The Reactivity of Enantiopure (S )-6-Oxopipecolic Acid and Corresponding Pyridoisoquinolines Under Acidic Conditions-Reference-Cited by-同舟云学术

The Reactivity of Enantiopure (S )-6-Oxopipecolic Acid and Corresponding Pyridoisoquinolines Under Acidic Conditions

Published:2018-10-18 Issue:40 Volume:2018 Page:5499-5511
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Šafář Peter¹,Marchalín Štefan¹²,Balónová Barbora³,Šoral Michal⁴,Moncol Ján⁵,Ghinet Alina⁶⁷⁸,Rigo Benoît⁶⁷,Daïch Adam²^ORCID

Affiliation:

1. Department of Organic Chemistry; Faculty of Chemical and Food Technology; Slovak University of Technology; 81237 Bratislava Slovakia

2. Normandie Univ.; UNILEHAVRE, FR 3038 CNRS, URCOM, 76600 Le Havre, France EA 3221, INC3M CNRS-FR 3038, UFR ST; BP: 1123; BP: 1123, 25 rue Philipe Lebon 76063 Le Havre Cedex France

3. University of Kent School of Physical Sciences; Ingram 307 CT2 7NH Canterbury Kent UK

4. Central Laboratories; Faculty of Chemical and Food Technology; Slovak University of Technology; 81237 Bratislava Slovakia

5. Department of Inorganic Chemistry; Faculty of Chemical and Food Technology; Slovak University of Technology; 81237 Bratislava Slovakia

6. HEI, Yncréa Hauts-de-France; Laboratoire de Pharmacochimie; 13 rue de Toul 59046 Lille France

7. INSERM; U995-LIRIC; CHRU de Lile; Faculté de Médecine-Pôle Recherche Université Lille; U995-LIRIC, CHRU de Lille -59045 Lille France

8. Alexandru Ioan Cuza' University of Iasi; Faculty of Chemistry; Bd. Carol I nr. 11 700506 Iasi Romania

Funder

ERDF

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201800908/fullpdf

Reference96 articles.

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4. Total Synthesis of (S)-(+)-Tylophorine Via Enantioselective Intramolecular Alkene Carboamination

5. A general approach to triphenylenes and azatriphenylenes: total synthesis of dehydrotylophorine and tylophorine

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