| Year |
Citation |
Score |
| 2022 |
Li JK, Qu G, Li X, Tian Y, Cui C, Zhang FG, Zhang W, Ma JA, Reetz MT, Sun Z. Rational enzyme design for enabling biocatalytic Baldwin cyclization and asymmetric synthesis of chiral heterocycles. Nature Communications. 13: 7813. PMID 36535947 DOI: 10.1038/s41467-022-35468-y |
0.667 |
|
| 2020 |
Li D, Wu Q, Reetz MT. Focused rational iterative site-specific mutagenesis (FRISM). Methods in Enzymology. 643: 225-242. PMID 32896283 DOI: 10.1016/Bs.Mie.2020.04.055 |
0.309 |
|
| 2020 |
Li A, Acevedo-Rocha CG, D'Amore L, Chen J, Peng Y, Garcia-Borràs M, Gao C, Zhu J, Rickerby H, Osuna S, Zhou J, Reetz MT. Regio- and Stereoselective Steroid Hydroxylation at the C7-Position by Cytochrome P450 Monooxygenase Mutants. Angewandte Chemie (International Ed. in English). PMID 32243054 DOI: 10.1002/Anie.202003139 |
0.308 |
|
| 2020 |
Wang JB, Huang Q, Peng W, Wu P, Yu D, Chen B, Wang B, Reetz MT. P450-BM3 Catalyzed Sulfoxidation versus Hydroxylation: A Common or Two Different Catalytically Active Species? Journal of the American Chemical Society. PMID 31927987 DOI: 10.1021/Jacs.9B13061 |
0.325 |
|
| 2019 |
Cen Y, Singh W, Arkin M, Moody TS, Huang M, Zhou J, Wu Q, Reetz MT. Artificial cysteine-lipases with high activity and altered catalytic mechanism created by laboratory evolution. Nature Communications. 10: 3198. PMID 31324776 DOI: 10.1038/S41467-019-11155-3 |
0.347 |
|
| 2019 |
Xu J, Cen Y, Singh W, Fan J, Wu L, Lin X, Zhou J, Huang M, Reetz MT, Wu Q. Stereodivergent Protein Engineering of a Lipase to Access All Possible Stereoisomers of Chiral Esters with Two Stereo-centers. Journal of the American Chemical Society. PMID 31023008 DOI: 10.1021/Jacs.9B02709 |
0.362 |
|
| 2019 |
Yu D, Wang JB, Reetz MT. Exploiting Designed Oxidase-Peroxygenase Mutual Benefit System for Asymmetric Cascade Reactions. Journal of the American Chemical Society. PMID 30920820 DOI: 10.1021/Jacs.9B01939 |
0.36 |
|
| 2019 |
Reetz MT. Directed Evolution of Artificial Metalloenzymes: A Universal Means to Tune the Selectivity of Transition Metal Catalysts? Accounts of Chemical Research. PMID 30689339 DOI: 10.1021/Acs.Accounts.8B00582 |
0.333 |
|
| 2018 |
Li G, Garcia-Borràs M, Fürst MJLJ, Ilie A, Fraaije MW, Houk KN, Reetz MT. Overriding Traditional Electronic Effects in Biocatalytic Baeyer-Villiger Reactions by Directed Evolution. Journal of the American Chemical Society. PMID 30044629 DOI: 10.1021/Jacs.8B04742 |
0.365 |
|
| 2018 |
Li A, Acevedo-Rocha CG, Reetz MT. Boosting the efficiency of site-saturation mutagenesis for a difficult-to-randomize gene by a two-step PCR strategy. Applied Microbiology and Biotechnology. PMID 29785500 DOI: 10.1007/S00253-018-9041-2 |
0.306 |
|
| 2018 |
Ilie A, Harms K, Reetz MT. P450-Catalyzed Regio- and Stereoselective Oxidative Hydroxylation of 6-Iodo-tetralone: Preparative-Scale Synthesis of a Key Intermediate for Pd-Catalyzed Transformations. The Journal of Organic Chemistry. PMID 29313346 DOI: 10.1021/Acs.Joc.7B02878 |
0.373 |
|
| 2018 |
Acevedo-Rocha CG, Ferla M, Reetz MT. Directed Evolution of Proteins Based on Mutational Scanning. Methods in Molecular Biology (Clifton, N.J.). 1685: 87-128. PMID 29086305 DOI: 10.1007/978-1-4939-7366-8_6 |
0.308 |
|
| 2017 |
Li G, Yao P, Gong R, Li J, Liu P, Lonsdale R, Wu Q, Lin J, Zhu D, Reetz MT. Simultaneous engineering of an enzyme's entrance tunnel and active site: the case of monoamine oxidase MAO-N. Chemical Science. 8: 4093-4099. PMID 30155214 DOI: 10.1039/C6Sc05381E |
0.349 |
|
| 2017 |
Reetz MT, Li A, Acevedo-Rocha CG, Sun Z, Cox T, Xu JL. Beating Bias in Directed Evolution of Proteins: Combining High-Fidelity On-Chip Solid-Phase Gene Synthesis with Efficient Gene Assembly for Combinatorial Library Construction. Chembiochem : a European Journal of Chemical Biology. PMID 29171900 DOI: 10.1002/Cbic.201700540 |
0.331 |
|
| 2017 |
Li G, Fürst MJLJ, Mansouri HR, Ressmann AK, Ilie A, Rudroff F, Mihovilovic MD, Fraaije MW, Reetz MT. Manipulating the stereoselectivity of the thermostable Baeyer-Villiger monooxygenase TmCHMO by directed evolution. Organic & Biomolecular Chemistry. PMID 29130465 DOI: 10.1039/C7Ob02692G |
0.367 |
|
| 2017 |
Li G, Maria-Solano MA, Romero-Rivera A, Osuna S, Reetz MT. Inducing high activity of a thermophilic enzyme at ambient temperatures by directed evolution. Chemical Communications (Cambridge, England). PMID 28795696 DOI: 10.1039/C7Cc05377K |
0.321 |
|
| 2017 |
Wang JB, Ilie A, Yuan S, Reetz MT. Investigating Substrate Scope and Enantioselectivity of a Defluorinase by a Stereochemical Probe. Journal of the American Chemical Society. PMID 28741946 DOI: 10.1021/Jacs.7B06019 |
0.336 |
|
| 2017 |
Li G, Wang JB, Reetz MT. Biocatalysts for the pharmaceutical industry created by structure-guided directed evolution of stereoselective enzymes. Bioorganic & Medicinal Chemistry. PMID 28693917 DOI: 10.1016/J.Bmc.2017.05.021 |
0.376 |
|
| 2017 |
Li A, Wang B, Ilie A, Dubey KD, Bange G, Korendovych IV, Shaik S, Reetz MT. A redox-mediated Kemp eliminase. Nature Communications. 8: 14876. PMID 28348375 DOI: 10.1038/Ncomms14876 |
0.316 |
|
| 2017 |
Wang JB, Li G, Reetz MT. Enzymatic site-selectivity enabled by structure-guided directed evolution. Chemical Communications (Cambridge, England). PMID 28294248 DOI: 10.1039/C7Cc00368D |
0.3 |
|
| 2017 |
Acevedo JP, Reetz MT, Asenjo JA, Parra LP. One-step combined focused epPCR and saturation mutagenesis for thermostability evolution of a new cold-active xylanase. Enzyme and Microbial Technology. 100: 60-70. PMID 28284313 DOI: 10.1016/J.Enzmictec.2017.02.005 |
0.317 |
|
| 2017 |
Wang J, Ilie A, Reetz MT. Chemo- and Stereoselective Cytochrome P450-BM3-Catalyzed Sulfoxidation of 1-Thiochroman-4-ones Enabled by Directed Evolution Advanced Synthesis & Catalysis. 359: 2056-2060. DOI: 10.1002/Adsc.201700414 |
0.334 |
|
| 2016 |
Li A, Ilie A, Sun Z, Lonsdale R, Xu JH, Reetz MT. Whole-Cell-Catalyzed Multiple Regio- and Stereoselective Functionalizations in Cascade Reactions Enabled by Directed Evolution. Angewandte Chemie (International Ed. in English). PMID 27573978 DOI: 10.1002/Anie.201605990 |
0.355 |
|
| 2016 |
Sun Z, Lonsdale R, Li G, Reetz MT. Comparing Different Strategies in Directed Evolution of Enzyme Stereoselectivity: Single versus Double Code Saturation Mutagenesis. Chembiochem : a European Journal of Chemical Biology. PMID 27411213 DOI: 10.1002/Cbic.201600296 |
0.332 |
|
| 2016 |
Reetz MT. What are the Limitations of Enzymes in Synthetic Organic Chemistry? Chemical Record (New York, N.Y.). PMID 27301318 DOI: 10.1002/Tcr.201600040 |
0.322 |
|
| 2016 |
Wang JB, Lonsdale R, Reetz MT. Exploring substrate scope and stereoselectivity of P450 peroxygenase OleTJE in olefin-forming oxidative decarboxylation. Chemical Communications (Cambridge, England). PMID 27271555 DOI: 10.1039/C6Cc04345C |
0.345 |
|
| 2016 |
Sun Z, Wikmark Y, Bäckvall JE, Reetz MT. New Concepts for Increasing the Efficiency in Directed Evolution of Stereoselective Enzymes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26914401 DOI: 10.1002/Chem.201504406 |
0.344 |
|
| 2016 |
Krone KM, Warias R, Ritter C, Li A, Acevedo-Rocha CG, Reetz MT, Belder D. Analysis of enantioselective biotransformations using a few hundred cells on an integrated microfluidic chip. Journal of the American Chemical Society. PMID 26824299 DOI: 10.1021/Jacs.5B12443 |
0.309 |
|
| 2016 |
Sun Z, Lonsdale R, Ilie A, Li G, Zhou J, Reetz MT. Catalytic Asymmetric Reduction of Difficult-to-Reduce Ketones: Triple-Code Saturation Mutagenesis of an Alcohol Dehydrogenase Acs Catalysis. 6: 1598-1605. DOI: 10.1021/Acscatal.5B02752 |
0.348 |
|
| 2016 |
Sun Z, Lonsdale R, Wu L, Li G, Li A, Wang J, Zhou J, Reetz MT. Structure-Guided Triple-Code Saturation Mutagenesis: Efficient Tuning of the Stereoselectivity of an Epoxide Hydrolase Acs Catalysis. 6: 1590-1597. DOI: 10.1021/Acscatal.5B02751 |
