Year |
Citation |
Score |
2024 |
G-Simonian N, Spieß P, Riomet M, Maryasin B, Klose I, Beaton Garcia A, Pollesböck L, Kaldre D, Todorovic U, Minghua Liu J, Kaiser D, González L, Maulide N. Stereodivergent Synthesis of 1,4-Dicarbonyl Compounds through Sulfonium Rearrangement: Mechanistic Investigation, Stereocontrolled Access to γ-Lactones and γ-Lactams, and Total Synthesis of Paraconic Acids. Journal of the American Chemical Society. PMID 38741029 DOI: 10.1021/jacs.4c01755 |
0.331 |
|
2024 |
Saridakis I, Riomet M, Belleza OJV, Coussanes G, Singer NK, Kastner N, Xiao Y, Smith E, Tona V, de la Torre A, Lopes EF, Sánchez-Murcia PA, González L, Sitte HH, Maulide N. PyrAtes: Modular Organic Salts with Large Stokes Shifts for Fluo-rescence Microscopy. Angewandte Chemie (International Ed. in English). e202318127. PMID 38570814 DOI: 10.1002/anie.202318127 |
0.715 |
|
2024 |
Jones BT, Maulide N. Lewis Acid-Driven Inverse Hydride Shuttle Catalysis. Angewandte Chemie (International Ed. in English). e202320001. PMID 38551113 DOI: 10.1002/anie.202320001 |
0.304 |
|
2023 |
Lemmerer M, Maulide N. Lewis Base-Assisted Arylation of Unsaturated Carbonyls. Chemistry (Weinheim An Der Bergstrasse, Germany). e202302490. PMID 37647146 DOI: 10.1002/chem.202302490 |
0.306 |
|
2023 |
Spieß P, Shaaban S, Kaiser D, Maulide N. New Strategies for the Functionalization of Carbonyl Derivatives via α-Umpolung: From Enolates to Enolonium Ions. Accounts of Chemical Research. PMID 37226674 DOI: 10.1021/acs.accounts.3c00171 |
0.306 |
|
2023 |
Feng M, Fernandes AJ, Sirvent A, Spinozzi E, Shaaban S, Maulide N. Free Amino Group Transfer via α-Amination of Native Carbonyls. Angewandte Chemie (International Ed. in English). e202304990. PMID 37114555 DOI: 10.1002/anie.202304990 |
0.302 |
|
2023 |
Tiefenbrunner I, Brutiu BR, Stopka T, Maulide N. Isothiouronium-Mediated Conversion of Carboxylic Acids to Cyanomethyl Thioesters. The Journal of Organic Chemistry. 88: 3941-3944. PMID 36853206 DOI: 10.1021/acs.joc.2c02902 |
0.323 |
|
2022 |
Feng M, Tinelli R, Meyrelles R, González L, Maryasin B, Maulide N. Direct Synthesis of α-Amino Acid Derivatives by Hydrative Amination of Alkynes. Angewandte Chemie (International Ed. in English). PMID 36222199 DOI: 10.1002/anie.202212399 |
0.32 |
|
2022 |
Lemmerer M, Zhang H, Fernandes A, Fischer T, Miesskes M, Xiao Y, Maulide N. Synthesis of α-Aryl Acrylamides via Lewis Base Mediated Aryl/Hydrogen Exchange. Angewandte Chemie (International Ed. in English). PMID 35881564 DOI: 10.1002/anie.202207475 |
0.358 |
|
2022 |
Feng M, Mosiagin I, Kaiser D, Maryasin B, Maulide N. Deployment of Sulfinimines in Charge-Accelerated Sulfonium Rearrangement Enables a Surrogate Asymmetric Mannich Reaction. Journal of the American Chemical Society. PMID 35839521 DOI: 10.1021/jacs.2c05368 |
0.339 |
|
2022 |
Hsu CS, Goncalves C, Tona V, Pons A, Kaiser M, Maulide N. Leveraging electron-deficient iminium intermediates in a general synthesis of valuable amines. Angewandte Chemie (International Ed. in English). PMID 35103377 DOI: 10.1002/anie.202115435 |
0.325 |
|
2021 |
Spieß P, Berger M, Kaiser D, Maulide N. Direct Synthesis of Enamides via Electrophilic Activation of Amides. Journal of the American Chemical Society. PMID 34232035 DOI: 10.1021/jacs.1c04363 |
0.338 |
|
2021 |
Todorović U, Klose I, Maulide N. Straightforward Access to Thiocyanates via Dealkylative Cyanation of Sulfoxides. Organic Letters. PMID 33724046 DOI: 10.1021/acs.orglett.1c00460 |
0.307 |
|
2021 |
Martins BS, Kaiser D, Bauer A, Tiefenbrunner I, Maulide N. Formal Enone α-Arylation via I(III)-Mediated Aryl Migration/Elimination. Organic Letters. PMID 33635665 DOI: 10.1021/acs.orglett.1c00251 |
0.327 |
|
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 |
0.447 |
|
2020 |
Zawodny W, Teskey CJ, Mishevska M, Völkl M, Maryasin B, González L, Maulide N. α-Functionalisation of Ketones Through Metal-Free Electrophilic Activation. Angewandte Chemie (International Ed. in English). PMID 32914929 DOI: 10.1002/Anie.202006398 |
0.783 |
|
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 |
0.453 |
|
