| Year |
Citation |
Score |
| 2023 |
Jessen CH, Bendix J, Nannestad TB, Bordallo H, Pedersen MJ, Pedersen CM, Bols M. CO complexation with cyclodextrins. Beilstein Journal of Organic Chemistry. 19: 1021-1027. PMID 37497051 DOI: 10.3762/bjoc.19.78 |
0.402 |
|
| 2020 |
Bols M, Matassini C, Warren J, Wang B, Goti A, Cardona F, Morrone A. Imino- and azasugar protonation inside human acid β-glucosidase, the enzyme defective in Gaucher disease. Angewandte Chemie (International Ed. in English). PMID 32191378 DOI: 10.1002/Anie.202002850 |
0.309 |
|
| 2019 |
Madsen J, Viuf C, Bols M. A new method for the deprotection of benzyl ethers or the selective protection of alcohols Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 1140-6. PMID 10785798 DOI: 10.1002/(Sici)1521-3765(20000403)6:7<1140::Aid-Chem1140>3.0.Co;2-6 |
0.318 |
|
| 2018 |
Jørgensen FP, Bols M. An inexpensive and scalable synthesis of Shld. The Journal of Organic Chemistry. PMID 29749733 DOI: 10.1021/Acs.Joc.8B00698 |
0.361 |
|
| 2017 |
Wang B, Olsen JI, Laursen BW, Navarro Poulsen JC, Bols M. Determination of protonation states of iminosugar-enzyme complexes using photoinduced electron transfer. Chemical Science. 8: 7383-7393. PMID 29163889 DOI: 10.1039/C7Sc01540B |
0.355 |
|
| 2017 |
Bols M, Pedersen CM. Silyl-protective groups influencing the reactivity and selectivity in glycosylations. Beilstein Journal of Organic Chemistry. 13: 93-105. PMID 28228850 DOI: 10.3762/Bjoc.13.12 |
0.499 |
|
| 2017 |
Pedersen CM, Bols M. On the nature of the electronic effect of multiple hydroxyl groups in the 6-membered ring - the effects are additive but steric hindrance plays a role too. Organic & Biomolecular Chemistry. PMID 28084490 DOI: 10.1039/C6Ob02427K |
0.51 |
|
| 2017 |
Nielsen MM, Stougaard BA, Bols M, Glibstrup E, Pedersen CM. Glycosyl Fluorides as Intermediates in BF3·OEt2-Promoted Glycosylation with Trichloroacetimidates European Journal of Organic Chemistry. 2017: 1281-1284. DOI: 10.1002/Ejoc.201601439 |
0.502 |
|
| 2016 |
Bandara MD, Yasomanee JP, Rath NP, Pedersen CM, Bols M, Demchenko AV. Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot. Organic & Biomolecular Chemistry. PMID 27942674 DOI: 10.1039/C6Ob02498J |
0.556 |
|
| 2016 |
Olsen JI, Plata GB, Padrón JM, López Ó, Bols M, Fernández-Bolaños JG. Selenoureido-iminosugars: A new family of multitarget drugs. European Journal of Medicinal Chemistry. 123: 155-160. PMID 27474931 DOI: 10.1016/J.Ejmech.2016.07.021 |
0.312 |
|
| 2016 |
Olsen JI, Kowalska K, Pedersen CM, Bols M. Super arming of a glycosyl donor using a molecular lever Tetrahedron Letters. 57: 35-38. DOI: 10.1016/J.Tetlet.2015.11.052 |
0.5 |
|
| 2016 |
Frihed TG, Bols M, Pedersen CM. C-H Functionalization on Carbohydrates European Journal of Organic Chemistry. 2016: 2740-2756. DOI: 10.1002/Ejoc.201600121 |
0.466 |
|
| 2016 |
Frihed TG, Bols M, Pedersen CM. ChemInform Abstract: C-H Functionalization on Carbohydrates Cheminform. 47. DOI: 10.1002/CHIN.201635168 |
0.37 |
|
| 2015 |
Heuckendorff M, Bols PS, Barry CB, Frihed TG, Pedersen CM, Bols M. β-Mannosylation with 4,6-benzylidene protected mannosyl donors without preactivation. Chemical Communications (Cambridge, England). 51: 13283-5. PMID 26197760 DOI: 10.1039/C5Cc04716A |
0.517 |
|
| 2015 |
Lindbäck E, Laursen BW, Poulsen JC, Kilså K, Pedersen CM, Bols M. A fluorescence study of isofagomine protonation in β-glucosidase. Organic & Biomolecular Chemistry. 13: 6562-6. PMID 25978843 DOI: 10.1039/C5Ob00624D |
0.515 |
|
| 2015 |
Frihed TG, Bols M, Pedersen CM. Mechanisms of Glycosylation Reactions Studied by Low-Temperature Nuclear Magnetic Resonance. Chemical Reviews. 115: 4963-5013. PMID 25923428 DOI: 10.1021/Cr500434X |
0.442 |
|
| 2015 |
Frihed TG, Bols M, Pedersen CM. Synthesis of L-Hexoses. Chemical Reviews. 115: 3615-76. PMID 25893557 DOI: 10.1021/Acs.Chemrev.5B00104 |
0.474 |
|
| 2015 |
Heuckendorff M, Bols PS, Barry CB, Frihed TG, Pedersen CM, Bols M. β-Mannosylation with 4,6-benzylidene protected mannosyl donors without preactivation Chemical Communications. 51: 13283-13285. DOI: 10.1039/c5cc04716a |
0.432 |
|
| 2015 |
Frihed TG, Bols M, Pedersen CM. ChemInform Abstract: Mechanisms of Glycosylation Reactions Studied by Low-Temperature Nuclear Magnetic Resonance Cheminform. 46: no-no. DOI: 10.1002/CHIN.201533305 |
0.379 |
|
| 2015 |
