Synthetic Photochemistry. LX. One-pot Formation of Spirocyclic 3-Acetyl-2-hydroxy-2-cyclopentenone Derivatives from Methylenecycloalkanes and Methyl 2,4-Dioxopentanoate
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/66/3/66_3_870/_pdf
Reference16 articles.
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2. Synthetic Photochemistry. I. The Cycloaddition Reaction of Methyl Acetopyruvate with Olefins
3. Total synthesis of (±)-silphinene
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1. ChemInform Abstract: Synthetic Photochemistry. Part 60. One-Pot Formation of Spirocyclic 3- Acetyl-2-hydroxy-2-cyclopentenone Derivatives from Methylenecycloalkanes and Methyl 2,4-Dioxopentanoate.;ChemInform;2010-08-20
2. Cyclobutane Ring Opening Reactions of 1,2,2a,8b-Tetrahydrocyclobuta[c]-quinolin-3(4H)-ones;Synthesis;2008-06-18
3. Synthetic Photochemistry. LXVII. A Total Synthesis of (±)-Hinesol and (±)-Agarospirol viaretro-Benzilic Acid Rearrangement;Bulletin of the Chemical Society of Japan;1995-08
4. Photoaddition of methyl 2,4-dioxopentanoate to norbornadiene and quadricyclane;Journal of Photochemistry and Photobiology A: Chemistry;1995-04
5. Synthetic Photochemistry. LXIV. Mild Base-Inducedretro-Benzilic-Acid Rearrangement of Isolatedproto-Photocycloadducts of Methyl 2,4-Dioxopentanoate to Terpinolene. Facile Synthesis ofα-Chamigrene andα-Chamigren-3-one;Bulletin of the Chemical Society of Japan;1994-09
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