Stereochemical Requirements of Oxidative Cyclizations in Extended Iterative Organoiron-Mediated Routes to Alkaloids
Author:
Affiliation:
1. School of Chemistry, University of East Anglia, Norwich NR4 7TJ, U.K.
2. Institut für Anorganische Chemie, Karlsruhe Institute of Technology, Karlsruhe, Engesserstrasse Geb. 30.45, D-76128 Karlsruhe, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo301617f
Reference79 articles.
1. Transition metal mediated asymmetric synthesis, part 151 directing group competition in organoiron intermediates in the synthesis of (±)-O-methyljoubertiamine
2. Electrophilic C12 Building Blocks for Alkaloids: 1,1 Iterative Organoiron-Mediated Routes to (±)-Lycoramine and (±)-Maritidine
3. A Synthesis of (±)-Stemodinone: An Application of Organoiron Chemistry to the Construction of Sterically Congested Quaternary Carbon Centers
4. Synthetic studies directed toward guianolides: an organoiron route to the 5,7,5 tricyclic ring system
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