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 |
0.394 |
|
2020 |
Zhang H, Riomet M, Roller A, Maulide N. Synthesis of Novel Heterocycles by Amide Activation and Umpolung Cyclization. Organic Letters. PMID 32159354 DOI: 10.1021/Acs.Orglett.0C00571 |
0.467 |
|
2020 |
Brutiu BR, Klose I, Maulide N. Facile C–S Bond Cleavage of Aryl Sulfoxides Promoted by Brønsted Acid Synlett. 24. DOI: 10.1055/S-0040-1707109 |
0.327 |
|
2020 |
Stopka T, Schröder S, Maulide N, Niggemann M. The unusual migratory aptitude in a case of α-carbonyl cation-driven 1,2-migration Tetrahedron. 131460. DOI: 10.1016/J.Tet.2020.131460 |
0.38 |
|
2020 |
Berger M, Knittl-Frank C, Bauer S, Winter G, Maulide N. Application of Relay C−H Oxidation Logic to Polyhydroxylated Oleanane Triterpenoids Chem. 6: 1183-1189. DOI: 10.1016/J.Chempr.2020.04.007 |
0.34 |
|
2020 |
Zawodny W, Teskey CJ, Mishevska M, Völkl M, Maryasin B, González L, Maulide N. α‐Funktionalisierung von Ketonen durch metallfreie elektrophile Aktivierung Angewandte Chemie. DOI: 10.1002/Ange.202006398 |
0.692 |
|
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 |
0.413 |
|
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 |
0.761 |
|
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 |
0.459 |
|
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 |
0.399 |
|
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 |
0.437 |
|
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 |
0.403 |
|
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 |
0.366 |
|
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 |
0.469 |
|
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 |
0.429 |
|
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 |
0.313 |
|
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 |
0.461 |
|
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 |
0.766 |
|
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 |
0.448 |
|
2019 |
Di Mauro G, Drescher M, Tkaczyk S, Maulide N. Aminoxylation of Thioalkynes through Radical-Polar Crossover Synlett. 31: 592-594. DOI: 10.1055/S-0039-1689925 |
0.361 |
|
2019 |
Bauer A, Nam J, Maulide N. A Short, Efficient, and Stereoselective Synthesis of Piperine and its Analogues Synlett. 30: 413-416. DOI: 10.1055/S-0037-1611652 |
0.47 |
|
2019 |
Li J, Berger M, Zawodny W, Simaan M, Maulide N. A Chemoselective α-Oxytriflation Enables the Direct Asymmetric Arylation of Amides Chem. 5: 1883-1891. DOI: 10.1016/J.Chempr.2019.05.006 |
0.521 |
|
2019 |
Landeros JM, Suchy L, Ávila-Ortiz CG, Maulide N, Juaristi E. Dendrimeric α,β-dipeptidic conjugates as organocatalysts in the asymmetric Michael addition reaction of isobutyraldehyde to N-phenylmaleimides Monatshefte FüR Chemie - Chemical Monthly. 150: 777-788. DOI: 10.1007/S00706-018-2338-0 |
0.386 |
|
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 |
0.42 |
|
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 |
0.764 |
|
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 |
0.362 |
|
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 |
0.367 |
|
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 |
0.332 |
|
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 |
0.46 |
|
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 |
0.399 |
|
2018 |
Kaldre D, Klose I, Maulide N. Stereodivergent synthesis of 1,4-dicarbonyls by traceless charge-accelerated sulfonium rearrangement. Science (New York, N.Y.). 361: 664-667. PMID 30115803 DOI: 10.1126/Science.Aat5883 |
0.443 |
|
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 |
0.359 |
|
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 |
0.447 |
|
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 |
0.68 |
|
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 |
0.784 |
|
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 |
0.781 |
|
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 |
0.341 |
|
2018 |
Bauer A, Maulide N. A Stereoselective Reductive Hosomi-Sakurai Reaction. Organic Letters. PMID 29469578 DOI: 10.1021/Acs.Orglett.8B00276 |
0.43 |
|
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 |
0.332 |
|
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 |
