A Minimalist NMR Approach for the Structural Revision of Mucoxin
Author:
Publisher
Wiley
Subject
General Chemistry,Catalysis,Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201001619/fullpdf
Reference24 articles.
1. Synthesis of the Proposed Structure of Mucoxin via Regio- and Stereoselective Tetrahydrofuran Ring-Forming Strategies
2. Validation of the proton NMR chemical shift method for determination of stereochemistry in the bistetrahydrofuranyl moiety of uvaricin-related acetogenins from Annonaceae: rolliniastatin 1 (and asimicin)
3. On the stereochemistry of the bistetrahydrofuranyl moiety of uvaricin. Proton chemical shifts can play a crucial role in complex structure determination
4. On the Proof and Disproof of Natural Product Stereostructures: Characterization and Analysis of a Twenty-Eight Member Stereoisomer Library of Murisolins and Their Mosher Ester Derivatives
5. Total Synthesis of a 28-Member Stereoisomer Library of Murisolins
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