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A Short‐Step Synthesis of 1,6‐Methano[10]annulene‐3,4‐dicarboximides and Their Benzene‐, Naphthalene‐, and Thiophene‐Annulated Compounds (Eur. J. Org. Chem. 27/2014)
Author(s) -
Oda Mitsunori,
Nakamura Tomomi,
Neha Miyako,
Miyawaki Daisuke,
Ohta Akira,
Kuroda Shigeyasu,
Miyatake Ryuta
Publication year - 2014
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201490075
Subject(s) - annulene , chemistry , thiophene , naphthalene , phosphorane , reagent , computational chemistry , medicinal chemistry , organic chemistry
The cover picture shows a rapid stream in a valley of the Hirayu area in the Gifu Prefecture located in the middle of the Japanese mainland. The schemes show an improved one‐pot reaction with phosphorane reagents, along the stream, and the previously reported multistep reactions from dicarbaldehydes to 1,6‐methano[10]annulene‐dicarboximides. The one‐pot procedure was successfully applied to the synthesis of the arene‐annulated 1,6‐methano[10]annulenes. Details are discussed in the article by M. Oda et al. on p. 5976 ff . Even after the eminent achievements by the late Dr. E. Vogel, the field of 1,6‐methano[10]annulene chemistry is still interesting and fertile. The authors thank Mr. Yoshimitsu Kumai in our laboratory for his great help in preparing this cover picture.

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