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1,3‐Dipolar cycloaddition reactions of cyclooctyne with azomethine ylides
Author(s) -
Matsumoto Kiyoshi,
Ohta Ryuji,
Uchida Takane,
Nishioka Hiroyasu,
Yoshida Maki,
Kakehi Akikazu
Publication year - 1995
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570320163
Subject(s) - pyridinium , chemistry , cycloaddition , 1,3 dipolar cycloaddition , azomethine ylide , organic chemistry , combinatorial chemistry , computational chemistry , catalysis
Cyclooctyne smoothly underwent 1,3‐dipolar cycloaddition with aziridines and pyridinium ylides to afford the corresponding pyrroles and indolizines in moderate to good yields.
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