0.307 |
|
| 2016 |
Sun Z, Li G, Ilie A, Reetz MT. Exploring the substrate scope of mutants derived from the robust alcohol dehydrogenase TbSADH Tetrahedron Letters. 57: 3648-3651. DOI: 10.1016/J.Tetlet.2016.06.134 |
0.379 |
|
| 2015 |
Lonsdale R, Reetz MT. Reduction of α,β-Unsaturated Ketones by Old Yellow Enzymes: Mechanistic Insights from Quantum Mechanics/Molecular Mechanics Calculations. Journal of the American Chemical Society. PMID 26521678 DOI: 10.1021/Jacs.5B08687 |
0.347 |
|
| 2015 |
Sun Z, Lonsdale R, Kong XD, Xu JH, Zhou J, Reetz MT. Reshaping an enzyme binding pocket for enhanced and inverted stereoselectivity: Use of smallest amino acid alphabets in directed evolution Angewandte Chemie - International Edition. PMID 25891639 DOI: 10.1002/Anie.201501809 |
0.316 |
|
| 2015 |
Parra LP, Acevedo JP, Reetz MT. Directed evolution of phenylacetone monooxygenase as an active catalyst for the baeyer-villiger conversion of cyclohexanone to caprolactone Biotechnology and Bioengineering. 112: 1354-1364. PMID 25675885 DOI: 10.1002/Bit.25564 |
0.328 |
|
| 2015 |
Agudo R, Roiban GD, Lonsdale R, Ilie A, Reetz MT. Biocatalytic route to chiral acyloins: P450-catalyzed regio- and enantioselective α-hydroxylation of ketones Journal of Organic Chemistry. 80: 950-956. PMID 25495724 DOI: 10.1021/Jo502397S |
0.381 |
|
| 2015 |
Hoebenreich S, Zilly FE, Acevedo-Rocha CG, Zilly M, Reetz MT. Speeding up directed evolution: Combining the advantages of solid-phase combinatorial gene synthesis with statistically guided reduction of screening effort Acs Synthetic Biology. 4: 317-331. PMID 24921161 DOI: 10.1021/sb5002399 |
0.674 |
|
| 2015 |
Ilie A, Lonsdale R, Agudo R, Reetz MT. A diastereoselective P450-catalyzed epoxidation reaction: Anti versus syn reactivity This Letter is dedicated to the memory of Harry Wasserman Tetrahedron Letters. 56: 3435-3437. DOI: 10.1016/J.Tetlet.2015.03.076 |
0.311 |
|
| 2015 |
Ilie A, Agudo R, Roiban GD, Reetz MT. P450-catalyzed regio- and stereoselective oxidative hydroxylation of disubstituted cyclohexanes: Creation of three centers of chirality in a single CH-activation event This paper is dedicated to the memory of Harry H. Wasserman Tetrahedron. 71: 470-475. DOI: 10.1016/J.Tet.2014.11.067 |
0.333 |
|
| 2015 |
Ilie A, Reetz MT. Directed evolution of artificial metalloenzymes Israel Journal of Chemistry. 55: 51-60. DOI: 10.1002/Ijch.201400087 |
0.302 |
|
| 2014 |
Zhang ZG, Lonsdale R, Sanchis J, Reetz MT. Extreme synergistic mutational effects in the directed evolution of a baeyer-villiger monooxygenase as catalyst for asymmetric sulfoxidation Journal of the American Chemical Society. 136: 17262-17272. PMID 25394568 DOI: 10.1021/Ja5098034 |
0.322 |
|
| 2014 |
Tielmann P, Kierkels H, Zonta A, Ilie A, Reetz MT. Increasing the activity and enantioselectivity of lipases by sol-gel immobilization: Further advancements of practical interest Nanoscale. 6: 6220-6228. PMID 24676487 DOI: 10.1039/C3Nr06317H |
0.322 |
|
| 2014 |
Roiban GD, Agudo R, Reetz MT. Cytochrome P450 catalyzed oxidative hydroxylation of achiral organic compounds with simultaneous creation of two chirality centers in a single C-H activation step Angewandte Chemie - International Edition. 53: 8659-8663. PMID 24590553 DOI: 10.1002/Anie.201310892 |
0.365 |
|
| 2014 |
Roiban GD, Mehler G, Reetz MT. Palladium-catalysed amination of aryl- and heteroaryl halides using tert-butyl tetraisopropylphosphorodiamidite as an easily accessible and air-stable ligand European Journal of Organic Chemistry. 2014: 2070-2076. DOI: 10.1002/Ejoc.201301789 |
0.315 |
|
| 2013 |
Parra LP, Agudo R, Reetz MT. Directed evolution by using iterative saturation mutagenesis based on multiresidue sites Chembiochem. 14: 2301-2309. PMID 24136881 DOI: 10.1002/Cbic.201300486 |
0.312 |
|
| 2013 |
Agudo R, Reetz MT. Designer cells for stereocomplementary de novo enzymatic cascade reactions based on laboratory evolution Chemical Communications. 49: 10914-10916. PMID 24135920 DOI: 10.1039/C3Cc46229C |
0.346 |
|
| 2013 |
Reetz MT. Practical protocols for lipase immobilization via sol-gel techniques. Methods in Molecular Biology (Clifton, N.J.). 1051: 241-54. PMID 23934809 DOI: 10.1007/978-1-62703-550-7_16 |
0.31 |
|
| 2013 |
Reetz MT. Biocatalysis in organic chemistry and biotechnology: Past, present, and future Journal of the American Chemical Society. 135: 12480-12496. PMID 23930719 DOI: 10.1021/Ja405051F |
0.321 |
|
| 2013 |
Kille S, Acevedo-Rocha CG, Parra LP, Zhang ZG, Opperman DJ, Reetz MT, Acevedo JP. Reducing codon redundancy and screening effort of combinatorial protein libraries created by saturation mutagenesis Acs Synthetic Biology. 2: 83-92. PMID 23656371 DOI: 10.1021/Sb300037W |
0.635 |
|
| 2013 |
Polyak I, Reetz MT, Thiel W. Quantum mechanical/molecular mechanical study on the enantioselectivity of the enzymatic baeyer-villiger reaction of 4-hydroxycyclohexanone Journal of Physical Chemistry B. 117: 4993-5001. PMID 23600847 DOI: 10.1021/Jp4018019 |
0.335 |
|
| 2013 |
Roiban GD, Reetz MT. Enzyme promiscuity: Using a P450 enzyme as a carbene transfer catalyst Angewandte Chemie - International Edition. 52: 5439-5440. PMID 23592495 DOI: 10.1002/Anie.201301083 |
0.311 |
|
| 2013 |
Wu Q, Soni P, Reetz MT. Laboratory evolution of enantiocomplementary Candida antarctica lipase B mutants with broad substrate scope Journal of the American Chemical Society. 135: 1872-1881. PMID 23301759 DOI: 10.1021/Ja310455T |
0.362 |
|
| 2013 |
Agudo R, Roiban GD, Reetz MT. Induced axial chirality in biocatalytic asymmetric ketone reduction Journal of the American Chemical Society. 135: 1665-1668. PMID 23075382 DOI: 10.1021/Ja3092517 |
0.332 |
|
| 2013 |
Roiban GD, Agudo R, Reetz MT. Stereo- and regioselectivity in the P450-catalyzed oxidative tandem difunctionalization of 1-methylcyclohexene Tetrahedron. 69: 5306-5311. DOI: 10.1016/J.Tet.2013.04.132 |
0.305 |
|
| 2013 |
Zilly FE, Acevedo JP, Augustyniak W, Deege A, Häusig UW, Reetz MT. Erratum: Tuning a P450 enzyme for methane oxidation (Angewandte Chemie - International Edition (2011) 50 (2720-2724) DOI: 10.1002/anie.201006587) Angewandte Chemie - International Edition. 52: 13503. DOI: 10.1002/Anie.201309655 |
0.692 |
|
| 2013 |
Zilly FE, Acevedo JP, Augustyniak W, Deege A, Häusig UW, Reetz MT. Berichtigung: Tuning a P450 Enzyme for Methane Oxidation Angewandte Chemie. 125: 13745-13745. DOI: 10.1002/Ange.201309655 |
0.692 |
|
| 2013 |
Zhang ZG, Roiban GD, Acevedo JP, Polyak I, Reetz MT. A new type of stereoselectivity in Baeyer-Villiger reactions: Access to E- and Z-olefins Advanced Synthesis and Catalysis. 355: 99-106. DOI: 10.1002/Adsc.201200759 |
0.327 |
|
| 2012 |
Reetz MT. Artificial metalloenzymes as catalysts in stereoselective diels-alder reactions Chemical Record. 12: 391-406. PMID 22711577 DOI: 10.1002/Tcr.201100043 |
0.339 |
|
| 2012 |
Agudo R, Roiban GD, Reetz MT. Achieving Regio- and Enantioselectivity of P450-Catalyzed Oxidative CH Activation of Small Functionalized Molecules by Structure-Guided Directed Evolution Chembiochem. 13: 1465-1473. PMID 22711296 DOI: 10.1002/Cbic.201200244 |
0.389 |
|
| 2012 |
Gumulya Y, Sanchis J, Reetz MT. Many Pathways in Laboratory Evolution Can Lead to Improved Enzymes: How to Escape from Local Minima Chembiochem. 13: 1060-1066. PMID 22522601 DOI: 10.1002/Cbic.201100784 |
0.738 |
|
| 2012 |
Feng X, Sanchis J, Reetz MT, Rabitz H. Enhancing the efficiency of directed evolution in focused enzyme libraries by the adaptive substituent reordering algorithm Chemistry - a European Journal. 18: 5646-5654. PMID 22434591 DOI: 10.1002/Chem.201103811 |
0.303 |
|
| 2012 |
Augustyniak W, Brzezinska AA, Pijning T, Wienk H, Boelens R, Dijkstra BW, Reetz MT. Biophysical characterization of mutants of Bacillus subtilis lipase evolved for thermostability: Factors contributing to increased activity retention Protein Science. 21: 487-497. PMID 22267088 DOI: 10.1002/Pro.2031 |
