Stereoselective synthesis of six- and seven-membered ether rings based on the ring expansion
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Isolation and structure of brevetoxin B from the "red tide" dinoflagellate Ptychodiscus brevis (Gymnodinium breve)
2. Stereocontrolled synthesis of cyclic ethers by intramolecular hetero-Michael addition. 3. Enantiomeric synthesis of highly functionalized and fused tetrahydropyrans
3. Stereocontrolled synthesis of cyclic ethers by intramolecular hetero-Michael addition. 4. Enantiomeric synthesis of substituted and fused oxepanes
4. Activation of 6-endo over 5-exo epoxide openings. Ring-selective formation of tetrahydropyran systems and stereocontrolled synthesis of the ABC ring framework of brevetoxin B
5. Activation of 6-endo over 5-exo hydroxy epoxide openings. Stereoselective and ring selective synthesis of tetrahydrofuran and tetrahydropyran systems
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