| Year |
Citation |
Score |
| 2017 |
Maupillier W, Journot G, Stoeckli‐Evans H, Neier R. An Efficient Synthetic Approach to Calix[n]furan[4‐n]pyrroles and the Calix[n]tetrahydrofuran[4‐n]pyrrolidines European Journal of Organic Chemistry. 2017: 6023-6037. DOI: 10.1002/Ejoc.201701156 |
0.305 |
|
| 2015 |
Yamada Y, Wehrli P, Miljkovic D, Wild HJ, Bühler N, Götschi E, Golding B, Löliger P, Gleason J, Pace B, Ellis L, Hunkeler W, Schneider P, Fuhrer W, Nordmann R, ... ... Neier R, et al. Corrin Syntheses. Part VI: Corrin Synthesis via A→D Ring Closure. the Construction of A/D-Secocorrin Chromophore Systems by the 'Sulfide Contraction' Method and the Photochemical A/B-Secocorrin→Corrin Cycloisomerization Helvetica Chimica Acta. 98: 1921-2054. DOI: 10.1002/Hlca.201500012 |
0.512 |
|
| 2014 |
Journot G, Neier R, Stoeckli-Evans H. Phase-transformation-induced twinning of an iron(III) calix[4]pyrrolidine complex. Acta Crystallographica. Section C, Structural Chemistry. 70: 644-9. PMID 24992103 DOI: 10.1107/S2053229614012157 |
0.309 |
|
| 2014 |
Neier R. Chemistry. A two-catalyst photochemistry route to homochiral rings. Science (New York, N.Y.). 344: 368-9. PMID 24763578 DOI: 10.1126/Science.1252965 |
0.359 |
|
| 2014 |
Kholod I, Vallat O, Buciumas A, Neier R. Preparation of precursors for the synthesis of analogues of rhazinilam Arkivoc. 2014. DOI: 10.3998/Ark.5550190.P008.497 |
0.382 |
|
| 2014 |
Kholod I, Vallat O, Buciumas A, Neels A, Neier R. Synthetic Strategies for the Synthesis and Transformation of Substituted Pyrrolinones as Advanced Intermediates for Rhazinilam Analogues European Journal of Organic Chemistry. 2014: 7865-7877. DOI: 10.1002/Ejoc.201402903 |
0.39 |
|
| 2012 |
Journot G, Neier R, Stoeckli-Evans H. 4-Chloro-benzoyl-meso-octa-methyl-calix[2]pyrrolidino[2]pyrrole: an acyl chloride derivative of a partially reduced calix[4] pyrrole. Acta Crystallographica. Section E, Structure Reports Online. 68: o976-7. PMID 22590031 DOI: 10.1107/S1600536812007003 |
0.312 |
|
| 2012 |
Journot G, Neier R, Stoeckli-Evans H. 2-[2-(pyrrolidin-2-yl)propan-2-yl]-1H-pyrrole and its amide derivative 1-{2-[2-(1H-pyrrol-2-yl)propan-2-yl]pyrrolidin-1-yl}ethanone. Acta Crystallographica. Section C, Crystal Structure Communications. 68: o119-22. PMID 22382545 DOI: 10.1107/S0108270112007603 |
0.331 |
|
| 2012 |
Journot G, Jones CR, Blangy V, Neier R. ■ The Hydrogenation of Heterocyclic Calix(4)arenes, a Transformation Leading to Novel Macrocyclic Ligands Heterocycles. 85: 749-797. DOI: 10.3987/Rev-11-Sr(P)8 |
0.326 |
|
| 2012 |
Pordea A, Stoeckli-Evans H, Dalvit C, Neier R. Synthesis and reactions of 2-[1-Methyl-1-(pyrrolidin-2-yl)ethyl]-1H-pyrrole and some derivatives with aldehydes: Chiral structures combining a secondary-amine group with an 1H-pyrrole moiety as excellent H-bond donor Helvetica Chimica Acta. 95: 2249-2264. DOI: 10.1002/Hlca.201200459 |
0.345 |
|
| 2012 |
