Pd‐Catalyzed Asymmetric N‐Allylation of Amino Acid Esters with Exceptional Levels of Catalyst Control: Stereo‐Divergent Synthesis of ProM‐15 and Related Bicyclic Dipeptide Mimetics-Reference-Cited by-同舟云学术

Pd‐Catalyzed Asymmetric N‐Allylation of Amino Acid Esters with Exceptional Levels of Catalyst Control: Stereo‐Divergent Synthesis of ProM‐15 and Related Bicyclic Dipeptide Mimetics

Published:2020-02-18 Issue:14 Volume:26 Page:3049-3053
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Dohmen Stephan¹,Reiher Martin¹,Albat Dominik¹,Akyol Sema¹,Barone Matthias²,Neudörfl Jörg‐Martin¹,Kühne Ronald²,Schmalz Hans‐Günther¹^ORCID

Affiliation:

1. Department of ChemistryUniversity of Cologne Greinstrasse 4 50939 Köln Germany

2. Leibniz-Institut für Molekulare Pharmakologie (FMP) 13125 Berlin Germany

Funder

Bundesministerium für Forschung und Technologie

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202000307

Reference67 articles.

2. Addressing Protein-Protein Interactions with Small Molecules: A Pro-Pro Dipeptide Mimic with a PPII Helix Conformation as a Module for the Synthesis of PRD-Binding Ligands

3. Adressierung von Protein-Protein-Wechselwirkungen durch niedermolekulare Verbindungen: ein Pro-Pro-Dipeptidmimetikum mit PPII-Helixkonformation als Modul für die Synthese PRD-bindender Liganden

4. Exercises in Pyrrolidine Chemistry: Gram Scale Synthesis of a Pro-Pro Dipeptide Mimetic with a Polyproline Type II Helix Conformation

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