Publications

[169] Mehl, L.-M.; Maier, M. E.: A Radical-Based Synthesis of Lingzhiol. J. Org. Chem. 2017, 82, asap. (article)

[168] Rengarasu, R.; Maier, M. E.: Total Synthesis of Lingzhiol and some Analogs via Wittig Reaction on an Oxocyclopentane Carboxylate. Asian J. Org. Chem. 2017, 6, 108-117. (article)

[167] Mishra, V. K.; Ravikumar, P. C.; Maier, M. E.: Formal Total Synthesis of Amphidinolide Q. J. Org. Chem. 2016, 81, 9728-9737. (article)

[166] Reinbold, J.; Hierlemann, T.; Hinkel, H.; Müller, I.; Maier, M. E.; Weindl, T.; Schlensak, C.; Wendel, H. P.; Krajewski, S.: Development and in vitro characterization of poly(lactide-co-glycolide) microspheres loaded with an antibacterial natural drug for the treatment of long-term bacterial infections. Drug Des. Devel. Ther. 2016, 10, 2823-2832. (article)

[165] Mishra, V. K.; Ravikumar, P. C.; Maier, M. E.: C–H-Activation approach towards the core structure of the alkaloid γ-lycorane. Tetrahedron 2016, 72, 6499-6509. (article)

[164] Reiss, A.; Maier, M. E.: Toward Leiodermatolide: Synthesis of the Core Structure. Org. Lett. 2016, 18, 3146-3149. (article)

[163] Morkunas, M.; Maier, M. E.: Alternative routes to the acylphloroglucinol rhodomyrtone. Tetrahedron 2015, 71, 9662-9666. (article)

[162] Zhdanko, A.; Maier, M. E.: Explanation of "Silver Effects" in Gold(I)-Catalyzed Hydroalkoxylation of Alkynes. ACS Catal. 2015, 5, 5994-6004. (article)

[161] Maier, M. E.: Design and Synthesis of Analogues of Natural Products. Org. Biomol. Chem. 2015, 13, 5302-5343. (article)

[160] Gündüz, S.; Power, A.; Maier, M. E.; Logothetis, N. K.; Angelovski, G.: Synthesis and Characterization of a Biotinylated Multivalent Targeted Contrast Agent. ChemPlusChem 2015, 80, 612-622. (article)

[159] Cotter, K.; Capecci, J.; Sennoune, S.; Huss, M.; Maier, M.; Martinez-Zaguilan, R.; Forgac, M.: Activity of Plasma Membrane V-ATPases is Critical for the Invasion of MDA-MB231 Breast Cancer Cells. J. Biol. Chem. 2015, 290, 3680-3692. (article)

[158] Gündüz, S.; Nitta, N.; Vibhute, S.; Shibata, S.; May(i)er, M. E.; Logothetis, N. K.; Aoki, I.; Angelovski, G.: Dendrimeric calcium-responsive MRI contrast agents with slow in vivo diffusion. Chem. Commun. 2015 51, 2782-2785. (article)

[157] Cavalcante, I. M.; Rocha, N. R. d. C.; Maier, M. E.; de Lima, A. P. D.; Andrade Neto, D. M.; de Brito, D. H. A.; Petzhold, C. L.; Schanz, M. T. G. F.; Ricardo, N. M. P. S.: Synthesis and characterization of new esters of oleic acid and glycerol analogues as potential lubricants. Ind. Crops Prod. 2014, 62, 453-459. (article)

[156] Zhdanko, A.; Maier, M. E.: Explanation of Counterion Effects in Gold(I)-Catalyzed Hydroalkoxylation of Alkynes. ACS Catal. 2014, 4, 2770-2775. (article)

[155] Zhdanko, A.; Maier, M. E.: Mechanistic Study of Gold(I)-Catalyzed Hydroamination of Alkynes: Outer or Inner Sphere Mechanism? Angew. Chem. 2014, 126, 7894-7898; Angew. Chem. Int. Ed. 2014, 53, 7760-7764. (article)

[154] Zhdanko, A.; Maier, M. E.: Gold(I)-, Palladium(II)-, Platinum(II)-, and Mercury(II)-Catalysed Spirocyclization of 1,3-Enynediols: Reaction Scope. Eur. J. Org. Chem. 2014, 3411-3422. (article)

[153] Müller, K. H.; Spoden, G. A.; Scheffer, K. D.; Brunnhöfer, R.; De Brabander, J. K.; Maier, M. E.; Florin, L.; Muller, C. P.: Inhibition by Cellular Vacuolar ATPase Impairs Human Papillomavirus Uncoating and Infection. Antimicrobiol. Agents Chemother. 2014, 58, 2905-2911. (article)

