Synthetic Studies and Mechanistic Insight in Nickel-Catalyzed [4+2+1] Cycloadditions-Reference-Cited by-同舟云学术

Synthetic Studies and Mechanistic Insight in Nickel-Catalyzed [4+2+1] Cycloadditions

Published:2006-02-03 Issue:8 Volume:128 Page:2609-2614
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ni Yike¹,Montgomery John¹

Affiliation:

1. Contribution from the Department of Chemistry, Wayne State University, Detroit, Michigan 48202-3489, and Department of Chemistry, University of Michigan, 930 North University, Ann Arbor, Michigan 48109-1055

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja057741q

Reference54 articles.

1. Nickel-catalyzed intramolecular [4 + 4]-cycloadditions: a new method for the synthesis of polycycles containing eight-membered rings

2. Transition Metal Catalyzed [5 + 2] Cycloadditions of Vinylcyclopropanes and Alkynes: A Homolog of the Diels-Alder Reaction for the Synthesis of Seven-Membered Rings

3. Transition metal template controlled cycloaddition reactions. An efficient chromium(0)-mediated [6.pi. + 2.pi.] cycloaddition

4. Metal-promoted higher-order cycloaddition reactions. Stereochemical, regiochemical, and mechanistic aspects of the [6.pi. + 4.pi.] reaction

5. Intermolecular Transition Metal-Catalyzed [4 + 2 + 2] Cycloaddition Reactions: A New Approach to the Construction of Eight-Membered Rings

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