0.306 |
|
| 2012 |
Polyak I, Reetz MT, Thiel W. Quantum mechanical/molecular mechanical study on the mechanism of the enzymatic Baeyer-Villiger reaction Journal of the American Chemical Society. 134: 2732-2741. PMID 22239272 DOI: 10.1021/Ja2103839 |
0.311 |
|
| 2012 |
Reetz MT. Laboratory evolution of stereoselective enzymes as a means to expand the toolbox of organic chemists Tetrahedron. 68: 7530-7548. DOI: 10.1016/J.Tet.2012.05.093 |
0.343 |
|
| 2012 |
Cesarini S, Bofill C, Pastor FIJ, Reetz MT, Diaz P. A thermostable variant of P. Aeruginosa cold-adapted LipC obtained by rational design and saturation mutagenesis Process Biochemistry. 47: 2064-2071. DOI: 10.1016/J.Procbio.2012.07.023 |
0.308 |
|
| 2011 |
Gumulya Y, Reetz MT. Enhancing the thermal robustness of an enzyme by directed evolution: Least favorable starting points and inferior mutants can map superior evolutionary Pathways Chembiochem. 12: 2502-2510. PMID 21913300 DOI: 10.1002/Cbic.201100412 |
0.722 |
|
| 2011 |
Kille S, Zilly FE, Acevedo JP, Reetz MT. Regio- and stereoselectivity of P450-catalysed hydroxylation of steroids controlled by laboratory evolution. Nature Chemistry. 3: 738-43. PMID 21860465 DOI: 10.1038/nchem.1113 |
0.701 |
|
| 2011 |
Reetz MT, Zheng H. Manipulating the Expression Rate and Enantioselectivity of an Epoxide Hydrolase by Using Directed Evolution Chembiochem. 12: 1529-1535. PMID 21567703 DOI: 10.1002/Cbic.201100078 |
0.329 |
|
| 2011 |
Prasad S, Bocola M, Reetz MT. Revisiting the lipase from pseudomonas aeruginosa: Directed evolution of substrate acceptance and enantioselectivity using iterative saturation mutagenesis Chemphyschem. 12: 1550-1557. PMID 21472964 DOI: 10.1002/Cphc.201100031 |
0.377 |
|
| 2011 |
Zilly FE, Acevedo JP, Augustyniak W, Deege A, Häusig UW, Reetz MT. Tuning a p450 enzyme for methane oxidation. Angewandte Chemie (International Ed. in English). 50: 2720-4. PMID 21387474 DOI: 10.1002/Anie.201006587 |
0.723 |
|
| 2011 |
Reetz MT. Laboratory evolution of stereoselective enzymes: A prolific source of catalysts for asymmetric reactions Angewandte Chemie - International Edition. 50: 138-174. PMID 20715024 DOI: 10.1002/Anie.201000826 |
0.363 |
|
| 2011 |
Reetz MT, Krebs GPL. Challenges in the directed evolution of stereoselective enzymes for use in organic chemistry Comptes Rendus Chimie. 14: 811-818. DOI: 10.1016/J.Crci.2011.02.002 |
0.335 |
|
| 2010 |
Opperman DJ, Reetz MT. Towards practical baeyer-villiger-monooxygenases: Design of cyclohexanone monooxygenase mutants with enhanced oxidative stability Chembiochem. 11: 2589-2596. PMID 21080396 DOI: 10.1002/Cbic.201000464 |
0.684 |
|
| 2010 |
Zheng H, Reetz MT. Manipulating the stereoselectivity of limonene epoxide hydrolase by directed evolution based on iterative saturation mutagenesis Journal of the American Chemical Society. 132: 15744-15751. PMID 20958062 DOI: 10.1021/Ja1067542 |
0.381 |
|
| 2010 |
Reetz MT, Soni P, Fernández L, Gumulya Y, Carballeira JD. Increasing the stability of an enzyme toward hostile organic solvents by directed evolution based on iterative saturation mutagenesis using the B-FIT method Chemical Communications. 46: 8657-8658. PMID 20957255 DOI: 10.1039/C0Cc02657C |
0.712 |
|
| 2010 |
Reetz MT, Prasad S, Carballeira JD, Gumulya Y, Bocola M. Iterative saturation mutagenesis accelerates laboratory evolution of enzyme stereoselectivity: Rigorous comparison with traditional methods Journal of the American Chemical Society. 132: 9144-9152. PMID 20536132 DOI: 10.1021/Ja1030479 |
0.743 |
|
| 2010 |
Wu S, Acevedo JP, Reetz MT. Induced allostery in the directed evolution of an enantioselective Baeyer-Villiger monooxygenase Proceedings of the National Academy of Sciences of the United States of America. 107: 2775-2780. PMID 20133612 DOI: 10.1073/Pnas.0911656107 |
0.325 |
|
| 2010 |
Feránndez L, Jiao N, Soni P, Gumulya Y, De Oliveira LG, Reetz MT. An efficient method for mutant library creation in Pichia pastoris useful in directed evolution Biocatalysis and Biotransformation. 28: 122-129. DOI: 10.3109/10242420903505834 |
0.765 |
|
| 2010 |
Reetz MT, Wu S, Zheng H, Prasad S. Directed evolution of enantioselective enzymes: An unceasing catalyst source for organic chemistry Pure and Applied Chemistry. 82: 1575-1584. DOI: 10.1351/Pac-Con-09-09-16 |
0.343 |
|
| 2010 |
Gavrilov KN, Safronov AS, Rastorguev EA, Groshkin NN, Zheglov SV, Shiryaev AA, Maksimova MG, Petrovskii PV, Davankov VA, Reetz MT. Phosphorodiamidite derivatives of 1,1'-bi-2-naphthol containing stereogenic phosphorus atoms as ligands in enantioselective catalysis Russian Chemical Bulletin. 59: 434-440. DOI: 10.1007/S11172-010-0097-0 |
0.333 |
|
| 2010 |
REETZ MT, BREINBAUER R, WANNINGER K. ChemInform Abstract: Suzuki and Heck Reactions Catalyzed by Preformed Palladium Clusters and Palladium/Nickel Bimetallic Clusters. Cheminform. 27: no-no. DOI: 10.1002/chin.199640066 |
0.486 |
|
| 2010 |
Zheng H, Kahakeaw D, Acevedo JP, Reetz MT. Directed Evolution of Enantioconvergency: The Case of an Epoxide Hydrolase-Catalyzed Reaction of a Racemic Epoxide Chemcatchem. 2: 958-961. DOI: 10.1002/Cctc.201000122 |
0.328 |
|
| 2010 |
Gavrilov KN, Zheglov SV, Rastorguev EA, Groshkin NN, Maksimova MG, Benetsky EB, Davankov VA, Reetz MT. Asymmetric catalytic reactions using P*-mono-, P*,N- and P*,P*-bidentate diamidophosphites with BINOL backbones and 1,3,2-diazaphospholidine moieties: Differences in the enantioselectivity Advanced Synthesis and Catalysis. 352: 2599-2610. DOI: 10.1002/Adsc.201000325 |
0.357 |
|
| 2009 |
Zilly FE, Taglieber A, Schulz F, Hollmann F, Reetz MT. Deazaflavins as mediators in light-driven cytochrome P450 catalyzed hydroxylations. Chemical Communications (Cambridge, England). 7152-4. PMID 19921013 DOI: 10.1039/B913863C |
0.769 |
|
| 2009 |
Reetz MT, Wu S. Laboratory evolution of robust and enantioselective Baeyer-Villiger monooxygenases for asymmetric catalysis Journal of the American Chemical Society. 131: 15424-15432. PMID 19807086 DOI: 10.1021/Ja906212K |
0.368 |
|
| 2009 |
Reetz MT, Bocola M, Wang LW, Sanchis J, Cronin A, Arand M, Zou J, Archelas A, Bottalla AL, Naworyta A, Mowbray SL. Directed evolution of an enantioselective epoxide hydrolase: Uncovering the source of enantioselectivity at each evolutionary stage Journal of the American Chemical Society. 131: 7334-7343. PMID 19469578 DOI: 10.1021/Ja809673D |
0.365 |
|
| 2009 |
Reetz MT, Guo H, Jun-An M, Goddard R, Mynott RJ. Helical triskelion monophosphites as ligands in asymmetric catalysis Journal of the American Chemical Society. 131: 4136-4142. PMID 19249837 DOI: 10.1021/Ja809297A |
0.345 |
|
| 2009 |
Reetz MT, Kahakeaw D, Sanchis J. Shedding light on the efficacy of laboratory evolution based on iterative saturation mutagenesis Molecular Biosystems. 5: 115-122. PMID 19156255 DOI: 10.1039/B814862G |
0.323 |
|
| 2009 |
Reetz MT, Zonta A, Simpelkamp J. Efficient immobilization of lipases by entrapment in hydrophobic sol-gel materials. Biotechnology and Bioengineering. 49: 527-34. PMID 18623614 DOI: 10.1002/(Sici)1097-0290(19960305)49:5<527::Aid-Bit5>3.0.Co;2-L |
0.371 |
|
| 2009 |
Lamm AS, Khare A, Rosazza JPN, Taglieber A, Schulz F, Hollmann F, Rusek M, Reetz MT, Gefflaut T, Sagot E, Bolte J, Mihara H, Esaki N, Conway P, Paradisi F, et al. Reduction of Functional Groups Practical Methods For Biocatalysis and Biotransformations. 295-298. DOI: 10.1002/9780470748589.ch10 |
0.395 |
|
| 2008 |
Reetz MT, Höbenreich H, Soni P, Fernández L. A genetic selection system for evolving enantioselectivity of enzymes Chemical Communications. 5502-5504. PMID 18997932 DOI: 10.1039/B814538E |
0.343 |
|
| 2008 |
