A Short Olefin Metathesis-Based Route to Enantiomerically Pure Arylated Dihydropyrans and α,β-Unsaturated δ-Valero Lactones-Reference-Cited by-同舟云学术

A Short Olefin Metathesis-Based Route to Enantiomerically Pure Arylated Dihydropyrans and α,β-Unsaturated δ-Valero Lactones

Published:2002-12-13 Issue:3 Volume:68 Page:799-804
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wildemann Holger¹,Dünkelmann Pascal¹,Müller Michael¹,Schmidt Bernd¹

Affiliation:

1. FB Chemie der Universität Dortmund, Organische Chemie, D-44221 Dortmund, Germany, and Institut für Biotechnologie 2, Forschungszentrum Jülich GmbH, D-52425 Jülich, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0264729

Reference28 articles.

1. Methoxytetrahydropyrans. A new series of selective and orally potent 5-lipoxygenase inhibitors

2. Stereocontrolled Syntheses of Epimeric 3-Aryl-6-phenyl-1-oxa-7-azaspiro[4.5]decane NK-1 Receptor Antagonist Precursors

3. A Double Ring Closing Metathesis Reaction in the Rapid, Enantioselective Synthesis of NK-1 Receptor Antagonists

4. SAR Studies of Piperidine-Based Analogues of Cocaine. 4. Effect of N-Modification and Ester Replacement

5. Dynamic Kinetic Resolution of Racemic γ-Aryl-δ-oxoesters. Enantioselective Synthesis of 3-Arylpiperidines

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