0.357 |
|
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 |
0.332 |
|
2018 |
Stopka T, Adler P, Hagn G, Zhang H, Tona V, Maulide N. Electrophilic Activation of Amides for the Preparation of Polysubstituted Pyrimidines Synthesis. 51: 194-202. DOI: 10.1055/S-0037-1610411 |
0.407 |
|
2018 |
Bauer A, Maulide N. Development of a reductive Hosomi-Sakurai reaction Tetrahedron. 74: 6883-6889. DOI: 10.1016/J.Tet.2018.10.033 |
0.364 |
|
2018 |
Lemmerer M, Teskey CJ, Kaiser D, Maulide N. Correction to: Regioselective synthesis of pyridines by redox alkylation of pyridine N-oxides with malonates Monatshefte FüR Chemie - Chemical Monthly. 149: 721-722. DOI: 10.1007/S00706-018-2149-3 |
0.735 |
|
2018 |
Martin HJ, Kampatsikas I, Oost R, Pretzler M, Al-Sayed E, Roller A, Giester G, Rompel A, Maulide N. Cover Feature: Total Synthesis, Stereochemical Assignment, and Divergent Enantioselective Enzymatic Recognition of Larreatricin (Chem. Eur. J. 59/2018) Chemistry - a European Journal. 24: 15694-15694. DOI: 10.1002/Chem.201805128 |
0.336 |
|
2018 |
Teskey CJ, Adler P, Gonçalves CR, Maulide N. Chemoselektive α,β‐Dehydrierung von gesättigten Amiden Angewandte Chemie. 131: 456-460. DOI: 10.1002/Ange.201808794 |
0.72 |
|
2018 |
Adler P, Pons A, Li J, Heider J, Brutiu BR, Maulide N. Chemoselektive Aktivierung von Diethylphosphonaten: modulare Synthese von biologisch relevanten phosphonylierten Grundgerüsten Angewandte Chemie. 130: 13514-13518. DOI: 10.1002/Ange.201806343 |
0.387 |
|
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 |
0.766 |
|
2017 |
Niyomchon S, Oppedisano A, Aillard P, Maulide N. A three-membered ring approach to carbonyl olefination. Nature Communications. 8: 1091. PMID 29061994 DOI: 10.1038/S41467-017-01036-Y |
0.412 |
|
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 |
0.776 |
|
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 |
0.322 |
|
2017 |
Stopka T, Niggemann M, Maulide N. α-Carbonyl Cations in Sulfoxide-Driven, Oxidative Cyclizations. Angewandte Chemie (International Ed. in English). PMID 28834106 DOI: 10.1002/Anie.201705964 |
0.429 |
|
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 |
0.413 |
|
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 |
0.382 |
|
2017 |
Pototschnig G, Maulide N, Schnürch M. Direct Functionalization of C-H Bonds by Iron, Nickel, and Cobalt Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28590552 DOI: 10.1002/Chem.201605657 |
0.361 |
|
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 |
0.772 |
|
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 |
0.782 |
|
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 |
0.783 |
|
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 |
0.772 |
|
2017 |
Merad J, Maier T, Rodrigues CA, Maulide N. Synthesis of γ-pyrones via decarboxylative condensation of β-ketoacids. Monatshefte Fur Chemie. 148: 57-62. PMID 28127091 DOI: 10.1007/S00706-016-1851-2 |
0.425 |
|
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 |
0.39 |
|
2017 |
Shaaban S, Maulide N. Metal-Free Redox Transformations for C–C and C–N Bond Construction Synlett. 28: 2707-2713. DOI: 10.1055/S-0036-1588776 |
0.373 |
|
2017 |
Oost R, Neuhaus JD, Merad J, Maulide N. Sulfur Ylides in Organic Synthesis and Transition Metal Catalysis Structure and Bonding. 73-115. DOI: 10.1007/430_2017_14 |
0.374 |
|
2017 |
Baldassari LL, de la Torre A, Li J, Lüdtke DS, Maulide N. Regio- und stereoselektive Synthese α,β-disubstituierter Enamide durch Voraktivierung von Inamiden Angewandte Chemie. 129: 15929-15933. DOI: 10.1002/Ange.201709128 |
0.358 |
|
2017 |
de la Torre A, Tona V, Maulide N. Umkehr der Polarität: α-Aminierungen von Carbonylverbindungen mit Stickstoffnukleophilen Angewandte Chemie. 129: 12588-12596. DOI: 10.1002/Ange.201702937 |
0.302 |
|
2017 |
Kaiser D, de la Torre A, Shaaban S, Maulide N. Metallfreie formale oxidative C-C-Kupplung durch In-situ-Erzeugung einer elektrophilen Enoloniumspezies Angewandte Chemie. 129: 6015-6019. DOI: 10.1002/Ange.201701538 |
0.319 |
|
2017 |
