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Synlett 2017; 28(01): 1-11
DOI: 10.1055/s-0036-1588372
DOI: 10.1055/s-0036-1588372
account
Pardon the Interruption: A Modification of Fischer’s Venerable Reaction for the Synthesis of Heterocycles and Natural Products
Further Information
Publication History
Received: 17 November 2016
Accepted: 21 November 2016
Publication Date:
08 December 2016 (online)
‡ These authors contributed equally.
Abstract
This account provides an overview of our laboratory’s studies of an unusual variant of the Fischer indolization reaction. We describe the discovery of the so-called ‘interrupted Fischer indolization’ and the development of the reaction from a methodological standpoint. In addition, our efforts to evaluate and apply this methodology in the context of akuammiline alkaloid total synthesis are discussed.
1 Introduction
2 Interrupted Fischer Indolization Methodology
3 Applications in Akuammiline Alkaloid Total Synthesis
4 Concluding Thoughts
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References
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For select studies on physovenine, see:
For a recent review of pyrrolidinoindoline natural product syntheses, see:
See also:
For syntheses of physostigmine since Alvarez’s review (ref. 6a), see:
For a pertinent review, see:
For a seminal and influential study by Stoltz and co-workers, see:
For the classic Fischer indole synthesis, see:
Lactols and hemiaminals had previously been employed in modifications of the Fischer indole synthesis, see:
List’s laboratory ultimately developed an asymmetric Fischer indolization, see:
For other total syntheses of akuammiline alkaloids, see:
For our laboratory’s total syntheses of akuammilines, see:
For the initial isolation of picrinine, see:
For more recent isolation reports, see:
For the initial isolation of strictamine, see:
For previous synthetic studies on strictamine or related methanoquinolizidine akuammilines, see:
For additional examples of the Fischer indolization in late-stage total synthesis of complex alkaloids, see: