Electroauxiliary-Assisted Sequential Introduction of Two Carbon Nucleophiles on the Same α-Carbon of Nitrogen: Application to the Synthesis of Spiro Compounds-Reference-Cited by-同舟云学术

Electroauxiliary-Assisted Sequential Introduction of Two Carbon Nucleophiles on the Same α-Carbon of Nitrogen: Application to the Synthesis of Spiro Compounds

Published:2002-11-21 Issue:50 Volume:124 Page:14824-14825
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Suga Seiji¹,Watanabe Mitsuru¹,Yoshida Jun-ichi¹

Affiliation:

1. Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 606-8501, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja028663z

Reference31 articles.

1. Electroorganic chemistry. 46. A new carbon-carbon bond forming reaction at the .alpha.-position of amines utilizing anodic oxidation as a key step

2. A new [3 + 3]-type annelation useful for the formation of piperidine skeletons

3. Synthetic Applications of Anodic Electrochemistry

4. Regioselective, Diastereoselective, and Enantioselective Lithiation−Substitution Sequences: Reaction Pathways and Synthetic Applications

5. Complex Induced Proximity Effects: Enantioselective Syntheses Based on Asymmetric Deprotonations of N-Boc-pyrrolidines

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