Isolation, biosynthesis, and chemical syntheses of the hasubanan and acutumine alkaloids: A historical perspective

Enantioselective Total Synthesis of (+)-Stephadiamine

(2023) Baochao Yang et al.   Journal of the American Chemical Society

Enantioselective Synthesis of (−)‐10‐Hydroxyacutuminine

(2022) Denise C. Grünenfelder et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Alkaloids in genus stephania (Menispermaceae): A comprehensive review of its ethnopharmacology, phytochemistry, pharmacology and toxicology

(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