| Year |
Citation |
Score |
| 2022 |
Smith SN, Trujillo C, Connon SJ. Catalytic, asymmetric azidations at carbonyls: achiral and -anhydride desymmetrisation affords enantioenriched γ-lactams. Organic & Biomolecular Chemistry. PMID 35861618 DOI: 10.1039/d2ob01040b |
0.687 |
|
| 2021 |
Litvajova M, Sorrentino E, Twamley B, Connon SJ. Base-free enantioselective S2 alkylation of 2-oxindoles via bifunctional phase-transfer catalysis. Beilstein Journal of Organic Chemistry. 17: 2287-2294. PMID 34621391 DOI: 10.3762/bjoc.17.146 |
0.439 |
|
| 2021 |
Cronin SA, Connon SJ. The kinetic resolution of oxazinones by alcoholysis: access to orthogonally protected β-amino acids. Organic & Biomolecular Chemistry. 19: 7348-7352. PMID 34387643 DOI: 10.1039/d1ob01306h |
0.309 |
|
| 2020 |
Delany EG, Connon SJ. Enantioselective N-heterocyclic carbene-catalysed intermolecular crossed benzoin condensations: improved catalyst design and the role of racemisation. Organic & Biomolecular Chemistry. PMID 33289760 DOI: 10.1039/d0ob02017f |
0.488 |
|
| 2020 |
Smith SN, Craig R, Connon SJ. Divergent Synthesis of γ-Amino Acid and γ-Lactam Derivatives from meso-Glutaric Anhydrides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32996163 DOI: 10.1002/chem.202003280 |
0.611 |
|
| 2019 |
Maguire AC, Kumar V, Connon SJ. Highly chemoselective, sterically sensitive NHC-catalysed amine acylation with pyridil. Chemical Communications (Cambridge, England). PMID 31650988 DOI: 10.1039/C9Cc06937B |
0.572 |
|
| 2019 |
Lockett-Walters B, Trujillo C, Twamley B, Connon S. The base-catalysed Tamura cycloaddition reaction: calculation, mechanism, isolation of intermediates and asymmetric catalysis. Chemical Communications (Cambridge, England). PMID 31475708 DOI: 10.1039/C9Cc05064G |
0.52 |
|
| 2019 |
Connon S, Farid U, Aiello ML. Highly Enantioselective Catalytic Kinetic Resolution of α-Branched Aldehydes via Formal Cycloaddition with Homophthalic Anhydrides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31173400 DOI: 10.1002/chem.201902422 |
0.45 |
|
| 2019 |
Collar AG, Trujillo C, Lockett-Walters B, Twamley B, Connon SJ. Catalytic Asymmetric γ-Lactam Synthesis from Enolisable Anhydrides and Imines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31050082 DOI: 10.1002/chem.201901028 |
0.443 |
|
| 2019 |
Collar AG, Trujillo C, Connon SJ. Highly Enantio- and Diastereoselective Catalytic Asymmetric Tamura Cycloaddition Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31050071 DOI: 10.1002/chem.201900119 |
0.456 |
|
| 2019 |
Trujillo C, Litvajova M, Cronin SA, Craig R, Connon SJ. The Steglich Rearrangement of 2‐Oxindole Derivatives Promoted by Anion‐based Nucleophilic Catalysis Chemcatchem. 11: 3776-3780. DOI: 10.1002/cctc.201900756 |
0.346 |
|
| 2018 |
Aiello ML, Farid U, Trujillo C, Twamley B, Connon SJ. Catalytic asymmetric cycloadditions between aldehydes and enolizable anhydrides: cis-selective dihydroisocoumarin formation. The Journal of Organic Chemistry. PMID 30461274 DOI: 10.1021/acs.joc.8b02332 |
0.458 |
|
| 2018 |
Claveau R, Twamley B, Connon SJ. Synthesis of α-alkylated γ-butyrolactones with concomitant anhydride kinetic resolution using a sulfamide-based catalyst. Organic & Biomolecular Chemistry. 16: 7574-7578. PMID 30307019 DOI: 10.1039/c8ob02248h |
0.457 |
|
| 2018 |
Craig R, Litvajova M, Cronin SA, Connon SJ. Enantioselective acyl-transfer catalysis by fluoride ions. Chemical Communications (Cambridge, England). PMID 30124692 DOI: 10.1039/c8cc05692g |
0.315 |
|
| 2018 |
Claveau R, Twamley B, Connon SJ. Dynamic kinetic resolution of bis-aryl succinic anhydrides: enantioselective synthesis of densely functionalised γ-butyrolactones. Chemical Communications (Cambridge, England). 54: 3231-3234. PMID 29533401 DOI: 10.1039/c8cc00609a |
0.338 |
|
| 2018 |
Craig R, Sorrentino E, Connon SJ. Enantioselective Alkylation of 2-Oxindoles Catalyzed by a Bifunctional Phase-Transfer Catalyst: Synthesis of (-)-Debromoflustramine B. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 4528-4531. PMID 29513404 DOI: 10.1002/chem.201800313 |
0.495 |
|
| 2018 |
Delany EG, Connon SJ. Highly chemoselective intermolecular cross-benzoin reactions using an ad hoc designed novel N-heterocyclic carbene catalyst. Organic & Biomolecular Chemistry. 16: 780-786. PMID 29319099 DOI: 10.1039/c7ob03005c |
0.447 |
|
| 2018 |
