On the stereoselectivity of the intramolecular dioxenone photocycloaddition
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Intramolecural Photocycloaddition on Dioxolenones: An Efficient Method for the Synthesis of Medium-sized Rings
2. Inside-outside stereoisomerism. II. Synthesis of the carbocyclic ring system of the ingenane diterpenes via the intramolecular dioxolenone photocycloaddition
3. Inside-outside stereoisomerism III: The synthesis of trans-bicyclo[4.3.1]decan-10-one+
4. Inside-outside stereoisomerism. 5. Synthesis and reactivity of trans-bicyclo[n.3.1] alkanones prepared via the intramolecular photocycloaddition of dioxenones
5. Winkler, J.; Hong, B.; Bahador, A.; Kazanietz, M.; Blumberg, P. Bioorg. Med. Chem. Lett., in press.
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1. A Biocatalytic Route to Highly Enantioenriched β-Hydroxydioxinones;Advanced Synthesis & Catalysis;2017-03-02
2. ChemInform Abstract: On the Stereoselectivity of the Intramolecular Dioxenone Photocycloaddition.;ChemInform;2010-08-20
3. Photochemistry of Compounds Containing CC Double Bonds;PATAI'S Chemistry of Functional Groups;2009-12-15
4. Asymmetric Photoreactions of Conjugated Enones and Esters;Advances in Photochemistry;2007-01-05
5. Synthetic approaches to ingenol;Tetrahedron;2006-02
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