Hydrogen-bonding directed, regioselective photocycloaddition reactions of cyanonaphthalenes with furanmethanols
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2011/PP/C1PP05060E
Reference22 articles.
1. Photoadditions of aromatic compounds
2. The meta photocycloaddition of arenes to alkenes
3. THE PHOTOCHEMICAL (4 + 4) CYCLOADDITIOM OF FURAN TO α-NAPHTHONITRILE
4. NEGATIVE TEMPERATURE DEPENDENCE OF THE PHOTOCHEMICAL (4+4) CYCLOADDITION OF FURAN TO α-NAPHTHONITRILE : EVIDENCE FOR EXCIPLEX INTERMEDIACY
5. X-Ray Molecular Structure of 1-Cyano-7,8-benzo-11-oxatricyclo[4.2.2.12,5]undeca-3,7,9-triene
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1. Hydroxy group-enabled highly regio- and stereo-selective hydrocarboxylation of alkynes;Chemical Science;2019
2. Synthesis of Polycyclic Compounds by Using Photocycloaddition Reactions to Aromatic Rings;Journal of Synthetic Organic Chemistry, Japan;2018
3. Diastereoselective photocycloaddition reactions of 2-naphthalenecarboxylates and 2,3-naphthalenedicarboxylates with furans governed by chiral auxiliaries and hydrogen bonding interactions;Journal of Photochemistry and Photobiology A: Chemistry;2017-12
4. Intermolecular hydrogen bonding controlled stereoselective photocycloaddition of vinyl ethers to 1-cyanonaphthalenes;Photochemical & Photobiological Sciences;2016
5. Photochemistry of aromatic compounds;Photochemistry
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