23 results on '"Pesquet, Anthony"'
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2. Access to 3-spiroindolizines containing an isoindole ring through intra-molecular arylation of spiro- N -acyliminium species: a new family of potent farnesyltransferase inhibitors
3. General and versatile entry to 4,5-fused polycyclic imidazolones systems. Use of the tandem transposition/pi-cyclization of N-acyliminium species
4. Combining α-amidoalkylation reactions of N-acyliminium ions with ring-closing metathesis: access to versatile novel isoindolones spirocyclic compounds
5. An Unusual Polyheterocyclic Diversity by the π-Cyclisation of N -Carbamoyliminium Ion, with or without Tandem N , N -Acetal Cleavage, from Spiro(imidazolidinoquinazolinones)
6. General and Versatile Entry to Polycyclic Imidazolidinones: Use of N-acyliminium Chemistry in Domino Process
7. Access to the New Isoindolo[1,3]benzothiazocinones via the Combination of N-Acyliminium Chemistry and Friedel—Crafts Type π-Cyclization
8. Heterocyclization-Transposition-Isomerisation of N-acyliminium ion. Domino Process to Accede New Tricyclic Thiolactams
9. Use of the Newly Heterocyclization/Double Transposition/Isomerisation of N-acyliminium ion Cascade to Access Tricyclic Thiolactams
10. Use of the Newly Heterocyclization/ Double Transposition/Isomerisation of N-acyliminium ion Cascade to Access Tricyclic Thiolactams
11. ChemInform Abstract: Combining α‐Amidoalkylation Reactions of N‐Acyliminium Ions with Ring‐Closing Metathesis: Access to Versatile Novel Isoindolones Spirocyclic Compounds.
12. Use of the cascade α-oxo-amidoalkylation/transposition/ p-cationic cyclization of N-acyliminium ions in the synthesis of novel fused heterocyclic N,O-acetals
13. An Unusual Polyheterocyclic Diversity by the π-Cyclisation of N-Carbamoyliminium Ion, with or without Tandem N,N-Acetal Cleavage, from Spiro(imidazolidinoquinazolinones)
14. General and Versatile Entry to 4,5‐Fused Polycyclic Imidazolones Systems. Use of the Tandem Transposition/π‐Cyclization of N‐Acyliminium Species.
15. Acid-Catalyzed Formation of Tricyclic N,S-Acetals in Imidazolinone Series Based on the Use of the Unprecedented N-Acyliminium Ion Cascade Reaction Involving Transposition, Heterocyclization and π-Cyclization.
16. Exocyclic–Endocyclic N‐Acyliminium Ion Equilibration via an Intramolecular α‐Thioamidoalkylation in the Synthesis of Fused N,S‐Heterocyclic Systems: Some New Parameters
17. Acid-catalysed formation of tricyclic N,S-acetals in imidazolinone series based on the use of the unprecedented N-acyliminium ion cascade reaction involving transposition, heterocyclisation and π-cyclisation
18. Evaluation of N-Hydroxymethylphthalimide in Alkaline Medium: Novel Entry to the Tricyclic [1,3]Oxazepine Core via an Intramolecular π and O-Cationic Cyclization.
19. Use of the cascade α-oxo-amidoalkylation / transposition / π-cationic cyclization of N-acyliminium ions in the synthesis of novel fused heterocyclic N,O-acetals.
20. Evaluation of N-hydroxymethylphthalimide in alkaline medium: Novel entry to the tricyclic [1,3]oxazepine core via an intramolecular π and O-cationic cyclization.
21. Evaluation of Nhydroxymethylphthalimide in alkaline medium: Novel entry to the tricyclic 1,3oxazepine core viaan intramolecular π and Ocationic cyclization
22. Access to 3-spiroindolizines containing an isoindole ring through intra-molecular arylation of spiro-N-acyliminium species: a new family of potent farnesyltransferase inhibitors.
23. Acid-catalysed formation of tricyclic N,S-acetals in imidazolinone series based on the use of the unprecedented N-acyliminium ion cascade reaction involving transposition, heterocyclisation and pi-cyclisation.
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