| Year |
Citation |
Score |
| 2022 |
Zhang ZX, Bell C, Ding M, Willis MC. Modular Two-Step Route to Sulfondiimidamides. Journal of the American Chemical Society. PMID 35729783 DOI: 10.1021/jacs.2c04404 |
0.351 |
|
| 2022 |
McKnight J, Shavnya A, Sach NW, Blakemore DC, Moses IB, Willis MC. Reductant-Free Cross-Electrophile Synthesis of Di(hetero)arylmethanes by Palladium-Catalyzed Desulfinative C-C Coupling. Angewandte Chemie (International Ed. in English). e202116775. PMID 35229419 DOI: 10.1002/anie.202116775 |
0.442 |
|
| 2022 |
Iwumene NUN, Moseley DF, Pullin RDC, Willis MC. Diverse saturated heterocycles from a hydroacylation/conjugate addition cascade. Chemical Science. 13: 1504-1511. PMID 35222935 DOI: 10.1039/d1sc06900d |
0.391 |
|
| 2022 |
Ding M, Zhang ZX, Davies TQ, Willis MC. A Silyl Sulfinylamine Reagent Enables the Modular Synthesis of Sulfonimidamides via Primary Sulfinamides. Organic Letters. 24: 1711-1715. PMID 35188396 DOI: 10.1021/acs.orglett.2c00347 |
0.383 |
|
| 2021 |
Moseley DF, Kalepu J, Willis MC. Azine-N-oxides as effective controlling groups for Rh-catalysed intermolecular alkyne hydroacylation. Chemical Science. 12: 13068-13073. PMID 34745537 DOI: 10.1039/d1sc03915f |
0.441 |
|
| 2021 |
Tilby MJ, Dewez DF, Hall A, Martínez Lamenca C, Willis MC. Exploiting Configurational Lability in Aza-Sulfur Compounds for the Organocatalytic Enantioselective Synthesis of Sulfonimidamides. Angewandte Chemie (International Ed. in English). PMID 34558788 DOI: 10.1002/anie.202109160 |
0.341 |
|
| 2021 |
Lo PKT, Willis MC. Nickel(II)-Catalyzed Addition of Aryl and Heteroaryl Boroxines to the Sulfinylamine Reagent TrNSO: The Catalytic Synthesis of Sulfinamides, Sulfonimidamides, and Primary Sulfonamides. Journal of the American Chemical Society. PMID 34533921 DOI: 10.1021/jacs.1c08052 |
0.473 |
|
| 2021 |
Cook XAF, Pantaine LRE, Blakemore DC, Moses IB, Sach NW, Shavnya A, Willis MC. Base-Activated Latent Heteroaromatic Sulfinates as Nucleophilic Coupling Partners in Palladium-Catalyzed Cross-Coupling Reactions. Angewandte Chemie (International Ed. in English). PMID 34342107 DOI: 10.1002/anie.202109146 |
0.448 |
|
| 2021 |
Seo S, Gao M, Paffenholz E, Willis MC. Sequential Catalytic Functionalization of Aryltriazenyl Aldehydes for the Synthesis of Complex Benzenes. Acs Catalysis. 11: 6091-6098. PMID 34306807 DOI: 10.1021/acscatal.1c01722 |
0.465 |
|
| 2021 |
Davies TQ, Willis MC. Rediscovering Sulfinylamines as Reagents for Organic Synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33857343 DOI: 10.1002/chem.202100321 |
0.395 |
|
| 2020 |
Davies TQ, Tilby MJ, Skolc D, Hall A, Willis MC. Primary Sulfonamide Synthesis Using the Sulfinylamine Reagent -Sulfinyl--(-butyl)hydroxylamine, -BuONSO. Organic Letters. PMID 33237777 DOI: 10.1021/acs.orglett.0c03505 |
0.366 |
|
| 2020 |
Willis MC, Cook XAF, de Gombert A, McKnight J, Pantaine LRE. The 2-Pyridyl Problem: Challenging Nucleophiles in Cross-Coupling Arylations. Angewandte Chemie (International Ed. in English). PMID 32940402 DOI: 10.1002/Anie.202010631 |
0.758 |
|
| 2020 |
Davies TQ, Tilby MJ, Ren J, Parker NA, Skolc D, Hall A, Duarte F, Willis MC. Harnessing Sulfinyl Nitrenes: A Unified One-Pot Synthesis of Sulfoximines and Sulfonimidamides. Journal of the American Chemical Society. PMID 32841007 DOI: 10.1021/Jacs.0C06986 |
0.517 |
|
| 2020 |
Pal R, O'Brien S, Willis MC. a-Amidoaldehydes as substrates in rhodium-catalyzed intermolecular alkyne hydroacylation: The synthesis of a-amidoketones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32449532 DOI: 10.1002/Chem.202002478 |
0.489 |
|
| 2020 |
Lo PKT, Oliver GA, Willis MC. Sulfinamide Synthesis Using Organometallic Reagents, DABSO, and Amines. The Journal of Organic Chemistry. PMID 32286844 DOI: 10.1021/Acs.Joc.0C00334 |
0.522 |
|
| 2020 |
Hell SM, Meyer CF, Misale A, Sap JBI, Christensen KK, Willis MC, Trabanco AA, Gouverneur V. Hydrosulfonylation of Alkenes with Sulfonyl Chlorides under Visible Light Activation. Angewandte Chemie (International Ed. in English). PMID 32286720 DOI: 10.1002/Anie.202004070 |
0.412 |
|
| 2020 |
de Gombert A, McKay AI, Davis CJ, Wheelhouse KM, Willis MC. Mechanistic Studies of the Palladium-Catalyzed Desulfinative Cross-Coupling of Aryl Bromides and (Hetero)Aryl Sulfinate Salts. Journal of the American Chemical Society. PMID 32031375 DOI: 10.1021/Jacs.9B13260 |
0.768 |
|
| 2020 |
de Gombert A, Willis MC. Palladium-Catalyzed Desulfinative Cross-Couplings Trends in Chemistry. 2: 865-866. DOI: 10.1016/j.trechm.2020.04.004 |
0.321 |
|
| 2020 |
Lou TS, Willis MC. Arylsulfonyl fluoride boronic acids: Preparation and coupling reactivity Tetrahedron. 76: 130782. DOI: 10.1016/J.Tet.2019.130782 |
0.529 |
|
| 2019 |
Hell SM, Meyer CF, Laudadio G, Misale A, Willis MC, Noël T, Trabanco AA, Gouverneur V. Silyl Radical-Mediated Activation of Sulfamoyl Chlorides Enables Direct Access to Aliphatic Sulfonamides from Alkenes. Journal of the American Chemical Society. PMID 31881153 DOI: 10.1021/Jacs.9B13071 |
0.388 |
|
| 2019 |
McKay A, Barwick-Silk J, Savage M, Willis M, Weller AS. Synthesis of highly fluorinated arene complexes of [Rh(chelating phosphine)]+ cations, and their use in synthesis and catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31749160 DOI: 10.1002/Chem.201904668 |
0.423 |
|
| 2019 |
Lou TS, Bagley SW, Willis MC. Cyclic Alkenylsulfonyl Fluorides: Palladium-Catalyzed Synthesis and Functionalization of Compact Multi-functional Reagents. Angewandte Chemie (International Ed. in English). PMID 31613041 DOI: 10.1002/Anie.201910871 |