Roucan M, Kielmann M, Connon SJ, Bernhard SSR, Senge MO. Conformational control of nonplanar free base porphyrins: towards bifunctional catalysts of tunable basicity. Chemical Communications (Cambridge, England). 54: 26-29. PMID 29226923 DOI: 10.1039/C7Cc08099A |
0.352 |
|
| 2017 |
Kumar V, Connon SJ. Direct, efficient NHC-catalysed aldehyde oxidative amidation: in situ formed benzils as unconventional acylating agents. Chemical Communications (Cambridge, England). PMID 28861574 DOI: 10.1039/C7Cc05561G |
0.544 |
|
| 2017 |
Trujillo C, Rozas I, Botte A, Connon SJ. A DFT mechanistic study of the organocatalytic asymmetric reaction of aldehydes and homophthalic anhydride. Chemical Communications (Cambridge, England). PMID 28737812 DOI: 10.1039/c7cc04596d |
0.462 |
|
| 2017 |
Manoni F, Farid U, Trujillo C, Connon SJ. Catalytic asymmetric Tamura cycloadditions involving nitroalkenes. Organic & Biomolecular Chemistry. 15: 1463-1474. PMID 28112763 DOI: 10.1039/c6ob02637k |
0.439 |
|
| 2016 |
Sorrentino E, Connon SJ. Enantioselective Alkylative Kinetic Resolution of 2-Oxindole-Derived Enolates Promoted by Bifunctional Phase Transfer Catalysts. Organic Letters. PMID 27700121 DOI: 10.1021/acs.orglett.6b02398 |
0.464 |
|
| 2016 |
Cronin SA, Gutiérrez Collar A, Gundala S, Cornaggia C, Torrente E, Manoni F, Botte A, Twamley B, Connon SJ. The first catalytic asymmetric cycloadditions of imines with an enolisable anhydride. Organic & Biomolecular Chemistry. 14: 6955-9. PMID 27381361 DOI: 10.1039/c6ob00048g |
0.462 |
|
| 2016 |
Cornaggia C, Gundala S, Manoni F, Gopalasetty N, Connon SJ. Catalytic formal cycloadditions between anhydrides and ketones: excellent enantio and diastereocontrol, controllable decarboxylation and the formation of adjacent quaternary stereocentres. Organic & Biomolecular Chemistry. 14: 3040-6. PMID 26891029 DOI: 10.1039/c6ob00089d |
0.478 |
|
| 2015 |
Tallon S, Manoni F, Connon SJ. A practical aryl unit for azlactone dynamic kinetic resolution: orthogonally protected products and a ligation-inspired coupling process. Angewandte Chemie (International Ed. in English). 54: 813-7. PMID 25425156 DOI: 10.1002/anie.201406857 |
0.377 |
|
| 2014 |
Manoni F, Connon SJ. Catalytic asymmetric Tamura cycloadditions. Angewandte Chemie (International Ed. in English). 53: 2628-32. PMID 24573916 DOI: 10.1002/anie.201309297 |
0.422 |
|
| 2014 |
Connon SJ. Diaminocyclopropenylidene organocatalysts: beyond N-heterocyclic carbenes. Angewandte Chemie (International Ed. in English). 53: 1203-5. PMID 24285465 DOI: 10.1002/anie.201309256 |
0.484 |
|
| 2013 |
Myles L, Gathergood N, Connon SJ. The catalytic versatility of low toxicity dialkyltriazolium salts: in situ modification facilitates diametrically opposed catalysis modes in one pot. Chemical Communications (Cambridge, England). 49: 5316-8. PMID 23646348 DOI: 10.1039/C3Cc41588K |
0.342 |
|
| 2013 |
Kavanagh SA, Piccinini A, Connon SJ. The asymmetric synthesis of terminal aziridines by methylene transfer from sulfonium ylides to imines. Organic & Biomolecular Chemistry. 11: 3535-40. PMID 23598787 DOI: 10.1039/c3ob27271k |
0.427 |
|
| 2013 |
Connon S, Gleeson O, Gun'ko Y. (S)-Proline-Derived Catalysts for the Acylative Kinetic Resolution of Alcohols: A Remote Structural Change Allows a Complete Selectivity Switch Synlett. 24: 1728-1734. DOI: 10.1055/S-0033-1339286 |
0.352 |
|
| 2013 |
Gore RG, Myles L, Spulak M, Beadham I, Garcia TM, Connon SJ, Gathergood N. A new generation of aprotic yet Brønsted acidic imidazolium salts: effect of ester/amide groups in the C-2, C-4 and C-5 on antimicrobial toxicity and biodegradation Green Chemistry. 15: 2747. DOI: 10.1039/C3Gc40992A |
0.305 |
|
| 2013 |
Myles L, Gore RG, Gathergood N, Connon SJ. A new generation of aprotic yet Brønsted acidic imidazolium salts: low toxicity, high recyclability and greatly improved activity Green Chemistry. 15: 2740. DOI: 10.1039/C3Gc40975A |
0.358 |
|
| 2013 |
Palacio C, Connon SJ. C-5′-Substituted Cinchona Alkaloid Derivatives Catalyse the First Highly Enantioselective Dynamic Kinetic Resolutions of Azlactones by Thiolysis European Journal of Organic Chemistry. 2013: 5398-5413. DOI: 10.1002/EJOC.201300451 |
0.32 |
|
| 2013 |
Palacio C, Connon SJ. ChemInform Abstract: C-5′-Substituted Cinchona Alkaloid Derivatives Catalyse the First Highly Enantioselective Dynamic Kinetic Resolutions of Azlactones by Thiolysis. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201402049 |
0.321 |
|
