Metal-Free α-Amination of Secondary Amines: Computational and Experimental Evidence for Azaquinone Methide and Azomethine Ylide Intermediates-Reference-Cited by-同舟云学术

Metal-Free α-Amination of Secondary Amines: Computational and Experimental Evidence for Azaquinone Methide and Azomethine Ylide Intermediates

Published:2013-04-02 Issue:8 Volume:78 Page:4132-4144
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dieckmann Arne¹,Richers Matthew T.²,Platonova Alena Yu.²³,Zhang Chen²,Seidel Daniel²,Houk K. N.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States

2. Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, United States

3. Department of Organic Synthesis Technology, Ural Federal University, Yekaterinburg, 620002, Russia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo400483h

Reference147 articles.

1. Hiersemann, M.InComprehensive Organic Functional Group Transformations II;Katritzky, A. R. T., Richard, J. K., Ed.Elsevier:Oxford, 2005; Vol.4, p411.

2. aHino, T.; Nakagawa, M.InAlkaloids;Academic Press:New York, 1988; Vol.34, p1.

3. Total Synthesis of (±)-Isoschizogamine

4. Total Syntheses of (−)-Fumiquinazolines C, E, and H

5. Concise Total Synthesis of (−)-Calycanthine, (+)-Chimonanthine, and (+)-Folicanthine

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