Bruyneel F, Letondor C, Bastürk B, Gualandi A, Pordea A, Stoeckli-Evans H, Neier R. Catalytic epoxidation of alkenes by the manganese complex of a reduced porphyrinogen macrocycle Advanced Synthesis and Catalysis. 354: 428-440. DOI: 10.1002/Adsc.201100433 |
0.587 |
|
| 2011 |
Thevenet D, Neier R. An Efficient Photoinduced Deprotection of Aromatic Acetals and Ketals Helvetica Chimica Acta. 94: 331-346. DOI: 10.1002/Hlca.201000333 |
0.368 |
|
| 2010 |
Thevenet D, Neier R, Stoeckli-Evans H. 1,4-Bis[4-(tert-butyl-diphenyl-silyl)buta-1,3-diyn-yl]benzene. Acta Crystallographica. Section E, Structure Reports Online. 66: o839-40. PMID 21580665 DOI: 10.1107/S160053681000351X |
0.307 |
|
| 2010 |
Thevenet D, Neier R, Sereda O, Neels A, Stoeckli-Evans H. 1,4-Bis(hex-yloxy)-2,5-diiodo-benzene. Acta Crystallographica. Section E, Structure Reports Online. 66: o837-8. PMID 21580664 DOI: 10.1107/S1600536810005258 |
0.301 |
|
| 2010 |
Thevenet D, Neier R, Stoeckli-Evans H. 2-(2-Naphth-yl)-1,3-dioxane. Acta Crystallographica. Section E, Structure Reports Online. 66: o473-4. PMID 21579883 DOI: 10.1107/S1600536810000644 |
0.306 |
|
| 2010 |
Journot G, Neier R, Stoeckli-Evans H. 4,4-Bis(1H-pyrrol-2-yl)penta-nol. Acta Crystallographica. Section E, Structure Reports Online. 66: o393. PMID 21579814 DOI: 10.1107/S1600536809054269 |
0.312 |
|
| 2010 |
Journot G, Neier R, Stoeckli-Evans H. 2,2'-(Propane-2,2-di-yl)bis-(1H-pyrrole). Acta Crystallographica. Section E, Structure Reports Online. 66: o392. PMID 21579813 DOI: 10.1107/S1600536809054701 |
0.312 |
|
| 2010 |
Journot G, Letondor C, Neier R, Stoeckli-Evans H, Savoia D, Gualandi A. Catalytic hydrogenation of meso-octamethylporphyrinogen (calix[4]pyrrole). Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 4224-30. PMID 20222096 DOI: 10.1002/Chem.200903464 |
0.595 |
|
| 2010 |
Loiseau F, Kholod I, Neier R. Thione Esters as Substrates for the Stereoselective Alkylation of Model Compounds of Nonactic Acids European Journal of Organic Chemistry. 2010: 4642-4661. DOI: 10.1002/Ejoc.200901513 |
0.364 |
|
| 2009 |
Vallat O, Buciumas AM, Neier R, Stoeckli-Evans H. rac-Methyl 4-azido-3-hydr-oxy-3-(2-nitro-phen-yl)butanoate. Acta Crystallographica. Section E, Structure Reports Online. 65: o396-7. PMID 21581990 DOI: 10.1107/S1600536808043857 |
0.311 |
|
| 2009 |
Vallat O, Buciumas AM, Neier R, Stoeckli-Evans H. 5-Hydroxyalkyl derivatives of tert-butyl 2-oxo-2,5-dihydro-1H-pyrrole-1-carboxylate: diastereoselectivity of the Mukaiyama crossed-aldol-type reaction. Acta Crystallographica. Section C, Crystal Structure Communications. 65: o171-5. PMID 19346616 DOI: 10.1107/S0108270109008877 |
0.359 |
|
| 2009 |
Vallat O, Buciumas A, Neier R, Stoeckli-Evans H. Rac-(2R*,3R*)-S-Ethyl-4-Chloro-3-Hydroxy-2-Phenylbuthanethioate and Rac-(2R*,3R*)-S-Ethyl-2-Phenyl-3-(tosyloxy)buthanethioate: Dichotomy of the Stereoselectivity of the Mukaiyama Reaction Journal of Chemical Crystallography. 40: 10-14. DOI: 10.1007/S10870-009-9596-Y |
