An intramolecular [2+2] photocycloaddition-fragmentation approach towards the total synthesis of Asteriscanolide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Model studies towards the total synthesis of asteriscanolide
2. Nucleophilic substitution of 5,5-dimethyl-2-cyclopentenyl derivatives. Lack of SN2′ reaction
3. Intramolecular [2+2] photocycloaddition of enone-acetals
4. Stereocontrol in the intramolecular Diels-Alder reaction. 4. A remarkable effect of overlap requirements in the connecting chain
5. Annelative ring expansion via intramolecular [2 + 2] photocycloaddition of .alpha.,.beta.-unsaturated .gamma.-lactones and reductive cleavage: synthesis of hydrocyclopentacyclooctene-5-carboxylates
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3. Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions;Chemical Reviews;2016-03-28
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