Highly Diastereoselective Synthesis of Tetrahydropyridines by a C–H Activation–Cyclization–Reduction Cascade-Reference-Cited by-同舟云学术

Highly Diastereoselective Synthesis of Tetrahydropyridines by a C–H Activation–Cyclization–Reduction Cascade

Published:2012-02-22 Issue:9 Volume:134 Page:4064-4067
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Duttwyler Simon¹,Lu Colin¹,Rheingold Arnold L.²,Bergman Robert G.³,Ellman Jonathan A.¹

Affiliation:

1. Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States

2. Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093, United States

3. Division of Chemical Sciences, Lawrence Berkeley National Laboratory, and Department of Chemistry, University of California, Berkeley, California 94720, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja2119833

Reference69 articles.

1. One-Pot Synthesis of Isoquinolinium Salts by Rhodium-Catalyzed CH Bond Activation: Application to the Total Synthesis of Oxychelerythrine

2. Regioselective Pd-Catalyzed Aerobic Aza-Wacker Cyclization for Preparation of Isoindolinones and Isoquinolin-1(2H)-ones

3. N-Fused Indolines through Non-Carbonyl-Stabilized Rhodium Carbenoid CH Insertion of N-Aziridinyl Imines

4. Rhodium(III)-Catalyzed Heterocycle Synthesis Using an Internal Oxidant: Improved Reactivity and Mechanistic Studies

5. The Vinyl Moiety as a Handle for Regiocontrol in the Preparation of Unsymmetrical 2,3-Aliphatic-Substituted Indoles and Pyrroles

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