Reetz MT, Wu S. Greatly reduced amino acid alphabets in directed evolution: Making the right choice for saturation mutagenesis at homologous enzyme positions Chemical Communications. 5499-5501. PMID 18997931 DOI: 10.1039/B813388C |
0.358 |
|
| 2008 |
Sanchis J, Fernández L, Carballeira JD, Drone J, Gumulya Y, Höbenreich H, Kahakeaw D, Kille S, Lohmer R, Peyralans JJP, Podtetenieff J, Prasad S, Soni P, Taglieber A, Wu S, ... ... Reetz MT, et al. Improved PCR method for the creation of saturation mutagenesis libraries in directed evolution: Application to difficult-to-amplify templates Applied Microbiology and Biotechnology. 81: 387-397. PMID 18820909 DOI: 10.1007/S00253-008-1678-9 |
0.771 |
|
| 2008 |
Reetz MT, Kahakeaw D, Lohmer R. Addressing the numbers problem in directed evolution Chembiochem. 9: 1797-1804. PMID 18567049 DOI: 10.1002/Cbic.200800298 |
0.347 |
|
| 2008 |
Taglieber A, Schulz F, Hollman F, Rusek M, Reetz MT. Light-driven biocatalytic oxidation and reduction reactions: Scope and limitations Chembiochem. 9: 565-572. PMID 18288667 DOI: 10.1002/Cbic.200700435 |
0.678 |
|
| 2008 |
Reetz MT, Rentzsch M, Pletsch A, Taglieber A, Hollman F, Mondière RJG, Dickman N, Höcker B, Cerrone S, Hagaer MC, Sterner R. A robust protein host for anchoring chelating ligands and organocatalysts Chembiochem. 9: 552-564. PMID 18273849 DOI: 10.1002/Cbic.200700413 |
0.323 |
|
| 2007 |
Carballeira JD, Krumlinde P, Bocola M, Vogel A, Reetz MT, Bäckvall JE. Directed evolution and axial chirality: Optimization of the enantioselectivity of Pseudomonas aeruginosa lipase towards the kinetic resolution of a racemic allene Chemical Communications. 1913-1915. PMID 17695227 DOI: 10.1039/B700849J |
0.334 |
|
| 2007 |
Reetz MT, Carballeira JD. Iterative saturation mutagenesis (ISM) for rapid directed evolution of functional enzymes Nature Protocols. 2: 891-903. PMID 17446890 DOI: 10.1038/Nprot.2007.72 |
0.324 |
|
| 2007 |
Hollmann F, Taglieber A, Schulz F, Reetz MT. A light-driven stereoselective biocatalytic oxidation Angewandte Chemie - International Edition. 46: 2903-2906. PMID 17352446 DOI: 10.1002/Anie.200605169 |
0.69 |
|
| 2007 |
Reetz MT, Puls M, Carballeira JD, Vogel A, Jaeger KE, Eggert T, Thiel W, Bocola M, Otte N. Learning from directed evolution: Further lessons from theoretical investigations into cooperative mutations in lipase enantioselectivity. Chembiochem : a European Journal of Chemical Biology. 8: 106-12. PMID 17133645 DOI: 10.1002/Cbic.200600359 |
0.306 |
|
| 2007 |
Reetz MT. Evolution in the test-tube as a means to create selective biocatalysts Chimia. 61: 100-103. DOI: 10.2533/Chimia.2007.100 |
0.338 |
|
| 2007 |
Reetz MT, Mondière R, Carballeira JD. Enzyme promiscuity: first protein-catalyzed Morita-Baylis-Hillman reaction Tetrahedron Letters. 48: 1679-1681. DOI: 10.1016/J.Tetlet.2007.01.063 |
0.338 |
|
| 2007 |
Reetz MT, Rentzsch M, Pletsch A, Maywald M, Maiwald P, Peyralans JJP, Maichele A, Fu Y, Jiao N, Hollmann F, Mondière R, Taglieber A. Directed evolution of enantioselective hybrid catalysts: a novel concept in asymmetric catalysis Tetrahedron. 63: 6404-6414. DOI: 10.1016/J.Tet.2007.03.177 |
0.644 |
|
| 2007 |
Gavrilov KN, Lyubimov SE, Bondarev OG, Maksimova MG, Zheglov SV, Petrovskii PV, Davankov VA, Reetz MT. Chiral ionic phosphites and diamidophosphites: A novel group of efficient ligands for asymmetric catalysis Advanced Synthesis and Catalysis. 349: 609-616. DOI: 10.1002/Adsc.200600372 |
0.353 |
|
| 2006 |
Reetz MT, Peyralans JJ, Maichele A, Fu Y, Maywald M. Directed evolution of hybrid enzymes: Evolving enantioselectivity of an achiral Rh-complex anchored to a protein. Chemical Communications (Cambridge, England). 4318-20. PMID 17047853 DOI: 10.1039/B610461D |
0.306 |
|
| 2006 |
Reetz MT, Carballeira JD, Peyralans J, Höbenreich H, Maichele A, Vogel A. Expanding the substrate scope of enzymes: combining mutations obtained by CASTing. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 6031-8. PMID 16789057 DOI: 10.1002/Chem.200600459 |
0.352 |
|
| 2006 |
Reetz MT, Wang LW. High-throughput selection system for assessing the activity of epoxide hydrolases. Combinatorial Chemistry & High Throughput Screening. 9: 295-9. PMID 16724920 DOI: 10.2174/138620706776843156 |
0.34 |
|
| 2006 |
Reetz MT, Jiao N. Copper-phthalocyanine conjugates of serum albumins as enantioselective catalysts in Diels-Alder reactions. Angewandte Chemie (International Ed. in English). 45: 2416-9. PMID 16528766 DOI: 10.1002/Anie.200504561 |
0.505 |
|
| 2006 |
Mihovilovic MD, Rudroff F, Winninger A, Schneider T, Schulz F, Reetz MT. Microbial Baeyer-Villiger oxidation: stereopreference and substrate acceptance of cyclohexanone monooxygenase mutants prepared by directed evolution. Organic Letters. 8: 1221-4. PMID 16524308 DOI: 10.1021/Ol0601040 |
0.68 |
|
| 2006 |
Dröge MJ, Boersma YL, van Pouderoyen G, Vrenken TE, Rüggeberg CJ, Reetz MT, Dijkstra BW, Quax WJ. Directed evolution of Bacillus subtilis lipase A by use of enantiomeric phosphonate inhibitors: crystal structures and phage display selection. Chembiochem : a European Journal of Chemical Biology. 7: 149-57. PMID 16342303 DOI: 10.1002/Cbic.200500308 |
0.351 |
|
| 2006 |
Reetz MT, Surowiec M. Extending the concept of mixtures of chiral monodentate P-ligands in asymmetric Rh-catalyzed olefin-hydrogenation: Use of oxazaphospholidines Heterocycles. 67: 567-574. DOI: 10.3987/Com-05-S(T)74 |
0.335 |
|
| 2006 |
Reetz MT, Guo H. Transposition of allylic alcohols into carbonyl compounds catalyzed by rhodium-phosphinine complexes Synlett. 2127-2129. DOI: 10.1055/S-2006-948180 |
0.319 |
|
| 2005 |
Schulz F, Leca F, Hollmann F, Reetz MT. Towards practical biocatalytic Baeyer-Villiger reactions: applying a thermostable enzyme in the gram-scale synthesis of optically-active lactones in a two-liquid-phase system. Beilstein Journal of Organic Chemistry. 1: 10. PMID 16542025 DOI: 10.1186/1860-5397-1-10 |
0.742 |
|
| 2005 |
Reetz MT, Guo H. Mixtures of monodentate P-ligands as a means to control the diastereoselectivity in Rh-catalyzed hydrogenation of chiral alkenes. Beilstein Journal of Organic Chemistry. 1: 3. PMID 16542016 DOI: 10.1186/1860-5397-1-3 |
0.315 |
|
| 2005 |
Reetz MT, Meiswinkel A, Mehler G, Angermund K, Graf M, Thiel W, Mynott R, Blackmond DG. Why are BINOL-based monophosphites such efficient ligands in Rh-catalyzed asymmetric olefin hydrogenation? Journal of the American Chemical Society. 127: 10305-13. PMID 16028942 DOI: 10.1021/Ja052025+ |
0.335 |
|
| 2005 |
Bernsmann H, van den Berg M, Hoen R, Minnaard AJ, Mehler G, Reetz MT, De Vries JG, Feringa BL. PipPhos and MorfPhos: privileged monodentate phosphoramidite ligands for rhodium-catalyzed asymmetric hydrogenation. The Journal of Organic Chemistry. 70: 943-51. PMID 15675853 DOI: 10.1021/Jo048374O |
0.305 |
|
| 2005 |
Reetz MT, Bondarev OG, Gais HJ, Bolm C. BINOL-derived N-phosphino sulfoximines as ligands for asymmetric catalysis Tetrahedron Letters. 46: 5643-5646. DOI: 10.1016/j.tetlet.2005.06.107 |
0.336 |
|
| 2005 |
Bocola M, Schulz F, Leca F, Vogel A, Fraaije MW, Reetz MT. Converting phenylacetone monooxygenase into phenylcyclohexanone monooxygenase by rational design: Towards practical Baeyer-Villiger monooxygenases Advanced Synthesis and Catalysis. 347: 979-986. DOI: 10.1002/Adsc.200505069 |
0.657 |
|
| 2004 |
Reetz MT, Brunner B, Schneider T, Schulz F, Clouthier CM, Kayser MM. Directed evolution as a method to create enantioselective cyclohexanone monooxygenases for catalysis in Baeyer-Villiger reactions. Angewandte Chemie (International Ed. in English). 43: 4075-8. PMID 15300699 DOI: 10.1002/Anie.200460272 |
0.671 |
|
| 2004 |
Reetz MT. Changing the enantioselectivity of enzymes by directed evolution. Methods in Enzymology. 388: 238-56. PMID 15289076 DOI: 10.1016/S0076-6879(04)88021-2 |
0.388 |
|
| 2004 |
