Trimethylsilyl triflate catalysed Diels-Alder reaction of TMS ethers of conjugated dienols with cyclic enones: Evidence for an endo transition state, and first application to synthesis of enantiopure octalins
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference74 articles.
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3. THE SYNTHESIS OF CONDENSED RING COMPOUNDS. X. cis-9-METHYL-8-KETO-2-OCTALIN AND cis-10-METHYL-1-VINYL-1,7-NAPHTHITADIENE1
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2. Cationic Cyclization of 2-Alkenyl-1,3-dithiolanes: Diastereoselective Synthesis of trans-Decalins;The Journal of Organic Chemistry;2011-04-13
3. ChemInform Abstract: Trimethylsilyl Triflate Catalyzed Diels-Alder Reaction of TMS Ethers of Conjugated Dienols with Cyclic Enones: Evidence for an endo Transition State, and First Application to Synthesis of Enantiopure Octalins.;ChemInform;2010-06-15
4. Diastereoselective formal total synthesis of (±)-triptolide via a novel cationic cyclization of 2-alkenyl-1,3-dithiolane;Chemical Communications;2010
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