0.513 |
|
| 2019 |
Zhang ZX, Davies TQ, Willis MC. Modular Sulfondiimine Synthesis Using a Stable Sulfinylamine Reagent. Journal of the American Chemical Society. 141: 13022-13027. PMID 31398023 DOI: 10.1021/Jacs.9B06831 |
0.516 |
|
| 2019 |
Arambasic M, Majhail MK, Straker RN, Neuhaus JD, Willis MC. A rhodium-catalysed Sonogashira-type coupling exploiting C-S functionalisation: orthogonality with palladium-catalysed variants. Chemical Communications (Cambridge, England). 55: 2757-2760. PMID 30762057 DOI: 10.1039/C9Cc00092E |
0.46 |
|
| 2019 |
Willis MC. New catalytic reactions using sulfur dioxide Phosphorus, Sulfur, and Silicon and the Related Elements. 194: 654-657. DOI: 10.1080/10426507.2019.1602623 |
0.474 |
|
| 2019 |
Lo PKT, Chen Y, Willis MC. Nickel(II)-Catalyzed Synthesis of Sulfinates from Aryl and Heteroaryl Boronic Acids and the Sulfur Dioxide Surrogate DABSO Acs Catalysis. 9: 10668-10673. DOI: 10.1021/Acscatal.9B04363 |
0.486 |
|
| 2018 |
Markovic T, Murray PRD, Rocke BN, Shavnya A, Blakemore DC, Willis MC. Heterocyclic Allylsulfones as Latent Heteroaryl Nucleophiles in Palladium-Catalyzed Cross-Coupling Reactions. Journal of the American Chemical Society. PMID 30412397 DOI: 10.1021/Jacs.8B09595 |
0.566 |
|
| 2018 |
Tan QW, Chovatia P, Willis MC. Copper-catalysed synthesis of alkylidene 2-pyrrolinone derivatives from the combination of α-keto amides and alkynes. Organic & Biomolecular Chemistry. PMID 30327813 DOI: 10.1039/C8Ob02205D |
0.477 |
|
| 2018 |
Vedovato V, Talbot EPA, Willis MC. Copper-Catalyzed Synthesis of Activated Sulfonate Esters from Boronic Acids, DABSO, and Pentafluorophenol. Organic Letters. PMID 30152703 DOI: 10.1021/Acs.Orglett.8B02445 |
0.495 |
|
| 2018 |
Chen Y, Murray PRD, Davies AT, Willis MC. Direct Copper-Catalyzed Three-Component Synthesis of Sulfonamides. Journal of the American Chemical Society. PMID 29965736 DOI: 10.1021/Jacs.8B04532 |
0.539 |
|
| 2018 |
Barwick-Silk J, Hardy S, Willis MC, Weller AS. Rh(DPEPhos)-Catalyzed Alkyne Hydroacylation using β-Carbonyl Substituted Aldehydes. Mechanistic Insight Leads to Low Catalyst Loadings that Enables Selective Catalysis on Gram-Scale. Journal of the American Chemical Society. PMID 29763563 DOI: 10.1021/Jacs.8B04086 |
0.434 |
|
| 2018 |
Markovic T, Rocke BN, Blakemore DC, Mascitti V, Willis MC. Correction to "Catalyst Selection Facilitates the Use of Heterocyclic Sulfinates as General Nucleophilic Coupling Partners in Palladium-Catalyzed Coupling Reactions". Organic Letters. PMID 29741085 DOI: 10.1021/acs.orglett.8b01120 |
0.428 |
|
| 2018 |
Griffiths RJ, Kong WC, Richards SA, Burley GA, Willis MC, Talbot EPA. Oxidative β-C-H sulfonylation of cyclic amines. Chemical Science. 9: 2295-2300. PMID 29719703 DOI: 10.1039/C7Sc04900E |
0.389 |
|
| 2018 |
Johnson TC, Elbert BL, Farley AJM, Gorman TW, Genicot C, Lallemand B, Pasau P, Flasz J, Castro JL, MacCoss M, Dixon DJ, Paton RS, Schofield CJ, Smith MD, Willis MC. Direct sulfonylation of anilines mediated by visible light. Chemical Science. 9: 629-633. PMID 29629128 DOI: 10.1039/C7Sc03891G |
0.701 |
|
| 2018 |
Straker RN, Formica M, Lupton JD, Niu J, Willis MC. An enamine controlling group for rhodium-catalyzed intermolecular hydroacylation Tetrahedron. 74: 5408-5414. DOI: 10.1016/J.Tet.2018.04.068 |
0.493 |
|
| 2017 |
Straker RN, Majhail MK, Willis MC. Exploiting rhodium-catalysed ynamide hydroacylation as a platform for divergent heterocycle synthesis. Chemical Science. 8: 7963-7968. PMID 29568442 DOI: 10.1039/C7Sc03795C |
0.491 |
|
| 2017 |
Markovic T, Rocke BN, Blakemore DC, Mascitti V, Willis MC. Catalyst Selection Facilitates the Use of Heterocyclic Sulfinates as General Nucleophilic Coupling Partners in Palladium-Catalyzed Coupling Reactions. Organic Letters. PMID 29043813 DOI: 10.1021/Acs.Orglett.7B02944 |
0.535 |
|
| 2017 |
Markovic T, Rocke BN, Blakemore DC, Mascitti V, Willis MC. Pyridine sulfinates as general nucleophilic coupling partners in palladium-catalyzed cross-coupling reactions with aryl halides. Chemical Science. 8: 4437-4442. PMID 28936330 DOI: 10.1039/C7Sc00675F |
0.547 |
|
| 2017 |
Davies TQ, Hall A, Willis MC. One-pot, Three-Component Sulfonimidamide Synthesis exploiting the Sulfinylamine Reagent N-Sulfinyltritylamine, TrNSO. Angewandte Chemie (International Ed. in English). PMID 28929561 DOI: 10.1002/Anie.201708590 |
0.494 |
|
| 2017 |
Elbert B, Farley A, Gorman T, Johnson T, Genicot C, Lallemand B, Pasau P, Flasz J, Castro J, Maccoss M, Paton R, Schofield C, Smith M, Willis M, Dixon DJ. A C-H Cyanation of 6-Ring N-Containing Heteroaromatics. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28833674 DOI: 10.1002/Chem.201703931 |
0.651 |
|
| 2017 |
Seo S, Willis MC. A Copper(I)-Catalyzed Addition/Annulation Sequence for the Two-Component Synthesis of γ-Ylidenebutenolides. Organic Letters. PMID 28809495 DOI: 10.1021/Acs.Orglett.7B02151 |
0.497 |
|
| 2017 |
Coxon TJ, Fernández M, Barwick-Silk J, McKay AI, Britton LE, Weller AS, Willis MC. Exploiting Carbonyl Groups to Control Intermolecular Rhodium-Catalyzed Alkene and Alkyne Hydroacylation. Journal of the American Chemical Society. PMID 28715214 DOI: 10.1021/Jacs.7B05713 |
0.504 |
|
| 2017 |
Chen Y, Willis MC. Copper(i)-catalyzed sulfonylative Suzuki-Miyaura cross-coupling. Chemical Science. 8: 3249-3253. PMID 28553528 DOI: 10.1039/C6Sc05483H |
0.565 |
|
| 2017 |
Gao M, Willis MC. Enantioselective Three-Component Assembly of β'-Aryl Enones Using a Rhodium-Catalyzed Alkyne Hydroacylation/Aryl Boronic Acid Conjugate Addition Sequence. Organic Letters. PMID 28485946 DOI: 10.1021/Acs.Orglett.7B01087 |
