Nuno Maulide - Publications

Affiliations: 
University of Vienna, Wien, Wien, Austria 
Area:
Organic Chemistry, Asymmetric Catalysis, Total Synthesis
Website:
http://maulide.univie.ac.at

175 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Saridakis I, Kaiser D, Maulide N. Unconventional Macrocyclizations in Natural Product Synthesis. Acs Central Science. 6: 1869-1889. PMID 33274267 DOI: 10.1021/acscentsci.0c00599  1
2020 Porte V, Di Mauro G, Schupp M, Kaiser D, Maulide N. Chemoselective Alpha-Deuteration of Amides Via Retro-ene Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33035360 DOI: 10.1002/chem.202004103  1
2020 Bauer A, Borsos E, Maulide N. A Novel Class of 7-Membered Heterocyclic Compounds. European Journal of Organic Chemistry. 2020: 3971-3974. PMID 32982576 DOI: 10.1002/ejoc.202000363  0.44
2020 Bauer A, Di Mauro G, Li J, Maulide N. An α-Cyclopropanation of Carbonyl Derivatives by Oxidative Umpolung. Angewandte Chemie (International Ed. in English). PMID 32808419 DOI: 10.1002/anie.202007439  1
2020 Maulide N, Knittl-Frank C, Saridakis I, Stephens T, Gomes R, Neuhaus J, Misale A, Oost R, Oppedisano A. Gold-catalyzed cycloisomerization of sulfur ylides to dihydrobenzothiepines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32227380 DOI: 10.1002/chem.202000622  1
2019 Bauer A, Maulide N. Chemoselective formal β-functionalization of substituted aliphatic amides enabled by a facile stereoselective oxidation event. Chemical Science. 10: 9836-9840. PMID 32015806 DOI: 10.1039/c9sc03715b  0.44
2019 Zangerl-Plessl EM, Berger M, Drescher M, Chen Y, Wu W, Maulide N, Sanguinetti M, Stary-Weinzinger A. Towards a structural view of hERG activation by the small molecule activator ICA-105574. Journal of Chemical Information and Modeling. PMID 31877041 DOI: 10.1021/acs.jcim.9b00737  1
2019 Gonçalves CR, Lemmerer M, Teskey CJ, Adler P, Kaiser D, Maryasin B, González L, Maulide N. Unified Approach to the Chemoselective α-Functionalization of Amides with Heteroatom Nucleophiles. Journal of the American Chemical Society. PMID 31714077 DOI: 10.1021/jacs.9b06956  1
2019 Pons A, Michalland J, Zawodny W, Chen Y, Tona V, Maulide N. Vinyl Cation Stabilization by Silicon Enables a Formal Metal-Free α-Arylation of Alkyl Ketones. Angewandte Chemie (International Ed. in English). PMID 31638738 DOI: 10.1002/anie.201909381  1
2019 Spinozzi E, Bauer A, Maulide N. A Mild Synthesis of Bicyclic Alkoxyoxazolium Salts from Proline and Pipecolic Acid Derivatives. European Journal of Organic Chemistry. 2019: 5230-5233. PMID 31598092 DOI: 10.1002/ejoc.201900985  0.44
2019 Kaiser D, Tona V, Gonçalves CR, Shaaban S, Oppedisano A, Maulide N. A General Acid-Mediated Hydroaminomethylation of Unactivated Alkenes and Alkynes. Angewandte Chemie (International Ed. in English). PMID 31482639 DOI: 10.1002/anie.201906910  1
2019 Chen Y, Coussanes G, Souris C, Aillard P, Kaldre D, Runggatscher K, Kubicek S, Di Mauro G, Maryasin B, Maulide N. A Domino 10-Step Total Synthesis of FR252921 and Its Analogues, Complex Macrocyclic Immunosuppressants. Journal of the American Chemical Society. PMID 31436963 DOI: 10.1021/jacs.9b07185  1
2019 Kaiser D, Klose I, Oost R, Neuhaus J, Maulide N. Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts. Chemical Reviews. PMID 31243998 DOI: 10.1021/acs.chemrev.9b00111  1
2019 Li J, Oost R, Maryasin B, González L, Maulide N. A redox-neutral synthesis of ketones by coupling of alkenes and amides. Nature Communications. 10: 2327. PMID 31127092 DOI: 10.1038/s41467-019-10151-x  1
2019 Li J, Bauer A, Di Mauro G, Maulide N. a-Arylation of Carbonyl Compounds by Oxidative C-C Bond Activation. Angewandte Chemie (International Ed. in English). PMID 31112360 DOI: 10.1002/anie.201904899  1
2019 Maryasin B, Maulide N. On the Stability of Disubstituted Cyclobutenes - A Computational Study. European Journal of Organic Chemistry. 2019: 338-341. PMID 31007572 DOI: 10.1002/ejoc.201801243  0.36
2019 Li J, Preinfalk A, Maulide N. Diastereo- and Enantioselective Access to Stereotriads through a Flexible Coupling of Substituted Aldehydes and Alkenes. Angewandte Chemie (International Ed. in English). PMID 30919530 DOI: 10.1002/anie.201900801  1
2019 Adler P, Teskey CJ, Kaiser D, Holy M, Sitte HH, Maulide N. α-Fluorination of carbonyls with nucleophilic fluorine. Nature Chemistry. PMID 30833720 DOI: 10.1038/s41557-019-0215-z  1
2019 Brutiu BR, Bubeneck WA, Cvetkovic O, Li J, Maulide N. On the formation of seven-membered rings by arene-ynamide cyclization. Monatshefte Fur Chemie. 150: 3-10. PMID 30662090 DOI: 10.1007/s00706-018-2320-x  1
2018 Li J, Preinfalk A, Maulide N. Enantioselective Redox-Neutral Coupling of Aldehydes and Alkenes by an Iron-Catalyzed "Catch-Release" Tethering Approach. Journal of the American Chemical Society. PMID 30576130 DOI: 10.1021/jacs.8b12242  1
2018 Teskey C, Adler P, Goncalves C, Maulide N. Chemoselective α,β-Dehydrogenation of Saturated Amides. Angewandte Chemie (International Ed. in English). PMID 30332524 DOI: 10.1002/anie.201808794  0.44
