Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (±)-hippodamine and (±)-epi-hippodamine

Martin Rejzek; Robert A. Stockman; David L. Hughes

doi:10.1039/b413052a

Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (±)-hippodamine and (±)-epi-hippodamine

Martin Rejzek, Robert A. Stockman, David L. Hughes

School of Chemistry

Research output: Contribution to journal › Article › peer-review

29 Citations (Scopus)

Abstract

Two-directional total stereoselective syntheses of (±)-hippodamine and (±)-epi-hippodamine, utilising a tandem deprotection/intramolecular double Michael addition sequence as the key step, are presented.

Original language	English
Pages (from-to)	73-83
Number of pages	11
Journal	Organic & Biomolecular Chemistry
Volume	3
Issue number	1
DOIs	https://doi.org/10.1039/b413052a
Publication status	Published - 1 Jan 2005

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10.1039/b413052a

Cite this

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abstract = "Two-directional total stereoselective syntheses of (±)-hippodamine and (±)-epi-hippodamine, utilising a tandem deprotection/intramolecular double Michael addition sequence as the key step, are presented.",

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