Gold(I)-Catalyzed 7-exo-dig Cyclization: A Key Step to Access the Bicyclo[4.2.1]nonane Skeleton of Vibsatin A, a Neurotrophic Diterpenoid
Author:
Affiliation:
1. UMR CNRS 8038, Faculté de Pharmacie, Université de Paris, 4 avenue de l’Observatoire, 75270 Paris cedex 06, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c01757
Reference38 articles.
1. Neuere Entwicklungen in der Chemie der Naturstoffe
2. Biologically Active Indole Alkaloids from Kopsia arborea
3. Echinopines A and B: Sesquiterpenoids Possessing an Unprecedented Skeleton from Echinops spinosus
4. Vibsatins A and B, Two New Tetranorvibsane-Type Diterpenoids from Viburnum tinus cv. variegatus
5. Neurotrophic Natural Products: Chemistry and Biology
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1. Discovery of the Caged-Vibsane Norditerpenoids with Unprecedented Chemical Architectures and Exploration of Their Various Acid Tolerances;The Journal of Organic Chemistry;2023-08-16
2. Cinchonidine-Catalyzed Synthesis of Oxazabicyclo[4.2.1]nonanones from N-Aryl-α,β-unsaturated Nitrones and 1-Ethynylnaphthalen-2-ols;Organic Letters;2022-06-06
3. Vibsanoids A–D, four new subtypes of vibsane diterpenoids with a distinctive tricyclo[8.2.1.02,9]tridecane core from Viburnum odoratissimum;Organic Chemistry Frontiers;2022
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