2018 Oost R, Neuhaus JD, Misale A, Meyrelles R, Veiros LF, Maulide N. Catalyst-dependent selectivity in sulfonium ylide cycloisomerization reactions. Chemical Science. 9: 7091-7095. PMID 30310629 DOI: 10.1039/c8sc02815j  1
2018 Neuhaus J, Bauer A, Pinto A, Maulide N. A Catalytic Cross-Olefination of Diazocompounds with Sulfoxonium Ylides. Angewandte Chemie (International Ed. in English). PMID 30264529 DOI: 10.1002/anie.201809934  0.44
2018 Alves LG, Madeira F, Munhá RF, Maulide N, Veiros LF, Martins AM. Cooperative Metal-Ligand Hydroamination Catalysis Supported by C-H Activation in Cyclam Zr(IV) Complexes. Inorganic Chemistry. PMID 30240206 DOI: 10.1021/acs.inorgchem.8b02396  1
2018 Baldassari LL, Mantovani AC, Senoner S, Maryasin B, Maulide N, Lüdtke DS. Redox-Neutral Synthesis of Selenoesters by Oxyarylation of Selenoalkynes under Mild Conditions. Organic Letters. PMID 30183318 DOI: 10.1021/acs.orglett.8b02544  1
2018 Kaiser D, Bauer A, Lemmerer M, Maulide N. Amide activation: an emerging tool for chemoselective synthesis. Chemical Society Reviews. PMID 30152510 DOI: 10.1039/c8cs00335a  1
2018 Martin H, Kampatsikas I, Oost R, Pretzler M, Al-Sayed E, Roller A, Giester G, Rompel A, Maulide N. Total Synthesis, Stereochemical Assignment and Divergent Enantioselective Enzymatic Recognition of Larreatricin. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30113748 DOI: 10.1002/chem.201803785  1
2018 Adler P, Pons A, Li J, Heider J, Brutiu BR, Maulide N. Chemoselective Activation of Diethyl Phosphonates: A Modular Synthesis of Biologically Relevant Phosphonylated Scaffolds. Angewandte Chemie (International Ed. in English). PMID 30067301 DOI: 10.1002/anie.201806343  1
2018 Maryasin B, Kaldre D, Galaverna R, Klose I, Ruider S, Drescher M, Kählig H, González L, Eberlin MN, Jurberg ID, Maulide N. Unusual mechanisms in Claisen rearrangements: an ionic fragmentation leading to a -selective rearrangement. Chemical Science. 9: 4124-4131. PMID 29780542 DOI: 10.1039/c7sc04736c  1
2018 O' Donovan DH, Aillard P, Berger M, de la Torre A, Petkova D, Knittl-Frank C, Geerdink D, Kaiser M, Maulide N. C-H Activation Enables a Concise Total Synthesis of Quinine and Analogues with Enhanced Antimalarial Activity. Angewandte Chemie (International Ed. in English). PMID 29761878 DOI: 10.1002/anie.201804551  1
2018 Maryasin B, Marquetand P, Maulide N. Machine Learning for Organic Synthesis: Are Robots Replacing Chemists? Angewandte Chemie (International Ed. in English). PMID 29701305 DOI: 10.1002/anie.201803562  0.36
2018 Lemmerer M, Teskey CJ, Kaiser D, Maulide N. Regioselective synthesis of pyridines by redox alkylation of pyridine -oxides with malonates. Monatshefte Fur Chemie. 149: 715-719. PMID 29681655 DOI: 10.1007/s00706-017-2081-y  1
2018 Neuhaus JD, Oost R, Merad J, Maulide N. Sulfur-Based Ylides in Transition-Metal-Catalysed Processes. Topics in Current Chemistry (Cham). 376: 15. PMID 29654469 DOI: 10.1007/s41061-018-0193-4  1
2018 Bauer A, Maulide N. A Stereoselective Reductive Hosomi-Sakurai Reaction. Organic Letters. PMID 29469578 DOI: 10.1021/acs.orglett.8b00276  0.44
2018 Berger M, Chen Y, Bampali K, Ernst M, Maulide N. Expeditious synthesis of polyacetylenic water hemlock toxins and their effects on the major GABAA receptor isoform. Chemical Communications (Cambridge, England). PMID 29411793 DOI: 10.1039/c7cc09801d  1
2018 Neuhaus JD, Angyal P, Oost R, Maulide N. (3+2) Cycloadditions of Thiouronium Ylides: A Room-Temperature, One-Pot Approach to Dihydrothiophenes. The Journal of Organic Chemistry. PMID 29405711 DOI: 10.1021/acs.joc.7b03255  1
2018 Pinto A, Kaiser D, Maryasin B, Di Mauro G, Gonzalez L, Maulide N. Hydrative Aminoxylation of Ynamides: One Reaction, Two Mechanisms. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29293283 DOI: 10.1002/chem.201706063  1
2017 Kaiser D, Teskey CJ, Adler P, Maulide N. Chemoselective Intermolecular Cross-Enolate-Type Coupling of Amides. Journal of the American Chemical Society. PMID 29099184 DOI: 10.1021/jacs.7b08813  1
2017 Baldassari LL, de la Torre A, Li J, Lüdtke DS, Maulide N. Ynamide Preactivation Allows a Regio- and Stereoselective Synthesis of α,β-disubstituted Enamides. Angewandte Chemie (International Ed. in English). PMID 29032598 DOI: 10.1002/anie.201709128  0.92
2017 Mota AJ, Neuhold J, Drescher M, Lemouzy S, González L, Maulide N. Intramolecular hydrogen bonding in conformationally semi-rigid α-acylmethane derivatives: a theoretical NMR study. Organic & Biomolecular Chemistry. PMID 28858370 DOI: 10.1039/c7ob01834g  0.36
2017 Di Mauro G, Maryasin B, Kaiser D, Shaaban S, González L, Maulide N. Mechanistic Pathways in Amide Activation: Flexible Synthesis of Oxazoles and Imidazoles. Organic Letters. PMID 28703599 DOI: 10.1021/acs.orglett.7b01678  1
