Enantioselective Synthesis of Pyrrolidine-, Piperidine-, and Azepane-Type N-Heterocycles with α-Alkenyl Substitution: The CpRu-Catalyzed Dehydrative Intramolecular N-Allylation Approach-Reference-Cited by-同舟云学术

Enantioselective Synthesis of Pyrrolidine-, Piperidine-, and Azepane-Type N-Heterocycles with α-Alkenyl Substitution: The CpRu-Catalyzed Dehydrative Intramolecular N-Allylation Approach

Published:2011-12-23 Issue:2 Volume:14 Page:608-611
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Seki Tomoaki¹,Tanaka Shinji¹,Kitamura Masato¹

Affiliation:

1. Research Center for Materials Science and the Department of Chemistry, Nagoya University, Chikusa, Nagoya 464-8602, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol203218d

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3. bVicario, J. L.; Badía, D.; Carrillo, L.; Ruiz, N.; Reyes, E.InTargets in Heterocyclic Systems: Chemistry & Properties;Spinelli, D.; Attanasi, O. A., Eds.Societá Chimica Italiana:Rome, 2008; Vol.12, pp302–327.

4. Chiral Oxazolopiperidone Lactams: Versatile Intermediates for the Enantioselective Synthesis of Piperidine-Containing Natural Products

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