Reetz MT. Controlling the enantioselectivity of enzymes by directed evolution: practical and theoretical ramifications. Proceedings of the National Academy of Sciences of the United States of America. 101: 5716-22. PMID 15079053 DOI: 10.1073/Pnas.0306866101 |
0.376 |
|
| 2004 |
Bocola M, Otte N, Jaeger KE, Reetz MT, Thiel W. Learning from directed evolution: Theoretical investigations into cooperative mutations in lipase enantioselectivity Chembiochem. 5: 214-223. PMID 14760743 DOI: 10.1002/Cbic.200300731 |
0.313 |
|
| 2004 |
Reetz MT, Torre C, Eipper A, Lohmer R, Hermes M, Brunner B, Maichele A, Bocola M, Arand M, Cronin A, Genzel Y, Archelas A, Furstoss R. Enhancing the Enantioselectivity of an Epoxide Hydrolase by Directed Evolution Organic Letters. 6: 177-180. PMID 14723522 DOI: 10.1021/Ol035898M |
0.362 |
|
| 2004 |
Reetz MT, Kuhling KM, Hinrichs H, Deege A. Circular dichroism as a detection method in the screening of enantioselective catalysts. Chirality. 12: 479-82. PMID 10824174 DOI: 10.1002/(Sici)1520-636X(2000)12:5/6<479::Aid-Chir32>3.0.Co;2-# |
0.312 |
|
| 2004 |
Reetz MT, Mehler G, Meiswinkel A. Mixtures of chiral monodentate phosphites, phosphonites and phosphines as ligands in Rh-catalyzed hydrogenation of N-acyl enamines: Extension of the combinatorial approach Tetrahedron Asymmetry. 15: 2165-2167. DOI: 10.1016/J.Tetasy.2004.04.038 |
0.322 |
|
| 2004 |
Reetz MT, Li X. Combinatorial approach to the asymmetric hydrogenation of β-acylamino acrylates: Use of mixtures of chiral monodentate P-ligands Tetrahedron. 60: 9709-9714. DOI: 10.1016/J.Tet.2004.07.042 |
0.323 |
|
| 2003 |
Dröge MJ, Rüggeberg CJ, Van der Sloot AM, Schimmel J, Dijkstra DS, Verhaert RMD, Reetz MT, Quax WJ. Binding of phage displayed Bacillus subtilis lipase A to a phosphonate suicide inhibitor Journal of Biotechnology. 101: 19-28. PMID 12523966 DOI: 10.1016/S0168-1656(02)00289-4 |
0.301 |
|
| 2003 |
Reetz MT, Sell T, Goddard R. Chiral phosphoric acid diesters as ligands in asymmetric transition metal catalyzed hydrogenation Chimia. 57: 290-292. DOI: 10.2533/000942903777679316 |
0.315 |
|
| 2003 |
Funke SA, Eipper A, Reetz MT, Otte N, Thiel W, Van Pouderoyen G, Dijkstra BW, Jaeger KE, Eggert T. Directed evolution of an enantioselective Bacillus subtilis lipase Biocatalysis and Biotransformation. 21: 67-73. DOI: 10.1080/1024242031000110847 |
0.373 |
|
| 2003 |
Cedrone F, Niel S, Roca S, Bhatnagar T, Ait-Abdelkader N, Torre C, Krumm H, Maichele A, Reetz MT, Baratti JC. Directed evolution of the epoxide hydrolase from Aspergillus niger Biocatalysis and Biotransformation. 21: 357-364. DOI: 10.1080/102420310001630137 |
0.324 |
|
| 2003 |
Reetz M, Sommer K. Cover Picture: Gold-Catalyzed Hydroarylation of Alkynes (Eur. J. Org. Chem. 18/2003) European Journal of Organic Chemistry. 2003: 3465-3465. DOI: 10.1002/Ejoc.200390239 |
0.326 |
|
| 2003 |
Reetz MT, Tielmann P, Wiesenhöfer W, Könen W, Zonta A. Second Generation Sol-Gel Encapsulated Lipases: Robust Heterogeneous Biocatalysts Advanced Synthesis and Catalysis. 345: 717-728. DOI: 10.1002/Adsc.200303016 |
0.345 |
|
| 2003 |
Reetz MT, Chatziiosifidis I, Hübner F, Heimbach H. α‐tert‐Alkylation of Ketones: 2‐tert‐Pentylcyclopentanone Organic Syntheses. 95-95. DOI: 10.1002/0471264180.Os062.12 |
0.331 |
|
| 2002 |
Reetz MT, Rüggeberg CJ. A screening system for enantioselective enzymes based on differential cell growth. Chemical Communications (Cambridge, England). 1428-9. PMID 12125587 DOI: 10.1039/B203916H |
0.309 |
|
| 2002 |
Reetz MT. Lipases as practical biocatalysts Current Opinion in Chemical Biology. 6: 145-150. PMID 12038997 DOI: 10.1016/S1367-5931(02)00297-1 |
0.34 |
|
| 2002 |
Reetz MT, Rentzsch M, Pletsch A, Maywald M. Towards the directed evolution of hybrid catalysts Chimia. 56: 721-723. DOI: 10.2533/000942902777679920 |
0.302 |
|
| 2002 |
Reetz MT. Directed evolution of enantioselective enzymes as catalysts in the production of chiral pharmaceuticals Pharmacochemistry Library. 32: 27-37. DOI: 10.1016/S0165-7208(02)80005-8 |
0.362 |
|
| 2002 |
Reetz MT, Rüggeberg CJ, Dröge MJ, Quax WJ. Immobilization of chiral enzyme inhibitors on solid supports by amide-forming coupling and olefin metathesis Tetrahedron. 58: 8465-8473. DOI: 10.1016/S0040-4020(02)01052-9 |
0.352 |
|
| 2002 |
Reetz MT. Directed evolution of selective enzymes and hybrid catalysts Tetrahedron. 58: 6595-6602. DOI: 10.1016/S0040-4020(02)00668-3 |
0.358 |
|
| 2001 |
Fürstner A, Voigtländer D, Schrader W, Giebel D, Reetz MT. A "hard/soft" mismatch enables catalytic Friedel-Crafts acylations. Organic Letters. 3: 417-20. PMID 11428028 DOI: 10.1021/Ol0069251 |
0.319 |
|
| 2001 |
Jaeger KE, Eggert T, Eipper A, Reetz MT. Directed evolution and the creation of enantioselective biocatalysts Applied Microbiology and Biotechnology. 55: 519-530. PMID 11414315 DOI: 10.1007/S002530100643 |
0.311 |
|
| 2001 |
Reetz MT, Winter M, Breinbauer R, Thurn-Albrecht T, Vogel W. Size-selective electrochemical preparation of surfactant-stabilized Pd-, Ni- and Pt/Pd colloids. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 1084-94. PMID 11303867 DOI: 10.1002/1521-3765(20010302)7:5<1084::Aid-Chem1084>3.0.Co;2-J |
0.518 |
|
| 2001 |
Reetz MT. Combinatorial and Evolution-Based Methods in the Creation of Enantioselective Catalysts. Angewandte Chemie. 40: 284-310. PMID 11180317 DOI: 10.1002/1521-3773(20010119)40:2<284::Aid-Anie284>3.0.Co;2-N |
0.352 |
|
| 2001 |
Zha D, Wilensek S, Hermes M, Karl-Erich-Jaeger, Reetz MT. Complete reversal of enantioselectivity of an enzyme-catalyzed reaction by directed evolution Chemical Communications. 2664-2665. DOI: 10.1039/B109913M |
0.347 |
|
| 2001 |
Reetz MT, Wilensek S, Zha D, Jaeger KE. Directed evolution of an enantioselective enzyme through combinatorial multiple-cassette mutagenesis Angewandte Chemie - International Edition. 40: 3589-3591. DOI: 10.1002/1521-3773(20011001)40:19<3589::Aid-Anie3589>3.0.Co;2-X |
0.358 |
|
| 2001 |
Reetz MT. Kombinatorische und evolutionsgesteuerte Methoden zur Bildung enantioselektiver Katalysatoren Angewandte Chemie. 113: 292-320. DOI: 10.1002/1521-3757(20010119)113:2<292::Aid-Ange292>3.0.Co;2-F |
0.305 |
|
| 2000 |
Reetz MT, Mehler G. Highly Enantioselective Rh-Catalyzed Hydrogenation Reactions Based on Chiral Monophosphite Ligands. Angewandte Chemie (International Ed. in English). 39: 3889-3890. PMID 29711714 DOI: 10.1002/1521-3773(20001103)39:21<3889::Aid-Anie3889>3.0.Co;2-T |
0.327 |
|
| 2000 |
Liebeton K, Zonta A, Schimossek K, Nardini M, Lang D, Dijkstra BW, Reetz MT, Jaeger KE. Directed evolution of an enantioselective lipase. Chemistry & Biology. 7: 709-18. PMID 10980451 DOI: 10.1016/S1074-5521(00)00015-6 |
0.381 |
|
| 2000 |
Jaeger KE, Reetz MT. Directed evolution of enantioselective enzymes for organic chemistry. Current Opinion in Chemical Biology. 4: 68-73. PMID 10679373 DOI: 10.1016/S1367-5931(99)00054-X |
0.344 |
|
| 2000 |
Reetz MT, Haderlein aG, Angermund K. Chiral Diketimines as Ligands in Pd-Catalyzed Reactions: Prediction of Catalyst Activity by the AMS Model Journal of the American Chemical Society. 122: 996-997. DOI: 10.1021/Ja9930566 |
0.3 |
|
| 2000 |
Reetz MT, Sostmann S. Kinetic resolution in Pd-catalyzed allylic substitution using the helical PHelix ligand Journal of Organometallic Chemistry. 603: 105-109. DOI: 10.1016/S0022-328X(00)00173-X |
0.332 |
|
| 1999 |
Blackmond DG, Rosner T, Neugebauer T, Reetz MT. Kinetic Influences on Enantioselectivity for Non-Diastereopure Catalyst Mixtures. Angewandte Chemie (International Ed. in English). 38: 2196-2199. PMID 10425479 DOI: 10.1002/(Sici)1521-3773(19990802)38:15<2196::Aid-Anie2196>3.0.Co;2-9 |
0.327 |
|
| 1999 |
Reetz MT. Strategies for the development of enantioselective catalysts Pure and Applied Chemistry. 71: 1503-1509. DOI: 10.1351/Pac199971081503 |
0.344 |
|
| 1999 |