2017 Shaaban S, Tona V, Peng B, Maulide N. Hydroxamic acids as chemoselective (ortho-amino)arylating reagents via sigmatropic rearrangement. Angewandte Chemie (International Ed. in English). PMID 28691189 DOI: 10.1002/anie.201703667  1
2017 de la Torre A, Tona V, Maulide N. Reversing polarity: Carbonyl α-aminations with nitrogen nucleophiles. Angewandte Chemie (International Ed. in English). PMID 28544574 DOI: 10.1002/anie.201702937  1
2017 Tona V, Maryasin B, de la Torre A, Sprachmann J, González L, Maulide N. Direct Regioselective Synthesis of Tetrazolium Salts by Activation of Secondary Amides under Mild Conditions. Organic Letters. PMID 28485608 DOI: 10.1021/acs.orglett.7b01004  1
2017 de la Torre A, Kaiser D, Maulide N. Flexible and Chemoselective Oxidation of Amides to α-Keto Amides and α-Hydroxy Amides. Journal of the American Chemical Society. PMID 28485589 DOI: 10.1021/jacs.7b02983  1
2017 Kaiser D, de la Torre A, Shaaban S, Maulide N. Metal-Free Formal Oxidative C-C Coupling by In Situ Generation of an Enolonium Species. Angewandte Chemie (International Ed. in English). PMID 28429392 DOI: 10.1002/anie.201701538  1
2017 Kaldre D, Maryasin B, Kaiser D, Gajsek O, González L, Maulide N. An Asymmetric Redox Arylation: Chirality Transfer from Sulfur to Carbon through a Sulfonium [3,3]-Sigmatropic Rearrangement. Angewandte Chemie (International Ed. in English). PMID 28097797 DOI: 10.1002/anie.201610105  1
2016 Tona V, Ruider SA, Berger M, Shaaban S, Padmanaban M, Xie LG, González L, Maulide N. Divergent ynamide reactivity in the presence of azides - an experimental and computational study. Chemical Science. 7: 6032-6040. PMID 30034744 DOI: 10.1039/c6sc01945e  1
2016 Rodrigues CA, Misale A, Schiel F, Maulide N. Direct synthesis of γ-pyrones by electrophilic condensation of β-ketoesters. Organic & Biomolecular Chemistry. PMID 27976773 DOI: 10.1039/c6ob01884j  1
2016 Chen X, Ruider SA, Hartmann RW, González L, Maulide N. Metal-Free meta-Selective Alkyne Oxyarylation with Pyridine N-Oxides: Rapid Assembly of Metyrapone Analogues. Angewandte Chemie (International Ed. in English). PMID 27862782 DOI: 10.1002/anie.201607988  1
2016 Misale A, Niyomchon S, Maulide N. Cyclobutenes: At a Crossroad between Diastereoselective Syntheses of Dienes and Unique Palladium-Catalyzed Asymmetric Allylic Substitutions. Accounts of Chemical Research. PMID 27797480 DOI: 10.1021/acs.accounts.6b00375  1
2016 Xie LG, Shaaban S, Chen X, Maulide N. Metal-Free Synthesis of Highly Substituted Pyridines by Formal [2+2+2] Cycloaddition under Mild Conditions. Angewandte Chemie (International Ed. in English). PMID 27623988 DOI: 10.1002/anie.201606604  1
2016 Preinfalk A, Misale A, Maulide N. A Gold(I)-Catalyzed Domino Coupling of Alcohols with Allenes Enables the Synthesis of Highly Substituted Indenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27596096 DOI: 10.1002/chem.201603154  1
2016 Klose I, Misale A, Maulide N. Synthesis and Photocatalytic Reactivity of Vinylsulfonium Ylides. The Journal of Organic Chemistry. PMID 27398692 DOI: 10.1021/acs.joc.6b01073  1
2016 Tona V, de la Torre A, Padmanaban M, Ruider S, González L, Maulide N. Chemo- and Stereoselective Transition-Metal-Free Amination of Amides with Azides. Journal of the American Chemical Society. PMID 27350334 DOI: 10.1021/jacs.6b04061  1
2016 Kaiser D, Maulide N. Making the Least Reactive Electrophile the First in Class: Domino Electrophilic Activation of Amides. The Journal of Organic Chemistry. PMID 27187724 DOI: 10.1021/acs.joc.6b00675  1
2016 Sabbatani J, Maulide N. Temporary Generation of a Cyclopropyl Oxocarbenium Ion Enables Highly Diastereoselective Donor-Acceptor Cyclopropane Cycloaddition. Angewandte Chemie (International Ed. in English). PMID 27099179 DOI: 10.1002/anie.201601340  0.6
2016 Xie LG, Niyomchon S, Mota AJ, González L, Maulide N. Metal-free intermolecular formal cycloadditions enable an orthogonal access to nitrogen heterocycles. Nature Communications. 7: 10914. PMID 26975182 DOI: 10.1038/ncomms10914  1
2016 Oost R, Misale A, Maulide N. Enantioconvergent Fukuyama Cross-Coupling of Racemic Benzylic Organozinc Reagents. Angewandte Chemie (International Ed. in English). PMID 26945899 DOI: 10.1002/anie.201600597  1
2016 Kaiser D, Veiros LF, Maulide N. Brønsted Acid-Mediated Hydrative Arylation of Unactivated Alkynes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26918863 DOI: 10.1002/chem.201600432  1
2016 Shaaban S, Oh J, Maulide N. Redox-Neutral α-Amino C-H Functionalization: When the Catalyst Is Also the Nucleophile. Organic Letters. PMID 26757174 DOI: 10.1021/acs.orglett.5b03431  1
2015 Xie LG, Bagutski V, Audisio D, Wolf LM, Schmidts V, Hofmann K, Wirtz C, Thiel W, Thiele CM, Maulide N. Dynamic behaviour of monohaptoallylpalladium species: internal coordination as a driving force in allylic alkylation chemistry. Chemical Science. 6: 5734-5739. PMID 29910865 DOI: 10.1039/c5sc01867f  1