[152] Zhdanko, A.; Maier, M. E.: The Mechanism of Gold(I)-Catalyzed Hydroalkoxylation of Alkynes: An Extensive Experimental Study. Chem. Eur. J. 2014, 20, 1918-1930. (article)

[151] Müller, S.; Sasse, F.; Maier, M. E.: Synthesis of Pladienolide B and Its 7-Epimer with Insights into the Role of the Allylic Acetate. Eur. J. Org. Chem. 2014, 1025-1036. (article)

[150] Ma, C. I.; Diraviyam, K.; Maier, M. E.; Sept, D.; Sibley, L. D.: Synthetic Chondramide A Analogues Stabilize Filamentous Actin and Block Invasion by Toxoplasma gondii. J. Nat. Prod. 2013, 76, 1565-1572. (article)

[149] Verma, K. D.; Forgács, A.; Uh, H.; Beyerlein, M.; Maier, M. E.; Petoud, S.; Botta, M.; Logothetis, N. K.: New Calcium-Selective Smart Contrast Agents for Magnetic Resonance Imaging. Chem. Eur. J. 2013, 19, 18011-18026. (article)

[148] Morkunas, M.; Dube, L.; Götz, F.; Maier, M. E.: Synthesis of the acylphloroglucinols rhodomyrtone and rhodomyrtosone B. Tetrahedron 2013, 69, 8559-8563. (article)

[147] Danner, P.; Morkunas, M.; Maier, M. E.: Synthesis of D-Abrines by Palladium-catalyzed Reaction of ortho-Iodoanilines with N-Boc-N-methylalanyl-substituted Acetaldehyde and Acetylene. Org. Lett. 2013, 15, 2474-2477. (article)

[146] Gaugele, D.; Maier, M., E.: Approach to the Core Structure of the Polycyclic Alkaloid Palhinine A. Synlett 2013, 24, 955-958. (article)

[145] Zhdanko, A.; Maier, M. E.: Quantitative Evaluation of the Stability of gem-Diaurated Species in Reactions with Nucleophiles. Organometallics 2013, 32, 2000-2006. (article)

[144] Ushakov, D. B.; Maier, M. E.: Studies Towards the Synthesis of Crotogoudin. Synlett 2013, 24, 705-708. (article)

[143] Zhdanko, A.; Maier, M. E.: Synthesis of gem-Diaurated Species from Alkynols. Chem. Eur. J. 2013, 19, 3932-3942. (article)

[142] Vibhute, S. M.; Engelmann, J.; Verbic, T.; Maier, M. E.; Logothetis, N. K.; Angelovski, G.: Synthesis and characterization of pH-sensitive, biotinylated MRI contrast agents and their conjugates with avidin. Org. Biomol. Chem. 2013, 11, 1294-1305. (article)

[141] Navickas, V.; Maier, M. E. Construction of anti-Me-OH Vicinal Relationships in Polyketides. In Asymmetric Synthesis II: More Methods and Applications; Christmann, M.; Bräse, S. Eds.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2012; pp. 131-137. (article)

[140] Dhingra Verma, K.; Mishra, A.; Engelmann, J.; Beyerlein, M.; Maier, M. E.; Logothetis, N. K.: Magnetic-Field-Dependent 1H Relaxivity Behavior of Biotin/Avidin-Based Magnetic Resonance Imaging Probes. ChemPlusChem 2012, 77, 758-769. (article)

[139] Sawant, P.; Maier, M. E.: Synthesis of Atorvastatin Lactone Linker Constructs for Target Fishing. Eur. J. Org. Chem. 2012, 6576-6585. (article)

[138] Zhdanko, A.; Ströbele, M.; Maier, M. E.: Coordination Chemistry of Gold Catalysts in Solution: A Detailed NMR Study. Chem. Eur. J. 2012, 18, 14732-14744. (article)

[137] Ushakov, D. B.; Raja, A.; Franke, R.; Sasse, F.; Maier, M. E.: Total Synthesis of (±)-Moluccanic Acid Methyl Ester. Synlett 2012, 23, 1358-1360. (article)

[136] Satyanarayana, G.; Maier, M. E.: Tricyclic isoindolines by Heck cyclization. Tetrahedron 2012, 68, 1745-1749. (article)

[135] Mallah, E.; Sweidan, K.; Engelmann, J.; Steimann, M.; Kuhn, N.; Maier, M. E.: Nucleophilic substitution approach towards 1,3-dimethylbarbituric acid derivatives new synthetic routes and crystal structures. Tetrahedron 2012, 68, 1005-1010. (article)

[134] Sawant, P.; Maier, M. E.: Synthesis of the C1-C13 Fragment of Biselyngbyaside. Synlett 2011, 3002-3004. (article)

