Publications
2024
Reductive Transamination of Pyridinium Salts to N-Aryl Piperidines.
Chen, Z., Song, G., Qi, L., Gunasekar, R., Aïssa, C., Robertson, C., . . . Xiao, J. (2024). Reductive Transamination of Pyridinium Salts to N-Aryl Piperidines.. The Journal of organic chemistry, 89(13), 9352-9359. doi:10.1021/acs.joc.4c00493
2023
Storage without strain
Aïssa, C. (n.d.). Storage without strain. Nature Synthesis, 2(6), 478-480. doi:10.1038/s44160-023-00290-x
Cyclic Sulfoxonium Ylides: Synthesis and Chemospecific Reactivity in the Catalytic Alkylation of Indoles
Caiuby, C. A. D., Vidal, L., Burtoloso, A. C. B., & Aissa, C. (2023). Cyclic Sulfoxonium Ylides: Synthesis and Chemospecific Reactivity in the Catalytic Alkylation of Indoles. CHEMCATCHEM, 15(7). doi:10.1002/cctc.202201643
2022
Enantioselective Intramolecular Iridium-Catalyzed Cyclopropanation of α-Carbonyl Sulfoxonium Ylides
Vidal, L., Chen, P. -P., Nicolas, E., Hackett, A., Robertson, C. M., Houk, K. N., & Aissa, C. (2022). Enantioselective Intramolecular Iridium-Catalyzed Cyclopropanation of α-Carbonyl Sulfoxonium Ylides. ORGANIC LETTERS, 24(46), 8503-8508. doi:10.1021/acs.orglett.2c03396
Synthesis of Sulfur-Substituted Bicyclo[1.1.1]pentanes by Iodo-Sulfenylation of [1.1.1]Propellane
Livesley, S., Trueman, B., Robertson, C. M., Goundry, W. R. F., Morris, J. A., & Aissa, C. (2022). Synthesis of Sulfur-Substituted Bicyclo[1.1.1]pentanes by Iodo-Sulfenylation of [1.1.1]Propellane. ORGANIC LETTERS, 24(38), 7015-7020. doi:10.1021/acs.orglett.2c02875
Tandem Nickel-Catalyzed Dimerization/(4+2) Cycloaddition of Terminal Alkynes with Four-Membered Ring Ketones
Barday, M., Nicolas, E., Higginson, B., Delmotte, F., Appelmans, M., & Aissa, C. (2022). Tandem Nickel-Catalyzed Dimerization/(4+2) Cycloaddition of Terminal Alkynes with Four-Membered Ring Ketones. SYNTHESIS-STUTTGART, 54(04), 1081-1090. doi:10.1055/a-1671-8497
Electrophilic Activation of [1.1.1]Propellane for the Synthesis of Nitrogen-Substituted Bicyclo[1.1.1]pentanes
Livesley, S., Sterling, A. J., Robertson, C. M., Goundry, W. R. F., Morris, J. A., Duarte, F., & Aissa, C. (2022). Electrophilic Activation of [1.1.1]Propellane for the Synthesis of Nitrogen-Substituted Bicyclo[1.1.1]pentanes. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 61(2). doi:10.1002/ange.202111291
Electrophilic Activation of [1.1.1]Propellane for the Synthesis of Nitrogen‐Substituted Bicyclo[1.1.1]pentanes
Livesley, S., Sterling, A. J., Robertson, C. M., Goundry, W. R. F., Morris, J. A., Duarte, F., & Aïssa, C. (2022). Electrophilic Activation of [1.1.1]Propellane for the Synthesis of Nitrogen‐Substituted Bicyclo[1.1.1]pentanes. Angewandte Chemie, 134(2). doi:10.1002/ange.202111291
2020
Palladium-Catalyzed Synthesis of α-Carbonyl-α′-(hetero)aryl Sulfoxonium Ylides: Scope and Insight into the Mechanism
Janot, C., Chagnoleau, J. -B., Halcovitch, N. R., Muir, J., & Aissa, C. (2020). Palladium-Catalyzed Synthesis of α-Carbonyl-α′-(hetero)aryl Sulfoxonium Ylides: Scope and Insight into the Mechanism. JOURNAL OF ORGANIC CHEMISTRY, 85(2), 1126-1137. doi:10.1021/acs.joc.9b03032
2019
Chemospecific Cyclizations of α‐Carbonyl Sulfoxonium Ylides on Aryls and Heteroaryls
Clare, D., Dobson, B. C., Inglesby, P. A., & Aïssa, C. (2019). Chemospecific Cyclizations of α‐Carbonyl Sulfoxonium Ylides on Aryls and Heteroaryls. Angewandte Chemie, 131(45), 16344-16348. doi:10.1002/ange.201910821
