The reactivity enhancement in Diels–Alder cycloaddition of 1,3-diene by cation encapsulation to C60: a computational insight
Author:
Funder
Ferdowsi University of Mashhad
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
https://link.springer.com/content/pdf/10.1007/s11224-020-01538-4.pdf
Reference44 articles.
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2. Wu J, Xu W, Yu Z-X, Wang J (2015) Ruthenium-catalyzed formal dehydrative [4 + 2] cycloaddition of Enamides and alkynes for the synthesis of highly substituted pyridines: reaction development and mechanistic study. J Am Chem Soc 137:9489–9496
3. Liu L, Kim H, Xie Y, Farès C, Kaib PSJ, Goddard R, List B (2017) Catalytic asymmetric [4+2]-cycloaddition of dienes with aldehydes. J Am Chem Soc 139:13656–13659
4. Kim HJ, Ruszczycky MW, Choi S-h, Liu Y-n, Liu H-w (2011) Enzyme-catalysed [4+2] cycloaddition is a key step in the biosynthesis of spinosyn a. Nature 473:109–112
5. Heravi MM, Ahmadi T, Ghavidel M, Heidari B, Hamidi H (2015) Recent applications of the hetero Diels–Alder reaction in the total synthesis of natural products. RSC Adv 5:101999–102075
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1. Diels–Alder cycloadditions of fullerene: Advances in mechanistic theory;Journal of Physical Organic Chemistry;2023-10-24
2. Reactivity of the superhalogen/superalkali ion encapsulating C60 fullerenes;Dalton Transactions;2022
3. Computational insights into the multi‐Diels–Alder reactions of neutral C 60 and its Li + encapsulated analogue: A density functional theory study;International Journal of Quantum Chemistry;2021-10-23
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