0.492 |
|
| 2017 |
Davies AT, Curto JM, Bagley SW, Willis MC. One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides. Chemical Science. 8: 1233-1237. PMID 28451264 DOI: 10.1039/C6Sc03924C |
0.543 |
|
| 2017 |
Fernández M, Castaing M, Willis MC. Sequential catalysis: exploiting a single rhodium(i) catalyst to promote an alkyne hydroacylation-aryl boronic acid conjugate addition sequence. Chemical Science. 8: 536-540. PMID 28451201 DOI: 10.1039/C6Sc03066A |
0.528 |
|
| 2016 |
Bouisseau A, Glancy J, Willis MC. Two-Component Assembly of Thiochroman-4-ones and Tetrahydrothiopyran-4-ones Using a Rhodium-Catalyzed Alkyne Hydroacylation/Thio-Conjugate-Addition Sequence. Organic Letters. PMID 27779887 DOI: 10.1021/Acs.Orglett.6B02909 |
0.448 |
|
| 2016 |
Bouisseau A, Gao M, Willis MC. Traceless Rhodium-Catalyzed Hydroacylation Using Alkyl Aldehydes: The Enantioselective Synthesis of β-Aryl Ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27666437 DOI: 10.1002/Chem.201604035 |
0.552 |
|
| 2016 |
Neuhaus JD, Willis MC. Homogeneous rhodium(i)-catalysis in de novo heterocycle syntheses. Organic & Biomolecular Chemistry. PMID 27197887 DOI: 10.1039/C6Ob00835F |
0.499 |
|
| 2016 |
Neuhaus JD, Morrow SM, Brunavs M, Willis MC. Correction to "Diversely Substituted Quinolines via Rhodium-Catalyzed Alkyne Hydroacylation". Organic Letters. PMID 27128686 DOI: 10.1021/Acs.Orglett.6B01218 |
0.516 |
|
| 2016 |
Majhail MK, Ylioja PM, Willis MC. Direct Synthesis of Highly Substituted Pyrroles and Dihydropyrroles Using Linear Selective Hydroacylation Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27106284 DOI: 10.1002/Chem.201600311 |
0.568 |
|
| 2016 |
Lenstra DC, Vedovato V, Ferrer Flegeau E, Maydom J, Willis MC. One-Pot Sulfoxide Synthesis Exploiting a Sulfinyl-Dication Equivalent Generated from a DABSO/Trimethylsilyl Chloride Sequence. Organic Letters. 18: 2086-9. PMID 27082825 DOI: 10.1021/Acs.Orglett.6B00712 |
0.529 |
|
| 2016 |
Neuhaus JD, Morrow SM, Brunavs M, Willis MC. Diversely Substituted Quinolines via Rhodium-Catalyzed Alkyne Hydroacylation. Organic Letters. 18: 1562-5. PMID 26974467 DOI: 10.1021/Acs.Orglett.6B00390 |
0.512 |
|
| 2016 |
Hooper JF, Seo S, Truscott FR, Neuhaus JD, Willis MC. α-Amino Aldehydes as Readily Available Chiral Aldehydes for Rh-Catalyzed Alkyne Hydroacylation. Journal of the American Chemical Society. PMID 26771104 DOI: 10.1021/Jacs.5B11892 |
0.499 |
|
| 2016 |
Lenstra DC, Vedovato V, Flegeau EF, Maydom J, Willis MC. One-Pot Sulfoxide Synthesis Synfacts. 12: 728-728. DOI: 10.1055/S-0035-1562318 |
0.454 |
|
| 2016 |
Flegeau EF, Harrison JM, Willis MC. One-Pot Sulfonamide Synthesis Exploiting the Palladium-Catalyzed Sulfination of Aryl Iodides Synlett. 27: 101-105. DOI: 10.1055/S-0035-1560578 |
0.529 |
|
| 2016 |
Niu J, Willis MC. Heterocycle-derived β-S-enals as bifunctional linchpins for the catalytic synthesis of saturated heterocycles Organic Chemistry Frontiers. 3: 625-629. DOI: 10.1039/C6Qo00057F |
0.56 |
|
| 2016 |
Ferrer Flegeau E, Harrison JM, Willis MC. ChemInform Abstract: One-Pot Sulfonamide Synthesis Exploiting the Palladium-Catalyzed Sulfination of Aryl Iodides. Cheminform. 47. DOI: 10.1002/CHIN.201623099 |
0.5 |
|
| 2015 |
Deeming AS, Russell CJ, Willis MC. Palladium(II)-Catalyzed Synthesis of Sulfinates from Boronic Acids and DABSO: A Redox-Neutral, Phosphine-Free Transformation. Angewandte Chemie (International Ed. in English). PMID 26596861 DOI: 10.1002/Anie.201508370 |
0.516 |
|
| 2015 |
Chen Y, Willis MC. An Aryne-Based Route to Substituted Benzoisothiazoles. Organic Letters. PMID 26376173 DOI: 10.1021/Acs.Orglett.5B02347 |
0.446 |
|
| 2015 |
Prades A, Fernández M, Pike SD, Willis MC, Weller AS. Well-Defined and Robust Rhodium Catalysts for the Hydroacylation of Terminal and Internal Alkenes. Angewandte Chemie (International Ed. in English). PMID 26069052 DOI: 10.1002/Anie.201503208 |
0.394 |
|
| 2015 |
Deeming AS, Russell CJ, Willis MC. Combining organometallic reagents, the sulfur dioxide surrogate DABSO, and amines: a one-pot preparation of sulfonamides, amenable to array synthesis. Angewandte Chemie (International Ed. in English). 54: 1168-71. PMID 25431118 DOI: 10.1002/Anie.201409283 |
0.442 |
|
| 2015 |
Grodner J, Golebiewski WM, Willis MC, Osborne JD, Gucma M. The first stereoselective synthesis of a dithiane derivative of the C18 β-diketodiene system proposed for an active compound isolated from Cantharellus cibarius (chanterelle) Synthesis (Germany). 47: 1181-1189. DOI: 10.1055/S-0034-1379984 |
0.459 |
|
| 2015 |
Emmett EJ, Willis MC. The Development and Application of Sulfur Dioxide Surrogates in Synthetic Organic Chemistry Asian Journal of Organic Chemistry. 4: 602-611. DOI: 10.1002/Ajoc.201500103 |
0.486 |
|
| 2014 |
Emmett EJ, Hayter BR, Willis MC. Palladium-catalyzed synthesis of ammonium sulfinates from aryl halides and a sulfur dioxide surrogate: a gas- and reductant-free process. Angewandte Chemie (International Ed. in English). 53: 10204-8. PMID 25066222 DOI: 10.1002/Anie.201404527 |
0.532 |
|
| 2014 |
Deeming AS, Russell CJ, Hennessy AJ, Willis MC. DABSO-based, three-component, one-pot sulfone synthesis. Organic Letters. 16: 150-3. PMID 24308313 DOI: 10.1021/Ol403122A |
0.417 |
|
| 2014 |
Deeming AS, Emmett EJ, Richards-Taylor CS, Willis MC. Rediscovering the Chemistry of Sulfur Dioxide: New Developments in Synthesis and Catalysis Synthesis (Germany). 46: 2701-2710. DOI: 10.1055/S-0034-1379042 |
0.468 |
|
| 2014 |
