4.7 Article

Total Syntheses of Iheyamines A and B

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 88, Issue 2, Pages 1256-1259

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.2c02583

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An efficient synthetic route to iheyamine A and its analogues was discovered, involving a crucial one-pot transformation that included C-C migration to form the characteristic seven-membered ring. Subsequent addition of acetone to iheyamine A initiated a cascade process to complete the total synthesis of iheyamine B.
An efficient synthetic route to iheyamine A and its analogues was discovered; the crucial one-pot transformation included a C-C migration to form the characteristic seven -membered ring. Subsequent addition of acetone to iheyamine A initiated a cascade process to complete the total synthesis of iheyamine B.

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