Kaldre D, Maryasin B, Kaiser D, Gajsek O, González L, Maulide N. Asymmetrische Redoxarylierung: Chiralitätstransfer von Schwefel zu Kohlenstoff durch sigmatrope Sulfonium-[3,3]-Umlagerung Angewandte Chemie. 129: 2248-2252. DOI: 10.1002/Ange.201610105 |
0.309 |
|
2017 |
Kaiser D, Veiros LF, Maulide N. Front Cover Picture: Redox-Neutral Arylations of Vinyl Cation Intermediates (Adv. Synth. Catal. 1/2017) Advanced Synthesis & Catalysis. 359: 1-1. DOI: 10.1002/Adsc.201601440 |
0.377 |
|
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 |
0.362 |
|
2016 |
Berger M, Roller A, Maulide N. Synthesis and antimicrobial evaluation of novel analogues of dehydroabietic acid prepared by CH-Activation. European Journal of Medicinal Chemistry. 126: 937-943. PMID 27997880 DOI: 10.1016/J.Ejmech.2016.12.012 |
0.332 |
|
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 |
0.395 |
|
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 |
0.359 |
|
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 |
0.475 |
|
2016 |
Berger M, Chauhan R, Rodrigues C, Maulide N. Bridging C-H activation: Mild and versatile cleavage of the 8-Aminoquinoline directing group. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27642704 DOI: 10.1002/Chem.201604344 |
0.384 |
|
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 |
0.463 |
|
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 |
0.419 |
|
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 |
0.413 |
|
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 |
0.802 |
|
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 |
0.365 |
|
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 |
0.357 |
|
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 |
0.362 |
|
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 |
0.437 |
|
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 |
0.449 |
|
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 |
0.433 |
|
2016 |
Preinfalk A, Misale A, Maulide N. Inside Back Cover: A Gold(I)-Catalyzed Domino Coupling of Alcohols with Allenes Enables the Synthesis of Highly Substituted Indenes (Chem. Eur. J. 41/2016) Chemistry - a European Journal. 22: 14755-14755. DOI: 10.1002/Chem.201604243 |
0.378 |
|
2016 |
Kaiser D, Veiros LF, Maulide N. Redox-Neutral Arylations of Vinyl Cation Intermediates Advanced Synthesis & Catalysis. 359: 64-77. DOI: 10.1002/Adsc.201600860 |
0.423 |
|
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 |
0.344 |
|
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 |
0.349 |
|
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 |
0.38 |
|
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 |
0.309 |
|
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 |
0.671 |
|
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 |
0.704 |
|
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 |
0.619 |
|
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 |
0.674 |
|
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 |
0.427 |
|
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 |
0.419 |
|
2015 |
Gomes LFR, Veiros LF, Maulide N, Afonso CAM. Back Cover: Diazo- and Transition-Metal-Free CH Insertion: A Direct Synthesis of β-Lactams (Chem. Eur. J. 4/2015) Chemistry - a European Journal. 21: 1820-1820. DOI: 10.1002/Chem.201590014 |
0.328 |
|
2015 |
Klimczyk S, Misale A, Huang X, Maulide N. Dimere TADDOL-Phosphoramidite in der asymmetrischen Katalyse: Domino-Deracemisierung/Cyclopropanierung von Sulfoniumyliden Angewandte Chemie. 127: 10507-10511. DOI: 10.1002/Ange.201503851 |
0.607 |
|
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 |
0.448 |
|
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 |
0.699 |
|
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 |
0.446 |
|
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 |
0.452 |
|
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 |
0.696 |
|
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 |
0.665 |
|
2014 |
Peng B, Huang X, Xie L, Maulide N. Inside Back Cover: A Brønsted Acid Catalyzed Redox Arylation (Angew. Chem. Int. Ed. 33/2014) Angewandte Chemie International Edition. 53: 8789-8789. DOI: 10.1002/Anie.201406163 |
0.65 |
|
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 |
0.62 |