Frihed TG, Bols M, Pedersen CM. ChemInform Abstract: Synthesis of L-Hexoses Cheminform. 46: no-no. DOI: 10.1002/CHIN.201532248 |
0.418 |
|
| 2014 |
Frihed TG, Pedersen CM, Bols M. Synthesis of all eight L-glycopyranosyl donors using C-H activation. Angewandte Chemie (International Ed. in English). 53: 13889-93. PMID 25303081 DOI: 10.1002/Ange.201408209 |
0.518 |
|
| 2014 |
Hogendorf WF, Gisch N, Schwudke D, Heine H, Bols M, Pedersen CM. Total Synthesis of Five Lipoteichoic acids of Clostridium difficile. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 13511-6. PMID 25168290 DOI: 10.1002/Chem.201404336 |
0.483 |
|
| 2014 |
Heuckendorff M, Bendix J, Pedersen CM, Bols M. β-Selective mannosylation with a 4,6-silylene-tethered thiomannosyl donor. Organic Letters. 16: 1116-9. PMID 24502365 DOI: 10.1021/Ol403722F |
0.526 |
|
| 2014 |
Zhou Y, Lindbäck E, Pedersen CM, Bols M. Cyclodextrin-based artificial oxidases with high rate accelerations and selectivity Tetrahedron Letters. 55: 2304-2307. DOI: 10.1016/J.Tetlet.2014.02.100 |
0.507 |
|
| 2014 |
Frihed TG, Pedersen CM, Bols M. Synthesis of All Eight Stereoisomeric 6-Deoxy-L-hexopyranosyl Donors - Trends in Using Stereoselective Reductions or Mitsunobu Epimerizations European Journal of Organic Chemistry. 2014: 7924-7939. DOI: 10.1002/Ejoc.201403074 |
0.494 |
|
| 2014 |
Frihed TG, Pedersen CM, Bols M. Synthesis of All EightL-Glycopyranosyl Donors Using CH Activation Angewandte Chemie. 126: 14109-14113. DOI: 10.1002/ANGE.201408209 |
0.443 |
|
| 2013 |
Hogendorf WF, Jagalski V, Pomorski TG, Bols M, Cárdenas M, Pedersen CM. Synthesis and thermotropic phase behavior of four glycoglycerolipids. Molecules (Basel, Switzerland). 18: 13546-73. PMID 24189295 DOI: 10.3390/Molecules181113546 |
0.482 |
|
| 2013 |
Heuckendorff M, Premathilake HD, Pornsuriyasak P, Madsen AØ, Pedersen CM, Bols M, Demchenko AV. Superarming of glycosyl donors by combined neighboring and conformational effects. Organic Letters. 15: 4904-7. PMID 24006853 DOI: 10.1021/Ol402371B |
0.494 |
|
| 2013 |
Heuckendorff M, Pedersen CM, Bols M. Conformationally armed 3,6-tethered glycosyl donors: synthesis, conformation, reactivity, and selectivity. The Journal of Organic Chemistry. 78: 7234-48. PMID 23786671 DOI: 10.1021/Jo4012464 |
0.548 |
|
| 2013 |
López Ó, Qing FL, Pedersen CM, Bols M. Enzyme inhibition by iminosugars: analysis and insight into the glycosidase-iminosugar dependency of pH. Bioorganic & Medicinal Chemistry. 21: 4755-61. PMID 23583693 DOI: 10.1016/J.Bmc.2013.03.003 |
0.484 |
|
| 2013 |
Frihed TG, Walvoort MT, Codée JD, van der Marel GA, Bols M, Pedersen CM. Influence of O6 in mannosylations using benzylidene protected donors: stereoelectronic or conformational effects? The Journal of Organic Chemistry. 78: 2191-205. PMID 23336427 DOI: 10.1021/Jo302455D |
0.541 |
|
| 2013 |
Zhou Y, Pedersen CM, Bols M. Artificial enzyme activity from cyclodextrins with cyanohydrins on the secondary rim Tetrahedron Letters. 54: 2458-2461. DOI: 10.1016/J.Tetlet.2013.02.091 |
0.554 |
|
| 2013 |
Pedersen CM, Bols M, Qiao Y. ChemInform Abstract: Total Synthesis of Biologically Active Lipoteichoic Acids Cheminform. 44: no-no. DOI: 10.1002/chin.201316228 |
0.435 |
|
| 2012 |
Frihed TG, Heuckendorff M, Pedersen CM, Bols M. Easy access to L-mannosides and L-galactosides by using C-H activation of the corresponding 6-deoxysugars. Angewandte Chemie (International Ed. in English). 51: 12285-8. PMID 23109259 DOI: 10.1002/Anie.201206880 |
0.45 |
|
| 2012 |
Heuckendorff M, Pedersen CM, Bols M. Rhamnosylation: diastereoselectivity of conformationally armed donors. The Journal of Organic Chemistry. 77: 5559-68. PMID 22639871 DOI: 10.1021/Jo300591K |
0.531 |
|
| 2012 |
Pedersen CM, Bols M, Qiao Y. Total synthesis of biologically active lipoteichoic acids Arkivoc. 2013. DOI: 10.3998/Ark.5550190.0014.220 |
0.504 |
|
| 2012 |
Lindbäck E, Zhou Y, Pedersen CM, Bols M. Artificial enzymes based on cyclodextrin with phenol as the catalytic group Tetrahedron Letters. 53: 5023-5026. DOI: 10.1016/J.Tetlet.2012.07.050 |
0.499 |
|
| 2012 |
Lindbäck E, Zhou Y, López Ó, Fernández-Bolaños JG, Pedersen CM, Bols M. A uronic acid analogue of isofagomine lactam as a nanomolar glucuronidase inhibitor Tetrahedron Letters. 53: 2045-2047. DOI: 10.1016/J.Tetlet.2012.02.009 |
0.52 |
|
| 2012 |