0.34 |
|
| 2009 |
Eng C, Simone J, Hartenbach A, Loiseau F, Neier R. Macrocyclisation of 2-(5-(2-hydroxyethyl)furan-2-yl)acetic acid model compounds of nonactic acid Monatshefte Fur Chemie. 140: 349-354. DOI: 10.1007/S00706-008-0031-4 |
0.333 |
|
| 2008 |
Vallinayagam R, Weber J, Neier R. Novel bioconjugates of aminolevulinic acid with vitamins. Organic Letters. 10: 4453-5. PMID 18798636 DOI: 10.1021/Ol801496J |
0.317 |
|
| 2008 |
Soldermann CP, Vallinayagam R, Tzouros M, Neier R. Facile synthesis of a "ready to use" precursor of porphobilinogen and its amino Acid derivatives. The Journal of Organic Chemistry. 73: 764-7. PMID 18081349 DOI: 10.1021/Jo702319N |
0.377 |
|
| 2008 |
Gurba P, Vallinayagam R, Schmitt F, Furrer J, Juillerat-Jeanneret L, Neier R. Novel Bioconjugates of AminolevulinicAcid with Nucleosides Synthesis. 2008: 3957-3962. DOI: 10.1055/S-0028-1083241 |
0.308 |
|
| 2007 |
Gacond S, Frère F, Nentwich M, Faurite JP, Frankenberg-Dinkel N, Neier R. Synthesis of bisubstrate inhibitors of porphobilinogen synthase from Pseudomonas aeruginosa. Chemistry & Biodiversity. 4: 189-202. PMID 17311232 DOI: 10.1002/Cbdv.200790024 |
0.336 |
|
| 2007 |
Vallinayagam R, Bertschy H, Berger Y, Wenger V, Neier R. Synthesis of novel and stable 5-aminolevulinic acid derivatives for the efficient synthesis of 5-aminolevulinic acid based prodrugs Synthesis. 3731-3735. DOI: 10.1055/S-2007-990825 |
0.367 |
|
| 2007 |
Simone J, Loiseau F, Carcache D, Bobal P, Jeanneret-Gris J, Neier R. Malonylation/Decarbalkoxylation of Furan Derivatives as Key Steps for the Preparation of Nonactic Acid Derivatives. Part II [1] Monatshefte Fur Chemie. 138: 141-147. DOI: 10.1007/S00706-006-0579-9 |
0.379 |
|
| 2007 |
Loiseau F, Simone J, Carcache D, Bobal P, Neier R. Radical Couplings as Key Steps for the Preparation of Derivatives of Nonactic Acid Monatshefte Fur Chemie. 138: 121-129. DOI: 10.1007/S00706-006-0578-X |
0.348 |
|
| 2007 |
Soldermann N, Velker J, Neels A, Stoeckli-Evans H, Neier R. The high stereoselectivity of the tandem sequence Diels-Alder reaction : Ireland-Claisen rearrangement starting from substituted O-(E)-buta-1,3-dienyl ketene acetals and cyclic dienophiles Synthesis. 2007: 2379-2387. DOI: 10.1002/CHIN.200748108 |
0.356 |
|
| 2006 |
Loiseau F, Neier R, Labat G, Stoeckli-Evans H. rac-(Z)-Ethyl 2-bromo-2-[(3R,5R)-3-bromo-5-methyltetrahydrofuran-2-ylidene]acetate. Acta Crystallographica. Section C, Crystal Structure Communications. 62: o636-8. PMID 17088631 DOI: 10.1107/S0108270106037127 |
0.31 |
|
| 2006 |
Frère F, Nentwich M, Gacond S, Heinz DW, Neier R, Frankenberg-Dinkel N. Probing the active site of Pseudomonas aeruginosa porphobilinogen synthase using newly developed inhibitors. Biochemistry. 45: 8243-53. PMID 16819823 DOI: 10.1021/Bi052611F |
0.337 |
|
| 2006 |
Loiseau F, Neier R, Stoeckli‐Evans H. rac-(R)-2-[(2R,5R)-5-Methyltetrahydrofuran-2-yl]propanoic acid Acta Crystallographica Section E: Crystallographic Communications. 62. DOI: 10.1107/S160053680602705X |
