Highly Diastereoselective Arylations of Substituted Piperidines-Reference-Cited by-同舟云学术

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Highly Diastereoselective Arylations of Substituted Piperidines

Published:2011-03-09 Issue:13 Volume:133 Page:4774-4777
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Seel Stephanie¹,Thaler Tobias¹,Takatsu Keishi²,Zhang Cong¹,Zipse Hendrik¹,Straub Bernd F.³,Mayer Peter¹,Knochel Paul¹

Affiliation:

1. Department Chemie, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, Haus F, 81377 Munich, Germany

2. Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan

3. Organisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja201008e

Reference56 articles.

1. Recent advances in the stereoselective synthesis of trans-3,4-disubstituted-piperidines: applications to (−)-paroxetine

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

3. Synthesis of piperidines

4. Recent Advances in the Total Synthesis of Piperidine and Pyrrolidine Natural Alkaloids with Ring‐Closing Metathesis as a Key Step

5. Stereoselective Synthesis of Piperidines

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