[1.3], [3.3] and Tandem [1.3]–[3.3] rearrangements of 11- and 12-membered trienolides
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910001699
Reference30 articles.
1. The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation
2. Alicyclic Claisen rearrangement. A general carbocycle synthesis based on four-atom-ring contractions of lactones
3. Model studies on the synthesis of medium-sized and large carbocycles using the Ireland enolate Claisen rearrangement
4. Claisen-rearrangement-mediated ring contraction of macrocyclic lactones
5. Novel Synthesis of Ketolactones by Intramolecular Reverse Dieckmann Reaction1
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3. ChemInform Abstract: (1.3), (3.3), and Tandem (1.3)-(3.3) Rearrangements of 11- and 12- Membered Trienolides.;ChemInform;2010-08-22
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