Reetz MT, Willuhn M, Psiorz C, Goddard R. Donor complexes of bis(1-indenyl)phenylborane dichlorozirconium as isospecific catalysts in propene polymerization Chemical Communications. 1105-1106. DOI: 10.1039/A902543J |
0.312 |
|
| 1999 |
Reetz MT, Beuttenmüller EW, Goddard R, Pastó M. A new class of chiral diphosphines having planar chirality Tetrahedron Letters. 40: 4977-4980. DOI: 10.1016/S0040-4039(99)00947-8 |
0.306 |
|
| 1999 |
Huskens J, Reetz MT. Observation of Stereotopic Group Recognition in Chiral Borate Complexes in Solution European Journal of Organic Chemistry. 1999: 1775-1786. DOI: 10.1002/(Sici)1099-0690(199908)1999:8<1775::Aid-Ejoc1775>3.0.Co;2-1 |
0.465 |
|
| 1998 |
Reetz MT, Becker MH, Kühling KM, Holzwarth A. Time-Resolved IR-Thermographic Detection and Screening of Enantioselectivity in Catalytic Reactions. Angewandte Chemie (International Ed. in English). 37: 2647-2650. PMID 29711629 DOI: 10.1002/(Sici)1521-3773(19981016)37:19<2647::Aid-Anie2647>3.0.Co;2-I |
0.338 |
|
| 1998 |
Reetz MT, Lohmer G, Schwickardi R. A New Catalyst System for the Heck Reaction of Unreactive Aryl Halides. Angewandte Chemie (International Ed. in English). 37: 481-483. PMID 29711154 DOI: 10.1002/(Sici)1521-3773(19980302)37:4<481::Aid-Anie481>3.0.Co;2-I |
0.31 |
|
| 1998 |
Reetz MT, Jaeger KE. Overexpression, immobilization and biotechnological application of Pseudomonas lipases. Chemistry and Physics of Lipids. 93: 3-14. PMID 9720245 DOI: 10.1016/S0009-3084(98)00033-4 |
0.354 |
|
| 1998 |
Huskens J, Goddard R, Reetz MT. Direct Observation of Stereotopic Group Recognition in Solution and Solid State Journal of the American Chemical Society. 120: 6617-6618. DOI: 10.1021/Ja980215X |
0.422 |
|
| 1998 |
Reetz MT, Zonta A, Vijayakrishnan V, Schimossek K. Entrapment of lipases in hydrophobic magnetite-containing sol-gel materials: magnetic separation of heterogeneous biocatalysts Journal of Molecular Catalysis a-Chemical. 134: 251-258. DOI: 10.1016/S1381-1169(98)00043-0 |
0.326 |
|
| 1998 |
Reetz MT. Supramolecular transition metal catalysts in two-phase systems Catalysis Today. 42: 399-411. DOI: 10.1016/S0920-5861(98)00122-9 |
0.304 |
|
| 1998 |
Reetz MT, Westermann E, Lohmer R, Lohmer G. A highly active phosphine-free catalyst system for Heck reactions of aryl bromides Tetrahedron Letters. 39: 8449-8452. DOI: 10.1016/S0040-4039(98)01967-4 |
0.325 |
|
| 1998 |
Reetz MT, Demuth R, Goddard R. 2-Pyrimidylphosphines: A new class of ligands for transition metal catalysis Tetrahedron Letters. 39: 7089-7092. DOI: 10.1016/S0040-4039(98)01545-7 |
0.317 |
|
| 1998 |
Reetz MT, Breinbauer R, Wedemann P, Binger P. Nanostructured Nickel-clusters as catalysts in [3+2]cycloaddition reactions Tetrahedron. 54: 1233-1240. DOI: 10.1016/S0040-4020(97)10221-6 |
0.553 |
|
| 1998 |
Reetz MT. New supramolecular transition metal catalysts Journal of Heterocyclic Chemistry. 35: 1065-1073. DOI: 10.1002/Jhet.5570350506 |
0.306 |
|
| 1997 |
Reetz MT, Wanninger K, Hermes M. Regioselective palladium-catalysed coupling reactions of vinyl chlorides with carbon nucleophiles Chemical Communications. 535-536. DOI: 10.1039/A608371D |
0.325 |
|
| 1997 |
Jaeger KE, Schneidinger B, Rosenau F, Werner M, Lang D, Dijkstra BW, Schimossek K, Zonta A, Reetz MT. Bacterial lipases for biotechnological applications Journal of Molecular Catalysis - B Enzymatic. 3: 3-12. DOI: 10.1016/S1381-1177(96)00039-2 |
0.316 |
|
| 1997 |
Reetz MT, Merk C, Naberfeld G, Rudolph J, Griebenow N, Goddard R. 3,3′-dinitro-octahydrobinaphthol: A new chiral ligand for metal-catalyzed enantioselective reactions Tetrahedron Letters. 38: 5273-5276. DOI: 10.1016/S0040-4039(97)01149-0 |
0.34 |
|
| 1997 |
Reetz MT, Beuttenmüller EW, Goddard R. First enantioselective catalysis using a helical diphosphane Tetrahedron Letters. 38: 3211-3214. DOI: 10.1016/S0040-4039(97)00562-5 |
0.318 |
|
| 1997 |
Reetz MT, Haning H. Ligand effects in selective addition reactions of organoindium reagents with carbonyl compounds Journal of Organometallic Chemistry. 541: 117-120. DOI: 10.1016/S0022-328X(97)00021-1 |
0.314 |
|
| 1996 |
Reetz MT, Strack TJ, Kanand J, Goddard R. Stereospecific synthesis of chiral alkinylogous amino acids Chemical Communications. 733-734. DOI: 10.1039/Cc9960000733 |
0.317 |
|
| 1996 |
Reetz MT, Strack TJ, Mutulis F, Goddard R. Asymmetric dihydroxylation of chiral γ-amino α,β-unsaturated esters: Turning the mismatched into the matched case via protective group tuning Tetrahedron Letters. 37: 9293-9296. DOI: 10.1016/S0040-4039(97)82945-0 |
0.307 |
|
| 1996 |
Reetz MT, Breinbauer R, Wanninger K. Suzuki and Heck reactions catalyzed by preformed palladium clusters and palladium/nickel bimetallic clusters Tetrahedron Letters. 37: 4499-4502. DOI: 10.1016/0040-4039(96)00924-0 |
0.534 |
|
| 1996 |
Jaeger K-, Liebeton K, Zonta A, Schimossek K, Reetz MT. Biotechnological application of Pseudomonas aeruginosa lipase: efficient kinetic resolution of amines and alcohols Applied Microbiology and Biotechnology. 46: 99-105. DOI: 10.1007/S002530050789 |
0.344 |
|
| 1996 |
Reetz MT, Hütte S, Herzog HM, Goddard R. Synthetic and mechanistic aspects of metal‐free polymerizations of acrylates Macromolecular Symposia. 107: 209-217. DOI: 10.1002/Masy.19961070120 |
0.311 |
|
| 1996 |
Reetz MT, Hütte S, Goddard R, Robyr C. Synthesis, Structure, and Stereoselective Reaction of a Chiral Hydroxy-Stabilized Metal-Free Enolate Chemistry - a European Journal. 2: 382-384. DOI: 10.1002/Chem.19960020405 |
0.32 |
|
| 1996 |
Reetz MT, Quaiser SA, Breinbauer R, Tesche B. A New Strategy in Heterogeneous Catalysis: The Design of Cortex Catalysts Angewandte Chemie. 34: 2728-2730. DOI: 10.1002/Anie.199527281 |
0.538 |
|
| 1995 |
Reetz MT, Griebenow N, Goddard R. Stereoselective syntheses of α-hydroxy-γ-amino acids: possible γ-turn mimetics Journal of the Chemical Society, Chemical Communications. 1605-1606. DOI: 10.1039/C39950001605 |
0.302 |
|
| 1995 |
Reetz MT, Kindler A. The Kharasch reaction revisited: CuX3Li2-catalyzed conjugate addition reactions of Grignard reagents Journal of Organometallic Chemistry. 502. DOI: 10.1016/0022-328X(95)05699-P |
0.363 |
|
| 1995 |
Reetz MT, Quaiser SA, Breinbauer R, Tesche B. Eine neue Strategie in der heterogenen Katalyse: das Design von Cortex-Katalysatoren Angewandte Chemie. 107: 2956-2958. DOI: 10.1002/Ange.19951072348 |
0.498 |
|
| 1994 |
Reetz MT, Hübel M, Jaeger R, Schwickardi R, Goddard R. Stereoselective synthesis of α,β-diamino nitriles from amino acids Synthesis. 1994: 733-738. DOI: 10.1055/S-1994-25559 |
0.325 |
|
| 1994 |
Reetz MT, Röhrig D, Harms K, Frenking G. Stereoselective synthesis of β-amino hydroxylamines Tetrahedron Letters. 35: 8765-8768. DOI: 10.1016/S0040-4039(00)78492-9 |
0.327 |
|
| 1994 |
Reetz MT, Rölfing K, Griebenow N. A simple method for chelation controlled additions to α-amino aldehydes Tetrahedron Letters. 35: 1969-1972. DOI: 10.1016/S0040-4039(00)73024-3 |
0.346 |
|
| 1993 |
Reetz MT, Raguse B, Seitz T. First direct NMR spectroscopic observation of a cram-chelate involving a chiral α-alkoxy aldehyde Tetrahedron. 49: 8561-8568. DOI: 10.1016/S0040-4020(01)96262-3 |
0.335 |
|
| 1993 |
Reetz MT, Gansäuer A. Catalysis by lithium perchlorate in dichloromethane: Diels-Alder reactions and 1,3-Claisen rearrangements Tetrahedron. 49: 6025-6030. DOI: 10.1016/S0040-4020(01)87187-8 |
0.332 |
|
| 1992 |
Reetz MT, Kayser F, Harms K. Cycloaddition reactions of λ-amino α,β-didehydro amino acid esters: a test case for the principle of 1,3-allylic strain Tetrahedron Letters. 33: 3453-3456. DOI: 10.1016/S0040-4039(00)92661-3 |
0.306 |
|
| 1992 |
Reetz MT, Kayser F. Stereoselective synthesis of α,γ-diamino acid esters Tetrahedron-Asymmetry. 3: 1377-1380. DOI: 10.1016/0957-4166(92)80010-T |
0.344 |
|
| 1992 |
