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Total Synthesis of the Akuammiline Alkaloid Picrinine
Author(s) -
Joel M. Smith,
Jesus Moreno,
Ben W. Boal,
Neil K. Garg
Publication year - 2014
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja501780w
Subject(s) - chemistry , total synthesis , alkaloid , natural product , stereochemistry , indole alkaloid
We report the first total synthesis of the complex akuammiline alkaloid picrinine, which was first isolated nearly five decades ago. Our synthetic approach features a concise assembly of the [3.3.1]-azabicyclic core, a key Fischer indolization reaction to forge the natural product's carbon framework, and a series of delicate late-stage transformations to complete the synthesis. Our synthesis of picrinine also constitutes a formal synthesis of the related polycyclic alkaloid strictamine.

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