Stereoselective Approach to Tetrahydropyran by Iodoetherifications of (2S,3S)-2,3-Bis(t-butyldimethylsilyloxy)-5-alkene-1-ol
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1995-5035.pdf
Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Asymmetric synthesis of (−)-(R)-massoia lactone, (R)-δ-decalactone, and (+)-(3R,5R)-3-hydroxydecano-5-lactone. Formal synthesis of verbalactone;Russian Journal of Organic Chemistry;2012-07
2. Stereoselective Synthesis of 2,6-trans-Tetrahydropyran via Primary Diamine-Catalyzed Oxa-Conjugate Addition Reaction of α,β-Unsaturated Ketone: Total Synthesis of Psymberin;Organic Letters;2011-10-11
3. ChemInform Abstract: Stereoselective Approach to Tetrahydropyran by Iodoetherifications of ( 2S,3S)-2,3-Bis(tert-butyldimethylsilyloxy)-5-alken-1-ol.;ChemInform;2010-08-17
4. A Facile and Efficient Synthesis of 4-Hydroxy-2,6-cis-tetrahydropyrans via Tandem Cross-Metathesis/Thermal SN2′ Reaction: Protecting-Group-Free Synthesis of (±)-Diospongin A;Organic Letters;2009-10-13
5. 2,6-Disubstituted Tetrahydropyrans by Tandem Cross-Metathesis/Iodocyclisation;European Journal of Organic Chemistry;2008-02
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