Jadhav H, Taarning E, Pedersen CM, Bols M. Conversion of d-glucose into 5-hydroxymethylfurfural (HMF) using zeolite in [Bmim]Cl or tetrabutylammonium chloride (TBAC)/CrCl2 Tetrahedron Letters. 53: 983-985. DOI: 10.1016/J.Tetlet.2011.12.059 |
0.49 |
|
| 2012 |
Zhou Y, Marinescu L, Pedersen CM, Bols M. Synthesis of Tin-Containing Cyclodextrins as Potential Enzyme Models European Journal of Organic Chemistry. 2012: 6383-6389. DOI: 10.1002/Ejoc.201200756 |
0.543 |
|
| 2012 |
Lindbäck E, Zhou Y, Pedersen CM, Bols M. Two Diastereomeric Artificial Enzymes with Different Catalytic Activity European Journal of Organic Chemistry. 2012: 5366-5372. DOI: 10.1002/Ejoc.201200699 |
0.55 |
|
| 2012 |
Zhou Y, Lindbäck E, Marinescu LG, Pedersen CM, Bols M. Synthesis of Cyclodextrins with Carboxylic Acids at the Secondary Rim and an Evaluation of Their Properties as Chemzymes for Glycoside Hydrolysis European Journal of Organic Chemistry. 2012: 4063-4070. DOI: 10.1002/Ejoc.201200404 |
0.532 |
|
| 2011 |
Heuckendorff M, Pedersen CM, Bols M. The influence of neighboring group participation on the hydrolysis of 2-O-substituted methyl glucopyranosides. Organic Letters. 13: 5956-9. PMID 22007683 DOI: 10.1021/Ol202308Y |
0.504 |
|
| 2011 |
Jadhav V, Pedersen CM, Bols M. A study of anhydrocelluloses--is a cellulose structure with residues in a 1C4-conformation more prone to hydrolysis? Organic & Biomolecular Chemistry. 9: 7525-34. PMID 21931923 DOI: 10.1039/C1Ob06085F |
0.531 |
|
| 2011 |
Jadhav H, Pedersen CM, Sølling T, Bols M. 3-Deoxy-glucosone is an intermediate in the formation of furfurals from D-glucose. Chemsuschem. 4: 1049-51. PMID 21717583 DOI: 10.1002/Cssc.201100249 |
0.464 |
|
| 2011 |
Amorim L, Marcelo F, Rousseau C, Nieto L, Jiménez-Barbero J, Marrot J, Rauter AP, Sollogoub M, Bols M, Blériot Y. Direct experimental evidence for the high chemical reactivity of α- and β-xylopyranosides adopting a (2,5)B conformation in glycosyl transfer. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 7345-56. PMID 21567492 DOI: 10.1002/Chem.201003251 |
0.33 |
|
| 2011 |
Lindbäck E, López O, Fernández-Bolaños JG, Sauer SP, Bols M. An isofagomine analogue with an amidine at the pseudoanomeric position. Organic Letters. 13: 2908-11. PMID 21548609 DOI: 10.1021/Ol200942G |
0.358 |
|
| 2011 |
Pedersen CM, Olsen J, Brka AB, Bols M. Quantifying the electronic effects of carbohydrate hydroxy groups by using aminosugar models. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 7080-6. PMID 21542038 DOI: 10.1002/Chem.201100020 |
0.547 |
|
| 2011 |
Yang Y, Zheng F, Bols M, Marinescu LG, Qing FL. Synthesis of monofluorinated isofagomine analogues and evaluation as glycosidase inhibitors Journal of Fluorine Chemistry. 132: 838-845. DOI: 10.1016/J.Jfluchem.2011.05.031 |
0.337 |
|
| 2011 |
Pedersen CM, Marinescu LG, Bols M. Glycosyl donors in “unusual” conformations – influence on reactivity and selectivity Comptes Rendus Chimie. 14: 17-43. DOI: 10.1016/J.Crci.2010.03.030 |
0.519 |
|
| 2011 |
Christensen HS, Sigurskjold BW, Frihed TG, Marinescu LG, Pedersen CM, Bols M. Recognition of Peptides by Cyclodextrin Trimers European Journal of Organic Chemistry. 2011: 5279-5290. DOI: 10.1002/Ejoc.201100671 |
0.456 |
|
| 2011 |
Fenger TH, Marinescu LG, Bols M. Cyclodextrin Ketones with the Catalytic Group at the Secondary Rim and Their Effectiveness in Enzyme-Like Epoxidation of Stilbenes European Journal of Organic Chemistry. 2011: 2339-2345. DOI: 10.1002/Ejoc.201001696 |
0.372 |
|
| 2011 |
Kumari N, Olesen JK, Pedersen CM, Bols M. Synthesis of 5-Bromomethylfurfural from Cellulose as a Potential Intermediate for Biofuel European Journal of Organic Chemistry. 2011: 1266-1270. DOI: 10.1002/Ejoc.201001539 |
0.507 |
|
| 2011 |
Pedersen CM, Marinescu LG, Bols M. ChemInform Abstract: Glycosyl Donors in “Unusual” Conformations - Influence on Reactivity and Selectivity Cheminform. 42: no-no. DOI: 10.1002/CHIN.201134241 |
0.43 |
|
| 2010 |
Heuckendorff M, Pedersen CM, Bols M. Quantifying electronic effects of common carbohydrate protecting groups in a piperidine model system. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 13982-94. PMID 21132699 DOI: 10.1002/Chem.201002313 |
0.523 |
|
| 2010 |
Fenger TH, Bols M. Substrate control through per-O-methylation of cyclodextrin acids. Chemical Communications (Cambridge, England). 46: 7769-71. PMID 20871875 DOI: 10.1039/C0Cc02071K |