0.316 |
|
| 2005 |
Erskine PT, Coates L, Newbold R, Brindley AA, Stauffer F, Beaven GDE, Gill R, Coker A, Wood SP, Warren MJ, Shoolingin-Jordan PM, Neier R, Cooper JB. Structure of yeast 5-aminolaevulinic acid dehydratase complexed with the inhibitor 5-hydroxylaevulinic acid Acta Crystallographica Section D: Biological Crystallography. 61: 1222-1226. PMID 16131755 DOI: 10.1107/S0907444905018834 |
0.311 |
|
| 2005 |
Lanaspèze S, Neier R. Synthesis of Substituted 1-Thiocyanatobutadienes and their Application in a Diels-Alder/[3,3] Sigmatropic Rearrangement Tandem Reaction Monatshefte Fur Chemie. 136: 597-607. DOI: 10.1007/S00706-004-0258-7 |
0.37 |
|
| 2003 |
Berger Y, Ingrassia L, Neier R, Juillerat-Jeanneret L. Evaluation of dipeptide-derivatives of 5-aminolevulinic acid as precursors for photosensitizers in photodynamic therapy. Bioorganic & Medicinal Chemistry. 11: 1343-51. PMID 12628660 DOI: 10.1016/S0968-0896(02)00619-3 |
0.312 |
|
| 2003 |
Chaperon A, Bertschy H, Franz-Schrumpf A, Hugelet B, Neels A, Stoeckli-Evans H, Neier R. The Synthesis of a Pyrazol Analogon of Porphobilinogen with the Help of the Mukaiyama Aldol Reaction Chimia. 57: 601-606. DOI: 10.2533/000942903777678812 |
0.342 |
|
| 2002 |
Frère F, Schubert WD, Stauffer F, Frankenberg N, Neier R, Jahn D, Heinz DW. Structure of porphobilinogen synthase from Pseudomonas aeruginosa in complex with 5-fluorolevulinic acid suggests a double Schiff base mechanism. Journal of Molecular Biology. 320: 237-47. PMID 12079382 DOI: 10.1016/S0022-2836(02)00472-2 |
0.323 |
|
| 2002 |
Jaffe EK, Kervinen J, Martins J, Stauffer F, Neier R, Wlodawer A, Zdanov A. Species-specific inhibition of porphobilinogen synthase by 4-oxosebacic acid. The Journal of Biological Chemistry. 277: 19792-9. PMID 11909869 DOI: 10.1074/Jbc.M201486200 |
0.341 |
|
| 2001 |
Kervinen J, Jaffe EK, Stauffer F, Neier R, Wlodawer aA, Zdanov A. Mechanistic basis for suicide inactivation of porphobilinogen synthase by 4,7-dioxosebacic acid, an inhibitor that shows dramatic species selectivity. Biochemistry. 40: 8227-8236. PMID 11444968 DOI: 10.1021/Bi010656K |
0.34 |
|
| 2001 |
Berger Y, Greppi A, Siri O, Neier R, Juillerat-Jeanneret L. Ethylene glycol and amino acid derivatives of 5-aminolevulinic acid as new photosensitizing precursors of protoporphyrin IX in cells. Journal of Medicinal Chemistry. 43: 4738-46. PMID 11123982 DOI: 10.1021/Jm000981Q |
0.593 |
|
| 2000 |
Stauffer F, Neier R. Synthesis of Tri- and Tetrasubstituted Furans Catalyzed by Trifluoroacetic Acid Organic Letters. 2: 3535-3537. PMID 11073638 DOI: 10.1021/Ol0063205 |
0.368 |
|
| 2000 |
Jarret C, Stauffer F, Henz ME, Marty M, Lüönd RM, Bobálová J, Schürmann P, Neier R. Inhibition of Escherichia coli porphobilinogen synthase using analogs of postulated intermediates Chemistry & Biology. 7: 185-196. PMID 10712932 DOI: 10.1016/S1074-5521(00)00089-2 |