[133] Zhdanko, A.; Schmauder, A.; Ma, C. I.; Sibley, L. D.; Sept, D.; Sasse, F.; Maier, M. E.: Synthesis of Chondramide A Analogues with Modified b-Tyrosine and Their Biological Evaluation. Chem. Eur. J. 2011, 17, 13349-13357. (article)

[132] Müller, S.; Mayer, T.; Sasse, F.; Maier, M. E.: Synthesis of a Pladienolide B Analogue with the Fully Functionalized Core Structure. Org. Lett. 2011, 13, 3940-3943. (article)

[131] Wohland, M.; Maier, M. E.: 2,6-Disubstituted Tetrahydropyrans by Tandem Meyer-Schuster Rearrangement/Hetero Michael Addition of 6-Alkyne-1,5-diols. Synlett 2011, 1523-1526. (article)

[130] Rink, C.; Navickas, V.; Maier, M. E.: An Approach to the Core Structure of Leiodermatolide. Org. Lett. 2011, 13, 2334–2337. (article)

[129] Ushakov, D. B.; Navickas, V.; Ströbele, M.; Maichle-Mössmer, C.; Sasse, F.; Maier, M. E.: Total Synthesis and Biological Evaluation of (–)-9-Deoxy-englerin A. Org. Lett. 2011, 13, 2090-2093. (article)

[128] Jha, D.; Mishra, R.; Gottschalk, S.; Wiesmüller, K.-H.; Ugurbil, K.; Maier, M. E.; Engelmann, J.: CyLoP-1: A Novel Cysteine-Rich Cell-Penetrating Peptide for Cytosolic Delivery of Cargoes. Bioconjugate Chem. 2011, 22 319-328. (article)

[127] Navickas, V.; Rink, C.; Maier, M. E.: Synthetic Studies towards Leiodermatolide: Rapid Stereoselective Syntheses of Key Fragments. Synlett 2011, 191-194. (article)

[126] Neumaier, J.; Maier, M. E.: Synthesis of the Spirofungin A Core via a Domino Strategy Consisting of Olefinic Ester Ring-Closing Metathesis and Iodospiroacetalization. Synlett 2011, 187-190. (article)

[125] Rink, C.; Sasse, F.; Matulis, D.; Zubriene, A.; Maier, M. E.: Probing the influence of an allylic methyl group in zearlenone analogues on binding to Hsp90. Chem. Eur. J. 2010, 16, 14469-14478. (article)

[124] Sawant, P.; Maier, M. E.: A novel strategy towards the atorvastatin lactone. Tetrahedron 2010, 66, 9738-9744. (article)

[123] Schwehm, C.; Wohland, M.; Maier, M. E.: Tetrahydrofurans from Substituted Hex-5-yne-1,4-diols. Synlett 2010, 1789-1792. (article)

[122] Navickas, V.; Ushakov, D. B.; Maier, M. E.; Ströbele, M.; Meyer, H.-J.: Synthesis of the Guaianolide Ring System via Cycloaddition of a Bicyclic Carbonyl Ylide with Allyl Propiolate. Org. Lett. 2010, 12, 3418-3421. (article)

[121] Schmauder, A.; Sibley, L. D.; Maier, M. E.: Total Synthesis and Configurational Assignment of Chondramide A. Chem. Eur. J. 2010, 16, 4328-4336.(article)

[120] Ugele, M.; Maier, M. E.: Synthesis of the alkaloid tyroscherin by an aldol/Curtius strategy. Tetrahedron 2010, 66, 2633-2641. (article)

[119] Navickas, Vaidotas; Maier, M. E.: Synthesis of the proposed structure of queenslandon. Tetrahedron 2010, 66, 94-101. (article)

[118] Ugele, M.; Sasse, F.; Knapp, S.; Fedorov, O.; Zubriene, A.; Matulis, D.; Maier, M. E.: Propionate Analogs of Zearalenone Bind to Hsp90. ChemBioChem 2009, 10, 2203-2212.

[117] Jägel, J.; Maier, M. E.: Formal Total Synthesis of Palmerolide A. Synthesis 2009, 2881-2892.

[116] Maier, M. E.: Structural revisions of natural products by total synthesis. Nat. Prod. Rep. 2009, 26, 1105-1124.

[115] Varseev, G. N.; Maier, M. E.: Formal total synthesis of platencin. Angew. Chem. 2009, 121, 3739-3742; Angew. Chem. Int. Ed. 2009, 48, 3685-3688.

[114] Satyanarayana, G.; Maichle-Mössmer, C.; Maier, M. E.: Formation of pentacyclic structures by a domino sequence on cyclic enamides. Chem. Commun. 2009, 1571-1573.

[113] Zimmermann, T. J.; Niesen, F. H.; Pilka, E. S.; Knapp, S.; Oppermann, U.; Maier, M. E.: Discovery of a potent and selective inhibitor for human carbonyl reductase 1 from propionate scanning applied to the macrolide zearalenone. Bioorg. Med. Chem. 2009, 17, 530-536.

