RhI-Catalyzed Cycloaddition between Allenyl π-Bonds and C-C Triple Bonds
Author:
Affiliation:
1. Division of Pharmaceutical Sciences, Graduate School of Medical Sciences, Kanazawa University
Publisher
The Society of Synthetic Organic Chemistry, Japan
Subject
Organic Chemistry
Link
https://www.jstage.jst.go.jp/article/yukigoseikyokaishi/74/11/74_1108/_pdf
Reference136 articles.
1. 1) (a) Landor, S. R. The chemistry of the allenes; Academic: London, 1982.
2. (b) Schuster, H. F.; Coppola, G. M. Allenes in Organic Synthesis; Wiley: New York, 1984.
3. (c) Pasto, D. J. Tetrahedron 1984, 40, 2805.
4. (d) Zimmer, R.; Dinesh, C. U.; Nandanan, E.; Khan, F. A. Chem. Rev. 2000, 100, 3067.
5. (e) Hashmi, A. S. K. Angew. Chem. Int. Ed. 2000, 39, 3590.
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2. Computational Study on Mechanisms and Origins of Selectivities in Rh(I)-Catalyzed Cycloisomerizations of 1,6-Allenynes with Tethered Unsaturated Carbon–Carbon Bonds;ACS Catalysis;2021-04-05
3. A Comparison between the Cycloadditions of Allenyl- and Vinyl-Cyclopentanes Using Density Functional Theory and GRRM Program;Chemical and Pharmaceutical Bulletin;2020-08-01
4. Enantioselective Rhodium-Catalyzed Cycloisomerization of 1,6-Allenynes to access 5/6-Fused Bicycle[4.3.0]nonadienes;Nature Communications;2019-02-27
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