0.324 |
|
| 2000 |
Neier R. A novel synthesis of porphobilinogen: Synthetic and biosynthetic studies Journal of Heterocyclic Chemistry. 37: 487-508. DOI: 10.1002/Jhet.5570370307 |
0.333 |
|
| 2000 |
Neuschütz K, Simone J, Thyrann T, Neier R. Amino‐Claisen Rearrangements and Diels‐Alder Reactions of Ketene N,O‐Acetals: Reactivity Studies. On the Way to a Novel Tandem Process? Helvetica Chimica Acta. 83: 2712-2737. DOI: 10.1002/1522-2675(20001004)83:10<2712::Aid-Hlca2712>3.0.Co;2-D |
0.335 |
|
| 2000 |
Soldermann N, Velker J, Vallat O, Stoeckli-Evans H, Neier R. Application of the Novel Tandem Process Diels-Alder Reaction/Ireland-Claisen Rearrangement to the Synthesis of rac-Juvabione and rac-Epijuvabione Helvetica Chimica Acta. 83: 2266-2276. DOI: 10.1002/1522-2675(20000906)83:9<2266::Aid-Hlca2266>3.0.Co;2-T |
0.341 |
|
| 1999 |
Rubin Y, Ganapathi PS, Franz A, An Y, Qian W, Neier R. Tandem Nucleophilic Addition/Diels-Alder Reaction ofN-ButadienylN,O-Ketene Silyl Acetals with C60: Stereoselective Formation of Bicyclic Octahydroquinolino-1,2,3,4-Tetrahydrobuckminsterfullerenes and Combined NMR Spectroscopic and Computational Evaluation of the Functionalization Reactions Chemistry - a European Journal. 5: 3162-3184. DOI: 10.1002/(Sici)1521-3765(19991105)5:11<3162::Aid-Chem3162>3.0.Co;2-H |
0.354 |
|
| 1998 |
Chaperon AR, Engeloch TM, Neier R. A Biomimetic Synthesis of a Porphobilinogen Precursor Using a Mukaiyama Aldol Reaction. Angewandte Chemie (International Ed. in English). 37: 358-360. PMID 29711252 DOI: 10.1002/(Sici)1521-3773(19980216)37:3<358::Aid-Anie358>3.0.Co;2-Y |
0.372 |
|
| 1998 |
Neuschütz K, Velker J, Neier R. Tandem Reactions Combining Diels-Alder Reactions With Sigmatropic Rearrangement Processes And Their Use In Synthesis Synthesis. 1998: 227-255. DOI: 10.1055/S-1998-2021 |
0.322 |
|
| 1998 |
Chaperon AR, Engeloch TM, Neier R. Biomimetische Synthese eines Porphobilinogenvorläufers mit Hilfe der Mukaiyama‐Aldolreaktion Angewandte Chemie. 110: 369-371. DOI: 10.1002/(Sici)1521-3757(19980202)110:3<369::Aid-Ange369>3.0.Co;2-3 |
0.307 |
|
| 1996 |
Lüönd RM, Neier R. On the formation of the mixed pyrrole catalysed by porphobilinogen synthase from Rhodobacter spheroides Biochimica Et Biophysica Acta. 1289: 83-86. PMID 8605237 DOI: 10.1016/0304-4165(95)00146-8 |
0.341 |
|
| 1996 |
Franz A, Eschler P, Tharin M, Neier R. The preparation and the cascade reactions of N-butadienyl-N-alkylketeneN,O-tert-butyldimethylsilyl acetals Tetrahedron. 52: 11643-11656. DOI: 10.1016/0040-4020(96)00646-1 |
0.332 |
|
| 1996 |
Marty M, Stoeckli-Evans H, Neier R. Diastereoselective synthesis of (1S,2S,3R,6S) 3-Chloro-3-methyl-6-isopropenyl-1,2-cyclohexanediol via Prins reaction induced by zinc and trimethylsilyl chloride Tetrahedron. 52: 4645-4658. DOI: 10.1016/0040-4020(96)00167-6 |
0.312 |
|
| 1994 |
