Synthesis of a possible kallolide a precursor via [2,3] wittig ring contraction of a macrocyclic furan diether
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Kallolide A, a new antiinflammatory diterpenoid, and related lactones from the Caribbean octocoral Pseudopterogorgia kallos (Bielschowsky)
2. [2,3]-Wittig ring contraction. A new route to cembranoid natural products
3. [2,3]-Wittig rearrangement of a 13-membered diallylic ether. Six-step synthesis of costunolide
4. Total synthesis of the germacranolide (±)-aristolactone via [2,3] wittig ring contraction
5. Stereoselective total synthesis of (.+-.)-aristolactone and (.+-.)-epiaristolactone via [2,3] Wittig ring contraction
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1. Catalytic C−H Functionalization of Unreactive Furan Cores in Bio‐Derived Platform Chemicals;ChemSusChem;2020-12-03
2. Directing-Group-Free, Carbonyl Group-Promoted Catalytic C–H Arylation of Bio-Based Furans;ACS Catalysis;2020-09-21
3. Synthetic approaches to phomactins: on the stereoselectivity of some [2,3]-Wittig rearrangements;Tetrahedron;2015-09
4. Asymmetric synthesis of the C(6–18) bis(tetrahydropyran)spiroacetal fragment of the lituarines;Tetrahedron;2011-07
5. The Natural Products Chemistry of the Gorgonian Genus Pseudopterogorgia (Octocorallia: Gorgoniidae);Comprehensive Natural Products II;2010
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