[112] Vintonyak, V. V.; Kunze, B.; Sasse, F.; Maier, M. E.: Total Synthesis and Biological Activity of Neopeltolide and Analogues. Chem. Eur. J. 2008, 14, 11132-11140.

[111] Maier, M. E.; Ritschel, J.: A second generation synthesis of the cruentaren A core structure based on oxetane and oxirane opening reactions. ARKIVOC 2008, 14, 314-329.

[110] Satyanarayana, G.; Maier, M. E.: Unsymmetrical Biaryls by Palladium-Catalyzed Coupling of Aryl Halides with Internal Reduction. Eur. J. Org. Chem. 2008, 5543-5552.

[109] Dhingra, K.; Maier, M. E.; Beyerlein, M.; Angelovski, G.; Logothetis, N. K.: Synthesis and characterization of a smart contrast agent sensitive to calcium. Chem. Commun. 2008, 3444-3446.

[108] Satyanarayana, G.; Maier, M. E.: Formation of Spirocyclic Compounds from Heck Cyclizations Invoking Cyclic Enamides. J. Org. Chem. 2008, 73, 5410-5415.

[107] Satyanarayana, G.; Maier, M. E.: Biaryl Formation from 5-(2-Bromobenzyl)-Substituted Piperidin-2-ones via Palladacycles. Org. Lett. 2008, 10, 2361-2364.

[106] Schmauder, A.; Müller, S.; Maier, M. E.: Concise route to defined stereoisomers of the hydroxy acid of the chondramides. Tetrahedron 2008, 64, 6263-6269.

[105] Vintonyak Viktor, V.; Cala, M.; Lay, F.; Kunze, B.; Sasse, F.; Maier Martin, E.: Synthesis and biological evaluation of cruentaren a analogues. Chem. Eur. J. 2008, 14, 3709-3720.

[104] Satyanarayana, G.; Müller, S.; Maier, M. E.: Benzoazabicyclo[4.3.1] derivatives by intramolecular Michael addition of piperidinone enolates to enoates. Tetrahedron Lett. 2008, 49, 3279-3282.

[103] Vintonyak, V. V.; Maier, M. E.: Formal Total Synthesis of Neopeltolide. Org. Lett. 2008, 10, 1239-1242.

[102] Dhingra, K.; Fousková, P.; Angelovski, G.; Maier, M. E.; Logothetis, N. K.; Tóth, É.: Towards extracellular Ca2+ sensing by MRI: synthesis and calcium-dependent 1H and 17O relaxation studies of two novel bismacrocyclic Gd3+ complexes. J. Biol. Inorg. Chem. 2008, 13, 35-46.

[101] Satyanarayana, G.; Maier, M. E.: Synthesis of 1,5-methano-3-benzazocines by intramolecular Buchwald-Hartwig arylation of 2-piperidinones. Tetrahedron 2008, 64, 356-363.

[100] Jägel, J.; Schmauder, A.; Binanzer, M.; Maier, M. E.: A concise route to the C3-C23 fragment of the macrolide palmerolide A. Tetrahedron 2007, 63, 13006-13017.

[99] Mayer, T.; Maier, M. E.: Design and Synthesis of a Tag-Free Chemical Probe for Photoaffinity Labeling. Eur. J. Org. Chem. 2007, 4711-4720.

[98] Prusov, E.; Maier, M. E.: Synthesis of nitrogen-containing spirocyclic scaffolds via aminoallylation/RCM sequence. Tetrahedron 2007, 63, 10486-10496.

[97] Vintonyak, V. V.; Maier, M. E.: Total Synthesis of Cruentaren A. Angew. Chem. 2007, 119, 5301-5303; Angew. Chem. Int. Ed. 2007, 46, 5209-5211.

[96] Marimganti, S.; Wieneke, R.; Geyer, A.; Maier, M. E.: Synthesis and Conformational Analysis of Geodiamolide Analogues. Eur. J. Org. Chem. 2007, 2779-2790.

[95] Varseev, G. N.; Maier, M. E.: Enantioselective total synthesis of (+)-neosymbioimine. Org. Lett. 2007, 9, 1461-1464.

[94] Vintonyak, V. V.; Maier, M. E.: Synthesis of the Core Structure of Cruentaren A. Org. Lett. 2007, 9, 655-658.

[93] Maier, M. E.: Product Class 6: Lactones. Science of Synthesis; Panek, J. S. Ed.; Georg Thieme Verlag, Stuttgart, 2007; Vol. 20b; pp. 1421-1551.

[92] Ritschel, J.; Sasse, F.; Maier, M. E.: Synthesis of a Benzolactone Collection using Click Chemistry. Eur. J. Org. Chem. 2007, 78-87.