Chemospecific Cyclizations of α-Carbonyl Sulfoxonium Ylides on Aryls and Heteroaryls
Clare, D., Dobson, B. C., Inglesby, P. A., & Aissa, C. (2019). Chemospecific Cyclizations of α-Carbonyl Sulfoxonium Ylides on Aryls and Heteroaryls. Angewandte Chemie (International Edition), 58(45), 16198-16202. doi:10.1002/anie.201910821
Palladium-Catalyzed Synthesis of Bis-Substituted Sulfoxonium Ylides
Janot, C., Palamini, P., Dobson, B. C., Muir, J., & Aissa, C. (2019). Palladium-Catalyzed Synthesis of Bis-Substituted Sulfoxonium Ylides. ORGANIC LETTERS, 21(1), 296-299. doi:10.1021/acs.orglett.8b03744
Regioselective cycloaddition of potassium alkynyltrifluoroborates with 3-azetidinones and 3-oxetanone by nickel-catalysed C-C bond activation
Elwrfalli, F., Esvan, Y. J., Robertson, C. M., & Aissa, C. (2019). Regioselective cycloaddition of potassium alkynyltrifluoroborates with 3-azetidinones and 3-oxetanone by nickel-catalysed C-C bond activation. CHEMICAL COMMUNICATIONS, 55(4), 497-500. doi:10.1039/c8cc09241a
2017
Cross-Coupling of α-Carbonyl Sulfoxonium Ylides with C-H Bonds
Barday, M., Janot, C., Halcovitch, N. R., Muir, J., & Aïssa, C. (2017). Cross-Coupling of α-Carbonyl Sulfoxonium Ylides with C-H Bonds. Angewandte Chemie International Edition, 56(42), 13117-13121. doi:10.1002/anie.201706804
Cross-Coupling of α-carbonyl sulfoxonium ylides with C-H bonds
Barday, M., Janot, C., Halcovitch, N. R., Muir, J., & Aïssa, C. (2017). Cross‐Coupling of α‐Carbonyl Sulfoxonium Ylides with C−H Bonds. Angewandte Chemie, 129(42), 13297-13301. doi:10.1002/ange.201706804
On the Regioselectivity of the Nickel-Catalyzed Insertion of Alkynes into the Carbon-Carbon Bond of Oxetan-3-one
Barday, M., Janot, C., Clare, D., Carr-Knox, C., Higginson, B., Ho, K. Y. T., & Aissa, C. (2017). On the Regioselectivity of the Nickel-Catalyzed Insertion of Alkynes into the Carbon-Carbon Bond of Oxetan-3-one. SYNTHESIS-STUTTGART, 49(16), 3582-3589. doi:10.1055/s-0036-1589052
2016
Cleavage of Carbon–Carbon Single Bonds by Transition Metals. Herausgegeben von Masahiro Murakami und Naoto Chatani.
Aïssa, C. (2016). Cleavage of Carbon–Carbon Single Bonds by Transition Metals. Herausgegeben von Masahiro Murakami und Naoto Chatani.. Angewandte Chemie, 128(26), 7409. doi:10.1002/ange.201604142
Regioselective Synthesis of 3-Hydroxy-4,5-alkyl-Substituted Pyridines Using 1,3-Enynes as Alkynes Surrogates
Barday, M., Ho, K. Y. T., Halsall, C. T., & Aissa, C. (2016). Regioselective Synthesis of 3-Hydroxy-4,5-alkyl-Substituted Pyridines Using 1,3-Enynes as Alkynes Surrogates. Organic Letters, 18(8), 1756-1759. doi:10.1021/acs.orglett.6b00451
The synthesis and biological evaluation of a kabiramide C fragment modified with a WH2 consensus actin-binding motif as a potential disruptor of the actin cytoskeleton
Tetlow, D. J., Winder, S. J., & Aissa, C. (2016). The synthesis and biological evaluation of a kabiramide C fragment modified with a WH2 consensus actin-binding motif as a potential disruptor of the actin cytoskeleton. CHEMICAL COMMUNICATIONS, 52(4), 807-810. doi:10.1039/c5cc06081h
2015
ChemInform Abstract: Isomerization of Olefins Triggered by Rhodium‐Catalyzed C—H Bond Activation: Control of Endocyclic β‐Hydrogen Elimination.