2015 Ruider SA, Maulide N. Strong Bonds Made Weak: Towards the General Utility of Amides as Synthetic Modules. Angewandte Chemie (International Ed. in English). PMID 26460213 DOI: 10.1002/anie.201508536  1
2015 Souris C, Misale A, Chen Y, Luparia M, Maulide N. From Stereodefined Cyclobutenes to Dienes: Total Syntheses of Ieodomycin D and the Southern Fragment of Macrolactin A. Organic Letters. PMID 26349917 DOI: 10.1021/acs.orglett.5b02149  1
2015 Shaaban S, Jolit A, Petkova D, Maulide N. A family of low molecular-weight, organic catalysts for reductive C-C bond formation. Chemical Communications (Cambridge, England). 51: 13902-5. PMID 26239300 DOI: 10.1039/c5cc03580e  1
2015 Klimczyk S, Misale A, Huang X, Maulide N. Dimeric TADDOL Phosphoramidites in Asymmetric Catalysis: Domino Deracemization and Cyclopropanation of Sulfonium Ylides. Angewandte Chemie (International Ed. in English). PMID 26138505 DOI: 10.1002/anie.201503851  1
2015 Klimczyk S, Huang X, Kählig H, Veiros LF, Maulide N. Stereoselective gold(I) domino catalysis of allylic isomerization and olefin cyclopropanation: mechanistic studies. The Journal of Organic Chemistry. 80: 5719-29. PMID 26017800 DOI: 10.1021/acs.joc.5b00666  1
2015 Gomes LF, Veiros LF, Maulide N, Afonso CA. Diazo- and transition-metal-free C-H insertion: a direct synthesis of β-lactams. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 1449-53. PMID 25412838 DOI: 10.1002/chem.201404990  1
2015 Xie LG, Bagutski V, Audisio D, Wolf LM, Schmidts V, Hofmann K, Wirtz C, Thiel W, Thiele CM, Maulide N. Dynamic behaviour of monohaptoallylpalladium species: Internal coordination as a driving force in allylic alkylation chemistry Chemical Science. 6: 5734-5739. DOI: 10.1039/c5sc01867f  1
2015 Klimczyk S, Huang X, Kählig H, Veiros LF, Maulide N. Stereoselective gold(I) domino catalysis of allylic isomerization and olefin cyclopropanation: Mechanistic studies Journal of Organic Chemistry. 80: 5719-5729. DOI: 10.1021/acs.joc.5b00666  1
2015 Padmanaban M, Carvalho LCR, Petkova D, Lee JW, Santos AS, Marques MMB, Maulide N. Investigation of cationic Claisen-type electrophilic rearrangements of amides Tetrahedron. 71: 5994-6005. DOI: 10.1016/j.tet.2015.06.027  1
2015 Shaaban S, Roller A, Maulide N. Visible-Light, Metal-Free α-Amino C(sp3)-H Activation through 1,5-Hydrogen Migration: A Concise Method for the Preparation of Bis(indolyl)alkanes European Journal of Organic Chemistry. DOI: 10.1002/ejoc.201501149  1
2014 Maulide N, Souris C, Frébault F, Luparia M, Audisio D. Direct synthesis of stereodefined and functionalized dienes as valuable building blocks Chimia. 68: 248-251. PMID 24983608 DOI: 10.2533/chimia.2014.248  1
2014 Sabbatani J, Huang X, Veiros LF, Maulide N. Gold-catalyzed intermolecular synthesis of alkylidenecyclopropanes through catalytic allene activation. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 10636-9. PMID 24976605 DOI: 10.1002/chem.201402935  1
2014 Misale A, Niyomchon S, Luparia M, Maulide N. Asymmetric palladium-catalyzed allylic alkylation using dialkylzinc reagents: a remarkable ligand effect. Angewandte Chemie (International Ed. in English). 53: 7068-73. PMID 24888236 DOI: 10.1002/anie.201309074  1
2014 Peng B, Geerdink D, Farès C, Maulide N. Chemoselective intermolecular α-arylation of amides. Angewandte Chemie (International Ed. in English). 53: 5462-6. PMID 24740762 DOI: 10.1002/anie.201402229  0.76
2014 Peng B, Huang X, Xie LG, Maulide N. A Brønsted acid catalyzed redox arylation. Angewandte Chemie (International Ed. in English). 53: 8718-21. PMID 24590501 DOI: 10.1002/anie.201310865  1
2014 Sabbatani J, Huang X, Veiros LF, Maulide N. Gold-catalyzed intermolecular synthesis of alkylidenecyclopropanes through catalytic allene activation Chemistry - a European Journal. 20: 10636-10639. DOI: 10.1002/chem.201402935  1
2014 Peng B, Geerdink D, Farès C, Maulide N. Chemoselective intermolecular α-arylation of amides Angewandte Chemie - International Edition. 53: 5462-5466. DOI: 10.1002/anie.201402229  1
2014 Peng B, Huang X, Xie LG, Maulide N. A Brønsted acid catalyzed redox arylation Angewandte Chemie - International Edition. 53: 8718-8721. DOI: 10.1002/anie.201310865  1
2014 Misale A, Niyomchon S, Luparia M, Maulide N. Asymmetric palladium-catalyzed allylic alkylation using dialkylzinc reagents: A remarkable ligand effect Angewandte Chemie - International Edition. 53: 7068-7073. DOI: 10.1002/anie.201309074  1
2013 Oliveira MT, Luparia M, Audisio D, Maulide N. Dual catalysis becomes diastereodivergent. Angewandte Chemie (International Ed. in English). 52: 13149-52. PMID 24130132 DOI: 10.1002/anie.201305933  1
2013 Peng B, Geerdink D, Maulide N. Electrophilic rearrangements of chiral amides: a traceless asymmetric α-allylation. Journal of the American Chemical Society. 135: 14968-71. PMID 24079481 DOI: 10.1021/ja408856p  0.76
2013 Peng B, Maulide N. The redox-neutral approach to C-H functionalization. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 13274-87. PMID 24027042 DOI: 10.1002/chem.201301522  0.76
