Brønsted acid-mediated annulations of pyrroles featuring N-tethered α,β-unsaturated ketones and esters: Total syntheses of (±)-tashiromine and (±)-indolizidine 209I-Reference-Cited by-同舟云学术

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Brønsted acid-mediated annulations of pyrroles featuring N-tethered α,β-unsaturated ketones and esters: Total syntheses of (±)-tashiromine and (±)-indolizidine 209I

Published:2018-09 Issue:38 Volume:74 Page:5436-5441
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Olivier Wesley J.,Gardiner Michael G.,Bissember Alex C.,Smith Jason A.

Funder

University of Tasmania

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference41 articles.

1. Biological formation of pyrroles: Nature's logic and enzymatic machinery

2. Pyrrole and its Derivatives in Heterocycles in Natural Product Synthesis;Mal,2011

3. Five-membered Heterocycles: Pyrrole and Related Systems in Modern Heterocyclic Chemistry;Bergman,2011

4. Pyrrolizidine alkaloids

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2. Metal-Free, Adjustable, and Recyclable Catalytic Systems for the Construction of C–C Bonds by Activating Propargylic Alcohols;The Journal of Organic Chemistry;2022-08-23

3. Structural Revision of Parvistemoamide: Informing Biosynthetic Proposals of Stemona Alkaloids;Organic Letters;2022-07-28

4. Strategies for the synthesis of Stemona alkaloids: an update;Natural Product Reports;2022

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