Synthetic routes to crinine and vittatine
Author:
Affiliation:
1. Department of Applied Chemistry National Yang Ming Chiao Tung University Hsinchu Taiwan
Funder
Ministry of Science and Technology, Taiwan
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jccs.202100270
Reference34 articles.
1. Alkaloids of the Amaryllidaceae. IV. Crystalline Alkaloids of Ammocharis coranica (Ker-Gawl.) Herb., Brunsvigia rosea (Lam.) Hannibal and Two Crinum Species
2. XVI. Mitteil. über Amaryllidaceen‐Alkaloide. Alkaloide von Nerine Corusca, N. Flexuosa, Pancratium Illyricum, Lycoris Aurea und L. Incarnata
3. Heterocyclic Amaryllidaceae Alkaloids: Biosynthesis and Pharmacological Applications
4. Phytochemical and biological investigations of Amaryllidaceae alkaloids: a review
5. Biosynthesis of alkaloids in Amaryllidaceae plants: a review
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2. Enantioselective Construction of Tetrahydroindole Skeletons by Rh‐Catalyzed [2+2+2] Cycloaddition of Homopropargyl Enamides with Alkynes;Angewandte Chemie;2024-08-13
3. Chiral Bisphosphine-Catalyzed Asymmetric Staudinger/aza-Wittig Reaction: An Enantioselective Desymmetrizing Approach to Crinine-Type Amaryllidaceae Alkaloids;Journal of the American Chemical Society;2024-04-20
4. Corrigendum;Journal of the Chinese Chemical Society;2021-12
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