Total Synthesis of the Fungal Metabolite Trienylfuranol A through Nucleophilic Diastereodivergent Additions to Oxocarbenium Ions
Author:
Affiliation:
1. Institut de Chimie des Substances Naturelles, CNRS UPR 2301 Université Paris-Saclay 1 avenue de la Terrasse 91198 Gif-sur-Yvette Cedex France
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202100265
Reference60 articles.
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2. Sporothriolide-Related Compounds from the Fungus Hypoxylon monticulosum CLL-205 Isolated from a Sphaerocladina Sponge from the Tahiti Coast
3. Sporochartines A–E, A New Family of Natural Products from the Marine Fungus Hypoxylon monticulosum Isolated from a Sphaerocladina Sponge
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1. Regio- and Chemoselective Double Allylic Substitution of Alkenyl vic-Diols;Organic Letters;2024-03-15
2. Biomimetic-inspired synthesis of sporochartines through Diels–Alder reaction between enantiopure (−)-sporothriolide and (+)-trienylfuranol A;Organic Chemistry Frontiers;2023
3. Seven-Step Total Synthesis of Sporothriolide;The Journal of Organic Chemistry;2021-08-23
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