Reetz MT, Raguse B, Marth CF, Hügel HM, Bach T, Fox DNA. A rapid injection NMR study of the chelation controlled Mukaiyama aldol addition: TiCl4 versus LiClO4 as the Lewis acid Tetrahedron. 48: 5731-5742. DOI: 10.1016/0040-4020(92)80024-A |
0.51 |
|
| 1992 |
Reetz MT, Kanand J, Griebenow N, Harms K. Stereoselektive nucleophile Additionsreaktionen an reaktiven Pseudopeptiden Angewandte Chemie. 104: 1638-1641. DOI: 10.1002/Ange.19921041217 |
0.324 |
|
| 1991 |
Reetz MT, Wang F, Harms K. Novel 1,4-asymmetric induction in nucleophilic 1,2-additions to chiral γ-amino enals Journal of the Chemical Society, Chemical Communications. 1309-1311. DOI: 10.1039/C39910001309 |
0.306 |
|
| 1991 |
Reetz MT. New Approaches to the Use of Amino Acids as Chiral Building Blocks in Organic Synthesis[New Synthetic Methods(85)] Angewandte Chemie International Edition in English. 30: 1531-1546. DOI: 10.1002/Anie.199115313 |
0.352 |
|
| 1991 |
Reetz MT, Jaeger R, Drewlies R, Hübel M. Stereoselective Synthesis of Vicinal Diamines Angewandte Chemie. 30: 103-106. DOI: 10.1002/Anie.199101031 |
0.305 |
|
| 1990 |
Reetz M, Rivadeneira E, Niemeyer C. Reagent control in the aldol addition of chiral boron enolates based on the 2,5-diphenylborolane ligand system Tetrahedron Letters. 31: 3863-3866. DOI: 10.1016/S0040-4039(00)97489-6 |
0.318 |
|
| 1990 |
Reetz MT, Drewes MW, Lennick K, Schmitz A, Holdgrün X. Non-racemizing synthesis and stereoselective reduction of chiral α-amino ketones Tetrahedron-Asymmetry. 1: 375-378. DOI: 10.1016/0957-4166(90)90037-B |
0.319 |
|
| 1990 |
Reetz MT, Wünsch T, Harms K. Stereoselective synthesis of α,γ-diamino-β-hydroxy amino acid esters: A new class of amino acids Tetrahedron-Asymmetry. 1: 371-374. DOI: 10.1016/0957-4166(90)90036-A |
0.316 |
|
| 1990 |
Reetz MT, Sauerwald M. Stereoselective α-alkylation of carbonyl compounds using tricarbonylchromium-complexed benzyl acetates Journal of Organometallic Chemistry. 382: 121-128. DOI: 10.1016/0022-328X(90)85221-J |
0.306 |
|
| 1989 |
Reetz MT, Drewes MW, Matthews BR, Lennick K. A simple synthetic route to statine and statine analogues Journal of the Chemical Society, Chemical Communications. 1474-1475. DOI: 10.1039/C39890001474 |
0.3 |
|
| 1989 |
Reetz MT, Schmitz A, Holdgrün X. Tandem aldolization/lactonization/dyotropic rearrangement of α-amino-aldehydes Tetrahedron Letters. 30: 5421-5424. DOI: 10.1016/S0040-4039(01)80583-9 |
0.334 |
|
| 1988 |
Reetz MT, Drewes MW, Schmitz A, Holdgrün X, Wünsch T, Binder J. Stereoselective reactions of chiral α-amino aldehydes Philosophical Transactions of the Royal Society A. 326: 573-578. DOI: 10.1098/Rsta.1988.0108 |
0.315 |
|
| 1988 |
Reetz M, Drewes M, Harms K, Reif W. Stereoselective cyanohydrin-forming reactions of chiral α-amino aldehydes Tetrahedron Letters. 29: 3295-3298. DOI: 10.1016/0040-4039(88)85144-X |
0.342 |
|
| 1987 |
Reetz MT, Sauerwald M. α-Alkylation of carbonyl compounds using 1-acetoxy-1-ferrocenylethane Journal of Organometallic Chemistry. 328: 155-160. DOI: 10.1016/S0022-328X(00)99775-4 |
0.349 |
|
| 1987 |
REETZ MT, KYUNG SH, BOLM C, ZIERKE T. ChemInform Abstract: Enantioselective C-C Bond Formation with Chiral Lewis Acids. Cheminform. 18. DOI: 10.1002/chin.198719082 |
0.356 |
|
| 1987 |
Reetz MT, Peter R, Itzstein MV. Titanium‐Mediated Stereoselective Knoevenagel Condensation of Ethyl (Diethoxyphosphoryl)acetate with Aldehydes Chemische Berichte. 120: 121-122. DOI: 10.1002/Cber.19871200123 |
0.335 |
|
| 1987 |
Reetz MT, Seitz T. Regio‐ and Stereoselective Carbosulfenylation of Olefins Angewandte Chemie. 26: 1028-1029. DOI: 10.1002/Anie.198710281 |
0.344 |
|
| 1986 |
Reetz MT, Hüllmann M. Non-chelation-controlled nucleophilic addition to chiral α-siloxyketones Journal of the Chemical Society, Chemical Communications. 1600-1602. DOI: 10.1039/C39860001600 |
0.301 |
|
| 1985 |
Reetz MT, Kyung S. A Simple Access to α,β‐Diketoesters. Tetrahedron Letters. 26: 6333-6336. DOI: 10.1016/S0040-4039(01)84591-3 |
0.31 |
|
| 1985 |
Reetz MT, Steinbach R, Westermann J, Peter R, Wenderoth B. Stereoselective Addition of Organotitanium Reagents to Carbonyl Compounds Chemische Berichte. 118: 1441-1454. DOI: 10.1002/Cber.19851180413 |
0.335 |
|
| 1985 |
Reetz MT, Westermann J, Kyung S. Direct geminal dimethylation of ketones and exhaustive methylation of carboxylic acid chlorides using dichlorodimethyltitanium Chemische Berichte. 118: 1050-1057. DOI: 10.1002/Cber.19851180322 |
0.332 |
|
| 1984 |
Reetz MT, Kesseler K, Jung A. Concerning the role of Lewis acids in chelation controlled addition to chiral alkoxy aldehydes Tetrahedron Letters. 25: 729-732. DOI: 10.1016/S0040-4039(01)80011-3 |
0.325 |
|
| 1984 |
Reetz MT, Heimbach H, Schwellnus K. A mild and variable synthesis of α-ketoesters Tetrahedron Letters. 25: 511-514. DOI: 10.1016/S0040-4039(00)99924-6 |
0.306 |
|
| 1984 |
Reetz MT, Walz P, Huebner F, Huettenhain SH, Heimbach H, Schwellnus K. REGIOSELECTIVE LEWIS ACID-MEDIATED α-SEC-ALKYLATION OF CARBONYL COMPOUNDS Cheminform. 15. DOI: 10.1002/Chin.198412139 |
0.312 |
|
| 1984 |
Reetz MT, Hübner F, Hüttenhain SH, Heimbach H, Schwellnus K, Walz P. Regioselektive Lewis‐Säure‐bedingte α‐sek‐Alkylierung von Carbonylverbindungen Chemische Berichte. 117: 322-335. DOI: 10.1002/Cber.19841170123 |
0.352 |
|
| 1984 |
Reetz MT. Chelation or Non-Chelation Control in Addition Reactions of Chiral ?- and ?- Alkoxy Carbonyl Compounds [New Synthetic Methods (44)] Angewandte Chemie International Edition in English. 23: 556-569. DOI: 10.1002/Anie.198405561 |
0.331 |
|
| 1983 |
Reetz MT, Wenderoth B, Peter R. Chemoselective in situ protection of aldehydes and ketones using titanium tetrakis(dialkylamides) Journal of the Chemical Society, Chemical Communications. 406-408. DOI: 10.1039/C39830000406 |
0.317 |
|
| 1983 |
Reetz MT, Sauerwald M. Stereoselective α-alkylation of ketones and esters using chromiumtricarbonyl-complexed benzyl acetates Tetrahedron Letters. 24: 2837-2840. DOI: 10.1016/S0040-4039(00)88037-5 |
0.307 |
|
| 1983 |
Reetz MT, Chatziiosifidis I, Künzer H, Müller-Starke H. Trimethylsilyl cyanide promoted cyanation of tertiary alkyl chlorides and other SN1 active compounds Tetrahedron. 39: 961-965. DOI: 10.1016/S0040-4020(01)88594-X |
0.327 |
|
| 1983 |
Reetz MT, Müller-Starke H. Lewis‐Säure‐bedingte α‐Alkoxyalkylierung von Carbonyl‐verbindungen mit α‐Halogen‐ und α‐Acetoxyethern. Synthese von C‐Glycosiden European Journal of Organic Chemistry. 1983: 1726-1738. DOI: 10.1002/Jlac.198319831008 |
0.31 |
|
| 1983 |
Reetz MT, Kesseler K, Schmidtberger S, Wenderoth B, Steinbach R. Chelation or Non-Chelation Control in Stereoselective Reactions of Titanium Reagents with Chiral Alkoxycarbonyl Compounds Angewandte Chemie International Edition in English. 22: 989-990. DOI: 10.1002/Chin.198412272 |
0.311 |
|
| 1983 |
Reetz MT, Wenderoth B, Peter R. Chemoselective In Situ Protection Of Aldehydes And Ketones Using Titanium Tetrakis(Dialkylamides) Cheminform. 14. DOI: 10.1002/Chin.198333146 |
0.306 |
|
| 1983 |
Reetz MT, Schwellnus K, Hübner F, Massa W, Schmidt RE. Lewis‐Säure‐bedingte α‐tert‐Alkylierung von Carbonsäuren und Carbonsäureestern Chemische Berichte. 116: 3708-3724. DOI: 10.1002/Cber.19831161119 |
0.314 |
|
| 1983 |
Reetz MT, Heimbach H. Regioselektive Lewis‐Säure‐bedingte α‐tert‐Alkylierung von Acyloinen und Glycolsäure Chemische Berichte. 116: 3702-3707. DOI: 10.1002/Cber.19831161118 |
0.317 |
|
| 1982 |
Reetz MT, Steinbach R, Westermann J, Urz R, Wenderoth B, Peter R. Stereoselectivity and Relative Reactivity in the Reaction of Organotitanium and -zirconium Reagents with Carbonyl Compounds Angewandte Chemie International Edition in English. 21: 135-135. DOI: 10.1002/Chin.198221257 |
0.302 |
|
| 1982 |
Reetz MT. Lewis Acid Induced ?-Alkylation of Carbonyl Compounds Angewandte Chemie International Edition in English. 21: 96-108. DOI: 10.1002/Anie.198200961 |
0.363 |
|
| 1981 |
