Central‐to‐Axial Chirality Conversion Approach Designed on Organocatalytic Enantioselective Povarov Cycloadditions: First Access to Configurationally Stable Indole–Quinoline Atropisomers-Reference-Cited by-同舟云学术

Central‐to‐Axial Chirality Conversion Approach Designed on Organocatalytic Enantioselective Povarov Cycloadditions: First Access to Configurationally Stable Indole–Quinoline Atropisomers

Published:2019-12-05 Issue:68 Volume:25 Page:15694-15701
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Bisag Giorgiana Denisa¹^ORCID,Pecorari Daniel¹,Mazzanti Andrea¹^ORCID,Bernardi Luca¹^ORCID,Fochi Mariafrancesca¹^ORCID,Bencivenni Giorgio¹^ORCID,Bertuzzi Giulio¹^ORCID,Corti Vasco¹^ORCID

Affiliation:

1. Department of Industrial Chemistry “Toso Montanari”Alma Mater Studiorum–University of Bologna Viale Risorgimento 4 40136 Bologna Italy

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201904213

Reference152 articles.

2. The Challenge of Atropisomerism in Drug Discovery

3. Atropisomerie als Herausforderung in der Medikamentenentwicklung

4. Assessing Atropisomer Axial Chirality in Drug Discovery and Development

5. Recent encounters with atropisomerism in drug discovery

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