|
2014 |
Peng B, Huang X, Xie L, Maulide N. Innenrücktitelbild: Eine Brønsted-Säure-katalysierte Redox-Arylierung (Angew. Chem. 33/2014) Angewandte Chemie. 126: 8933-8933. DOI: 10.1002/Ange.201406163 |
0.604 |
|
2014 |
Peng B, Geerdink D, Farès C, Maulide N. Chemoselektive intermolekulare α-Arylierung von Amiden Angewandte Chemie. 126: 5566-5570. DOI: 10.1002/Ange.201402229 |
0.317 |
|
2014 |
Peng B, Huang X, Xie L, Maulide N. Eine Brønsted-Säure-katalysierte Redox-Arylierung Angewandte Chemie. 126: 8862-8866. DOI: 10.1002/Ange.201310865 |
0.624 |
|
2014 |
Misale A, Niyomchon S, Luparia M, Maulide N. Asymmetrische Palladium-katalysierte allylische Alkylierung mit Dialkylzinkreagentien: ein bemerkenswerter Ligandeneffekt Angewandte Chemie. 126: 7188-7193. DOI: 10.1002/Ange.201309074 |
0.387 |
|
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 |
0.302 |
|
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 |
0.461 |
|
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 |
0.317 |
|
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 |
0.358 |
|
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 |
0.67 |
|
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 |
0.44 |
|
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 |
0.416 |
|
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 |
0.312 |
|
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 |
0.648 |
|
2013 |
Shaaban S, Peng B, Maulide N. Base-promoted internal redox-cyclisation reactions Synlett. 24: 1722-1724. DOI: 10.1055/S-0033-1339313 |
0.432 |
|
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 |
0.387 |
|
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 |
0.674 |
|
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 |
0.584 |
|
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 |
0.396 |
|
2013 |
Audisio D, Gopakumar G, Xie L, Alves LG, Wirtz C, Martins AM, Thiel W, Farès C, Maulide N. Palladium-katalysierte allylische Substitution an viergliedrigen Ringen: Bildung von η1-Allylkomplexen und elektrocyclische Ringöffnung Angewandte Chemie. 125: 6434-6438. DOI: 10.1002/Ange.201301034 |
0.407 |
|
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 |
0.733 |
|
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 |
0.708 |
|
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 |
0.32 |
|
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 |
0.666 |
|
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 |
0.319 |
|
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 |
0.67 |
|
2012 |
Huang X, Klimczyk S, Maulide N. Charge-accelerated sulfonium [3,3]-sigmatropic rearrangements Synthesis. 2012: 175-183. DOI: 10.1055/S-0031-1289632 |
0.662 |
|
2012 |
Huang X, Klimczyk S, Maulide N. Charge-accelerated sulfonium [3,3]-sigmatropic rearrangements Synthesis. 2012: 175-183. DOI: 10.1055/S-0031-1289632 |
0.662 |
|
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 |
0.594 |
|
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 |
0.704 |
|
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 |
0.351 |
|
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 |
0.351 |
|
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 |
0.304 |
|
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 |
0.304 |
|
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 |
0.646 |
|
2012 |
Huang X, Peng B, Luparia M, Gomes LFR, Veiros LF, Maulide N. Gold-katalysierte Synthese von Furanen und Furanonen aus Schwefel-Yliden Angewandte Chemie. 124: 9016-9020. DOI: 10.1002/Ange.201203637 |
0.615 |
|
2012 |
Jurberg ID, Peng B, Wöstefeld E, Wasserloos M, Maulide N. C-H-Funktionalisierung durch eine intramolekulare Redox-Strategie Angewandte Chemie. 124: 1986-1989. DOI: 10.1002/Ange.201108639 |
0.656 |
|
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 |
0.341 |
|
2011 |
Madelaine C, Valerio V, Maulide N. Revisiting keteniminium salts: more than the nitrogen analogs of ketenes. Chemistry, An Asian Journal. 6: 2224-39. PMID 21721132 DOI: 10.1002/Asia.201100108 |
0.403 |
|
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 |
0.685 |
|
2011 |