Reetz MT, Giannis A. Lewis Acid Mediated A-Thioalkylation of Ketones Synthetic Communications. 11: 315-322. DOI: 10.1080/00397918108063611 |
0.457 |
|
| 1981 |
Reetz MT, Steinbach R, Wenderoth B. Carbon-Carbon Bond Formation Using Alkyl-Titanium-(IV) Compounds Synthetic Communications. 11: 261-266. DOI: 10.1080/00397918108061870 |
0.312 |
|
| 1981 |
Reetz MT, Hüttenhain S, Hübner F. Lewis Acid Alkylation of Ketones Using SN1-reactive Acetates Synthetic Communications. 11: 217-222. DOI: 10.1080/00397918108061863 |
0.338 |
|
| 1981 |
Reetz MT, Westermann J, Steinbach R. Direct geminal dimethylation of ketones using dimethyltitanium dichloride Journal of the Chemical Society, Chemical Communications. 237-239. DOI: 10.1039/C39810000237 |
0.303 |
|
| 1981 |
Reetz MT, Sauerwald M, Walz P. Retention of configuration in Lewis acid mediated α-alkylation of carbonyl compounds using SN1 reactive alkyl halides Tetrahedron Letters. 22: 1101-1104. DOI: 10.1016/S0040-4039(01)90247-3 |
0.332 |
|
| 1981 |
REETZ MT, SAUERWALD M. ChemInform Abstract: SIMPLE SYNTHESIS OF NORTRICYCLYL CHLORIDE Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198137151 |
0.305 |
|
| 1981 |
Reetz MT, Westermann J, Steinbach R. Direct Geminal Dimethylation Of Ketones Using Dimethyltitanium Dichloride Cheminform. 12. DOI: 10.1002/Chin.198127139 |
0.309 |
|
| 1981 |
Reetz MT, Steinbach R, Westermann J, Peter R. Chemo‐ And Diastereoselective Addition Of Alkyl And Aryl Titanium(Iv) Compounds To Aldehydes And Ketones Cheminform. 12. DOI: 10.1002/Chin.198112132 |
0.312 |
|
| 1981 |
REETZ MT, MAIER WF, CHATZIIOSIFIDIS I, GIANNIS A, HEIMBACH H, LOEWE U. ChemInform Abstract: LEWIS ACID MEDIATED α-ALKYLATION OF CARBONYL COMPOUNDS. VII. REGIO AND POSITION SPECIFIC α-TERT-ALKYLATION OF KETONES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198109166 |
0.683 |
|
| 1981 |
REETZ MT, MAIER WF, HEIMBACH H, GIANNIS A, ANASTASSIOUS G. ChemInform Abstract: LEWIS ACID MEDIATED α-ALKYLATION OF CARBONYL COMPOUNDS. VI. OPTIMIZATION OF THE PROCEDURE FOR THE α-TERT-ALKYLATION OF KETONES AND ALDEHYDES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198109165 |
0.682 |
|
| 1981 |
REETZ MT, MAIER WF. ChemInform Abstract: SIMPLE SYNTHESIS OF LITHIUM DIISOPROPYLAMIDE IN MOLAR QUANTITIES Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198106290 |
0.527 |
|
| 1981 |
Reetz MT, Sauerwald M. Einfache Synthese von Nortricyclylchlorid Chemische Berichte. 114: 2355-2356. DOI: 10.1002/Cber.19811140631 |
0.324 |
|
| 1981 |
Reetz MT, Chatziiosifidis I. Cyanation of Tertiary Alkyl Chlorides: A Novel Method for the Geminal Dialkylation of Ketones Angewandte Chemie. 20: 1017-1018. DOI: 10.1002/Anie.198110172 |
0.307 |
|
| 1980 |
Reetz MT, Stephan V, Maier WF. Facile Hydride Ion Abstraction From Enamines, Allylamines And Imines Synthetic Communications. 10: 867-871. DOI: 10.1080/00397918008062771 |
0.473 |
|
| 1980 |
SCHWARZ H, REETZ MT, MAIER WF, WESDEMIOTIS C, CHATZIIOSIFIDIS I, SCHILLING M. ChemInform Abstract: ADAMANTANE IN THE VAPOR PHASE Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198012119 |
0.519 |
|
| 1980 |
Reetz MT, Maier WF, Chatziiosifidis I, Giannis A, Heimbach H, Löwe U. Lewis-Säure-bedingte α-Alkylierung von Carbonylverbindungen, VII. Regio- und positionsspezifische α-tert-Alkylierung von Ketonen Chemische Berichte. 113: 3741-3757. DOI: 10.1002/Cber.19801131208 |
0.555 |
|
| 1980 |
Reetz MT, Maier WF, Heimbach H, Giannis A, Anastassious G. Lewis-Säure-bedingte α-Alkylierung von Carbonylverbindungen, VI. Optimierung des Verfahrens zur α-tert-Alkylierung von Ketonen und Aldehyden Chemische Berichte. 113: 3734-3740. DOI: 10.1002/Cber.19801131207 |
0.562 |
|
| 1980 |
Reetz MT, Steinbach R, Westermann J, Peter R. Chemo‐ und diastereoselektive Addition von Alkyl‐ und Aryltitan(IV)‐Verbindungen an Aldehyde und Ketone Angewandte Chemie. 92: 1044-1045. DOI: 10.1002/Ange.19800921217 |
0.336 |
|
| 1979 |
Reetz MT, Maier WF, Schwellnus K, Chatziiosifidis I. General synthesis of potentially antiviral alpha-adamantyl carbonyl compounds. Angewandte Chemie (International Ed. in English). 18: 72. PMID 105650 DOI: 10.1002/Anie.197900721 |
0.545 |
|
| 1979 |
Reetz MT, Hüttenhain S, Walz P, Löwe U. Lewis and mediated α-alkylation of ketones using SN1 reactive alkylating agents Tetrahedron Letters. 20: 4971-4974. DOI: 10.1016/S0040-4039(01)86764-2 |
0.346 |
|
| 1979 |
Reetz M, Chatziliosifidis I, Löwe U, Maier W. Position specific α-tert-alkylation of ketones Tetrahedron Letters. 20: 1427-1428. DOI: 10.1016/S0040-4039(01)86168-2 |
0.599 |
|
| 1979 |
REETZ MT, MAIER WF, SCHWELLNUS K, CHATZIIOSIFIDIS I. ChemInform Abstract: GENERAL SYNTHESIS OF ACTIVE ANTIVIRAL α-ADAMANTYL CARBONYL COMPOUNDS Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197915194 |
0.583 |
|
| 1979 |
Reetz MT, Neumeier G. Diels‐Alder‐Reaktionen von 2,3‐Bis(trimethylsilyloxy)‐1,3–dienen Chemische Berichte. 112: 2209-2219. DOI: 10.1002/Cber.19791120628 |
0.313 |
|
| 1979 |
Schwarz H, Reetz MT, Maier WF, Wesdemiotis C, Chatziiosifidis I, Schilling M. Adamantene in the Gas Phase Angewandte Chemie International Edition in English. 18: 952-953. DOI: 10.1002/Anie.197909521 |
0.504 |
|
| 1979 |
Schwarz H, Reetz MT, Maier WF, Wesdemiotis C, Chatziiosifidis I, Schilling M. Adamanten in der Gasphase Angewandte Chemie. 91: 1019-1020. DOI: 10.1002/Ange.19790911225 |
0.527 |
|
| 1979 |
Reetz MT, Maier WF, Schwellnus K, Chatziiosifidis I. Allgemeine Synthese potentiell antiviral wirksamer α-Adamantyl-carbonylverbindungen Angewandte Chemie. 91: 78-79. DOI: 10.1002/Ange.19790910121 |
0.558 |
|
| 1978 |
REETZ MT, MAIER WF. ChemInform Abstract: TERT-ALKYLATION OF KETONES AND ALDEHYDES Chemischer Informationsdienst. 9. DOI: 10.1002/Chin.197814166 |
0.601 |
|
| 1978 |
Hoffmann RW, Kurz HR, Becherer J, Reetz MT. Bicyclofulvene, IV: Synthesen von Methylentricyclo[4.2.1.02,5]nonan- und -tricyclo[3.2.1.02,4]octan-Derivaten Chemische Berichte. 111: 1264-1274. DOI: 10.1002/Cber.19781110406 |
0.301 |
|
| 1978 |
Reetz MT, Maier WF. tert-Alkylation of Ketones and Aldehydes† Angewandte Chemie. 17: 48-49. DOI: 10.1002/Anie.197800481 |
0.6 |
|
| 1978 |
Reetz MT, Maier WF. tert‐Alkylierung von Ketonen und Aldehyden Angewandte Chemie. 90: 50-50. DOI: 10.1002/Ange.19780900110 |
0.534 |
|
| 1977 |
Reetz MT. Dyotrope Umlagerungen, XI. Mechnismus der thermischen Umlagerung von Allyl-(silymethyl)-ethern Chemische Berichte. 110: 965-978. DOI: 10.1002/Cber.19771100316 |
0.306 |
|
| 1977 |
Reetz MT. Dyotrope Umlagerungen, X. Synthese und thermische Umlagerung von Allyl‐(silylmethyl)‐ethern Chemische Berichte. 110: 954-964. DOI: 10.1002/Cber.19771100315 |
0.321 |
|
| 1977 |
Reetz MT, Schinzer D. Nucleophile Substitution von Vinyl‐Wasserstoffatomen durch Carbanionen Angewandte Chemie. 89: 46-47. DOI: 10.1002/Ange.19770890113 |
0.321 |
|
| 1976 |
Reetz MT, Kliment M, Plachky M. Dyotrope Umlagerungen, VII: Synthese und thermische Umlagerung von (Silyl) methyl‐silyl‐äthern Chemische Berichte. 109: 2716-2727. DOI: 10.1002/Cber.19761090808 |
0.304 |
|
| 1975 |
Maier WF, Reetz MT. Ab initio study of acyloxy cations Journal of the American Chemical Society. 97: 3687-3690. DOI: 10.1021/Ja00846A021 |
0.528 |
|
| 1975 |
MAIER WF, REETZ MT. ChemInform Abstract: AN AB INITIO STUDY OF ACYLOXY CATIONS Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197536085 |
0.543 |
|
| 1974 |
Reetz MT, Maier WF. The electronic structure and energy of acyloxy and dioxacyclopropyl cations Theoretical Chemistry Accounts. 35: 163-167. DOI: 10.1007/Bf00551404 |
0.531 |
|
| 1973 |
Reetz M, Schöllkopf U, Bánhidai B. Untersuchungen über Heterocarbene, XIII1) Brom-, Jod- und Chlor-äthoxycarbonylcarben aus Brom-, Jod- und Chlor-diazoessigsäure-äthylester Justus Liebigs Annalen Der Chemie. 1973: 599-610. DOI: 10.1002/Jlac.197319730409 |
0.519 |
|
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