of Talatisamine and Cammaconine by Correlation with Isotalatizidine. Tetrahedron 27 (1971) 819−822
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