Intramolecular diels-alder reactions of silyl acetal trienes. The effect of stereoselectivity of allylic substitution
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Stereochemical aspects of the intramolecular Diels–Alder reaction
2. Pericyclic umpolung. Reversal of regioselectivity in the diels-alder reaction
3. Disposable tethers in type 2 intramolecular diels-alder cycloaddition reactions. Applications in stereochemical control
4. The unsymmetrical silaketal as a neutral, removable tether for effecting intramolecular diels-alder reactions.
5. A novel strategy for regio- and stereocontrol in [4 + 2] cycloadditions. Intramolecular diels-alder reaction of a sllyl acetal triene
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2. Formation of Alkenes by Diels-Alder Reactions;Comprehensive Organic Transformations;2018-02-28
3. ChemInform Abstract: Intramolecular Diels-Alder Reactions of Silyl Acetal Trienes. The Effect on Stereoselectivity of Allylic Substitution.;ChemInform;2010-08-21
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5. Selectivity Controls in the [4+2] Cycloadditions of 1-Oxygenated Dienes;Synlett;2006-09
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