0.312 |
|
| 2010 |
Petrillo M, Marinescu L, Bols M. Regioselective difunctionalization of cyclodextrins Journal of Inclusion Phenomena and Macrocyclic Chemistry. 69: 425-431. DOI: 10.1007/S10847-010-9775-7 |
0.377 |
|
| 2010 |
Fenger TH, Bols M. Simple cyclodextrin aldehydes as excellent artificial oxidases Journal of Inclusion Phenomena and Macrocyclic Chemistry. 69: 397-402. DOI: 10.1007/S10847-010-9771-Y |
0.304 |
|
| 2010 |
Bjerre J, Bols M. Substantial Spatial Flexibility and Hydrogen Bonding within the Catalysis Exerted by Cyclodextrin Artificial Glycosidases European Journal of Organic Chemistry. 2010: 3487-3500. DOI: 10.1002/Ejoc.201000380 |
0.329 |
|
| 2010 |
Lindbäck E, Zhou Y, Marinescu L, Pedersen CM, Bols M. The Grignard Reaction of Cyclodextrin-6-aldehydes Revisited: A Study of the Stereoselectivity Upon Addition of Organometallic Reagents to Aldehydes and Ketones European Journal of Organic Chemistry. 2010: 3883-3896. DOI: 10.1002/Ejoc.201000295 |
0.515 |
|
| 2009 |
Wang RW, Xu J, Lopez O, Bols M, Qing FL. Difluoromethylenated polyhydroxylated pyrrolidines: facile synthesis, crystal structure and biological evaluation. Future Medicinal Chemistry. 1: 991-7. PMID 21426093 DOI: 10.4155/Fmc.09.82 |
0.304 |
|
| 2009 |
Nielsen S, Pedersen CM, Hansen SG, Petersen MD, Sinning S, Wiborg O, Jensen HH, Bols M. An extended study of dimeric phenyl tropanes. Bioorganic & Medicinal Chemistry. 17: 4900-9. PMID 19560930 DOI: 10.1016/J.Bmc.2009.06.007 |
0.516 |
|
| 2009 |
Fenger TH, Marinescu LG, Bols M. Cyclodextrin ketones as oxidation catalysts: investigation of bridged derivatives. Organic & Biomolecular Chemistry. 7: 933-43. PMID 19225677 DOI: 10.1039/B814245A |
0.321 |
|
| 2009 |
Li R, Bols M, Rousseau C, Zhang X, Wang R, Qing F. Synthesis and biological evaluation of potent glycosidase inhibitors: 4-deoxy-4,4-difluoroisofagomine and analogues Tetrahedron. 65: 3717-3727. DOI: 10.1016/J.Tet.2009.02.079 |
0.326 |
|
| 2009 |
Marinescu LG, Doyagüez EG, Petrillo M, Fernández-Mayoralas A, Bols M. Amino-Acetone-Bridged Cyclodextrins ― Artificial Alcohol Oxidases European Journal of Organic Chemistry. 2010: 157-167. DOI: 10.1002/Ejoc.200901099 |
0.362 |
|
| 2008 |
Pedersen CM, Marinescu LG, Bols M. Conformationally armed glycosyl donors: reactivity quantification, new donors and one pot reactions. Chemical Communications (Cambridge, England). 2465-7. PMID 18491016 DOI: 10.1039/B801305E |
0.498 |
|
| 2008 |
López Ó, Bols M. Effective synthesis of negatively charged cyclodextrins. Selective access to phosphate cyclodextrins Tetrahedron. 64: 7587-7593. DOI: 10.1016/J.Tet.2008.05.094 |
0.376 |
|
| 2008 |
Bjerre J, Nielsen EH, Bols M. Hydrolysis of Toxic Natural Glucosides Catalyzed by Cyclodextrin Dicyanohydrins European Journal of Organic Chemistry. 2008: 745-752. DOI: 10.1002/Ejoc.200700954 |
0.373 |
|
| 2007 |
Boye SV, Ortega-Caballero F, Sinning S, Wiborg O, Jensen HH, Bols M. High dopamine transporter selectivity can be displayed by remarkably simple non-nitrogen containing inhibitors. Bioorganic & Medicinal Chemistry Letters. 17: 6019-25. PMID 17869101 DOI: 10.1016/J.Bmcl.2007.07.076 |
0.302 |
|
| 2007 |
Jensen HH, Pedersen CM, Bols M. Going to extremes: "super" armed glycosyl donors in glycosylation chemistry. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 7576-82. PMID 17705330 DOI: 10.1002/Chem.200700947 |
0.504 |
|
| 2007 |
Pedersen CM, Nordstrøm LU, Bols M. "Super armed" glycosyl donors: conformational arming of thioglycosides by silylation. Journal of the American Chemical Society. 129: 9222-35. PMID 17602482 DOI: 10.1021/Ja071955L |
0.53 |
|
| 2007 |
Petersen MD, Boye SV, Nielsen EH, Willumsen J, Sinning S, Wiborg O, Bols M. Synthesis, inhibition and binding of simple non-nitrogen inhibitors of monoamine transporters. Bioorganic & Medicinal Chemistry. 15: 4159-74. PMID 17446076 DOI: 10.1016/J.Bmc.2007.03.069 |
0.314 |
|
| 2007 |
Lopez OL, Bols M. Anomer-selective glycosidase inhibition by 2-N-alkylated 1-azafagomines Chembiochem. 8: 657-661. PMID 17352429 DOI: 10.1002/Cbic.200700012 |
0.36 |
|
| 2007 |
Lopez OL, Marinescu L, Bols M. New cup-shaped α-cyclodextrin derivatives and a study of their catalytic properties in oxidation reactions Tetrahedron. 63: 8872-8880. DOI: 10.1016/J.Tet.2007.06.018 |
0.332 |
|
| 2007 |