| 2012 |
Curran SP, Connon SJ. The thiolate-catalyzed intermolecular crossed Tishchenko reaction: highly chemoselective coupling of two different aromatic aldehydes. Angewandte Chemie (International Ed. in English). 51: 10866-70. PMID 23011755 DOI: 10.1002/anie.201206343 |
0.355 |
|
| 2012 |
Piccinini A, Kavanagh SA, Connon SJ. Highly enantioselective ylide-mediated synthesis of terminal epoxides. Chemical Communications (Cambridge, England). 48: 7814-6. PMID 22785555 DOI: 10.1039/c2cc32101g |
0.459 |
|
| 2012 |
Manoni F, Cornaggia C, Murray J, Tallon S, Connon SJ. Catalytic, enantio- and diastereoselective synthesis of γ-butyrolactones incorporating quaternary stereocentres. Chemical Communications (Cambridge, England). 48: 6502-4. PMID 22622626 DOI: 10.1039/c2cc32147e |
0.485 |
|
| 2012 |
Cornaggia C, Manoni F, Torrente E, Tallon S, Connon SJ. A catalytic asymmetric reaction involving enolizable anhydrides. Organic Letters. 14: 1850-3. PMID 22449206 DOI: 10.1021/ol300453s |
0.448 |
|
| 2012 |
RodrÃguez-Docampo Z, Quigley C, Tallon S, Connon SJ. The dynamic kinetic resolution of azlactones with thiol nucleophiles catalyzed by arylated, deoxygenated cinchona alkaloids. The Journal of Organic Chemistry. 77: 2407-14. PMID 22353170 DOI: 10.1021/jo202662d |
0.431 |
|
| 2012 |
Palacio C, Connon SJ. A novel C-5' substituted cinchona alkaloid-derived catalyst promotes additions of alkyl thiols to nitroolefins with excellent enantioselectivity. Chemical Communications (Cambridge, England). 48: 2849-51. PMID 22322277 DOI: 10.1039/c2cc17965b |
0.492 |
|
| 2012 |
Curran SP, Connon SJ. Selenide ions as catalysts for homo- and crossed-Tishchenko reactions of expanded scope. Organic Letters. 14: 1074-7. PMID 22304722 DOI: 10.1021/ol203439g |
0.455 |
|
| 2012 |
Quigley C, RodrÃguez-Docampo Z, Connon SJ. Highly tunable arylated cinchona alkaloids as bifunctional catalysts. Chemical Communications (Cambridge, England). 48: 1443-5. PMID 21897955 DOI: 10.1039/c1cc14684j |
0.416 |
|
| 2012 |
Rose CA, Gundala S, Fagan C, Franz JF, Connon SJ, Zeitler K. ChemInform Abstract: NHC-Catalyzed, Chemoselective Crossed-Acyloin Reactions. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201229046 |
0.347 |
|
| 2012 |
Rodriquez-Docampo Z, Connon SJ. ChemInform Abstract: Organocatalytic Asymmetric Additions to meso-Anhydrides and Azlactones Cheminform. 43: no-no. DOI: 10.1002/CHIN.201216244 |
0.371 |
|
| 2011 |
Gleeson O, Davies GL, Peschiulli A, Tekoriute R, Gun'ko YK, Connon SJ. The immobilisation of chiral organocatalysts on magnetic nanoparticles: the support particle cannot always be considered inert. Organic & Biomolecular Chemistry. 9: 7929-40. PMID 21989817 DOI: 10.1039/C1Ob06110K |
0.486 |
|
| 2011 |
Palacio C, Connon SJ. A new class of urea-substituted cinchona alkaloids promote highly enantioselective nitroaldol reactions of trifluoromethylketones. Organic Letters. 13: 1298-301. PMID 21338077 DOI: 10.1021/ol103089j |
0.55 |
|
| 2011 |
O'Toole SE, Rose CA, Gundala S, Zeitler K, Connon SJ. Highly chemoselective direct crossed aliphatic-aromatic acyloin condensations with triazolium-derived carbene catalysts. The Journal of Organic Chemistry. 76: 347-57. PMID 20977280 DOI: 10.1021/jo101791w |
0.498 |
|
| 2011 |
Rose CA, Gundala S, Connon SJ, Zeitler K. Chemoselective crossed acyloin condensations: Catalyst and substrate control Synthesis. 190-198. DOI: 10.1055/s-0030-1258363 |
0.466 |
|
| 2011 |
O'Connor CJ, Manoni F, Curran SP, Connon SJ. Microwave-assisted efficient thiolate-catalysed homo- and crossed intermolecular Tishchenko reactions New Journal of Chemistry. 35: 551-553. DOI: 10.1039/c0nj00790k |
0.329 |
|
| 2011 |
O'Connor CJ, Manoni F, Curran SP, Connon SJ. ChemInform Abstract: Microwave-Assisted Efficient Thiolate-Catalyzed Homo- and Crossed Intermolecular Tishchenko Reactions. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201127077 |
0.376 |
|
| 2011 |
Rodriguez-Docampo Z, Connon SJ. Organocatalytic Asymmetric Additions tomeso-Anhydrides and Azlactones Chemcatchem. 4: 151-168. DOI: 10.1002/cctc.201100266 |
0.492 |
|
| 2010 |
Peschiulli A, Procuranti B, O' Connor CJ, Connon SJ. Synergistic organocatalysis in the kinetic resolution of secondary thiols with concomitant desymmetrization of an anhydride. Nature Chemistry. 2: 380-4. PMID 20414238 DOI: 10.1038/nchem.584 |
0.362 |
|
| 2010 |
