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Stereoselective synthesis of the tricyclic core ABC-rings of nakadomarin and manzamine from a common intermediate

✍ Scribed by Philip Magnus; Mark R Fielding; Charles Wells; Vince Lynch


Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
263 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


Pauson-Khand cyclization of the enamide 9 proceeds in trifluoroethanol to give cyclopentenone 10, which on hydrogenation gives 11, having the core ABC-rings of nakadomarin 1.


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