Schoepfer J, Marquis C, Pasquier C, Neier R. Lewis-acid catalysed tandem reaction Diels–Alder–[3,3] sigmatropic shift between buta-1,3-dienyl thiocyanic acid ester and acryloyl chloride: application in the synthesis of 2-azabicyclo[2.2.2]oct-5-ene derivatives Journal of the Chemical Society, Chemical Communications. 8: 1001-1002. DOI: 10.1039/C39940001001 |
0.399 |
|
| 1991 |
Guerry P, Blanco P, Brodbeck H, Pasteris O, Neier R. 1‐Methoxycarbonyl‐substituiertes 2,3‐Dihydropyridin‐4(1H)‐on (= Methyl‐1,2,3,4‐tetrahydro‐4‐oxopyridin‐1‐carboxylat) als Chromophor für die photochemische [2 + 2]‐Cycloaddition Helvetica Chimica Acta. 74: 163-178. DOI: 10.1002/Hlca.19910740118 |
0.374 |
|
| 1991 |
Lüönd R, Neier R. Michael reactions of α-unsubstituted trisubstituted 1H-pyrroles Helvetica Chimica Acta. 74: 91-102. DOI: 10.1002/Hlca.19910740111 |
0.334 |
|
| 1990 |
Bertschy H, Meunier A, Neier R. A Novel Pyrrole Synthesis Angewandte Chemie. 29: 777-778. DOI: 10.1002/Anie.199007771 |
0.329 |
|
| 1989 |
Guerry P, Neier R. The photochemical[2 + 2]cycloaddition to N-methoxycarbonyl-5,6-dihydro-4-pyridone Journal of the Chemical Society, Chemical Communications. 22: 1727-1728. DOI: 10.1039/C39890001727 |
0.311 |
|
| 1988 |
Meunier A, Neier R. Synthesis of Pyrroles via the Cross-Aldol Reaction Synthesis. 5: 381-383. DOI: 10.1055/S-1988-27581 |
0.321 |
|
| 1986 |
Brodbeck H, Bourgin D, Neier R. Photochemical ring closure of muconic acid anhydride Tetrahedron Letters. 27: 343-344. DOI: 10.1016/S0040-4039(00)84013-7 |
0.363 |
|
| 1986 |
Huber S, Stamouli P, Jenny T, Neier R. 1,3-Butadienyl-thiocyanate in der Diels-Alder-Reaktion mit anschliessender [3,3]-sigmatroper Umlagerung Helvetica Chimica Acta. 69: 1898-1915. DOI: 10.1002/Hlca.19860690817 |
0.329 |
|
| 1985 |
Huber S, Stamouli P, Neier R. Synthesis of (E)- and (Z)-1-thiocyanatobuta-1,3-dienes and their Diels–Alder reaction Journal of the Chemical Society, Chemical Communications. 9: 533-534. DOI: 10.1039/C39850000533 |
0.343 |
|
| 1985 |
Huber S, Stamouli P, Neier R. Synthesis Of (E)- And (Z)-1-Thiocyanatobuta-1,3-Dienes And Their Diels-Alder Reaction Cheminform. 16. DOI: 10.1002/Chin.198533214 |
0.325 |
|
| 1978 |
PFALTZ A, BUEHLER N, NEIER R, HIRAI K, ESCHENMOSER A. ChemInform Abstract: CORRINOIDS. 4. PHOTOCHEMICAL AND NON-PHOTOCHEMICAL A D-SECOCORRIN → CORRIN CYCLIZATIONS OF 19-CARBOXY- AND 19-FORMYL-1-METHYLIDENE-1,19-SECOCORRINATES. DECARBOXYLATION AND DEFORMYLATION OF NICKEL(II) 19-CARBOXY(AND 19-FORMYL)CORRINATE Chemischer Informationsdienst. 9. DOI: 10.1002/Chin.197817330 |
0.593 |
|
| 1977 |
Pfaltz A, Bühler N, Neier R, Hirai K, Eschenmoser A. Photochemische und nicht-photochemische A/D-Secocorrin→Corrin-Cyclisierungen bei 19-Carboxy- und 19-Formyl-1-methyliden-1,19-secocorrinaten. Decarboxylierbarkeit und Deformylierbarkeit von Nickel (II)-19-carboxy- bzw. 19-formyl-corrinaten. Vorläufige Mitt Helvetica Chimica Acta. 60: 2653-2672. DOI: 10.1002/Hlca.19770600817 |
0.628 |
|
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