Cronin L, Manoni F, O'Connor CJ, Connon SJ. Tunable bromomagnesium thiolate Tishchenko reaction catalysts: intermolecular aldehyde-trifluoromethylketone coupling. Angewandte Chemie (International Ed. in English). 49: 3045-8. PMID 20301157 DOI: 10.1002/anie.200907167 |
0.457 |
|
| 2010 |
Piccinini A, Kavanagh SA, Connon PB, Connon SJ. Catalytic (asymmetric) methylene transfer to aldehydes. Organic Letters. 12: 608-11. PMID 20055441 DOI: 10.1021/ol902816w |
0.507 |
|
| 2010 |
Connon S, Kavanagh S, Piccinini A. Organocatalytic Corey-Chaykovsky Reaction of Ketones Synfacts. 2010: 1418-1418. DOI: 10.1055/s-0030-1258931 |
0.364 |
|
| 2010 |
Myles L, Gore R, Špulák M, Gathergood N, Connon SJ. Highly recyclable, imidazolium derived ionic liquids of low antimicrobial and antifungal toxicity: A new strategy for acid catalysis Green Chemistry. 12: 1157. DOI: 10.1039/C003301D |
0.376 |
|
| 2010 |
Kavanagh SA, Piccinini A, Connon SJ. ChemInform Abstract: Efficient Catalytic Corey-Chaykovsky Reactions Involving Ketone Substrates. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201103096 |
0.448 |
|
| 2010 |
Randl S, Buschmann N, Connon SJ, Blechert S. ChemInform Abstract: Highly Efficient and Recyclable Polymer-Bound Catalyst for Olefin Metathesis Reactions. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200206063 |
0.611 |
|
| 2010 |
Randl S, Connon SJ, Blechert S. ChemInform Abstract: Ring Opening-Cross Metathesis of Unstrained Cycloalkenes. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200202079 |
0.441 |
|
| 2010 |
Connon SJ, Hegarty AF. ChemInform Abstract: Substituted 3,4-Pyridynes: Clean Cycloadditions. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200033142 |
0.602 |
|
| 2010 |
Kavanagh S, Piccinini A, Connon S. Efficient Catalytic Corey–Chaykovsky Reactions Involving Ketone Substrates Advanced Synthesis & Catalysis. 352: 2089-2093. DOI: 10.1002/ADSC.201000255 |
0.436 |
|
| 2009 |
Baragwanath L, Rose CA, Zeitler K, Connon SJ. Highly enantioselective benzoin condensation reactions involving a bifunctional protic pentafluorophenyl-substituted triazolium precatalyst. The Journal of Organic Chemistry. 74: 9214-7. PMID 19950884 DOI: 10.1021/jo902018j |
0.494 |
|
| 2009 |
O'Toole SE, Connon SJ. The enantioselective benzoin condensation promoted by chiral triazolium precatalysts: stereochemical control via hydrogen bonding. Organic & Biomolecular Chemistry. 7: 3584-93. PMID 19675916 DOI: 10.1039/b908517c |
0.398 |
|
| 2009 |
Gleeson O, Tekoriute R, Gun'ko YK, Connon SJ. The first magnetic nanoparticle-supported chiral DMAP analogue: highly enantioselective acylation and excellent recyclability. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 5669-73. PMID 19388038 DOI: 10.1002/chem.200900532 |
0.385 |
|
| 2009 |
Connon S, Procuranti B, Myles L, Gathergood N. Pyridinium Ion Catalysis of Carbonyl Protection Reactions Synthesis. 2009: 4082-4086. DOI: 10.1055/S-0029-1217022 |
0.406 |
|
| 2009 |
O'Toole SE, Connon SJ. The enantioselective benzoin condensation promoted by chiral triazolium precatalysts: Stereochemical control via hydrogen bonding Organic and Biomolecular Chemistry. 7: 3584-3593. DOI: 10.1039/b908517c |
0.4 |
|
| 2008 |
Procuranti B, Connon SJ. Unexpected catalysis: aprotic pyridinium ions as active and recyclable Brønsted acid catalysts in protic media. Organic Letters. 10: 4935-8. PMID 18837552 DOI: 10.1021/ol802008m |
0.459 |
|
| 2008 |
Peschiulli A, Quigley C, Tallon S, Gun'ko YK, Connon SJ. Organocatalytic asymmetric addition of alcohols and thiols to activated electrophiles: efficient dynamic kinetic resolution and desymmetrization protocols. The Journal of Organic Chemistry. 73: 6409-12. PMID 18646859 DOI: 10.1021/jo801158g |
0.523 |
|
| 2008 |
Connon SJ. Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts. Chemical Communications (Cambridge, England). 2499-510. PMID 18506226 DOI: 10.1039/b719249e |
0.431 |
|
| 2008 |
Kavanagh SA, Piccinini A, Fleming EM, Connon SJ. Urea derivatives are highly active catalysts for the base-mediated generation of terminal epoxides from aldehydes and trimethylsulfonium iodide. Organic & Biomolecular Chemistry. 6: 1339-43. PMID 18385839 DOI: 10.1039/b719767e |
0.701 |
|
| 2008 |
Peschiulli A, Gun'ko Y, Connon SJ. Highly enantioselective desymmetrization of meso anhydrides by a bifunctional thiourea-based organocatalyst at low catalyst loadings and room temperature. The Journal of Organic Chemistry. 73: 2454-7. PMID 18275219 DOI: 10.1021/jo702639h |
