Stereodivergent Synthesis of Alkaloid (±)-223A and (±)-6-<i>epi</i>-223A via Rh-Catalyzed Hydroformylation Double Cyclization-Reference-Cited by-同舟云学术

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Stereodivergent Synthesis of Alkaloid (±)-223A and (±)-6-epi-223A via Rh-Catalyzed Hydroformylation Double Cyclization

Published:2024-03-08 Issue:7 Volume:89 Page:5091-5097
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Huang Wen-Wei¹,Cheng Jui-Teng¹,Hsiao Wei-Ting¹,Chiou Wen-Hua¹^ORCID

Affiliation:

1. Department of Chemistry, National Chung-Hsing University, Taichung 402202, Taiwan, R.O.C.

Funder

National Chung-Hsing University

Ministry of Science and Technology, Taiwan

National center for High-performance computing

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02366

Reference20 articles.

1. Alkaloid 223A: The First Trisubstituted Indolizidine from Dendrobatid Frogs

2. Alkaloids Indolizidine 235B′, Quinolizidine 1-epi-207I, and the Tricyclic 205B are Potent and Selective Noncompetitive Inhibitors of Nicotinic Acetylcholine Receptors

3. Synthesis of Poison-Frog Alkaloids and Their Pharmacological Effects at Neuronal Nicotinic Acetylcholine Receptors

4. Synthesis of Alkaloid 223A and a Structural Revision

5. Stereodivergent synthesis of the 2,3,5,6-tetrasubstituted piperidine ring system: an application to the synthesis of alkaloids and from poison frogs

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