New Piperidine Scaffolds via Nucleophilic Reactivity of (−)-Phenyloxazolopiperidine-Reference-Cited by-同舟云学术

New Piperidine Scaffolds via Nucleophilic Reactivity of (−)-Phenyloxazolopiperidine

Published:2004-05-01 Issue:11 Volume:69 Page:3836-3841
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Poupon Erwan¹,François David¹,Kunesch Nicole¹,Husson Henri-Philippe¹

Affiliation:

1. Laboratoire de Pharmacognosie Associé au CNRS, UMR 8076 (BioCIS), Centre d'Études Pharmaceutiques, Université Paris-Sud 11, 5, Rue Jean-Baptiste Clément, 92296 Châtenay-Malabry CEDEX, France, and Laboratoire de Chimie Thérapeutique et Laboratoire de Pharmacognosie, Faculté des Sciences Pharmaceutiques et Biologiques, UMR 8638 Associée au CNRS et à l'Université René-Descartes (Paris 5), 4, Avenue de l'Observatoire, 75256 Paris CEDEX 06, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0499524

Reference23 articles.

1. A Method for Palladium-Catalyzed Cross-Couplings of Simple Alkyl Chlorides: Suzuki Reactions Catalyzed by [Pd2(dba)3]/PCy3 dba=(E,E)-dibenzylideneacetone, Cy=cyclohexyl. We thank Dr. Matthew R. Netherton for helpful discussions and Johnson Matthey Inc. for supplying palladium compounds. Support has been provided by the Deutsche Akademie der Naturforscher Leopoldina (Leopoldina fellowship to J.H.K., BMBF-LPD 9901/8-48), Bristol-Myers Squibb, the National Institutes of Health (National Institute of General Medical Sciences, R01-GM62871), the Natural Sciences and Engineering Research Council of Canada (postdoctoral fellowship to C.D.), and Novartis. Funding for the MIT Department of Chemistry Instrumentation Facility has been provided in part by NSF CHE-9808061 and NSF DBI-9729592.

2. Die Umlagerung von α‐Tripiperidein in Isotripiperidein

3. A convenient synthesis of 6-acetyl-1,2,3,4-tetrahydropyridine, the principle bread flavor component

4. The relative stabilities of 6-membered cyclic allylamine/enamine systems

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