2013 Souris C, Frébault F, Patel A, Audisio D, Houk KN, Maulide N. Stereoselective synthesis of dienyl-carboxylate building blocks: formal synthesis of inthomycin C. Organic Letters. 15: 3242-5. PMID 23763296 DOI: 10.1021/ol401226y  1
2013 Souris C, Frébault F, Patel A, Audisio D, Houk KN, Maulide N. Stereoselective synthesis of dienyl-carboxylate building blocks: formal synthesis of inthomycin C. Organic Letters. 15: 3242-5. PMID 23763296 DOI: 10.1021/ol401226y  1
2013 Audisio D, Gopakumar G, Xie LG, Alves LG, Wirtz C, Martins AM, Thiel W, Farès C, Maulide N. Palladium-catalyzed allylic substitution at four-membered-ring systems: formation of η1-allyl complexes and electrocyclic ring opening. Angewandte Chemie (International Ed. in English). 52: 6313-6. PMID 23649642 DOI: 10.1002/anie.201301034  1
2013 Huang X, Patil M, Farès C, Thiel W, Maulide N. Sulfur(IV)-mediated transformations: From ylide transfer to metal-free arylation of carbonyl compounds Journal of the American Chemical Society. 135: 7312-7323. PMID 23641807 DOI: 10.1021/ja4017683  1
2013 Niyomchon S, Audisio D, Luparia M, Maulide N. Regio- and enantioselective cyclobutene allylations. Organic Letters. 15: 2318-21. PMID 23614852 DOI: 10.1021/ol401033g  1
2013 Souris C, Luparia M, Frébault F, Audisio D, Farès C, Goddard R, Maulide N. An atom-economical and stereoselective domino synthesis of functionalised dienes. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 6566-70. PMID 23576421 DOI: 10.1002/chem.201300776  1
2013 Valerio V, Petkova D, Madelaine C, Maulide N. Direct room-temperature lactonisation of alcohols and ethers onto amides: an "amide strategy" for synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 2606-10. PMID 23307662 DOI: 10.1002/chem.201203906  1
2013 Huang X, Goddard R, Maulide N. Facile carbon-sulfur bond cleavage in diarylsulfonium ylides: a catalytic sulfur-to-silicon group transfer. Chemical Communications (Cambridge, England). 49: 4292-4. PMID 23011230 DOI: 10.1039/c2cc35762c  1
2013 Shaaban S, Peng B, Maulide N. Base-promoted internal redox-cyclisation reactions Synlett. 24: 1722-1724. DOI: 10.1055/s-0033-1339313  1
2013 Shaaban S, Peng B, Maulide N. Base-promoted internal redox-cyclisation reactions Synlett. 24: 1722-1724. DOI: 10.1055/s-0033-1339313  1
2013 Souris C, Frébault F, Audisio D, Farès C, Maulide N. Direct domino synthesis of azido-dienoic acids: Potential linker units Synlett. 24: 1286-1290. DOI: 10.1055/s-0033-1338452  1
2013 Souris C, Frébault F, Audisio D, Farès C, Maulide N. Direct domino synthesis of azido-dienoic acids: Potential linker units Synlett. 24: 1286-1290. DOI: 10.1055/s-0033-1338452  1
2013 Huang X, Klimczyk S, Veiros LF, Maulide N. Stereoselective intramolecular cyclopropanation through catalytic olefin activation Chemical Science. 4: 1105-1110. DOI: 10.1039/c2sc21914j  1
2013 Huang X, Klimczyk S, Veiros LF, Maulide N. Stereoselective intramolecular cyclopropanation through catalytic olefin activation Chemical Science. 4: 1105-1110. DOI: 10.1039/c2sc21914j  1
2013 Huang X, Goddard R, Maulide N. Facile carbon-sulfur bond cleavage in diarylsulfonium ylides: A catalytic sulfur-to-silicon group transfer Chemical Communications. 49: 4292-4294. DOI: 10.1039/c2cc35762c  1
2013 Huang X, Goddard R, Maulide N. Facile carbon-sulfur bond cleavage in diarylsulfonium ylides: A catalytic sulfur-to-silicon group transfer Chemical Communications. 49: 4292-4294. DOI: 10.1039/c2cc35762c  1
2013 Niyomchon S, Audisio D, Luparia M, Maulide N. Regio- and enantioselective cyclobutene allylations Organic Letters. 15: 2318-2321. DOI: 10.1021/ol401033g  1
2013 Niyomchon S, Audisio D, Luparia M, Maulide N. Regio- and enantioselective cyclobutene allylations Organic Letters. 15: 2318-2321. DOI: 10.1021/ol401033g  1
2013 Peng B, Geerdink D, Maulide N. Electrophilic rearrangements of chiral amides: A traceless asymmetric α-allylation Journal of the American Chemical Society. 135: 14968-14971. DOI: 10.1021/ja408856p  1
2013 Peng B, Geerdink D, Maulide N. Electrophilic rearrangements of chiral amides: A traceless asymmetric α-allylation Journal of the American Chemical Society. 135: 14968-14971. DOI: 10.1021/ja408856p  0.76
2013 Peng B, Maulide N. The redox-neutral approach to C-H functionalization Chemistry - a European Journal. 19: 13274-13287. DOI: 10.1002/chem.201301522  1
2013 Peng B, Maulide N. The redox-neutral approach to C-H functionalization Chemistry - a European Journal. 19: 13274-13287. DOI: 10.1002/chem.201301522  0.76
2013 Souris C, Luparia M, Frébault F, Audisio D, Farès C, Goddard R, Maulide N. An atom-economical and stereoselective domino synthesis of functionalised dienes Chemistry - a European Journal. 19: 6566-6570. DOI: 10.1002/chem.201300776  1
2013 Souris C, Luparia M, Frébault F, Audisio D, Farès C, Goddard R, Maulide N. An atom-economical and stereoselective domino synthesis of functionalised dienes Chemistry - a European Journal. 19: 6566-6570. DOI: 10.1002/chem.201300776  1
