A Regio- and Diastereoselective Anodic Aryl-Aryl Coupling in the Biomimetic Total Synthesis of (−)-Thebaine-Reference-Cited by-同舟云学术

A Regio- and Diastereoselective Anodic Aryl-Aryl Coupling in the Biomimetic Total Synthesis of (−)-Thebaine

Published:2018-06-14 Issue:34 Volume:57 Page:11055-11059
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Lipp Alexander¹,Ferenc Dorota¹,Gütz Christoph¹,Geffe Mario¹,Vierengel Nina¹,Schollmeyer Dieter¹,Schäfer Hans J.²,Waldvogel Siegfried R.¹,Opatz Till¹^ORCID

Affiliation:

1. Johannes Gutenberg-Universität; Institut für Organische Chemie; Duesbergweg 10-14 55128 Mainz Germany

2. Westfälische Wilhelms-Universität; Institut für Organische Chemie; Corrensstraße 40 48149 Münster Germany

Funder

Carl-Zeiss-Stiftung

Rhineland Palatinate Center for Natural Products Research

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201803887/fullpdf

Reference100 articles.

1. Morphine Synthesis and Biosynthesis-An Update

2. Recent advances in process development for opiate-derived pharmaceutical agents

3. Recent Developments in the Chemistry of Thebaine and its Transformation Products as Pharmacological Targets

4. Conversion of Thebaine to Oripavine and Other Useful Intermediates for the Semisynthesis of Opiate-Derived Agents: Synthesis of Hydromorphone

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