Emmett EJ, Hayter BR, Willis MC. Synthesis of Diaryl Sulfones: GSK 742457 Synfacts. 10: 117-117. DOI: 10.1055/S-0033-1340490 |
0.428 |
|
| 2014 |
Richards-Taylor CS, Blakemore DC, Willis MC. One-pot three-component sulfone synthesis exploiting palladium-catalysed aryl halide aminosulfonylation Chemical Science. 5: 222-228. DOI: 10.1039/C3Sc52332B |
0.565 |
|
| 2014 |
Deeming AS, Emmett EJ, Richards-Taylor CS, Willis MC. ChemInform Abstract: Rediscovering the Chemistry of Sulfur Dioxide: New Developments in Synthesis and Catalysis Cheminform. 46: no-no. DOI: 10.1002/CHIN.201502238 |
0.32 |
|
| 2014 |
Richards-Taylor CS, Blakemore DC, Willis MC. ChemInform Abstract: One-Pot Three-Component Sulfone Synthesis Exploiting Palladium-Catalyzed Aryl Halide Aminosulfonylation. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201426091 |
0.453 |
|
| 2014 |
Emmett EJ, Willis MC. DABCO‐bis(sulfur dioxide), DABSO, as an easy‐to‐handle source of SO2: Sulfonamide preparation Organic Syntheses. 91: 125-136. DOI: 10.1002/0471264229.Os091.12 |
0.436 |
|
| 2013 |
Castaing M, Wason SL, Estepa B, Hooper JF, Willis MC. 2-Aminobenzaldehydes as versatile substrates for rhodium-catalyzed alkyne hydroacylation: application to dihydroquinolone synthesis. Angewandte Chemie (International Ed. in English). 52: 13280-3. PMID 24222398 DOI: 10.1002/Anie.201308127 |
0.499 |
|
| 2013 |
Emmett EJ, Hayter BR, Willis MC. Palladium-catalyzed three-component diaryl sulfone synthesis exploiting the sulfur dioxide surrogate DABSO. Angewandte Chemie (International Ed. in English). 52: 12679-83. PMID 24115325 DOI: 10.1002/Anie.201305369 |
0.501 |
|
| 2013 |
Arambasic M, Hooper JF, Willis MC. Activating group recycling in action: a rhodium-catalyzed carbothiolation route to substituted isoquinolines. Organic Letters. 15: 5162-5. PMID 24083625 DOI: 10.1021/Ol402650Q |
0.504 |
|
| 2013 |
Hooper JF, Young RD, Weller AS, Willis MC. Traceless chelation-controlled rhodium-catalyzed intermolecular alkene and alkyne hydroacylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 3125-30. PMID 23325542 DOI: 10.1002/Chem.201204056 |
0.542 |
|
| 2013 |
Foster RA, Willis MC. Tandem inverse-electron-demand hetero-/retro-Diels-Alder reactions for aromatic nitrogen heterocycle synthesis. Chemical Society Reviews. 42: 63-76. PMID 23079670 DOI: 10.1039/C2Cs35316D |
0.487 |
|
| 2013 |
Hooper JF, Young RD, Pernik I, Weller AS, Willis MC. Carbon-carbon bond construction using boronic acids and aryl methyl sulfides: Orthogonal reactivity in Suzuki-type couplings Chemical Science. 4: 1568-1572. DOI: 10.1039/C3Sc00052D |
0.554 |
|
| 2013 |
Ball CJ, Willis MC. ChemInform Abstract: Cascade Palladium- and Copper-Catalyzed Aromatic Heterocycle Synthesis: The Emergence of General Precursors Cheminform. 44: no-no. DOI: 10.1002/CHIN.201321236 |
0.421 |
|
| 2013 |
Foster RAA, Willis MC. ChemInform Abstract: Tandem inverse-Electron-Demand hetero-/retro-Diels-Alder Reactions for Aromatic Nitrogen Heterocycle Synthesis Cheminform. 44: no-no. DOI: 10.1002/CHIN.201318240 |
0.397 |
|
| 2012 |
Snell RH, Durbin MJ, Woodward RL, Willis MC. Catalytic enantioselective desymmetrisation as a tool for the synthesis of hodgkinsine and hodgkinsine B. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 16754-64. PMID 23203932 DOI: 10.1002/Chem.201203150 |
0.431 |
|
| 2012 |
Sadig JE, Foster R, Wakenhut F, Willis MC. Palladium-catalyzed synthesis of benzimidazoles and quinazolinones from common precursors. The Journal of Organic Chemistry. 77: 9473-86. PMID 23030827 DOI: 10.1021/Jo301805D |
0.558 |
|
| 2012 |
Poingdestre SJ, Goodacre JD, Weller AS, Willis MC. Rhodium-catalysed linear-selective alkyne hydroacylation. Chemical Communications (Cambridge, England). PMID 22618331 DOI: 10.1039/C2Cc32713A |
0.415 |
|
| 2012 |
Ball CJ, Gilmore J, Willis MC. Copper-catalyzed tandem C-N bond formation: an efficient annulative synthesis of functionalized cinnolines. Angewandte Chemie (International Ed. in English). 51: 5718-22. PMID 22539417 DOI: 10.1002/Anie.201201529 |
0.429 |
|
| 2012 |
Emmett EJ, Richards-Taylor CS, Nguyen B, Garcia-Rubia A, Hayter BR, Willis MC. Palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides: scope of the three-component synthesis of N-aminosulfonamides. Organic & Biomolecular Chemistry. 10: 4007-14. PMID 22407213 DOI: 10.1039/C2Ob07034K |
0.416 |
|
| 2012 |
Chaplin AB, Hooper JF, Weller AS, Willis MC. Intermolecular hydroacylation: high activity rhodium catalysts containing small-bite-angle diphosphine ligands. Journal of the American Chemical Society. 134: 4885-97. PMID 22324763 DOI: 10.1021/Ja211649A |
0.401 |
|
| 2012 |
Hooper JF, Chaplin AB, González-RodrÃguez C, Thompson AL, Weller AS, Willis MC. Aryl methyl sulfides as substrates for rhodium-catalyzed alkyne carbothiolation: arene functionalization with activating group recycling. Journal of the American Chemical Society. 134: 2906-9. PMID 22296656 DOI: 10.1021/Ja2108992 |
0.467 |
|
| 2012 |
Hooper JF, Chaplin AB, González-Rodríguez C, Thompson AL, Weller AS, Willis MC. Rhodium-Catalyzed Alkyne Carbothiolations Synfacts. 8: 534-534. DOI: 10.1055/S-0031-1290904 |
0.58 |
|
| 2012 |
Pawley RJ, Huertos MA, Lloyd-Jones GC, Weller AS, Willis MC. Intermolecular alkyne hydroacylation. mechanistic insight from the isolation of the vinyl intermediate that precedes reductive elimination Organometallics. 31: 5650-5659. DOI: 10.1021/Om300647N |
0.365 |
|
| 2012 |
Pernik I, Hooper JF, Chaplin AB, Weller AS, Willis MC. Exploring small bite-angle ligands for the rhodium-catalyzed intermolecular hydroacylation of βs-substituted aldehydes with 1-octene and 1-octyne Acs Catalysis. 2: 2779-2786. DOI: 10.1021/Cs300541M |