[91] Khartulyari, A. S.; Maier, M. E.: Synthesis of Benzomorphan Analogues by Intramolecular Buchwald-Hartwig Cyclization. Eur. J. Org. Chem. 2007, 317-324.

[90] Khartulyari, A. S.; Manmohan, K.; Maier, M.: Concise Strategy to the Core Structure of the Macrolide Queenslandon. Org. Lett. 2006, 8, 5833-5836.

[89] Rajamalleswaramma, J.; Maier, M. E.: Synthesis of Luminacin D. J. Org. Chem. 2006, 71, 6999-7006.

[88] Maier, M. E.; Bayer, A.: A Formal Total Synthesis of Salvadione. Eur. J. Org. Chem. 2006, 4034-4043.

[87] Varseev, G. N.; Maier, M. E.: Total Synthesis of (±)-Symbioimine. Angew. Chem. 2006, 118, 4885-4889; Angew. Chem. Int. Ed. 2006, 45, 4767-4771.

[86] Kapur, M.; Khartulyari, A.; Maier, M. E.: Stereoselective Synthesis of Protected 1,2-Diols and 1,2,3-Triols by a Tandem Hydroboration-Coupling Sequence. Org. Lett. 2006, 8, 1629-1632.

[85] Jägel, J.; Maier, M. E.: An Efficient Synthesis of the C1-C9 Segment of Dictyostatin. Synlett 2006, 693-696.

[84] Prusov, E.; Röhm, H.; Maier, M. E.: Chemoenzymatic Synthesis of the C10-C23 Segment of Dictyostatin. Org. Lett. 2006, 8, 1025-1028.

[83] Marimganti, S.; Yasmeen, S.; Fischer, D.; Maier, M. E.: Synthesis of Jasplakinolide Analogues containing a Novel w-Amino Acid. Chem. Eur. J. 2005, 11, 6687-6700.

[82] Varseev, G. N.; Maier, M. E.: A Novel Palladium-Catalyzed Arylation-Dehydroaromatization Reaction: Synthesis of 7-Aryltetralones. Org. Lett. 2005 7, 3881-3884.

[81] Rath, J.-P.; Kinast, S.; Maier, M. E.: Synthesis of the Fully Functionalized Core Structure of the Antibiotic Abyssomicin C. Org. Lett. 2005, 7, 3089-3092.

[80] Petri, A. F.; Sasse, F.; Maier, M. E.: Synthesis and Biological Evaluation of Apicularen A Analogs. Eur. J. Org. Chem. 2005, 1865-1875.

[79] Herb, C.; Dettner, F.; Maier, M. E.: Synthesis of the Salicylihalamide Core Structure from Epichlorohydrin - Laying the Foundation to Macrolactone Collections. Eur. J. Org. Chem. 2005, 728-739.

[78] Rath, J.-P.; Eipert, M.; Kinast, S.; Maier, M. E.: Synthesis of the Tetronate-Containing Core Structure of the Antibiotic Abyssomicin C. Synlett 2005, 314-318.

[77] Danner, P.; Bauer, M.; Phukan, P.; Maier, M. E.: Total Synthesis of Cryptophycin 3. Eur. J. Org. Chem. 2005, 317-325.

[76] Petri, A. F.; Bayer, A.; Maier, M. E.: Total Synthesis of Apicularen A through Transannular Pyran Formation. Angew. Chem. 2004, 116, 5945-5947; Angew. Chem. Int Ed. 2004, 43, 5821-5823.

[75] Herb, C.; Bayer, A.; Maier, M. E.: Total Synthesis of Salicylihalamide A and B. Chem. Eur. J. 2004, 10, 5649-5660.

[74] Wattanasereekul, S.; Maier, M. E.: Synthesis of the 8-Hydroxy Acid of Jasplakinolide. Adv. Synth. Catal. 2004, 346, 855-861.

[73] Bayer, A.; Maier, M. E.: Synthesis of enamides from aldehydes and amides. Tetrahedron 2004, 60, 6665-6677.

[72] Herb, C.; Maier, M. E.: A Formal Total Synthesis of the Salicylihalamides. J. Org. Chem. 2003, 68, 8129-8135.

[71] Eipert, M.; Maichle-Mössmer, C.; Maier, M. E.: Use of epoxidation and epoxide opening reactions for the synthesis of highly functionalized 1-oxaspiro[4.5]decan-2-ones and related compounds. Tetrahedron 2003, 59, 7949-7960.

[70] Phukan, P.; Bauer, M.; Maier, M. E.: Facile Generation of Alkenes and Dienes from Tosylates. Synthesis 2003, 1324-1328.

