Mechanism of Stereo- and Regioselectivity in the Paternò−Büchi Reaction of Furan Derivatives with Aromatic Carbonyl Compounds: Importance of the Conformational Distribution in the Intermediary Triplet 1,4-Diradicals-Reference-Cited by-同舟云学术

Mechanism of Stereo- and Regioselectivity in the Paternò−Büchi Reaction of Furan Derivatives with Aromatic Carbonyl Compounds: Importance of the Conformational Distribution in the Intermediary Triplet 1,4-Diradicals

Published:2004-02-12 Issue:9 Volume:126 Page:2838-2846
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Abe Manabu¹,Kawakami Takanori¹,Ohata Shinji¹,Nozaki Koichi¹,Nojima Masatomo¹

Affiliation:

1. Contribution from the Department of Materials Chemistry, Graduate School of Engineering, Osaka University (HANDAI), Suita 565-0871, Osaka, Japan, and Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka 560-0043, Osaka, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja039491o

Reference72 articles.

1. Vierringsynthesen durch photosensibilisierte Cycloaddition von Dimethylmaleinsäureanhydrid an Olefine

2. Light-catalyzed Organic Reactions. I. The Reaction of Carbonyl Compounds with 2-Methyl-2-butene in the Presence of Ultraviolet Light

3. Organic Photochemical Reactions. I. The Synthesis of Substituted Oxetanes by the Photoaddition of Aldehydes to Furans

4. Synthesis of oxetanes by photoaddition of benzophenone to furans

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