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A total synthesis of magallanesinevia[1, 2]-Meisenheimer rearrangement

Authors
Journal
Tetrahedron Letters
0040-4039
Publisher
Elsevier
Publication Date
Volume
35
Issue
22
Identifiers
DOI: 10.1016/s0040-4039(00)73089-9

Abstract

Abstract A straightforward synthesis of magallanesine 1 from azetoisoquinoline 4 has been accomplished via [1,2]-Meisenheimer rearrangement and an intramolecular Heck cyclization as the key reactions.

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