2013 Valerio V, Petkova D, Madelaine C, Maulide N. Direct room-temperature lactonisation of alcohols and ethers onto amides: An "amide strategy" for synthesis Chemistry - a European Journal. 19: 2606-2610. DOI: 10.1002/chem.201203906  1
2013 Valerio V, Petkova D, Madelaine C, Maulide N. Direct room-temperature lactonisation of alcohols and ethers onto amides: An "amide strategy" for synthesis Chemistry - a European Journal. 19: 2606-2610. DOI: 10.1002/chem.201203906  1
2013 Oliveira MT, Audisio D, Niyomchon S, Maulide N. Diastereodivergent Processes in Palladium-Catalyzed Allylic Alkylation Chemcatchem. 5: 1239-1247. DOI: 10.1002/cctc.201200644  1
2013 Oliveira MT, Audisio D, Niyomchon S, Maulide N. Diastereodivergent Processes in Palladium-Catalyzed Allylic Alkylation Chemcatchem. 5: 1239-1247. DOI: 10.1002/cctc.201200644  1
2013 Oliveira MT, Luparia M, Audisio D, Maulide N. Dual catalysis becomes diastereodivergent Angewandte Chemie - International Edition. 52: 13149-13152. DOI: 10.1002/anie.201305933  1
2013 Audisio D, Gopakumar G, Xie LG, Alves LG, Wirtz C, Martins AM, Thiel W, Farès C, Maulide N. Palladium-catalyzed allylic substitution at four-membered-ring systems: Formation of η1-allyl complexes and electrocyclic ring opening Angewandte Chemie - International Edition. 52: 6313-6316. DOI: 10.1002/anie.201301034  1
2013 Audisio D, Gopakumar G, Xie LG, Alves LG, Wirtz C, Martins AM, Thiel W, Farès C, Maulide N. Palladium-catalyzed allylic substitution at four-membered-ring systems: Formation of η1-allyl complexes and electrocyclic ring opening Angewandte Chemie - International Edition. 52: 6313-6316. DOI: 10.1002/anie.201301034  1
2012 Peng B, O'Donovan DH, Jurberg ID, Maulide N. Dual nucleophilic/electrophilic capture of in situ generated iminium ethers: towards the synthesis of functionalized amide building blocks. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 16292-6. PMID 23154863 DOI: 10.1002/chem.201203293  0.76
2012 Huang X, Peng B, Luparia M, Gomes LF, Veiros LF, Maulide N. Gold-catalyzed synthesis of furans and furanones from sulfur ylides. Angewandte Chemie (International Ed. in English). 51: 8886-90. PMID 22847787 DOI: 10.1002/anie.201203637  1
2012 Audisio D, Luparia M, Oliveira MT, Klütt D, Maulide N. Diastereodivergent de-epimerization in catalytic asymmetric allylic alkylation. Angewandte Chemie (International Ed. in English). 51: 7314-7. PMID 22696160 DOI: 10.1002/anie.201202853  1
2012 Klimczyk S, Huang X, Farès C, Maulide N. Sulfoxide-mediated Umpolung of alkali halide salts. Organic & Biomolecular Chemistry. 10: 4327-9. PMID 22592400 DOI: 10.1039/c2ob25459j  1
2012 Frébault F, Maulide N. Total synthesis and structural revision of the piperarborenines: When photochemistry meets C-H activation Angewandte Chemie - International Edition. 51: 2815-2817. PMID 22331562 DOI: 10.1002/anie.201108592  1
2012 Jurberg ID, Peng B, Wöstefeld E, Wasserloos M, Maulide N. Intramolecular redox-triggered C-H functionalization. Angewandte Chemie (International Ed. in English). 51: 1950-3. PMID 22262631 DOI: 10.1002/anie.201108639  0.76
2012 Huang X, Klimczyk S, Maulide N. Charge-accelerated sulfonium [3,3]-sigmatropic rearrangements Synthesis. 2012: 175-183. DOI: 10.1055/s-0031-1289632  1
2012 Huang X, Klimczyk S, Maulide N. Charge-accelerated sulfonium [3,3]-sigmatropic rearrangements Synthesis. 2012: 175-183. DOI: 10.1055/s-0031-1289632  1
2012 Klimczyk S, Huang X, Farès C, Maulide N. Sulfoxide-mediated Umpolung of alkali halide salts Organic and Biomolecular Chemistry. 10: 4327-4329. DOI: 10.1039/c2ob25459j  1
2012 Klimczyk S, Huang X, Farès C, Maulide N. Sulfoxide-mediated Umpolung of alkali halide salts Organic and Biomolecular Chemistry. 10: 4327-4329. DOI: 10.1039/c2ob25459j  1
2012 Peng B, O'Donovan DH, Jurberg ID, Maulide N. Dual nucleophilic/electrophilic capture of in situ generated iminium ethers: Towards the synthesis of functionalized amide building blocks Chemistry - a European Journal. 18: 16292-16296. DOI: 10.1002/chem.201203293  1
2012 Peng B, O'Donovan DH, Jurberg ID, Maulide N. Dual nucleophilic/electrophilic capture of in situ generated iminium ethers: Towards the synthesis of functionalized amide building blocks Chemistry - a European Journal. 18: 16292-16296. DOI: 10.1002/chem.201203293  0.76
2012 Huang X, Peng B, Luparia M, Gomes LFR, Veiros LF, Maulide N. Gold-catalyzed synthesis of furans and furanones from sulfur ylides Angewandte Chemie - International Edition. 51: 8886-8890. DOI: 10.1002/anie.201203637  1
2012 Huang X, Peng B, Luparia M, Gomes LFR, Veiros LF, Maulide N. Gold-catalyzed synthesis of furans and furanones from sulfur ylides Angewandte Chemie - International Edition. 51: 8886-8890. DOI: 10.1002/anie.201203637  1
2012 Audisio D, Luparia M, Oliveira MT, Klütt D, Maulide N. Diastereodivergent de-epimerization in catalytic asymmetric allylic alkylation Angewandte Chemie - International Edition. 51: 7314-7317. DOI: 10.1002/anie.201202853  1
