Synthesis of 1-Oxadecalones via the Lewis Acid Catalyzed Dihydropyrone Diels−Alder Reaction
Author:
Affiliation:
1. Department of Chemistry, University of Iowa, Iowa City, Iowa 52242
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9911746
Reference6 articles.
1. Phomactin A; a novel PAF antagonist from a marine fungus Phoma sp
2. Synthetic studies towards phomactin A. Concise synthesis of the novel tricyclic furanochroman system
3. Dihydropyrones as Dienophiles in the Diels−Alder Reaction: Application to the Synthesis of 1-Oxadecalones
4. Reactions de diaziridines monosubstituees sur le carbone cyclique avec l'acetylene dicarboxylate de methyle
5. An Efficient Synthesis of Reduced Flavones via Diels-Alder Addition to 4H-Pyran-4-ones
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2. Enantioselective Synthesis of the ABC-Tricyclic Core of Phomactin A by a γ-Hydroxylation Strategy;Organic Letters;2015-04-10
3. The Phomactin Natural Products from Isolation to Total Synthesis: A Review;Organic Preparations and Procedures International;2014-05-04
4. Diastereoselective synthesis of highly functionalized cis-1-oxadecalines via 6-endo-tet-cyclizations of 2-C-branched sugars;RSC Adv.;2014
5. Constructing the architecturally distinctive ABD-tricycle of phomactin A through an intramolecular oxa-[3+3] annulation strategy;Tetrahedron;2011-12
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