0.456 |
|
| 2008 |
Connon SJ. The catalytic asymmetric Strecker reaction: ketimines continue to join the fold. Angewandte Chemie (International Ed. in English). 47: 1176-8. PMID 18175297 DOI: 10.1002/anie.200703879 |
0.416 |
|
| 2008 |
Fleming EM, Quigley C, Rozas I, Connon SJ. Computational study-led organocatalyst design: a novel, highly active urea-based catalyst for addition reactions to epoxides. The Journal of Organic Chemistry. 73: 948-56. PMID 18173286 DOI: 10.1021/jo702154m |
0.736 |
|
| 2008 |
Noonan C, Baragwanath L, Connon SJ. Nucleophilic carbene-catalysed oxidative esterification reactions Tetrahedron Letters. 49: 4003-4006. DOI: 10.1016/J.Tetlet.2008.04.097 |
0.639 |
|
| 2008 |
Kavanagh SA, Connon SJ. N-Alkyl salts derived from ephedrine do not promote enantioselective Corey–Chaykovsky reactions involving sulfonium methylides under phase-transfer conditions Tetrahedron: Asymmetry. 19: 1414-1417. DOI: 10.1016/J.TETASY.2008.05.029 |
0.35 |
|
| 2008 |
Noonan C, Baragwanath L, Connon SJ. ChemInform Abstract: Nucleophilic Carbene-Catalyzed Oxidative Esterification Reactions. Cheminform. 39. DOI: 10.1002/CHIN.200840053 |
0.338 |
|
| 2007 |
Connon SJ. Asymmetric organocatalytic reductions mediated by dihydropyridines. Organic & Biomolecular Chemistry. 5: 3407-17. PMID 17943197 DOI: 10.1039/b711499k |
0.392 |
|
| 2007 |
Dálaigh CO, Connon SJ. Nonenzymatic acylative kinetic resolution of Baylis-Hillman adducts. The Journal of Organic Chemistry. 72: 7066-9. PMID 17676808 DOI: 10.1021/Jo071223B |
0.8 |
|
| 2007 |
Procuranti B, Connon SJ. A reductase-mimicking thiourea organocatalyst incorporating a covalently bound NADH analogue: efficient 1,2-diketone reduction with in situ prosthetic group generation and recycling. Chemical Communications (Cambridge, England). 1421-3. PMID 17389979 DOI: 10.1039/b618792g |
0.335 |
|
| 2007 |
McCooey SH, Connon SJ. Readily accessible 9-epi-amino cinchona alkaloid derivatives promote efficient, highly enantioselective additions of aldehydes and ketones to nitroolefins. Organic Letters. 9: 599-602. PMID 17243708 DOI: 10.1021/ol0628006 |
0.808 |
|
| 2007 |
Fleming EM, McCabe T, Connon SJ. Novel Axially Chiral Bis-arylthiourea-Based Organocatalysts for Asymmetric Friedel—Crafts Type Reactions. Cheminform. 38. DOI: 10.1002/CHIN.200702112 |
0.699 |
|
| 2006 |
McCooey SH, McCabe T, Connon SJ. Stereoselective synthesis of highly functionalized nitrocyclopropanes via organocatalyic conjugate addition to nitroalkenes. The Journal of Organic Chemistry. 71: 7494-7. PMID 16958552 DOI: 10.1021/jo0613838 |
0.792 |
|
| 2006 |
Dálaigh CO, Hynes SJ, O'Brien JE, McCabe T, Maher DJ, Watson GW, Connon SJ. Asymmetric acyl-transfer promoted by readily assembled chiral 4-N,N-dialkylaminopyridine derivatives. Organic & Biomolecular Chemistry. 4: 2785-93. PMID 16826304 DOI: 10.1039/B604632K |
0.771 |
|
| 2006 |
Connon SJ. Chiral phosphoric acids: powerful organocatalysts for asymmetric addition reactions to imines. Angewandte Chemie (International Ed. in English). 45: 3909-12. PMID 16721892 DOI: 10.1002/anie.200600529 |
0.365 |
|
| 2006 |
Connon SJ. Organocatalysis mediated by (thio)urea derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 5418-27. PMID 16514689 DOI: 10.1002/chem.200501076 |
0.412 |
|
| 2006 |
Connon S. Highlights in Organic Chemistry ( Catalytic Asymmetric Acyl-transfer Mediated by Chiral Pyridine Derivatives ) Letters in Organic Chemistry. 3: 333-338. DOI: 10.2174/157017806776611908 |
0.387 |
|
| 2006 |
Fleming EM, McCabe T, Connon SJ. Novel axially chiral bis-arylthiourea-based organocatalysts for asymmetric Friedel-Crafts type reactions Tetrahedron Letters. 47: 7037-7042. DOI: 10.1016/j.tetlet.2006.07.112 |
0.73 |
|
| 2006 |
Connon SJ. Catalytic Asymmetric Acyl-Transfer Mediated by Chiral Pyridine Derivatives Cheminform. 37. DOI: 10.1002/CHIN.200642226 |
0.419 |
|
| 2006 |
Connon SJ. Chirale Phosphorsäuren: wirksame Organokatalysatoren für asymmetrische Additionen an Imine Angewandte Chemie. 118: 4013-4016. DOI: 10.1002/ANGE.200600529 |
0.339 |
|
| 2005 |
McCooey SH, Connon SJ. Urea- and thiourea-substituted cinchona alkaloid derivatives as highly efficient bifunctional organocatalysts for the asymmetric addition of malonate to nitroalkenes: inversion of configuration at C9 dramatically improves catalyst performance. Angewandte Chemie (International Ed. in English). 44: 6367-70. PMID 16136619 DOI: 10.1002/anie.200501721 |
