Revealing the cyclization selectivity in intramolecular [3 + 2] cycloaddition reactions of allenic nitrones from the molecular electron density theory perspective
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
https://link.springer.com/content/pdf/10.1007/s11224-023-02175-3.pdf
Reference60 articles.
1. Pinho e Melo TM (2009) Allenes as dipolarophiles and 1,3-dipole precursors: synthesis of carbocyclic and heterocyclic compounds. Curr Org Chem 13:1406–1431. https://doi.org/10.2174/138527209789055090
2. Padwa A, Tomioka Y, Venkatramanan MK (1987) A study of the 5-exo methylene-isoxazolidine to 3-pyrrolidinone rearrangement. Tetrahedron Lett 28:755–758. https://doi.org/10.1016/S0040-4039(01)80981-3
3. Padwa A, Matzinger M, Tomioka Y, Venkatramanan MK (1988) Study of the thermal transformation of the 5-exo methyleneisoxazolidines to 3-pyrrolidinones. J Org Chem 53:955–963. https://doi.org/10.1021/jo00240a005
4. Padwa A, Kline DN, Koehler KF, Matzinger M, Venkatramanan MK (1987) Cycloaddition of nitrones with allenes. An example of steric control of regiochemistry. J Org Chem 52:3909–3917. https://doi.org/10.1021/jo00226a035
5. Padwa A, Carter SP, Chiacchio U, Kline DN (1986) Dipolar cycloaddition reaction of (phenylsulfonyl)propadiene with nitrones and alkylation studies of the cycloadducts. Tetrahedron Lett 27:2683–2686. https://doi.org/10.1016/S0040-4039(00)84616-X
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