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Synthesis of an indole analog of magallanesine via the [1,2]-meisenheimer rearrangement

โœ Scribed by Ryuji Yoneda; Tetsuya Kimura; Junko Kinomoto; Shinya Harusawa; Takushi Kurihara

Book ID
112131705
Publisher
Journal of Heterocyclic Chemistry
Year
1996
Tongue
English
Weight
365 KB
Volume
33
Category
Article
ISSN
0022-152X

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๐Ÿ“œ SIMILAR VOLUMES

A total synthesis of magallanesine via [
A total synthesis of magallanesine via [1, 2]-Meisenheimer rearrangement
โœ Ryuji Yoneda; Yasuhiko Sakamoto; Yoshifumi Oketo; Kayoko Minami; Shinya Harusawa ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 257 KB

A straightforward synthesis of magallanesine 1 from azetoisoquinoline 4 has been accomplished via [ 1.21~Meisenheimer rearrangement and an intramolecular Heck cyclization as the key reactions. Members of the plant family Berberidaceae have long been known to contain a number of alkaloids, and recent