Sivertsen AC, Gasior M, Bjerring M, Hansen SU, Lopez OL, Nielsen NC, Bols M. Active site protonation of 1-azafagomine in glucosidases studied by solid-state NMR spectroscopy European Journal of Organic Chemistry. 1735-1742. DOI: 10.1002/Ejoc.200600816 |
0.326 |
|
| 2007 |
Bjerre J, Hauch Fenger T, Marinescu LG, Bols M. Synthesis of Some Trifluoromethylated Cyclodextrin Derivatives and Analysis of Their Properties as Artificial Glycosidases and Oxidases European Journal of Organic Chemistry. 2007: 704-710. DOI: 10.1002/Ejoc.200600762 |
0.367 |
|
| 2007 |
Jensen HH, Pedersen CM, Bols M. Going to Extremes: “Super” Armed Glycosyl Donors in Glycosylation Chemistry Cheminform. 38. DOI: 10.1002/CHIN.200750238 |
0.412 |
|
| 2007 |
Pedersen CM, Nordstroem LU, Bols M. “Super Armed” Glycosyl Donors: Conformational Arming of Thioglycosides by Silylation. Cheminform. 38. DOI: 10.1002/CHIN.200750201 |
0.413 |
|
| 2006 |
Wang RW, Qiu XL, Bols M, Ortega-Caballero F, Qing FL. Synthesis and biological evaluation of glycosidase inhibitors: gem-difluoromethylenated nojirimycin analogues. Journal of Medicinal Chemistry. 49: 2989-97. PMID 16686540 DOI: 10.1021/Jm060066Q |
0.312 |
|
| 2006 |
Jensen HH, Bols M. Stereoelectronic substituent effects. Accounts of Chemical Research. 39: 259-65. PMID 16618093 DOI: 10.1021/Ar050189P |
0.305 |
|
| 2006 |
Ortega-Caballero F, Bols M. Cyclodextrin derivatives with cyanohydrin and carboxylate groups as artificial glycosidases Canadian Journal of Chemistry. 84: 650-658. DOI: 10.1139/V06-039 |
0.364 |
|
| 2006 |
Kuntz DA, Liu H, Bols M, Rose DR. The role of the active site Zn in the catalytic mechanism of the GH38 Golgi α-mannosidase II: Implications from noeuromycin inhibition Biocatalysis and Biotransformation. 24: 55-61. DOI: 10.1080/10242420500533242 |
0.315 |
|
| 2006 |
Tagmose TM, Bols M. Synthesis of the 2-Deoxyisomaltose Analogue of Acarbose by an Improved Route to Chiral Valieneamines Chemistry - a European Journal. 3: 453-462. DOI: 10.1002/Chem.19970030318 |
0.353 |
|
| 2005 |
Ortega-Caballero F, Bjerre J, Laustsen LS, Bols M. Four orders of magnitude rate increase in artificial enzyme-catalyzed aryl glycoside hydrolysis. The Journal of Organic Chemistry. 70: 7217-26. PMID 16122240 DOI: 10.1021/Jo050861W |
0.35 |
|
| 2005 |
Rousseau C, Ortega-Caballero F, Nordstrøm LU, Christensen B, Petersen TE, Bols M. Artificial glycosyl phosphorylases. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 5094-101. PMID 15981287 DOI: 10.1002/Chem.200500364 |
0.306 |
|
| 2005 |
Gregersen A, Pedersen CM, Jensen HH, Bols M. On the electronic effects of OH groups. Synthesis and investigation of tetrahydroxylated azabicycloheptanes. Organic & Biomolecular Chemistry. 3: 1514-9. PMID 15827650 DOI: 10.1039/B419154D |
0.548 |
|
| 2005 |
Pedersen CM, Marinescu LG, Bols M. Radical substitution with azide: TMSN3-PhI(OAc)2 as a substitute of IN3. Organic & Biomolecular Chemistry. 3: 816-22. PMID 15731868 DOI: 10.1039/B500037H |
0.518 |
|
| 2005 |
Marinescu LG, Pedersen CM, Bols M. Safe Radical Azidonation Using Polystyrene Supported Diazidoiodate(I). Cheminform. 36. DOI: 10.1016/J.Tet.2004.10.040 |
0.489 |
|
| 2005 |
Marinescu LG, Pedersen CM, Bols M. Safe radical azidonation using polystyrene supported diazidoiodate(I) Tetrahedron. 61: 123-127. DOI: 10.1016/J.TET.2004.10.040 |
0.357 |
|
| 2005 |
Pedersen CM, Bols M. Stereochemical substituent effects: investigation of the cyano, amide and carboxylate group Tetrahedron. 61: 115-122. DOI: 10.1016/J.Tet.2004.10.039 |
0.471 |
|
| 2005 |
Rousseau C, Christensen B, Bols M. Artificial Epoxidase II. Synthesis of Cyclodextrin Ketoesters and Epoxidation of Alkenes European Journal of Organic Chemistry. 2005: 2734-2739. DOI: 10.1002/Ejoc.200500034 |
0.319 |
|
| 2005 |
Pedersen CM, Marinescu LG, Bols M. Radical Substitution with Azide: TMSN3—PhI(OAc)2 as a Substitute of IN3. Cheminform. 36. DOI: 10.1002/CHIN.200532062 |
0.437 |
|
| 2004 |
Rousseau C, Christensen B, Petersen TE, Bols M. Cyclodextrins containing an acetone bridge. Synthesis and study as epoxidation catalysts. Organic & Biomolecular Chemistry. 2: 3476-82. PMID 15565240 DOI: 10.1039/B410098K |
0.357 |
|
| 2004 |
Pedersen H, Sinning S, Bulow A, Wiborg O, Falborg L, Bols M. Combinatorial synthesis of benztropine libraries and their evaluation as monoamine transporter inhibitors. Organic & Biomolecular Chemistry. 2: 2861-9. PMID 15455161 DOI: 10.1039/B405768F |
