Photoracemization‐Based Viedma Ripening of a BINOL Derivative-Reference-Cited by-同舟云学术

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Photoracemization‐Based Viedma Ripening of a BINOL Derivative

Published:2019-12-12 Issue:4 Volume:26 Page:839-844
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Belletti Giuseppe¹^ORCID,Tortora Carola²^ORCID,Mellema Indradevi D.¹,Tinnemans Paul¹^ORCID,Meekes Hugo¹^ORCID,Rutjes Floris P. J. T.¹^ORCID,Tsogoeva Svetlana B.²^ORCID,Vlieg Elias¹^ORCID

Affiliation:

1. Radboud University Institute for Molecules and Materials Heyendaalseweg 135 6525 AJ Nijmegen The Netherlands

2. Chair of Organic Chemistry I Department of Chemistry and Pharmacy Friedrich-Alexander-Universität Erlangen-Nürnberg Nikolaus-Fiebiger-Str. 10 91058 Erlangen Germany

Funder

Horizon 2020 Framework Programme

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201904382

Reference38 articles.

1. Putting chirality to work: the strategy of chiral switches

2. Processes To Separate Enantiomers

3. Verfahren zur Enantiomerentrennung

4. Viedma ripening: a reliable crystallisation method to reach single chirality

5. Fast Attrition-Enhanced Deracemization of Naproxen by a Gradual In Situ Feed

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