[69] Phukan, P.; Sasmal, S.; Maier, M. E.: Flexible Routes to the 5-Hydroxy Acid of the Cryptophycins. Eur. J. Org. Chem. 2003, 1733-1740.

[68] Petri, A. F.; Kühnert, S. M.; Scheufler, F.; Maier, M. E.: Applications of Size-Selective Macrolactonizations to the Synthesis of Benzolactone-Enamide Core Structures. Synthesis 2003, 940-955.

[67] Sasmal, P. K.; Maier, M. E.: Acetal-Vinyl Sulfide Cyclization on Sugar Substrates: Effect of Structure and Substituent. J. Org. Chem. 2003, 68, 824-831.

[66] Eipert, M.; Maichle-Mössmer, C.; Maier, M. E.: Acid-induced Rearrangement Reactions of Reduced Benzoquinone Cyclopentadiene Cycloadducts. J. Org. Chem. 2002, 67, 8692-8695.

[65] Sasmal, S.; Geyer, A.; Maier, M. E.: Synthesis of Cyclic Peptidomimetics from Aldol Building Blocks. J. Org. Chem. 2002, 67, 6260-6263.

[64] Bauer, M.; Maier, M. E.: Synthesis of the Core Structure of Salicylihalamide A by Intramolecular Suzuki Reaction. Org. Lett. 2002, 4, 2205-2208.

[63] Richter, F.; Maichle-Mössmer, C.; Maier, M. E.: Intramolecular Diels-Alder Reactions with 6-Hydroxypyranone as Dienophile. Synlett 2002, 1097-1100.

[62] Hemmasi, B.; Maier, M. E.: One-pot procedure for the manufacture of swellable, functionalized crosslinked polyolefins by ring-opening metathesis copolymerization (ROMC). In Ger. Offen.: Germany, 2002; Vol. 10102086 A1; pp. 20 pp., issued: 20020307, CAN 136:232716

[61] Richter, F.; Bauer, M.; Perez, C.; Maichle-Mössmer, C.; Maier, M. E.: Intramolecular Diels-Alder Reactions Using a-Methylene Lactones as Dienophile. J. Org. Chem. 2002, 67, 2474-2480.

[60] Sasmal, P. K.; Maier, M. E.: Formation of Bicyclic Ethers from Lewis Acid Promoted Cyclizations of Cyclic Oxonium Ions. Org. Lett. 2002, 4, 1271-1274.

[59] Kühnert, S. M.; Maier, M. E.: Synthesis of the Core Structure of Apicularen A by Transannular Cyclization. Org. Lett. 2002, 4, 643-646.

[58] Hermann, C.; Giammasi, C.; Geyer, A.; Maier, M. E.: Syntheses of Hapalosin Analogs by Solid-phase Assembly of Acyclic Precursors. Tetrahedron 2001, 57, 8999-9010.

[57] Wahl, H. G.; Hong, Q.; Stübe, D.; Maier, M. E., Häring, H. U.; Liebich, H. M.: Simultaneous analysis of the di(2-ethylhexyl)phthalate metabolites 2-ethylhexanoic acid, 2-ethyl-3-hydroxyhexanoic acid and 2-ethyl-3-oxohexanoic acid in urine by gas chromatography-mass spectrometry. Journal of Chromatography B 2001, 2, 213-219.

[56] Scheufler, F.; Maier, M. E.: Synthesis of a Model System for the Macrocyclic Subunit of the Oximidines. Synlett 2001, 1221-1224.

[55] Paczkowski, R.; Maichle-Mössmer, C.; Maier, M. E.: A Formal Total Synthesis of Dysidiolide. Org. Lett. 2000, 2, 3967-3969.

[54] Scheufler, F.; Maier, M. E.: On the Diels-Alder Reaction of Allenes Bearing a Diphenylphosphoryl or (Trichloromethyl)sulfonyl Substituent. Eur. J. Org. Chem. 2000, 3945-3948.

[53] Hermann, C.; Pais, G. C. G.; Geyer, A.; Kühnert, S. M.; Maier, M. E.: Total Synthesis of Hapalosin and Two Ringexpanded Analogs. Tetrahedron 2000, 56, 8461-8471.

[52] Maier, M. E.: Synthesis of Medium-Sized Rings by the Ring-Closing Metathesis Reaction. Angew. Chem. 2000, 112, 2153-2157; Angew. Chem. Int. Ed. 2000, 39, 2073-2077 (Review).

[51] Maier, M. E.; Hermann, C.: Synthesis of the g-Amino-b-hydroxy Acid of Hapalosin via an Asymmetric Dihydroxylation Route. Tetrahedron 2000, 56, 557-561.

[50] Boße, F.; Maier, M. E.: Synthesis of a Tetrasubstituted Cyclohexene from a Bicyclo[2.2.2]octa-2,5-diene. J. Pract. Chem. 2000, 342, 6-9.