0.79 |
|
| 2005 |
Dálaigh CO, Hynes SJ, Maher DJ, Connon SJ. Kinetic resolution of sec-alcohols using a new class of readily assembled (S)-proline-derived 4-(pyrrolidino)-pyridine analogues. Organic & Biomolecular Chemistry. 3: 981-4. PMID 15750639 DOI: 10.1039/B419335K |
0.764 |
|
| 2005 |
Murtagh JE, McCooey SH, Connon SJ. Novel amine-catalysed hydroalkoxylation reactions of activated alkenes and alkynes. Chemical Communications (Cambridge, England). 227-9. PMID 15724194 DOI: 10.1039/b414895a |
0.788 |
|
| 2005 |
Connon S, McCooey S. Bifunctional Organocatalysts for the Asymmetric Addition of Malonate to Nitroalkenes Synfacts. 2006: 0077-0077. DOI: 10.1055/S-2005-921714 |
0.789 |
|
| 2004 |
Faltin C, Fleming EM, Connon SJ. Acrylamide in the Baylis-Hillman reaction: expanded reaction scope and the unexpected superiority of DABCO over more basic tertiary amine catalysts. The Journal of Organic Chemistry. 69: 6496-9. PMID 15357618 DOI: 10.1021/jo0490907 |
0.73 |
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| 2004 |
Maher DJ, Connon SJ. Acceleration of the DABCO-promoted Baylis-Hillman reaction using a recoverable H-bonding organocatalyst Tetrahedron Letters. 45: 1301-1305. DOI: 10.1016/j.tetlet.2003.11.062 |
0.388 |
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| 2004 |
Connon S, Hegarty A. Stabilised 2,3-Pyridyne Reactive Intermediates of Exceptional Dienophilicity European Journal of Organic Chemistry. 2004: 3477-3483. DOI: 10.1002/EJOC.200400232 |
0.558 |
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| 2003 |
Connon SJ, Blechert S. Recent developments in olefin cross-metathesis. Angewandte Chemie (International Ed. in English). 42: 1900-23. PMID 12730969 DOI: 10.1002/Anie.200200556 |
0.645 |
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| 2003 |
Zaja M, Connon SJ, Dunne AM, Rivard M, Buschmann N, Jiricek J, Blechert S. Ruthenium olefin metathesis catalysts with modified styrene ethers: influence of steric and electronic effects Tetrahedron. 59: 6545-6558. DOI: 10.1016/S0040-4020(03)01029-9 |
0.577 |
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| 2003 |
Zaja M, Connon SJ, Dunne AM, Rivard M, Buschmann N, Jiricek J, Blechert S. Ruthenium Olefin Metathesis Catalysts with Modified Styrene Ethers: Influence of Steric and Electronic Effects. Cheminform. 34. DOI: 10.1002/CHIN.200349060 |
0.345 |
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| 2003 |
Connon SJ, Dunne Aideen M. DAM, Blechert S. A Self-Generating, Highly Active, and Recyclable-Metathesis Catalyst. Cheminform. 34. DOI: 10.1002/CHIN.200306061 |
0.308 |
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| 2003 |
Connon SJ, Blechert S. Jüngste Entwicklungen bei der gekreuzten Olefinmetathese Angewandte Chemie. 115: 1944-1968. DOI: 10.1002/Ange.200200556 |
0.388 |
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| 2003 |
Connon S, Rivard M, Zaja M, Blechert S. Practical Olefin Metathesis in Protic Media under an Air Atmosphere Advanced Synthesis & Catalysis. 345: 572-575. DOI: 10.1002/Adsc.200202201 |
0.6 |
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| 2002 |
Connon SJ, Dunne AM, Blechert S. A self-generating, highly active, and recyclable olefin-metathesis catalyst. Angewandte Chemie (International Ed. in English). 41: 3835-8. PMID 12386863 DOI: 10.1002/1521-3773(20021018)41:20<3835::Aid-Anie3835>3.0.Co;2-4 |
0.552 |
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| 2002 |
Connon SJ, Blechert S. A solid-supported phosphine-free ruthenium alkylidene for olefin metathesis in methanol and water. Bioorganic & Medicinal Chemistry Letters. 12: 1873-6. PMID 12086837 DOI: 10.1016/S0960-894X(02)00260-3 |
0.621 |
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| 2002 |
Randl S, Lucas N, Connon S, Blechert S. A Mechanism Switch in Enyne Metathesis Reactions Involving Rearrangement: Influence of Heteroatoms in the Propargylic Position Advanced Synthesis & Catalysis. 344: 631. DOI: 10.1002/1615-4169(200208)344:6/7<631::Aid-Adsc631>3.0.Co;2-W |
0.558 |
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| 2002 |
Connon SJ, Dunne AM, Blechert S. Ein selbstgenerierender, hochaktiver und wiederverwendbarer Katalysator für die Olefinmetathese Angewandte Chemie. 114: 3989-3993. DOI: 10.1002/1521-3757(20021018)114:20<3989::Aid-Ange3989>3.0.Co;2-D |
0.363 |