0.396 |
|
| 2012 |
Gerelle M, Dalencon AJ, Willis MC. Palladium-catalyzed direct functionalization of benzoxazoles with alkenyl iodides Tetrahedron Letters. 53: 1954-1957. DOI: 10.1016/J.Tetlet.2012.02.014 |
0.507 |
|
| 2012 |
Ball CJ, Willis MC. Cascade Palladium- and Copper-Catalysed Aromatic Heterocycle Synthesis: The Emergence of General Precursors European Journal of Organic Chemistry. 2013: 425-441. DOI: 10.1002/Ejoc.201201386 |
0.52 |
|
| 2012 |
Gerelle M, Dalencon AJ, Willis MC. ChemInform Abstract: Palladium-Catalyzed Direct Functionalization of Benzoxazoles with Alkenyl Iodides. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201230141 |
0.363 |
|
| 2012 |
Snell RH, Durbin MJ, Woodward RL, Willis MC. Cover Picture: Catalytic Enantioselective Desymmetrisation as a Tool for the Synthesis of Hodgkinsine and Hodgkinsine B (Chem. Eur. J. 52/2012) Chemistry - a European Journal. 18: 16585-16585. DOI: 10.1002/Chem.201290220 |
0.389 |
|
| 2011 |
Lenden P, Entwistle DA, Willis MC. An alkyne hydroacylation route to highly substituted furans. Angewandte Chemie (International Ed. in English). 50: 10657-60. PMID 21932241 DOI: 10.1002/Anie.201105795 |
0.53 |
|
| 2011 |
Snell RH, Woodward RL, Willis MC. Catalytic enantioselective total synthesis of hodgkinsine B. Angewandte Chemie (International Ed. in English). 50: 9116-9. PMID 21919143 DOI: 10.1002/Anie.201103864 |
0.403 |
|
| 2011 |
Woolven H, González-RodrÃguez C, Marco I, Thompson AL, Willis MC. DABCO-bis(sulfur dioxide), DABSO, as a convenient source of sulfur dioxide for organic synthesis: utility in sulfonamide and sulfamide preparation. Organic Letters. 13: 4876-8. PMID 21866926 DOI: 10.1021/Ol201957N |
0.473 |
|
| 2011 |
González-Rodríguez C, Pawley RJ, Chaplin AB, Thompson AL, Weller AS, Willis MC. Rhodium-catalyzed branched-selective alkyne hydroacylation: a ligand-controlled regioselectivity switch. Angewandte Chemie (International Ed. in English). 50: 5134-8. PMID 21506226 DOI: 10.1002/Anie.201100956 |
0.36 |
|
| 2011 |
Parsons SR, Hooper JF, Willis MC. O-substituted alkyl aldehydes for rhodium-catalyzed intermolecular alkyne hydroacylation: the utility of methylthiomethyl ethers. Organic Letters. 13: 998-1000. PMID 21309521 DOI: 10.1021/Ol1030662 |
0.454 |
|
| 2011 |
González-Rodríguez C, Willis MC. Rhodium-catalyzed enantioselective intermolecular hydroacylation reactions Pure and Applied Chemistry. 83: 577-585. DOI: 10.1351/Pac-Con-10-09-23 |
0.557 |
|
| 2011 |
Snell RH, Woodward RL, Willis MC. Synthesis of (-)-Hodgkinsine B Synfacts. 2011: 1272-1272. DOI: 10.1055/S-0031-1289341 |
0.312 |
|
| 2011 |
Lenden P, Ylioja PM, González-Rodríguez C, Entwistle DA, Willis MC. Replacing dichloroethane as a solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions: the utility of propylene carbonate Green Chemistry. 13: 1980. DOI: 10.1039/C1Gc15293A |
0.447 |
|
| 2011 |
Pike SD, Pawley RJ, Chaplin AB, Thompson AL, Hooper JA, Willis MC, Weller AS. Exploring (Ph2PCH2CH2)2E ligand space (E = O, S, PPh) in RhI alkene complexes as potential hydroacylation catalysts European Journal of Inorganic Chemistry. 5558-5565. DOI: 10.1002/Ejic.201100958 |
0.37 |
|
| 2011 |
Gonzalez-Rodriguez C, Willis MC. ChemInform Abstract: Rhodium-Catalyzed Enantioselective Intermolecular Hydroacylation Reactions Cheminform. 43: no-no. DOI: 10.1002/CHIN.201203223 |
0.454 |
|
| 2011 |
Lenden P, Ylioja PM, Gonzalez-Rodriguez C, Entwistle DA, Willis MC. ChemInform Abstract: Replacing Dichloroethane as a Solvent for Rhodium-Catalyzed Intermolecular Alkyne Hydroacylation Reactions: The Utility of Propylene Carbonate. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201152076 |
0.378 |
|
| 2011 |
Sadig JER, Willis MC. ChemInform Abstract: Palladium- and Copper-Catalyzed Aryl Halide Amination, Etherification and Thioetherification Reactions in the Synthesis of Aromatic Heterocycles Cheminform. 42: no-no. DOI: 10.1002/CHIN.201112253 |
0.512 |
|
| 2010 |
Nguyen B, Emmett EJ, Willis MC. Palladium-catalyzed aminosulfonylation of aryl halides. Journal of the American Chemical Society. 132: 16372-3. PMID 21028814 DOI: 10.1021/Ja1081124 |
0.567 |
|
| 2010 |
Yagoubi M, Cruz AC, Nichols PL, Elliott RL, Willis MC. Cascade palladium-catalyzed direct intramolecular arylation/alkene isomerization sequences: synthesis of indoles and benzofurans. Angewandte Chemie (International Ed. in English). 49: 7958-62. PMID 20839211 DOI: 10.1002/Anie.201004097 |
0.518 |
|
| 2010 |
González-Rodríguez C, Parsons SR, Thompson AL, Willis MC. Rhodium-catalysed intermolecular alkyne hydroacylation: the enantioselective synthesis of α- and β-substituted ketones by kinetic resolution. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 10950-4. PMID 20715218 DOI: 10.1002/Chem.201001748 |
0.405 |
|
| 2010 |
Willis MC. Catalytic intramolecular ketone hydroacylation: enantioselective synthesis of phthalides. Angewandte Chemie (International Ed. in English). 49: 6026-7. PMID 20491100 DOI: 10.1002/Anie.201000159 |
0.55 |
|
| 2010 |
Byrne SJ, Fletcher AJ, Hebeisen P, Willis MC. Enantioselective desymmetrizing palladium catalyzed carbonylation reactions: the catalytic asymmetric synthesis of quaternary carbon center containing 1,3-dienes. Organic & Biomolecular Chemistry. 8: 758-60. PMID 20135030 DOI: 10.1039/B923186B |
0.581 |
|
| 2010 |
Willis MC. Transition metal catalyzed alkene and alkyne hydroacylation. Chemical Reviews. 110: 725-48. PMID 19873977 DOI: 10.1021/Cr900096X |
