Synthetic Studies toward the CD Spiroketal of Spongistatins
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.200901285/fullpdf
Reference126 articles.
1. Synthetic routes to tetrahydrofuran, tetrahydropyran, and spiroketal units of polyether antibiotics and a survey of spiroketals of other natural products
2. Chemistry of spiroketals
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1. Porifera (Sponges)-5;Encyclopedia of Marine Natural Products;2014-08-07
2. Application of The [4+3] Cycloaddition Reaction To The Synthesis of Natural Products;Methods and Applications of Cycloaddition Reactions in Organic Syntheses;2014-01-10
3. Stereoselective Synthesis of Difructose Dianhydrides by Use of the Xylylene Group as Stereodirecting Element in Spiroketalisation Reactions;European Journal of Organic Chemistry;2010-12-03
4. Short Diastereoselective Synthesis of the C1-C13 (AB Spiroacetal) and C17-C28 Fragments (CD Spiroacetal) of Spongistatin 1 and 2 through Double Chain-Elongation Reactions;Chemistry - A European Journal;2010-10-20
5. The (4+3)-cycloaddition reaction: heteroatom-substituted allylic cations as dienophiles;Chemical Communications;2010
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