Yip, S. Y. Y., & Aissa, C. (2015). ChemInform Abstract: Isomerization of Olefins Triggered by Rhodium‐Catalyzed C—H Bond Activation: Control of Endocyclic β‐Hydrogen Elimination.. ChemInform, 46(40). doi:10.1002/chin.201540040
Isomerization of Olefins Triggered by Rhodium-Catalyzed C-H Bond Activation: Control of Endocyclic beta-Hydrogen Elimination
Yip, Y. Y., & Aissa, C. (2015). Isomerization of Olefins Triggered by Rhodium-Catalyzed C-H Bond Activation: Control of Endocyclic beta-Hydrogen Elimination. Angewandte Chemie International Edition, 54(23), 6870-6873. doi:10.1002/anie.201500596
2014
Stereoselectivity of Metal-Catalyzed Cyclizations of 1,6-Dienes
Aissa, C. (2014). Stereoselectivity of Metal-Catalyzed Cyclizations of 1,6-Dienes. SYNLETT, 25(17), 2379-2384. doi:10.1055/s-0034-1378531
'Diastereoselective Carbocyclization of 1,6-Heptadienes Triggered by Rhodium-Catalyzed Activation of an Olefinic C-H Bond'
Aissa, C., Ho, K. Y. T., Tetlow, D. J., & Pin-No, M. (2014). 'Diastereoselective Carbocyclization of 1,6-Heptadienes Triggered by Rhodium-Catalyzed Activation of an Olefinic C-H Bond'. Angewandte Chemie International Edition, 53(16), 4209-4212. doi:10.1002/anie.201400080
5.35 Transition-Metal-Catalyzed Cycloaddition of Small Ring Compounds
Aïssa, C. (2014). 5.35 Transition-Metal-Catalyzed Cycloaddition of Small Ring Compounds. In Comprehensive Organic Synthesis II (pp. 1738-1771). Elsevier. doi:10.1016/b978-0-08-097742-3.00536-x
2013
Multiple Rhodium-Catalyzed Cleavages of Single C-C bonds
Aissa, C., Crepin, D., Tetlow, D. J., & Ho, K. Y. T. (2013). Multiple Rhodium-Catalyzed Cleavages of Single C-C bonds. ORGANIC LETTERS, 15(6), 1322-1325. doi:10.1021/ol400266g
2012
Regioselective Cycloaddition of 3-Azetidinones and 3-Oxetanones with Alkynes through Nickel-Catalysed Carbon-Carbon Bond Activation
Ho, K. Y. T., & Aissa, C. (2012). Regioselective Cycloaddition of 3-Azetidinones and 3-Oxetanones with Alkynes through Nickel-Catalysed Carbon-Carbon Bond Activation. CHEMISTRY-A EUROPEAN JOURNAL, 18(12), 3486-3489. doi:10.1002/chem.201200167
2011
Transition-Metal-Catalyzed Rearrangements of Small Cycloalkanes: Regioselectivity Trends in β-Carbon Elimination Reactions
Aissa, C. (2011). Transition-Metal-Catalyzed Rearrangements of Small Cycloalkanes: Regioselectivity Trends in β-Carbon Elimination Reactions. SYNTHESIS-STUTTGART, (21), 3389-3407. doi:10.1055/s-0030-1260233
Facile and chemoselective rhodium-catalysed intramolecular hydroacylation of α,α-disubstituted 4-alkylidenecyclopropanals.
Crépin, D., Tugny, C., Murray, J. H., & Aïssa, C. (2011). Facile and chemoselective rhodium-catalysed intramolecular hydroacylation of α,α-disubstituted 4-alkylidenecyclopropanals.. Chemical communications (Cambridge, England), 47(39), 10957-10959. doi:10.1039/c1cc14626b
2010
Combined Rhodium-Catalyzed Carbon-Hydrogen Activation and β-Carbon Elimination to access Eight-Membered Rings
Crepin, D., Dawick, J., & Aissa, C. (2010). Combined Rhodium-Catalyzed Carbon-Hydrogen Activation and β-Carbon Elimination to access Eight-Membered Rings. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 49(3), 620-623. doi:10.1002/anie.200904527
Combined Rhodium‐Catalyzed Carbon–Hydrogen Activation and β‐Carbon Elimination to access Eight‐Membered Rings
Crépin, D., Dawick, J., & Aïssa, C. (2010). Combined Rhodium‐Catalyzed Carbon–Hydrogen Activation and β‐Carbon Elimination to access Eight‐Membered Rings. Angewandte Chemie, 122(3), 630-633. doi:10.1002/ange.200904527
2009
Mechanistic Manifold and New Developments of the Julia–Kocienski Reaction
Aïssa, C. (2009). Mechanistic Manifold and New Developments of the Julia–Kocienski Reaction. European Journal of Organic Chemistry, 2009(12), 1831-1844. doi:10.1002/ejoc.200801117