0.316 |
|
| 2010 |
Willis M, Yagoubi M, Cruz A, Nichols P, Elliott R. Palladium-Catalyzed Heteroannulation Route to Indoles and Benzofurans Synfacts. 2011: 0027-0027. DOI: 10.1055/S-0030-1259203 |
0.529 |
|
| 2010 |
Willis M, Sadig J. Palladium- and Copper-Catalyzed Aryl Halide Amination, Etherification and Thioetherification Reactions in the Synthesis of Aromatic Heterocycles Synthesis. 2011: 1-22. DOI: 10.1055/S-0030-1258294 |
0.447 |
|
| 2010 |
Pawley RJ, Moxham GL, Dallanegra R, Chaplin AB, Brayshaw SK, Weller AS, Willis MC. Controlling Selectivity in Intermolecular Alkene or Aldehyde Hydroacylation Reactions Catalyzed by {Rh(L2)}+Fragments Organometallics. 29: 1717-1728. DOI: 10.1021/Om9011104 |
0.391 |
|
| 2010 |
Henderson LC, Lindon MJ, Willis MC. Palladium catalyzed tandem alkenyl- and aryl-C-N bond formation: A cascade N-annulation route to 4-, 5-, 6- and 7-chloroindoles Tetrahedron. 66: 6632-6638. DOI: 10.1016/J.Tet.2010.05.046 |
0.692 |
|
| 2010 |
Henderson LC, Lindon MJ, Willis MC. ChemInform Abstract: Palladium Catalyzed Tandem Alkenyl- and Aryl-C-N Bond Formation: A Cascade N-Annulation Route to 4-, 5-, 6- and 7-Chloroindoles. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201101093 |
0.595 |
|
| 2010 |
Evans DA, Scheidt KA, Johnston JN, Willis MC. ChemInform Abstract: Enantioselective and Diastereoselective Mukaiyama-Michael Reactions Catalyzed by Bis(oxazoline) Copper(II) Complexes. Cheminform. 32: no-no. DOI: 10.1002/chin.200137074 |
0.752 |
|
| 2010 |
Evans DA, Willis MC, Johnston JN. ChemInform Abstract: Catalytic Enantioselective Michael Additions to Unsaturated Ester Derivatives Using Chiral Copper(II) Lewis Acid Complexes. Cheminform. 30: no-no. DOI: 10.1002/chin.199948036 |
0.664 |
|
| 2010 |
SHELLHAMER DF, CARTER DL, CHIACO MC, HARRIS TE, HENDERSON RD, LOW WSC, METCALF BT, WILLIS MC, HEASLEY VL, CHAPMAN RD. ChemInform Abstract: Reaction of Xenon Difluoride with Indene in Aqueous 1,2- Dimethoxyethane and Tetrahydrofuran Cheminform. 22: no-no. DOI: 10.1002/CHIN.199124094 |
0.353 |
|
| 2010 |
Willis MC. Katalytische intramolekulare Hydroacylierung von Ketonen: eine enantioselektive Synthese von Phthaliden Angewandte Chemie. 122: 6162-6164. DOI: 10.1002/Ange.201000159 |
0.314 |
|
| 2009 |
Tadd AC, Fielding MR, Willis MC. Palladium-catalyzed aryl halide carbonylation-intramolecular O-enolate acylation: efficient isocoumarin synthesis, including the synthesis of thunberginol A. Chemical Communications (Cambridge, England). 6744-6. PMID 19885465 DOI: 10.1039/B917839B |
0.533 |
|
| 2009 |
Jauregui M, Perry WS, Allain C, Vidler LR, Willis MC, Kenwright AM, Snaith JS, Stasiuk GJ, Lowe MP, Faulkner S. Changing the local coordination environment in mono- and bi- nuclear lanthanide complexes through "click" chemistry. Dalton Transactions (Cambridge, England : 2003). 6283-5. PMID 19655058 DOI: 10.1039/B911588A |
0.362 |
|
| 2009 |
Ley SV, Tackett MN, Maddess ML, Anderson JC, Brennan PE, Cappi MW, Heer JP, Helgen C, Kori M, Kouklovsky C, Marsden SP, Norman J, Osborn DP, Palomero MA, Pavey JB, ... ... Willis MC, et al. Total synthesis of rapamycin. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 2874-914. PMID 19204960 DOI: 10.1002/Chem.200801656 |
0.634 |
|
| 2009 |
Hodgkinson RC, Schulz J, Willis MC. Tandem copper-catalysed aryl and alkenyl amination reactions: the synthesis of N-functionalised indoles. Organic & Biomolecular Chemistry. 7: 432-4. PMID 19156305 DOI: 10.1039/B817254D |
0.524 |
|
| 2009 |
Tadd AC, Matsuno A, Fielding MR, Willis MC. Cascade palladium-catalyzed alkenyl aminocarbonylation/ intramolecular aryl amidation: an annulative synthesis of 2-quinolones. Organic Letters. 11: 583-6. PMID 19125625 DOI: 10.1021/Ol802624E |
0.527 |
|
| 2009 |
Tadd AC, Matsuno A, Fielding MR, Willis MC. Palladium-Catalyzed Carbonylative Synthesis of 2-Quinolones Synfacts. 2009: 482-482. DOI: 10.1055/S-0029-1216614 |
0.564 |
|
| 2009 |
Willis M, Osborne J, Randell-Sly H, Currie G, Cowley A. Rhodium-Catalyzed Intermolecular Hydroacylation Synfacts. 2009: 0289-0289. DOI: 10.1055/S-0028-1087779 |
0.546 |
|
| 2009 |
Stainforth NE, Cutting GA, John MP, Willis MC. Direct catalytic diastereoselective Mannich reactions: the synthesis of protected α-hydroxy-β-aminoketones Tetrahedron: Asymmetry. 20: 741-743. DOI: 10.1016/J.Tetasy.2009.03.026 |
0.431 |
|
| 2009 |
Willis MC. Modern applications of transition metal catalysis in heterocycle synthesis Tetrahedron. 65: 8907. DOI: 10.1016/J.Tet.2009.08.065 |
0.326 |
|
| 2009 |
Hodgkinson RC, Schulz J, Willis MC. Palladium-catalysed tandem alkenyl- and aryl-C–N bond formation: a cascade N-annulation route to 1-functionalised 7-azaindoles Tetrahedron. 65: 8940-8949. DOI: 10.1016/J.Tet.2009.08.046 |
0.488 |
|
| 2009 |
Randell-Sly HE, Osborne JD, Woodward RL, Currie GS, Willis MC. Intermolecular rhodium catalyzed hydroacylation of allenes: the regioselective synthesis of β,γ-unsaturated ketones Tetrahedron. 65: 5110-5117. DOI: 10.1016/J.Tet.2009.03.054 |
0.491 |
|
| 2009 |
Randell-Sly HE, Osborne JD, Woodward RL, Currie GS, Willis MC. ChemInform Abstract: Intermolecular Rhodium-Catalyzed Hydroacylation of Allenes: The Regioselective Synthesis of β,γ-Unsaturated Ketones. Cheminform. 40. DOI: 10.1002/CHIN.200944078 |
0.326 |
|
| 2009 |
Stainforth NE, Cutting GA, John MP, Willis MC. ChemInform Abstract: Direct Catalytic Diastereoselective Mannich Reactions: The Synthesis of Protected α-Hydroxy-β-aminoketones. Cheminform. 40. DOI: 10.1002/CHIN.200939038 |
0.335 |
|
| 2008 |
