Isolation, biosynthesis, and chemical syntheses of the hasubanan and acutumine alkaloids: A historical perspective
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Title
Isolation, biosynthesis, and chemical syntheses of the hasubanan and acutumine alkaloids: A historical perspective
Authors
Keywords
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Journal
TETRAHEDRON
Volume -, Issue -, Pages 133709
Publisher
Elsevier BV
Online
2023-10-21
DOI
10.1016/j.tet.2023.133709
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Note: Only part of the references are listed.- Enantioselective Total Synthesis of (+)-Stephadiamine
- (2023) Baochao Yang et al. Journal of the American Chemical Society
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- (2022) Meng Wang et al. JOURNAL OF ETHNOPHARMACOLOGY
- Asymmetric Total Synthesis of Hasubanan Alkaloids: Periglaucines A–C, N,O ‐Dimethyloxostephine and Oxostephabenine
- (2022) Shaolei Ding et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Unified divergent strategy towards the total synthesis of the three sub-classes of hasubanan alkaloids
- (2021) Guang Li et al. Nature Communications
- Enantioselective Total Synthesis of (+)-Stephadiamine through Bioinspired Aza-Benzilic Acid Type Rearrangement
- (2021) Minami Odagi et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- The chloroalkaloid (−)-acutumine is biosynthesized via a Fe(II)- and 2-oxoglutarate-dependent halogenase in Menispermaceae plants
- (2020) Colin Y. Kim et al. Nature Communications
- Natural neuroprotective alkaloids from Stephania japonica (Thunb.) Miers
- (2019) Jiao Xiao et al. BIOORGANIC CHEMISTRY
- Total Synthesis of the Norhasubanan Alkaloid Stephadiamine
- (2018) Nina Hartrampf et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Memory of Chirality in Bromoalkyne Carbocyclization: Applications in Asymmetric Total Synthesis of Hasubanan Alkaloids
- (2018) Shenpeng Tan et al. ORGANIC LETTERS
- Substrate-Modified Functional Group Reactivity: Hasubanan and Acutumine Alkaloid Syntheses
- (2014) Sandra M. King et al. JOURNAL OF ORGANIC CHEMISTRY
- Total Syntheses of (−)-Acutumine and (−)-Dechloroacutumine
- (2013) Sandra M. King et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Three New Hasubanan Alkaloids fromStephania hernandifolia(Willd.)Walp.
- (2013) Li-Jia Tang et al. HELVETICA CHIMICA ACTA
- Development of Enantioselective Synthetic Routes to the Hasubanan and Acutumine Alkaloids
- (2013) Nicholas A. Calandra et al. JOURNAL OF ORGANIC CHEMISTRY
- Concise Synthesis of the Hasubanan Alkaloid (±)-Cepharatine A Using a Suzuki Coupling Reaction To Effect o,p-Phenolic Coupling
- (2013) Philip Magnus et al. ORGANIC LETTERS
- Efficient Entry to the Hasubanan Alkaloids: First Enantioselective Total Syntheses of (−)-Hasubanonine, (−)-Runanine, (−)-Delavayine, and (+)-Periglaucine B
- (2011) Seth B. Herzon et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Short, Enantioselective Total Syntheses of (−)-8-Demethoxyrunanine and (−)-Cepharatines A, C, and D
- (2011) Kangway V. Chuang et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Benzoquinone-derived sulfinyl imines as versatile intermediates for alkaloid synthesis: Total synthesis of (–)-3-demethoxyerythratidinone
- (2011) Kangway V. Chuang et al. Chemical Science
- Total Synthesis of (−)-Acutumine
- (2009) Fang Li et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Periglaucines A−D, Anti-HBV and -HIV-1 Alkaloids fromPericampylus glaucus
- (2008) Meng-Hong Yan et al. JOURNAL OF NATURAL PRODUCTS
- Synthesis of the Common Propellane Core Structure of the Hasubanan Alkaloids
- (2008) Thong X. Nguyen et al. JOURNAL OF ORGANIC CHEMISTRY
- Alkaloids inhibiting l-histidine decarboxylase from Sinomenium acutum
- (2008) Atsushi Kato et al. Phytochemistry Letters
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