0.364 |
|
| 2004 |
McDonnell C, López O, Murphy P, Fernández Bolaños JG, Hazell R, Bols M. Conformational effects on glycoside reactivity: study of the high reactive conformer of glucose. Journal of the American Chemical Society. 126: 12374-85. PMID 15453771 DOI: 10.1021/Ja047476T |
0.3 |
|
| 2004 |
Jensen HH, Nordstrøm LU, Bols M. The disarming effect of the 4,6-acetal group on glycoside reactivity: torsional or electronic? Journal of the American Chemical Society. 126: 9205-13. PMID 15281809 DOI: 10.1021/Ja047578J |
0.343 |
|
| 2004 |
Bülow A, Sinning S, Wiborg O, Bols M. Two- and three dimensional combinatorial chemistry from multicomponent Grignard reagents. Journal of Combinatorial Chemistry. 6: 509-19. PMID 15244412 DOI: 10.1021/Cc049947D |
0.328 |
|
| 2004 |
Andersch J, Bols M, Hazell A. Benzyl 4-C-nitrosomethyl-β-D-arabinopyranoside Acta Crystallographica Section E Structure Reports Online. 60: o660-o661. DOI: 10.1107/S1600536804006488 |
0.308 |
|
| 2004 |
Rousseau C, Nielsen N, Bols M. An artificial enzyme that catalyzes hydrolysis of aryl glycosides Tetrahedron Letters. 45: 8709-8711. DOI: 10.1016/J.Tetlet.2004.09.134 |
0.315 |
|
| 2004 |
Bülow A, Meyer T, Olszewski T, Bols M. The C-4 Configuration as a Probe for the Study of Glycosidation Reactions European Journal of Organic Chemistry. 2004: 323-329. DOI: 10.1002/Ejoc.200300540 |
0.33 |
|
| 2003 |
Marinescu L, Thinggaard J, Thomsen IB, Bols M. Radical azidonation of aldehydes. The Journal of Organic Chemistry. 68: 9453-5. PMID 14629171 DOI: 10.1021/Jo035163V |
0.326 |
|
| 2003 |
Lillelund VH, Liu H, Liang X, Søhoel H, Bols M. Isofagomine lactams, synthesis and enzyme inhibition. Organic & Biomolecular Chemistry. 1: 282-7. PMID 12929423 DOI: 10.1039/B208784G |
0.311 |
|
| 2003 |
Lopez OL, Fernández-Bolaños JG, Lillelund VH, Bols M. Aziridines as a structural motif to conformational restriction of azasugars Organic and Biomolecular Chemistry. 1: 478-482. PMID 12926248 DOI: 10.1039/B210038J |
0.335 |
|
| 2003 |
Ulgar V, López Ó, Maya I, Fernández-Bolaños JG, Bols M. Synthesis of furan 4′-thio-C-nucleosides, their methylsulfonium and sulfoxide derivatives. Evaluation as glycosidase inhibitors Tetrahedron. 59: 2801-2809. DOI: 10.1016/S0040-4020(03)00339-9 |
0.39 |
|
| 2002 |
Bols M, Liang X, Jensen HH. Equatorial contra axial polar substituents. The relation of a chemical reaction to stereochemical substituent constants. The Journal of Organic Chemistry. 67: 8970-4. PMID 12467416 DOI: 10.1021/Jo0205356 |
0.314 |
|
| 2002 |
Jensen HH, Lyngbye L, Jensen A, Bols M. Stereoelectronic substituent effects in polyhydroxylated piperidines and hexahydropyridazines. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 1218-26. PMID 11891910 DOI: 10.1002/1521-3765(20020301)8:5<1218::Aid-Chem1218>3.0.Co;2-X |
0.334 |
|
| 2002 |
Andersch J, Bols M. Efficient synthesis of isofagomine and noeuromycin. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 3744-7. PMID 11575775 DOI: 10.1002/1521-3765(20010903)7:17<3744::Aid-Chem3744>3.0.Co;2-3 |
0.356 |
|
| 2002 |
Hardlei T, Bols M. Unusual hydrogen-bonding differences in stereoisomeric 6-C-alkylated cyclodextrins Journal of the Chemical Society-Perkin Transactions 1. 2880-2885. DOI: 10.1039/B207033M |
0.355 |
|
| 2002 |
Ulgar V, Fernández-Bolaños JG, Bols M. Synthesis and evaluation of sulfonium analogues of isofucofagomine as glycosidase inhibitors Journal of the Chemical Society-Perkin Transactions 1. 1242-1246. DOI: 10.1039/B202021C |
0.333 |
|
| 2002 |
Jensen HH, Jensen A, Hazell RG, Bols M. Synthesis and investigation of L-fuco- and D-glucurono-azafagomine Journal of the Chemical Society-Perkin Transactions 1. 1190-1198. DOI: 10.1039/B200884J |
0.36 |
|
| 2002 |
Muldgaard L, Thomsen IB, Hazell RG, Bols M. Investigation of the base promoted tandem syn-elimination–Favorskii rearrangement of levoglucosan sulfonates Journal of the Chemical Society-Perkin Transactions 1. 1297-1301. DOI: 10.1039/B200064B |
0.37 |
|
| 2002 |
Baruah M, Bols M. Substitution of α-azido ethers with Grignard reagents and its use in combinatorial chemistry Journal of the Chemical Society-Perkin Transactions 1. 509-512. DOI: 10.1039/B110428B |
0.319 |
|
| 2002 |
Liang X, Bols M. Solution-phase combinatorial synthesis using multicomponent Grignard reagents Journal of the Chemical Society-Perkin Transactions 1. 503-508. DOI: 10.1039/B109952N |