[49] Pais, G. C. G.; Maier, M. E.: Efficient Synthesis of the g-Amino-b-hydroxy Acid Subunit of Hapalosin. J. Org. Chem. 1999, 64, 4551-4554.

[48] Namyslo, J.-C.; Schäfer, R.; Maier, M. E.: An Aldol Approach to the C21-C26-Part of FK506. J. Pract. Chem. 1999, 341, 557-561.

[47] Niestroj, A.; Bruhn, C.; Maier, M. E.: Synthesis of a dynemicin A analog without the nitrogen. New J. Chem. 1999, 23, 749-756.

[46] Maier, M. E.; Boße, F.; Niestroj, A. J.: Design and Synthesis of Dynemicin Analogs. Eur. J. Org. Chem. 1999, 1-13.

[45] Maier, M. E.; Lapeva, T.: Synthesis of Cyclohexenylamines by Ring Closing Metathesis. Synlett 1998, 891-893.

[44] Maier, M. E.; Perez, C.: Intramolecular Diels-Alder Reaction with an a-Methylene Lactone as Dienophile. Synlett 1998, 159-160.

[43] Niestroj, A. J.; Bruhn, C.; Maier, M. E.: Synthesis and Structural Characterization of 5-Bromo-2,3-dimethylphenol. J. Pract. Chem. 1998, 340, 175-177.

[42] Maier, M. E.; Bugl, M.: Synthesis of Spiro Ethers by Ring Closing Metathesis. Synlett 1998, 1390-1392.

[41] Kasyan, A.; Wagner, C.; Maier, M. E.: Regiochemistry of the Reductive Heck Coupling of 2-Azabicyclo[2.2.1]hept-5-ene. Synthesis of Epibatidine Analogues. Tetrahedron 1998, 54, 8047-8054.

[40] Haller, B.-U.; Kruber, S.; Maier, M. E.: A Practical Synthesis of the Cyclohexyl Part of FK506. J. Pract. Chem. 1998, 340, 656-661.

[39] Maier, M. E.; Reuter, S.: Zweidimensionale Synthese und asymmetrische Dihydroxylierung. GIT Labor-Fachzeitschrift 1997, 41, 1108-1112.

[38] Maier, M. E.; Reuter, S.: Double Asymmetric Dihydroxylation of 1,5-Hexadiene. Liebigs Ann./Recueil 1997, 2043-2046.

[37] Boße, F.; Tunoori, A. R.; Maier, M. E.: Cross-Coupling Approach towards Dynemicin Analogs without the Nitrogen. Tetrahedron 1997, 53, 9159-9168.

[36] Maier, M. E.; Langenbacher, D.: Synthesis of [7.3.2]-Enediynes. Synlett 1996, 682-684.

[35] Boße, F.; Tunoori, A. R.; Niestroj, A. J.; Gronwald, O.; Maier, M. E.: Palladium-catalyzed Cross-coupling Reactions of Arylmetal Compounds with b-Substituted a-Iodoenones and a Cyclohexyl Triflate. Tetrahedron 1996, 52, 9485-9498.

[34] Maier, M. E.; Reuter, S.: Combination of the ADH with a Two-dimensional Synthesis. Synlett 1995, 1029-1030.

[33] Maier, M. E.: Design of Enediyne Prodrugs. Synlett 1995, 13-26.

[32] Maier, M. E.; Abel, U.: On the Role of the Nitrogen Atom in Dynemicin A. Synlett 1995, 38-40.

[31] Maier, M. E.; Langenbacher, D.; Rebien, F.: Synthetic Routes to 1,4-Difunctionalized Cycloheptenes. Liebigs Ann. 1995, 1843-1848.

[30] Maier, M. E.; Oost, T.: Regio- and diastereoselectivity of the insertion of aldehydes into alkyne-zirconocene complexes. J. Organomet. Chem. 1995, 505, 95-107.

[29] Maier, M. E.; Langenbacher, D.: Synthesis of a Reactive [7.4.1]Enediyne and a Stable Eneyne-allene. Synlett 1994, 713-716.

[28] Brandstetter, T.; Maier, M. E.: Synthesis and Oxidative Activation of an Oxabicyclo[7.2.1] Enediyne. Tetrahedron 1994, 50, 1435-1448.

[27] Maier, M. E.: Strategies for the Generation of Reactive Enediynes from Stable Precursors. Kontakte (Darmstadt) 1994, 3-17.

[26] Maier, M. E.: Übersicht: Morphin-Synthesen. Nachr. Chem. Tech. Lab. 1993, 41, 1120-1128.

[25] Maier, M. E.: Übersicht: Gruppenselektive Reaktionen. Nachr. Chem. Tech. Lab. 1993, 41, 314-330.