2012 Audisio D, Luparia M, Oliveira MT, Klütt D, Maulide N. Diastereodivergent de-epimerization in catalytic asymmetric allylic alkylation Angewandte Chemie - International Edition. 51: 7314-7317. DOI: 10.1002/anie.201202853  1
2012 Jurberg ID, Peng B, Wöstefeld E, Wasserloos M, Maulide N. Intramolecular redox-triggered C-H functionalization Angewandte Chemie - International Edition. 51: 1950-1953. DOI: 10.1002/anie.201108639  1
2011 Luparia M, Oliveira MT, Audisio D, Frébault F, Goddard R, Maulide N. Catalytic asymmetric diastereodivergent deracemization. Angewandte Chemie (International Ed. in English). 50: 12631-5. PMID 22058047 DOI: 10.1002/anie.201106321  1
2011 Huang X, Maulide N. Sulfoxide-mediated α-arylation of carbonyl compounds. Journal of the American Chemical Society. 133: 8510-3. PMID 21574566 DOI: 10.1021/ja2031882  1
2011 Luparia M, Audisio D, Maulide N. Palladium-catalysed synthesis of stereodefined cyclobutenes Synlett. 735-740. DOI: 10.1055/s-0030-1259907  1
2011 Luparia M, Audisio D, Maulide N. Palladium-catalysed synthesis of stereodefined cyclobutenes Synlett. 735-740. DOI: 10.1055/s-0030-1259907  1
2011 Huang X, Maulide N. Sulfoxide-mediated α-arylation of carbonyl compounds Journal of the American Chemical Society. 133: 8510-8513. DOI: 10.1021/ja2031882  1
2011 Huang X, Maulide N. Sulfoxide-mediated α-arylation of carbonyl compounds Journal of the American Chemical Society. 133: 8510-8513. DOI: 10.1021/ja2031882  1
2011 Valerio V, Madelaine C, Maulide N. Steering reaction pathways: From benzyl Claisen rearrangements to powerful ionic shifts Chemistry - a European Journal. 17: 4742-4745. DOI: 10.1002/chem.201003591  1
2011 Madelaine C, Valerio V, Maulide N. Revisiting keteniminium salts: More than the nitrogen analogs of ketenes Chemistry - An Asian Journal. 6: 2224-2239. DOI: 10.1002/asia.201100108  1
2011 Luparia M, Oliveira MT, Audisio D, Frébault F, Goddard R, Maulide N. Catalytic asymmetric diastereodivergent deracemization Angewandte Chemie - International Edition. 50: 12631-12635. DOI: 10.1002/anie.201106321  1
2011 Luparia M, Oliveira MT, Audisio D, Frébault F, Goddard R, Maulide N. Catalytic asymmetric diastereodivergent deracemization Angewandte Chemie - International Edition. 50: 12631-12635. DOI: 10.1002/anie.201106321  1
2010 Frébault F, Oliveira MT, Wöstefeld E, Maulide N. A concise access to 3-substituted 2-pyrones Journal of Organic Chemistry. 75: 7962-7965. PMID 21033724 DOI: 10.1021/jo101843a  1
2010 Huang X, Goddard R, Maulide N. A direct ylide transfer to carbonyl derivatives and heteroaromatic compounds. Angewandte Chemie (International Ed. in English). 49: 8979-83. PMID 20939026 DOI: 10.1002/anie.201002919  1
2010 Frébault F, Luparia M, Oliveira MT, Goddard R, Maulide N. A versatile and stereoselective synthesis of fnnctionalized cyclobutenes Angewandte Chemie - International Edition. 49: 5672-5676. PMID 20629000 DOI: 10.1002/anie.201000911  1
2010 Barroso S, Abreu AM, Araújo AC, Coelho AM, Maulide N, Martins AM. Three-Component Mannich Couplings En Route to Substituted Aminophenol and Benzoxazine Derivatives Synlett. 2425-2428. DOI: 10.1055/s-0030-1258047  1
2010 Maulide N. A Feast and a reflection on organocatalysis - Notes from the ISOμ in Mülheim European Journal of Organic Chemistry. 6491-6493. DOI: 10.1002/ejoc.201001323  1
2010 Huang X, Goddard R, Maulide N. A direct ylide transfer to carbonyl derivatives and heteroaromatic compounds Angewandte Chemie - International Edition. 49: 8979-8983. DOI: 10.1002/anie.201002919  1
2010 Huang X, Goddard R, Maulide N. A direct ylide transfer to carbonyl derivatives and heteroaromatic compounds Angewandte Chemie - International Edition. 49: 8979-8983. DOI: 10.1002/anie.201002919  1
2010 Madelaine C, Valerio V, Maulide N. Unexpected electrophilic rearrangements of amides: A stereoselective entry to challenging substituted lactones Angewandte Chemie - International Edition. 49: 1583-1586. DOI: 10.1002/anie.200906416  1
2009 Trost BM, Maulide N, Rudd MT. Ruthenium-catalyzed cross-coupling of tertiary propargyl alcohols with omega-alkynenitriles: a regio- and stereoselective surrogate for an aldol condensation. Journal of the American Chemical Society. 131: 420-1. PMID 19099475 DOI: 10.1021/ja8077686  1
2009 Trost BM, Maulide N, Rudd MT. Ruthenium-catalyzed cross-coupling of tertiary propargyl alcohols with omega-alkynenitriles: a regio- and stereoselective surrogate for an aldol condensation. Journal of the American Chemical Society. 131: 420-1. PMID 19099475 DOI: 10.1021/ja8077686  1
2008 Trost BM, Maulide N, Livingston RC. A ruthenium-catalyzed, atom-economical synthesis of nitrogen heterocycles. Journal of the American Chemical Society. 130: 16502-3. PMID 19554686 DOI: 10.1021/ja807696e  1
2008 Trost BM, Maulide N, Livingston RC. A ruthenium-catalyzed, atom-economical synthesis of nitrogen heterocycles. Journal of the American Chemical Society. 130: 16502-3. PMID 19554686 DOI: 10.1021/ja807696e  1