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| 2001 |
Randl S, Buschmann N, Connon SJ, Blechert S. Highly Efficient and Recyclable Polymer-Bound Catalyst for Olefin Metathesis Reactions Synlett. 2001: 1547-1550. DOI: 10.1055/S-2001-17463 |
0.605 |
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| 2001 |
Connon SJ, Hegarty AF. Diels–Alder cycloadditions of stabilised 2,3-pyridynes Tetrahedron Letters. 42: 735-737. DOI: 10.1016/S0040-4039(00)02036-0 |
0.654 |
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| 2001 |
Connon SJ, Hegarty AF. ChemInform Abstract: Diels-Alder Cycloadditions of Stabilized 2,3-Pyridynes. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200118115 |
0.534 |
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| Low-probability matches (unlikely to be authored by this person) |
| 2014 |
Myles L, Gathergood N, Connon SJ. An Organocatalytic Process for the Hydrolytic Cleavage of Dithianes Mediated by Imidazolium Ions: No Harsh Agents Required European Journal of Organic Chemistry. 2015: 188-194. DOI: 10.1002/Ejoc.201402947 |
0.297 |
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| 2012 |
Rose CA, Gundala S, Fagan CL, Franz JF, Connon SJ, Zeitler K. NHC-catalysed, chemoselective crossed-acyloin reactions Chemical Science. 3: 735-740. DOI: 10.1039/c2sc00622g |
0.295 |
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| 2007 |
O Dálaigh C, Corr SA, Gun'ko Y, Connon SJ. A magnetic-nanoparticle-supported 4-N,N-dialkylaminopyridine catalyst: excellent reactivity combined with facile catalyst recovery and recyclability. Angewandte Chemie (International Ed. in English). 46: 4329-32. PMID 17476659 DOI: 10.1002/Anie.200605216 |
0.293 |
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| 2013 |
Delany EG, Fagan CL, Gundala S, Mari A, Broja T, Zeitler K, Connon SJ. NHC-catalysed aerobic aldehyde-esterifications with alcohols: no additives or cocatalysts required. Chemical Communications (Cambridge, England). 49: 6510-2. PMID 23764914 DOI: 10.1039/c3cc42596g |
0.291 |
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| 2013 |
Gore RG, Truong T, Pour M, Myles L, Connon SJ, Gathergood N. Tandem ionic liquid antimicrobial toxicity and asymmetric catalysis study: carbonyl-ene reactions with trifluoropyruvate Green Chemistry. 15: 2727. DOI: 10.1039/C3Gc40875B |
0.287 |
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| 2014 |
Gore R, Truong T, Spulak M, Connon S, Gathergood N. Low Antimicrobial Toxicity Ionic Liquids: Solvents for Asymmetric Carbonyl- Ene Reactions of Phenylglyoxal Current Green Chemistry. 1: 239-248. DOI: 10.2174/2213346101666140421220156 |
0.277 |
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| 2013 |
Delany EG, Fagan CL, Gundala S, Zeitler K, Connon SJ. Aerobic oxidation of NHC-catalysed aldehyde esterifications with alcohols: benzoin, not the Breslow intermediate, undergoes oxidation. Chemical Communications (Cambridge, England). 49: 6513-5. PMID 23770683 DOI: 10.1039/c3cc42597e |
0.255 |
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| 2002 |
Connon S. The Diels-Alder Reaction Selected Practical Methods Synthesis. 2002: 833-833. DOI: 10.1055/S-2002-25752 |
0.252 |
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| 2004 |
Maher DJ, Connon SJ. Acceleration of the DABCO-Promoted Baylis—Hillman Reaction Using a Recoverable H-Bonding Organocatalyst. Cheminform. 35. DOI: 10.1002/CHIN.200419078 |
0.241 |
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| 2010 |
Power DP, Lozach O, Meijer L, Grayson DH, Connon SJ. Concise synthesis and CDK/GSK inhibitory activity of the missing 9-azapaullones. Bioorganic & Medicinal Chemistry Letters. 20: 4940-4. PMID 20621478 DOI: 10.1016/j.bmcl.2010.06.024 |
0.21 |
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| 2010 |
Myles L, Gore R, Spulak M, Gathergood N, Connon SJ. ChemInform Abstract: Highly Recyclable, Imidazolium Derived Ionic Liquids of Low Antimicrobial and Antifungal Toxicity: A New Strategy for Acid Catalysis. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201048039 |
0.208 |
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| 2007 |
Connon S, Procuranti B. Reduction of Benzils Promoted by a New Class of Bifunctional Organocatalysts Synfacts. 2007: 0430-0430. DOI: 10.1055/S-2007-968352 |
0.171 |
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| 2020 |
