Stereodefined N,O-Acetals: Pd-Catalyzed Synthesis from Homopropargylic Amines and Utility in the Flexible Synthesis of 2,6-Substituted Piperidines-Reference-Cited by-同舟云学术

Stereodefined N,O-Acetals: Pd-Catalyzed Synthesis from Homopropargylic Amines and Utility in the Flexible Synthesis of 2,6-Substituted Piperidines

Published:2012-02-27 Issue:9 Volume:134 Page:4011-4014
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kim Haejin¹,Rhee Young Ho¹

Affiliation:

1. Department of Chemistry, Pohang University of Science and Technology, Hyoja-dong San 31, Pohang, Kyungbuk, Republic of Korea 790-784

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja2116298

Reference45 articles.

1. For a review on the use ofN,O-acetals, see:Warriner, S.Category 4: Compounds with Two Carbon-Heteroatom Bonds in Science of Synthesis: Houben-Weyl Methods of Molecular Transformations;Georg Thieme Verlag:Stuttguart; 2007; Vol30, p7.

2. A New Asymmetric Synthesis of trans-Hydroisoquinolones

3. A ring-closing metathesis-mediated route to novel enantiopure conformationally restricted cyclic amino acids

4. Catalytic N-Sulfonyliminium Ion-Mediated Cyclizations to α-Vinyl-Substituted Isoquinolines and β-Carbolines and Applications in Metathesis

5. Stereoselective reactions of N-acyl-N,O-acetals with 2-(trimethysilyloxy)furan

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