2008 Trost BM, Xie J, Maulide N. Stereoselective, dual-mode ruthenium-catalyzed ring expansion of alkynylcyclopropanols. Journal of the American Chemical Society. 130: 17258-9. PMID 19053484 DOI: 10.1021/ja807894t  1
2008 Trost BM, Xie J, Maulide N. Stereoselective, dual-mode ruthenium-catalyzed ring expansion of alkynylcyclopropanols. Journal of the American Chemical Society. 130: 17258-9. PMID 19053484 DOI: 10.1021/ja807894t  1
2008 Munhá RF, Alves LG, Maulide N, Teresa Duarte M, Markó IE, Fryzuk MD, Martins AM. trans-Disubstituted diamido/diamine cyclam zirconium complexes Inorganic Chemistry Communications. 11: 1174-1176. DOI: 10.1016/j.inoche.2008.07.002  1
2008 Munhá RF, Alves LG, Maulide N, Teresa Duarte M, Markó IE, Fryzuk MD, Martins AM. trans-Disubstituted diamido/diamine cyclam zirconium complexes Inorganic Chemistry Communications. 11: 1174-1176. DOI: 10.1016/j.inoche.2008.07.002  1
2007 Maulide N, Markó IE. Synthesis and ring expansions of functionalized spirocyclobutanones Organic Letters. 9: 3757-3760. PMID 17715931 DOI: 10.1021/ol7015753  1
2007 Maulide N, Vanherck JC, Gautier A, Markó IE. Mild and neutral deprotections catalyzed by cerium(IV) ammonium nitrate. Accounts of Chemical Research. 40: 381-92. PMID 17469793 DOI: 10.1021/ar600062b  1
2007 Maulide N, Vanherck JC, Gautier A, Markó IE. Mild and neutral deprotections catalyzed by cerium(IV) ammonium nitrate. Accounts of Chemical Research. 40: 381-92. PMID 17469793 DOI: 10.1021/ar600062b  1
2006 Maulide N, Markó IE. 2-(Trimethylsilyloxy)furan as a dianion equivalent: a two-step synthesis of functionalized spirocyclic butenolides. Organic Letters. 8: 3705-7. PMID 16898797 DOI: 10.1021/ol061284g  0.96
2006 Liao JH, Maulide N, Augustyns B, Markó IE. Tandem radical rearrangement/Pd-catalysed translocation of bicyclo[2.2.2]lactones. An efficient access to the oxa-triquinane core structure. Organic & Biomolecular Chemistry. 4: 1464-7. PMID 16604210 DOI: 10.1039/b518121f  0.96
2006 Maulide N, Markó IE. Stereoselective synthesis of bicyclic lactones by annelation with functionalised orthoesters Chemical Communications. 1200-1202. PMID 16518490 DOI: 10.1039/b600677a  1
2006 Liao JH, Maulide N, Augustyns B, Markó IE. Tandem radical rearrangement/Pd-catalysed translocation of bicyclo[2.2.2]lactones. An efficient access to the oxa-triquinane core structure Organic and Biomolecular Chemistry. 4: 1464-1467. DOI: 10.1039/b518121f  1
2006 Liao JH, Maulide N, Augustyns B, Markó IE. Tandem radical rearrangement/Pd-catalysed translocation of bicyclo[2.2.2]lactones. An efficient access to the oxa-triquinane core structure Organic and Biomolecular Chemistry. 4: 1464-1467. DOI: 10.1039/b518121f  0.96
2006 Maulide N, Markó IE. 2-(Trimethylsilyloxy)furan as a dianion equivalent: A two-step synthesis of functionalized spirocyclic butenolides Organic Letters. 8: 3705-3707. DOI: 10.1021/ol061284g  1
2006 Maulide N, Markó IE. 2-(Trimethylsilyloxy)furan as a dianion equivalent: A two-step synthesis of functionalized spirocyclic butenolides Organic Letters. 8: 3705-3707. DOI: 10.1021/ol061284g  0.96
2005 Maulide N, Markó IE. Cerium(IV) ammonium nitrate catalysed highly chemoselective deprotection of ketals and THP ethers in the presence of enol triflates Synlett. 2195-2198. DOI: 10.1055/s-2005-872257  1
2005 Maulide N, Markó IE. Cerium(IV) ammonium nitrate catalysed highly chemoselective deprotection of ketals and THP ethers in the presence of enol triflates Synlett. 2195-2198. DOI: 10.1055/s-2005-872257  0.96
2005 Augustyns B, Maulide N, Markó IE. Skeletal rearrangements of bicyclo[2.2.2]lactones: A short and efficient route towards Corey's lactone Tetrahedron Letters. 46: 3895-3899. DOI: 10.1016/j.tetlet.2005.03.204  1
2005 Augustyns B, Maulide N, Markó IE. Skeletal rearrangements of bicyclo[2.2.2]lactones: A short and efficient route towards Corey's lactone Tetrahedron Letters. 46: 3895-3899. DOI: 10.1016/j.tetlet.2005.03.204  0.96
2005 Heureux N, Marchant M, Maulide N, Berthon-Gelloz G, Hermans C, Hermant S, Kiss E, Leroy B, Wasnaire P, Markó IE. Preparation and applications of a novel bis(tributylstannyl)cyclopropane: A synthetic equivalent of a cyclopropane-1,2-dianion Tetrahedron Letters. 46: 79-83. DOI: 10.1016/j.tetlet.2004.11.036  1
2005 Heureux N, Marchant M, Maulide N, Berthon-Gelloz G, Hermans C, Hermant S, Kiss E, Leroy B, Wasnaire P, Markó IE. Preparation and applications of a novel bis(tributylstannyl)cyclopropane: A synthetic equivalent of a cyclopropane-1,2-dianion Tetrahedron Letters. 46: 79-83. DOI: 10.1016/j.tetlet.2004.11.036  0.96
2004 Maulide N, Vanherck JC, Markó IE. Connective synthesis of spirovetivanes: Total synthesis of (±)-agarospirol, (±)-hinesol and (±)-α-vetispirene European Journal of Organic Chemistry. 3962-3967. DOI: 10.1002/ejoc.200400236  1
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