Luparia M, Audisio D, Maulide N. Palladium-catalysed synthesis of stereodefined cyclobutenes Synlett. 735-740. DOI: 10.1055/S-0030-1259907 |
0.395 |
|
2011 |
Luparia M, Audisio D, Maulide N. Palladium-catalysed synthesis of stereodefined cyclobutenes Synlett. 735-740. DOI: 10.1055/s-0030-1259907 |
0.342 |
|
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 |
0.459 |
|
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 |
0.616 |
|
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 |
0.432 |
|
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 |
0.32 |
|
2010 |
Madelaine C, Valerio V, Maulide N. Unexpected electrophilic rearrangements of amides: a stereoselective entry to challenging substituted lactones. Angewandte Chemie (International Ed. in English). 49: 1583-6. PMID 20127923 DOI: 10.1002/Anie.200906416 |
0.427 |
|
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 |
0.398 |
|
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 |
0.314 |
|
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 |
0.314 |
|
2010 |
Huang X, Goddard R, Maulide N. Direkter Ylidtransfer auf Carbonylverbindungen und Heteroarene Angewandte Chemie. 122: 9163-9167. DOI: 10.1002/Ange.201002919 |
0.603 |
|
2010 |
Frébault F, Luparia M, Oliveira M, Goddard R, Maulide N. Eine vielseitige und stereoselektive Synthese funktionalisierter Cyclobutene Angewandte Chemie. 122: 5807-5811. DOI: 10.1002/Ange.201000911 |
0.352 |
|
2010 |
Madelaine C, Valerio V, Maulide N. Unerwartete nucleophile Umlagerung von Amiden: ein stereoselektiver Zugang zu anspruchsvoll substituierten Lactonen Angewandte Chemie. 122: 1628-1631. DOI: 10.1002/Ange.200906416 |
0.387 |
|
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 |
0.701 |
|
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 |
0.701 |
|
2009 |
Trost B, Xie J, Maulide N. Ring Expansion of Alkynylcyclopropanols Catalyzed by Ruthenium Synfacts. 2009: 0281-0281. DOI: 10.1055/s-0028-1087781 |
0.359 |
|
2009 |
Trost BM, Maulide N, Rudd MT. ChemInform Abstract: Ruthenium-Catalyzed Cross-Coupling of Tertiary Propargyl Alcohols with ω-Alkynenitriles: A Regio- and Stereoselective Surrogate for an Aldol Condensation. Cheminform. 40. DOI: 10.1002/chin.200921048 |
0.669 |
|
2009 |
Trost BM, Xie J, Maulide N. ChemInform Abstract: Stereoselective, Dual-Mode Ruthenium-Catalyzed Ring Expansion of Alkynylcyclopropanols. Cheminform. 40. DOI: 10.1002/chin.200919056 |
0.34 |
|
2009 |
Trost BM, Maulide N, Livingston RC. ChemInform Abstract: A Ruthenium-Catalyzed, Atom-Economical Synthesis of Nitrogen Heterocycles. Cheminform. 40. DOI: 10.1002/chin.200918115 |
0.374 |
|
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 |
0.369 |
|
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 |
0.369 |
|
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 |
0.399 |
|
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 |
0.399 |
|
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 |
0.508 |
|
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 |
0.508 |
|
2007 |
Maulide N, Markó IE. Synthesis and ring expansions of functionalized spirocyclobutanones Organic Letters. 9: 3757-3760. PMID 17715931 DOI: 10.1021/Ol7015753 |
0.57 |
|
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 |
0.675 |
|
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 |
0.675 |
|
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 |
0.63 |
|
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 |
0.577 |
|
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 |
0.709 |
|
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 |
0.336 |
|
2006 |
Markó I, Maulide N. Stereoselective Synthesis of Bicyclic Lactones from Furans Synfacts. 2006: 0429-0429. DOI: 10.1055/s-2006-934372 |
0.339 |
|
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 |
0.599 |
|
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 |
0.674 |
|
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 |
0.603 |
|
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 |
0.581 |
|
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 |
0.586 |
|
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 |
0.551 |
|
Show low-probability matches. |