Photochemistry of 1-allyl-naphthalen-2(1H)-ones: A revised mechanism for the formation of benzotricyclo[3.3.1.02,7]nonen-8-ones.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. The preparation and reactions of 1,3,4,5,6,7,8-heptafluoro-2-naphthyl prop-2-enyl ether: Formation of 1,3,4,5,6,7,8-heptafluoro-1-(prop-2-enyl)naphthalen-2-one and the photolysis and pyrolysis of this ketone [1].
2. Organic photochemistry. XV. Photochemistry of bichromophoric molecules. Intramolecular cycloaddition and cis-trans isomerization of 6-phenyl-2-hexene in solution
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1. Tandem RCM–Claisen Rearrangement–[2+2] Cycloaddition of O,O'-(But-2-en-1,4-diyl)-bridged Binaphthols;Molecules;2012-12-07
2. Intramolecular [2+2] Photocycloaddition Reactions as an Entry to the 2‐Oxatricyclo[4.2.1.04, 9]nonan‐3‐one Skeleton of Lactiflorin;Chemistry – An Asian Journal;2012-05-31
3. On the Regioselectivity of the Intramolecular [2 + 2]-Photocycloaddition of Alk-3-enyl Tetronates;The Journal of Organic Chemistry;2011-07-07
4. Photochemical [2 + 2] cycloaddition reactions of 6-alkenyl-3-phenylcyclohex-2-en-1-ones: using biradical conformation control to account for exceptions to the “rule of five”;Organic & Biomolecular Chemistry;2011
5. ChemInform Abstract: Photochemistry of 1-Allylnaphthalen-2(1H)-ones: A Revised Mechanism for the Formation of Benzotricyclo(3.3.1.02,7)nonen-8-ones.;ChemInform;1988-03-15
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