0.338 |
|
| 2001 |
Viuf C, Bols M. Radical Azidonation of Benzylic Positions with Iodonium Azide. Angewandte Chemie (International Ed. in English). 40: 623-625. PMID 29712008 DOI: 10.1002/1521-3773(20010202)40:3<623::Aid-Anie623>3.0.Co;2-G |
0.306 |
|
| 2001 |
Søndergaard K, Liang X, Bols M. Synthesis of 5-azacastanospermine, a conformationally restricted azafagomine analogue. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 2324-31. PMID 11446635 DOI: 10.1002/1521-3765(20010601)7:11<2324::Aid-Chem23240>3.0.Co;2-Y |
0.349 |
|
| 2001 |
Andreassen V, Svensson B, Bols M. Synthesis of an 1′-Azasugar Analogue of Maltose Synthesis. 2001: 0339-0342. DOI: 10.1055/S-2001-10799 |
0.345 |
|
| 2001 |
Søhoel H, Liang X, Bols M. Isogalactofagomine lactam. A neutral nanomolar galactosidase inhibitor Journal of the Chemical Society-Perkin Transactions 1. 1584-1585. DOI: 10.1039/B103831C |
0.312 |
|
| 2001 |
Liang X, Petersen BO, Duus JØ, Bols M. A bioisosteric oligosaccharide mimetic based on isofagomine-type monomers Journal of the Chemical Society-Perkin Transactions 1. 2764-2773. DOI: 10.1039/B103756K |
0.313 |
|
| 2001 |
Jensen HH, Bols M. Synthesis of 1-azagalactofagomine, a potent galactosidase inhibitor Journal of the Chemical Society-Perkin Transactions 1. 905-909. DOI: 10.1039/B007973L |
0.317 |
|
| 2000 |
Ernholt BV, Thomsen Ib B, Lohse A, Plesner IW, Jensen KB, Hazell RG, Liang X, Jakobsen A, Bols M. Enantiospecific synthesis of 1-azafagomine. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 278-87. PMID 11931107 DOI: 10.1002/(Sici)1521-3765(20000117)6:2<278::Aid-Chem278>3.0.Co;2-6 |
0.383 |
|
| 2000 |
Liang X, Lohse A, Bols M. Chemoenzymatic synthesis of isogalactofagomine. The Journal of Organic Chemistry. 65: 7432-7. PMID 11076600 DOI: 10.1021/Jo000699R |
0.377 |
|
| 2000 |
Jensen HH, Lohse A, Petersen BO, Duus JØ, Bols M. Synthesis of 3-C-hydroxymethyl- and 3-deoxyisofagomine and investigation of their binding to β-glucosidase Journal of the Chemical Society-Perkin Transactions 1. 667-670. DOI: 10.1039/A909869K |
0.318 |
|
| 2000 |
Lohse A, Jensen HH, Bach P, Bols M. Synthesis of 3-substituted isofagomine analogues using an unusual syn hydrogenation reaction Journal of the Chemical Society, Perkin Transactions 1. 659-665. DOI: 10.1039/A908340E |
0.37 |
|
| 1999 |
Lohse A, Jensen KB, Lundgren K, Bols M. Synthesis and deconvolution of the first combinatorial library of glycosidase inhibitors. Bioorganic & Medicinal Chemistry. 7: 1965-71. PMID 10530945 DOI: 10.1016/S0968-0896(99)00116-9 |
0.314 |
|
| 1999 |
Hansen SU, Bols M. Synthesis of labelled 1-azafagomine Journal of the Chemical Society-Perkin Transactions 1. 3323-3325. DOI: 10.1039/A907365E |
0.315 |
|
| 1999 |
Liang X, Bols M. Chemoenzymatic Synthesis of Enantiopure 1-Azafagomine The Journal of Organic Chemistry. 64: 8485-8488. DOI: 10.1021/Jo9907989 |
0.366 |
|
| 1999 |
Bach P, Bols M. Synthesis of an 1-azaglucose analogue with ring-oxygen retained Tetrahedron Letters. 40: 3461-3464. DOI: 10.1016/S0040-4039(99)00423-2 |
0.31 |
|
| 1999 |
Bach P, Lohse A, Bols M. Short synthesis of piperidine based hexopyranose minics. A remarkable example of syn hydrogenation Tetrahedron Letters. 40: 367-370. DOI: 10.1016/S0040-4039(98)02313-2 |
0.351 |
|
| 1998 |
Madsen J, Bols M. A New Intramolecular Reaction for the Regioselective Debenzylation or Protection of Alcohols. Angewandte Chemie (International Ed. in English). 37: 3177-3178. PMID 29711310 DOI: 10.1002/(Sici)1521-3773(19981204)37:22<3177::Aid-Anie3177>3.0.Co;2-A |
0.346 |
|
| 1998 |
Bols M. New branched carbohydrate building block from a tandem elimination-Farvorski rearrangement Chemical Communications. 1869-1870. DOI: 10.1039/A803397H |
0.324 |
|
| 1997 |
Byrgesen E, Nielsen J, Willert M, Bols M. Combinatorial chemistry of piperidine based carbohydrate mimics Tetrahedron Letters. 38: 5697-5700. DOI: 10.1016/S0040-4039(97)01249-5 |
0.317 |
|
| 1997 |
Thomsen I, Ernholt BV, Bols M. Synthetic studies of fluorinated analogues of 1-azafagomine: Remarkable nucleophilic substitution of fluorine by hydrazine Tetrahedron. 53: 9357-9364. DOI: 10.1016/S0040-4020(97)00588-7 |
0.349 |
|
| 1997 |
Lohse A, Bols M. Synthesis of 6-deoxy-6-phenylisofagomine derivatives Tetrahedron. 53: 6917-6924. DOI: 10.1016/S0040-4020(97)00392-X |
