Manfred T. Reetz - Publications

Bonn, Marburg, Mülheim 
organic chemistry

261 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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. 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, 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[,5]nonan- und -tricyclo[,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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