Alqasem MA, Fergus C, Southern JM, Connon SJ, Kelly VP. The eukaryotic tRNA-guanine transglycosylase enzyme inserts queuine into tRNA via a sequential bi-bi mechanism. Chemical Communications (Cambridge, England). PMID 32149287 DOI: 10.1039/c9cc09887a |
0.144 |
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| 2009 |
Connon SJ. ChemInform Abstract: The Design of Novel, Synthetically Useful (Thio)urea-Based Organocatalysts Cheminform. 40. DOI: 10.1002/chin.200921248 |
0.142 |
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| 2022 |
Cronin SA, Connon SJ. Correction: The kinetic resolution of oxazinones by alcoholysis: access to orthogonally protected β-amino acids. Organic & Biomolecular Chemistry. 20: 906. PMID 35022634 DOI: 10.1039/d1ob90184b |
0.121 |
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| 2009 |
Connon S. The Design of Novel, Synthetically Useful (Thio)urea-Based Organocatalysts Synlett. 2009: 0354-0376. DOI: 10.1055/S-0028-1087557 |
0.119 |
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| 2013 |
Connon SJ. Diaminocyclopropenyliden-Organokatalysatoren: jenseits N-heterocyclischer Carbene Angewandte Chemie. 126: 1225-1227. DOI: 10.1002/ANGE.201309256 |
0.118 |
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| 2013 |
Gundala S, Fagan C, Delany EG, Connon SJ. ChemInform Abstract: Organocatalytic Aerobic Oxidative Cleavage of Cyclic 1,2-Diketones. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201340030 |
0.112 |
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| 2023 |
Cotter M, Varghese S, Chevot F, Fergus C, Kelly V, Connon S, Southern JM. Queuine analogues incorporating the 7-aminomethyl-7-deazaguanine core: structure-activity relationships in the treatment of experimental autoimmune encephalomyelitis. Chemmedchem. e202300207. PMID 37350546 DOI: 10.1002/cmdc.202300207 |
0.1 |
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| 2022 |
McDonnell CM, Ghanim M, Mike Southern J, Kelly VP, Connon SJ. De-novo designed β-lysine derivatives can both augment and diminish the proliferation rates of E. coli through the action of Elongation Factor P. Bioorganic & Medicinal Chemistry Letters. 59: 128545. PMID 35032607 DOI: 10.1016/j.bmcl.2022.128545 |
0.096 |
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| 2015 |
Myles L, Gathergood N, Connon SJ. ChemInform Abstract: An Organocatalytic Process for the Hydrolytic Cleavage of Dithianes Mediated by Imidazolium Ions: No Harsh Agents Required. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201519096 |
0.09 |
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| 2013 |
Connon S, Gundala S, Fagan C, Delany E. Organocatalytic Aerobic Oxidative Cleavage of Cyclic 1,2-Diketones Synlett. 24: 1225-1228. DOI: 10.1055/S-0033-1338494 |
0.086 |
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| 2003 |
Connon SJ, Rivard M, Zaja M, Blechert S. Practical Olefin Metathesis in Protic Media under an Air Atmosphere. Cheminform. 34. DOI: 10.1002/CHIN.200334047 |
0.076 |
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| 2021 |
Fergus C, Al-Qasem M, Cotter M, McDonnell CM, Sorrentino E, Chevot F, Hokamp K, Senge MO, Southern JM, Connon SJ, Kelly VP. The human tRNA-guanine transglycosylase displays promiscuous nucleobase preference but strict tRNA specificity. Nucleic Acids Research. 49: 4877-4890. PMID 34009357 DOI: 10.1093/nar/gkab289 |
0.066 |
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| 2016 |
Varghese S, Cotter M, Chevot F, Fergus C, Cunningham C, Mills KH, Connon SJ, Southern JM, Kelly VP. In vivo modification of tRNA with an artificial nucleobase leads to full disease remission in an animal model of multiple sclerosis. Nucleic Acids Research. PMID 27664221 DOI: 10.1093/nar/gkw847 |
0.062 |
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| 2008 |
Connon S. Die katalytische asymmetrische Strecker-Reaktion: Fortschritte bei Ketiminen Angewandte Chemie. 120: 1194-1197. DOI: 10.1002/ANGE.200703879 |
0.031 |
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| 2017 |
Varghese S, Cotter M, Chevot F, Fergus C, Cunningham C, Mills KH, Connon SJ, Southern JM, Kelly VP. In vivo modification of tRNA with an artificial nucleobase leads to full disease remission in an animal model of multiple sclerosis. Nucleic Acids Research. 45: 2029-2039. PMID 28204548 DOI: 10.1093/nar/gkw847 |
0.015 |
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| Hide low-probability matches. |