Macroring contraction methodology. 6. transannular diels-alder reaction of the 14-members (E,E,E)-trienone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
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3. Transannular Diels-Alder reaction of 14-membered macrocyclic trienes. Part I: Theoretical analysis and stereochemical predictions
4. Transannular Diels-Alder reaction of 14-membered macrocyclic trienes. Part II: Experimental results and synthetic potential
5. Macroring contraction methodology. 4. A novel route to steroid A, B, C rings by the transannular Diels-Alder reaction of the 14-membered (E,E,E)-macrocyclic triene
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2. Synthesis of a trans,syn,trans-Dodecahydrophenanthrene via a Bicyclic Transannular Diels−Alder Reaction: Intermediate for the Synthesis of Fusidic Acid;The Journal of Organic Chemistry;2010-09-15
3. The ROBIA Program for Predicting Organic Reactivity;Journal of Chemical Information and Modeling;2006-01-21
4. Regio- and stereocontrolled Diels–Alder reaction tethered by Asp-Thr dipeptide;Chemical Communications;2005
5. First Experimental and Theoretical Evidence of a Deactivating Enone Dienophile in the Transannular Diels−Alder Reaction;The Journal of Organic Chemistry;2003-02-21
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