Osborne JD, Randell-Sly HE, Currie GS, Cowley AR, Willis MC. Catalytic enantioselective intermolecular hydroacylation: rhodium-catalyzed combination of beta-S-aldehydes and 1,3-disubstituted allenes. Journal of the American Chemical Society. 130: 17232-3. PMID 19053453 DOI: 10.1021/Ja8069133 |
0.457 |
|
| 2008 |
Osborne JD, Willis MC. Rhodium-catalysed hydroacylation or reductive aldol reactions: a ligand dependent switch of reactivity. Chemical Communications (Cambridge, England). 5025-7. PMID 18931774 DOI: 10.1039/B810935D |
0.522 |
|
| 2008 |
Moxham GL, Randell-Sly H, Brayshaw SK, Weller AS, Willis MC. Intermolecular alkene and alkyne hydroacylation with beta-S-substituted aldehydes: mechanistic insight into the role of a hemilabile P-O-P ligand. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 8383-97. PMID 18666296 DOI: 10.1002/Chem.200800738 |
0.351 |
|
| 2008 |
Durbin MJ, Willis MC. Palladium-catalyzed alpha-arylation of oxindoles. Organic Letters. 10: 1413-5. PMID 18321119 DOI: 10.1021/Ol800141T |
0.486 |
|
| 2008 |
Durbin MJ, Willis MC. ChemInform Abstract: Palladium-Catalyzed α-Arylation of Oxindoles. Cheminform. 39. DOI: 10.1002/CHIN.200835106 |
0.301 |
|
| 2008 |
Tadd AC, Fielding MR, Willis MC. ChemInform Abstract: Copper-Catalyzed Benzofuran Synthesis: Developing Aryl Bromide-Alkenyl Triflates as General Heterocycle Precursors. Cheminform. 39. DOI: 10.1002/CHIN.200807095 |
0.437 |
|
| 2008 |
Cutting GA, Stainforth NE, John MP, Kociok-Koehn G, Willis MC. ChemInform Abstract: Direct Catalytic Enantioselective Mannich Reactions: Synthesis of Protected anti-α,β-Diamino Acids. Cheminform. 39. DOI: 10.1002/CHIN.200801187 |
0.337 |
|
| 2007 |
Fletcher AJ, Bax MN, Willis MC. Palladium-catalysed N-annulation routes to indoles: the synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1. Chemical Communications (Cambridge, England). 4764-6. PMID 18004434 DOI: 10.1039/B712227F |
0.426 |
|
| 2007 |
Chapman CJ, Matsuno A, Frost CG, Willis MC. Site-selective modification of peptides using rhodium and palladium catalysis: complementary electrophilic and nucleophilic arylation. Chemical Communications (Cambridge, England). 3903-5. PMID 17896027 DOI: 10.1039/B711533D |
0.392 |
|
| 2007 |
Cruz AC, Miller ND, Willis MC. Intramolecular palladium-catalyzed direct arylation of alkenyl triflates. Organic Letters. 9: 4391-3. PMID 17850159 DOI: 10.1021/Ol702044Z |
0.549 |
|
| 2007 |
Cutting GA, Stainforth NE, John MP, Kociok-Köhn G, Willis MC. Direct catalytic enantioselective Mannich reactions: synthesis of protected anti-alpha,beta-diamino acids. Journal of the American Chemical Society. 129: 10632-3. PMID 17691788 DOI: 10.1021/Ja073473F |
0.537 |
|
| 2007 |
Willis MC. Palladium-catalyzed coupling of ammonia and hydroxide with aryl halides: the direct synthesis of primary anilines and phenols. Angewandte Chemie (International Ed. in English). 46: 3402-4. PMID 17351997 DOI: 10.1002/Anie.200605071 |
0.543 |
|
| 2007 |
Willis M, Snell R, Fletcher A, Woodward R. Pd-Catalyzed C-N Coupling. Synthesis of 2,4-Quinazolinediones Synfacts. 2007: 0140-0140. DOI: 10.1055/S-2006-955823 |
0.406 |
|
| 2007 |
Tadd AC, Fielding MR, Willis MC. Copper-catalysed benzofuran synthesis: developing aryl bromide–alkenyl triflates as general heterocycle precursors Tetrahedron Letters. 48: 7578-7581. DOI: 10.1016/J.Tetlet.2007.08.109 |
0.51 |
|
| 2006 |
Willis MC, Snell RH, Fletcher AJ, Woodward RL. Tandem palladium-catalyzed urea arylation-intramolecular ester amidation: regioselective synthesis of 3-alkylated 2,4-quinazolinediones. Organic Letters. 8: 5089-91. PMID 17048850 DOI: 10.1021/Ol062009X |
0.595 |
|
| 2006 |
Moxham GL, Randell-Sly HE, Brayshaw SK, Woodward RL, Weller AS, Willis MC. A second-generation catalyst for intermolecular hydroacylation of alkenes and alkynes using beta-S-substituted aldehydes: the role of a hemilabile P-O-P ligand. Angewandte Chemie (International Ed. in English). 45: 7618-22. PMID 17044106 DOI: 10.1002/Anie.200603133 |
0.342 |
|
| 2006 |
Willis MC, Randell-Sly HE, Woodward RL, McNally SJ, Currie GS. Rhodium-catalyzed intermolecular chelation controlled alkene and alkyne hydroacylation: synthetic scope of beta-S-substituted aldehyde substrates. The Journal of Organic Chemistry. 71: 5291-7. PMID 16808518 DOI: 10.1021/Jo060582O |
0.531 |
|
| 2006 |
Willis MC, Taylor D, Gillmore AT. Palladium-catalysed intramolecular enolate O-arylation and thio-enolate S-arylation: synthesis of benzo[b]furans and benzo[b]thiophenes Tetrahedron. 62: 11513-11520. DOI: 10.1016/J.Tet.2006.05.004 |
0.52 |
|
| 2006 |
Merle N, Frost CG, Kociok-Köhn G, Willis MC, Weller AS. Chelating Phosphane–Boranes as Hemilabile Ligands – Synthesis of[Mn(CO)3(η2-H3B·dppm)][BArF4] and [Mn(CO)4(η1-H3B·dppm)][BArF4] European Journal of Inorganic Chemistry. 2006: 4068-4073. DOI: 10.1002/Ejic.200600526 |
0.369 |
|
| 2006 |
Willis MC, Brace GN, Findlay TJK, Holmes IP. 2-(2-Haloalkenyl)-aryl Halides as Substrates for Palladium-Catalyzed Tandem C—N Bond Formation: Efficient Synthesis of 1-Substituted Indoles. Cheminform. 37. DOI: 10.1002/CHIN.200640112 |
0.424 |
|
| 2006 |
Willis MC, Brace GN, Holmes IP. Efficient Palladium-Catalyzed Enamide Synthesis from Enol Triflates and Enol Tosylates. Cheminform. 37. DOI: 10.1002/CHIN.200617048 |
0.44 |
|
| 2006 |
Willis MC, Brace GN, Findlay TJK, Holmes IP. 2-(2-Haloalkenyl)-aryl halides as substrates for palladium-catalysed tandem C-N bond formation: Efficient synthesis of 1-substituted indoles Advanced Synthesis and Catalysis. 348: 851-856. DOI: 10.1002/Adsc.200505484 |