0.333 |
|
| 1997 |
Bols M, Hazell RG, Thomsen IB. 1-Azafagomine: A Hydroxyhexahydropyridazine That Potently Inhibits Enzymatic Glycoside Cleavage Chemistry - a European Journal. 3: 940-947. DOI: 10.1002/Chem.19970030616 |
0.405 |
|
| 1996 |
Dong W, Jespersen T, Bols M, Skrydstrup T, Sierks MR. Evaluation of isofagomine and its derivatives as potent glycosidase inhibitors Biochemistry. 35: 2788-2795. PMID 8611585 DOI: 10.1021/Bi9522514 |
0.363 |
|
| 1996 |
Hansen A, Tagmose TM, Bols M. Synthesis of a new potent α-fucosidase inhibitor Chemical Communications. 2649-2650. DOI: 10.1039/Cc9960002649 |
0.324 |
|
| 1996 |
Skrydstrup T, Jespersen T, Beau J, Bols M. A new and convenient benzyloxyalkylating agent induced by samarium diiodide Chemical Communications. 515-516. DOI: 10.1039/Cc9960000515 |
0.319 |
|
| 1996 |
Hansen HC, Hindsgaul O, Bols M. Synthesis of tributyltinmethylated sugars, building blocks for tethered reactions Tetrahedron Letters. 37: 4211-4212. DOI: 10.1016/0040-4039(96)00798-8 |
0.351 |
|
| 1996 |
Bols M, Persson MP, Butt WM, Jørgensen M, Christensen P, Hansen LT. Synthesis of a ribofuranosyl cation mimic Tetrahedron Letters. 37: 2097-2100. DOI: 10.1016/0040-4039(96)00202-X |
0.353 |
|
| 1995 |
Thomas SS, Plenkiewicz J, Ison ER, Bols M, Zou W, Szarek WA, Kisilevsky R. Influence of monosaccharide derivatives on liver cell glycosaminoglycan synthesis: 3-deoxy-D-xylo-hexose (3-deoxy-D-galactose) and methyl (methyl 4-chloro-4-deoxy-beta-D-galactopyranosid) uronate. Biochimica Et Biophysica Acta. 1272: 37-48. PMID 7662718 DOI: 10.1016/0925-4439(95)00065-C |
0.35 |
|
| 1995 |
Mikkelsen G, Christensen TV, Bols M, Lundt I, Sierks MR. Aglycon mimicking: Glycoside bond cleavage transition state mimics based on hydroxypyrrolidine inhibitors Tetrahedron Letters. 36: 6541-6544. DOI: 10.1016/0040-4039(95)01281-L |
0.309 |
|
| 1995 |
Barbaud C, Bols M, Lundt I, Sierks MR. Synthesis of the first pseudosugar-C-disaccharide. A potential antigen for eliciting glycoside-bond forming antibodies with catalytic groups Tetrahedron. 51: 9063-9078. DOI: 10.1016/0040-4020(95)00505-3 |
0.361 |
|
| 1994 |
Bols M, Hansen HC. Long Range Intramolecular Glycosidation Chemistry Letters. 23: 1049-1052. DOI: 10.1246/Cl.1994.1049 |
0.346 |
|
| 1994 |
M. Jespersen T, Bols M, R. Sierks M, Skrydstrup T. Synthesis of isofagomine, a novel glycosidase inhibitor Tetrahedron. 50: 13449-13460. DOI: 10.1016/S0040-4020(01)89351-0 |
0.411 |
|
| 1993 |
Bols M. Application of intramolecular glycosidation to the stereocontrolled synthesis of disaccharides containing α-gluco and α-galacto linkages Journal of the Chemical Society, Chemical Communications. 791-792. DOI: 10.1039/C39930000791 |
0.332 |
|
| 1993 |
Bols M. Efficient stereocontrolled glycosidation of secondary sugar hydroxyls by silicon tethered intramolecular glycosidation Tetrahedron. 49: 10049-10060. DOI: 10.1016/S0040-4020(01)80200-3 |
0.307 |
|
| 1992 |
Bols M, Lundt I, Ottosen ER. Preparation of 2-, 3-, and 4-deoxy derivatives of L-rhamnose, and derivatives of 2-azido-2-deoxy-L-rhamnose and 2,6-dideoxy-2-fluoro-L-glucose, for use in glycosylation reactions. Carbohydrate Research. 222: 141-9. PMID 1813104 DOI: 10.1016/0008-6215(91)89013-6 |
0.324 |
|
| 1992 |
Bols M, Binderup L, Hansen J, Rasmussen P. Inhibition of collagenase by aranciamycin and aranciamycin derivatives. Journal of Medicinal Chemistry. 35: 2768-71. PMID 1322986 DOI: 10.1021/Jm00093A008 |
0.302 |
|
| 1992 |
Bols M. Stereocontrolled synthesis of α-glucosides by intramolecular glycosidation Journal of the Chemical Society, Chemical Communications. 913-914. DOI: 10.1039/C39920000913 |
0.341 |
|
| 1992 |
Bols M, Lundt I, Pedersen C. Simple synthesis of (R)-Carnitine from d-Galactono-1,4-lactone Tetrahedron. 48: 319-324. DOI: 10.1016/S0040-4020(01)88143-6 |
0.301 |
|
| 1991 |
Bols M. Stereoselective synthesis of 1-O-pivaloyl .beta.-D-glucopyranuronic acid The Journal of Organic Chemistry. 56: 5943-5945. DOI: 10.1021/Jo00020A044 |
0.307 |
|
| 1990 |
Bols M, Lundt I, Aksnes DW, Brekke T, Maartmann-Moe K, Tønnesen HH, Tokii T. Preparation of 2,3-Epoxyaldonolactones and their Conversion into 2-Fluoro-2-deoxy-aldonolactones and -sugars. Acta Chemica Scandinavica. 44: 252-256. DOI: 10.3891/Acta.Chem.Scand.44-0252 |
0.331 |
|
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