A DFT study on the mechanism and selectivity of [3 + 2] cycloaddition reactions leading to pyrole[2,1-a] phthalazine compounds
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry
Link
https://link.springer.com/content/pdf/10.1007/s00214-021-02756-7.pdf
Reference43 articles.
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2. Druta II, Andrei MA, Ganj CI, Aburel PS (1999) Synthesis of indolizine derivatives by the reaction of 2-(2′-pyridyl)-pyridinium ylides with ethylenic dipolarophiles. Tetrahedron 55:13063–13070. https://doi.org/10.1016/S0040-4020(99)00798-X
3. Elender K, Nöth H, Riebel P et al (2000) 1,3-Dipolar cycloaddition reactions of stable bicyclic and monocyclic azomethine ylides: preparative aspects. Tetrahedron 56:5443–5463. https://doi.org/10.1016/S0040-4020(00)00453-1
4. Tsuge O, Kanemasa S, Sakamoto K, Takenaka S (1988) Cycloaddition reactions of highly stabilized isoquinolinium methylides to nonactivated olefins and electron-rich olefins. Bull Chem Soc Jpn 61:2513–2524. https://doi.org/10.1246/bcsj.61.2513
5. Miki Y, Hachiken H, Takemura S, Ikeda M (1984) Novel synthesis and 1,3-dipolar cycloaddition reaction of pyridinium N-methylide. Heterocycles 22:701. https://doi.org/10.3987/R-1984-04-0701
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