0.542 |
|
| 2005 |
Willis MC, Woodward RL. Rhodium-catalyzed reductive aldol reactions using aldehydes as the stoichiometric reductants. Journal of the American Chemical Society. 127: 18012-3. PMID 16366546 DOI: 10.1021/Ja056130V |
0.491 |
|
| 2005 |
Willis MC, Chauhan J, Whittingham WG. A new reactivity pattern for vinyl bromides: cine-substitution via palladium catalysed C-N coupling/Michael addition reactions. Organic & Biomolecular Chemistry. 3: 3094-5. PMID 16106288 DOI: 10.1039/B508464D |
0.512 |
|
| 2005 |
Willis MC, Randell-Sly HE, Woodward RL, Currie GS. Chelation-controlled intermolecular alkene and alkyne hydroacylation: the utility of beta-thioacetal aldehydes. Organic Letters. 7: 2249-51. PMID 15901181 DOI: 10.1021/Ol050638L |
0.512 |
|
| 2005 |
Willis MC, Cutting GA, Piccio VJ, Durbin MJ, John MP. The direct catalytic enantioselective synthesis of protected aryl beta-hydroxy-alpha-amino acids. Angewandte Chemie (International Ed. in English). 44: 1543-5. PMID 15678437 DOI: 10.1002/Anie.200462125 |
0.47 |
|
| 2005 |
Willis MC, Brace GN, Holmes IP. Palladium-catalyzed tandem alkenyl and aryl C--N bond formation: a cascade N-annulation route to 1-functionalized indoles. Angewandte Chemie (International Ed. in English). 44: 403-6. PMID 15624185 DOI: 10.1002/Anie.200461598 |
0.404 |
|
| 2005 |
Willis MC, Brace GN, Holmes IP. Efficient palladium-catalysed enamide synthesis from enol triflates and enol tosylates Synthesis. 3229-3234. DOI: 10.1055/S-2005-918480 |
0.505 |
|
| 2005 |
Merle N, Frost CG, Kociok-Köhn G, Willis MC, Weller AS. Ruthenium (II) complexes of the chelating phosphine borane H2ClB·dppm Journal of Organometallic Chemistry. 690: 2829-2834. DOI: 10.1016/J.Jorganchem.2005.01.048 |
0.318 |
|
| 2004 |
Willis MC, Taylor D, Gillmore AT. Palladium-catalyzed intramolecular O-arylation of enolates: application to benzo[b]furan synthesis. Organic Letters. 6: 4755-7. PMID 15575678 DOI: 10.1021/Ol047993G |
0.538 |
|
| 2004 |
Sharman GJ, Jones IC, Parnell MP, Willis MC, Mahon MF, Carlson DV, Williams A, Elyashberg M, Blinov K, Molodtsov SG. Automated structure elucidation of two unexpected products in a reaction of an alpha,beta-unsaturated pyruvate. Magnetic Resonance in Chemistry : Mrc. 42: 567-72. PMID 15181625 DOI: 10.1002/Mrc.1396 |
0.306 |
|
| 2004 |
Willis MC, Powell LH, Claverie CK, Watson SJ. Enantioselective suzuki reactions: catalytic asymmetric synthesis of compounds containing quaternary carbon centers. Angewandte Chemie (International Ed. in English). 43: 1249-51. PMID 14991790 DOI: 10.1002/Anie.200352648 |
0.499 |
|
| 2004 |
Willis MC, McNally SJ, Beswick PJ. Chelation-controlled intermolecular hydroacylation: direct addition of alkyl aldehydes to functionalized alkenes. Angewandte Chemie (International Ed. in English). 43: 340-3. PMID 14705092 DOI: 10.1002/Anie.200352751 |
0.393 |
|
| 2004 |
Willis MC, Cutting GA, John MP. A Direct Catalytic and Diastereoselective Aldol Route to Protected α,β-Dihydroxyketones. Cheminform. 35. DOI: 10.1055/S-2004-822921 |
0.438 |
|
| 2003 |
Willis MC, Taylor D, Gillmore AT. Palladium catalysed aryl enol ether synthesis from vinyl triflates. Chemical Communications (Cambridge, England). 2222-3. PMID 13678211 DOI: 10.1039/B307574E |
0.439 |
|
| 2003 |
Willis MC, Flower SE. One-Pot Synthesis of Perhydrofuro[2,3-b]pyran Derivatives. Cheminform. 34. DOI: 10.1055/S-2003-40818 |
0.384 |
|
| 2003 |
Willis MC, Piccio VJ. A Direct Catalytic Aldol Route to Protected β-Hydroxy-α-amino Acids. Cheminform. 34. DOI: 10.1055/S-2002-34241 |
0.413 |
|
| 2003 |
Willis MC, Brace GN. Palladium-Catalyzed Enamine Synthesis from Vinyl Triflates. Cheminform. 34. DOI: 10.1002/CHIN.200307055 |
0.485 |
|
| 2002 |
Willis MC, Claverie CK, Mahon MF. Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling. Chemical Communications (Cambridge, England). 832-3. PMID 12123001 DOI: 10.1039/B200692H |
0.487 |
|
| 2002 |
Willis MC, Brace GN. Palladium catalysed enamine synthesis from vinyl triflates Tetrahedron Letters. 43: 9085-9088. DOI: 10.1016/S0040-4039(02)02249-9 |
0.434 |
|
| 2001 |
Evans DA, Scheidt KA, Johnston JN, Willis MC. Enantioselective and diastereoselective Mukaiyama-Michael reactions catalyzed by bis(oxazoline) copper(II) complexes. Journal of the American Chemical Society. 123: 4480-91. PMID 11457234 DOI: 10.1021/Ja010302G |
0.779 |
|
| 2001 |
Willis MC, Sapmaz S. Intermolecular hydroacylation of acrylate esters: a new route to 1,4-dicarbonyls Chemical Communications. 2558-2559. DOI: 10.1039/B107852F |
0.477 |
|
| 2001 |
Ingleson M, Patmore NJ, Ruggiero GD, Frost CG, Mahon MF, Willis MC, Weller AS. Chelating monoborane phosphines: Rational and high-yield synthesis of [(COD)Rh{(η2-BH3)Ph2PCH2PPh 2}][PF6] (COD = 1,5-cyclooctadiene) Organometallics. 20: 4434-4436. DOI: 10.1021/Om0103759 |
0.448 |
|
| 2001 |
Willis MC, Claverie CK. The selective preparation and Suzuki coupling reactivity of cyclic 1,3-dione derived mono- and ditriflates Tetrahedron Letters. 42: 5105-5107. DOI: 10.1016/S0040-4039(01)00933-9 |
0.464 |
|
| 1999 |
Evans DA, Willis MC, Johnston JN. Catalytic enantioselective Michael additions to unsaturated ester derivatives using chiral copper(II) Lewis acid complexes. Organic Letters. 1: 865-8. PMID 10823215 DOI: 10.1021/Ol9901570 |
0.695 |
|
| 1992 |
Berry MB, Blagg J, Craig D, Willis MC. An improved procedure for N-formylation of secondary amines using chlorotrimethylsilane-imidazole-N,N-dimethylformamide Synlett. 1992: 659-660. DOI: 10.1055/S-1992-21448 |
0.484 |
|
| Show low-probability matches. |