Synthetic Photochemistry. LIV. The Photoaddition Reaction of Methyl 2,4-Dioxopentanoate with 2,5-Dimethyl-2,4-hexadiene, a Sterically Crowded Conjugated Diene-Reference-Cited by-同舟云学术

Synthetic Photochemistry. LIV. The Photoaddition Reaction of Methyl 2,4-Dioxopentanoate with 2,5-Dimethyl-2,4-hexadiene, a Sterically Crowded Conjugated Diene

Published:1990-06 Issue:6 Volume:63 Page:1611-1616
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Hatsui Toshihide,Nojima Chitoshi,Takeshita Hitoshi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/63/6/63_6_1611/_pdf

Reference4 articles.

1. Synthetic Photochemistry. LI. Structure Elucidation of the Pyrolysates Formed by “Retro-Benzilic Acid Rearrangement” of the Proto-Photocycloadducts of Methyl 2,4-Dioxopentanoate-Olefins

2. Effect of UV irradiation on some β-dicarbonyl compounds in solution

3. Photoisomerization of the enol form of 1,3-dicarbonyl compounds

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