Strategies for the Formation of Tetrahydropyran Rings in the Synthesis of Natural Products
Author:
Affiliation:
1. School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK
2. Address from January 1, 2006: Department of Chemistry, University of York, Heslington, York, YO10 5DD, UK
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.200500964
Reference59 articles.
1. Oxonia-Cope Rearrangement and Side-Chain Exchange in the Prins Cyclization
2. Synthesis of (−)-Centrolobine by Prins Cyclizations that Avoid Racemization
3. Prins Cyclizations in Silyl Additives with Suppression of Epimerization: Versatile Tool in the Synthesis of the Tetrahydropyran Backbone of Natural Products
4. Synthesis of the C22−C26 Tetrahydropyran Segment of Phorboxazole by a Stereoselective Prins Cyclization
5. Synthesis of the C3−C19 Segment of Phorboxazole B
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