[24] Maier, M. E.: Übersicht: Furan als Synthesebaustein. Nachr. Chem. Tech. Lab. 1993, 41, 696-704.

[23] Maier, M. E.: Übersicht: Temporäre Silicium-Verknüpfungen. Nachr. Chem. Tech. Lab. 1993, 41, 442-451.

[22] Maier, M. E.: Übersicht: Totalsynthesen von Rapamycin. Nachr. Chem. Tech. Lab. 1993, 41, 1379-1384.

[21] Maier, M. E.; Haller, B.-U.; Stumpf, R.; Fischer, H.: A Stereoselective and Convergent Synthesis of a C21-C34 Fragment of FK506. Synlett 1993, 863-865.

[20] Maier, M. E.; Brandstetter, T.: Synthesis of 11-Membered Enediyne Ketones by the Intramolecular Nicholas Reaction. Liebigs Ann. Chem. 1993, 1009-1016.

[19] Maier, M. E.: Jahresrückblick: Enantioselektive Synthese. Nachr. Chem. Tech. Lab. 1993, 41, 154-159.

[18] Maier, M. E.: Rezension: Cycloaddition Reactions in Carbohydrate Chemistry, ACS Symposium Series, (Hrsg.: M. J. Comstock), Bd. 494 (Hrsg.: R. M. Giuliano), ACS, Washington, DC, 1992. Angew. Chem. 1993, 105, 1271.

[17] Maier, M. E.: Übersicht: C-C-Verknüpfungen mit Metallocenen der vierten Nebengruppe. Nachr. Chem. Tech. Lab. 1993, 41, 811-823.

[16] Maier, M. E.; Greiner, B.: Synthesis and Reactivity of a p-Methoxyphenyl-Substituted Enediyne. A Case of Electronic Influence on the Rate of the Bergman Cycloaromatization. Liebigs Ann. Chem. 1992, 855-861.

[15] Maier, M. E.: Jahresrückblick: Enantioselektive Synthese. Nachr. Chem. Tech. Lab. 1992, 40, 155-158.

[14] Maier, M. E.; Brandstetter, T.: Synthesis of an Oxabicyclo[7.2.1] Enediyne from a Furanoside Derivative. Tetrahedron Lett. 1992, 33, 7511-7514.

[13] Maier, M. E.; Schöffling, B.: An Enantioselective Synthesis of the C(10) to C(20) Fragment of FK506. Tetrahedron Lett. 1991, 32, 53-56.

[12] Maier, M. E.; Brandstetter, T.: Oxidative Generation of an Enediyne System from a 1,5-Diyne Precursor. A Novel Triggering Device for Enediynes. Tetrahedron Lett. 1991, 32, 3679-3682.

[11] Fang, F. G.; Maier, M. E.; Danishefsky, S. J.; Schulte, G.: New Routes to Functionalized Benzazepine Substructures: a Novel Transformation of an a Diketone Thioamide Induced by Trimethyl Phosphite. J. Org. Chem. 1990, 55, 831.

[10] Maier, M. E.; Kandler, H.; Haller, B.-U.; Hofmann, J. H.; Fischer, H.: Diastereoselectivity in the Halolactonization of 2-Alkoxy-4-alkenoic Acids and 4-alkenamides. Liebigs Ann. Chem. 1990, 323-330.

[9] Maier, M. E.; Schöffling, B.: Synthesis of the Cyclohexyl Fragment of FK 506 by Intramolecular Ene-Reaction. Tetrahedron Lett. 1990, 31, 3007-3010.

[8] Maier, M. E.; Schöffling, B.: Intramolecular Cycloadditions of Mesoionic Carbonyl Ylides with Alkynes. Synthesis of 5,6-Dihydro-4H-cyclopenta- and 4,5,6,7-Tetrahydrobenzo[b]furan Derivatives. Chem. Ber. 1989, 122, 1081-1087.

[7] Maier, M. E.; Evertz, K.: Intramolecular [3+2] Cycloadditions of Mesoionic Carbonyl Ylides. Tetrahedron Lett. 1988, 29, 1677-1680.

[6] Maier, M. E.; Schmidt, R. R.; Haag-Zeino, B.: Reactivity and Diastereoselectivity in Inverse-Type Hetero-Diels-Alder Dihydropyran Syntheses. Chem. Ber. 1987, 120, 1505.

[5] Apparao, S.; Maier, M. E.; Schmidt, R. R.: Reactivity and Diastereoselectivity in Inverse-Type Hetero-Diels-Alder Dihydropyran Syntheses. Synthesis 1987, 900-904.

[4] Schmidt, R. R.; Maier, M.: Diastereospecific Synthesis of 2,6 Dideoxy- and 2,4,6-Trideoxy-Sugars via Hetero-Diels-Alder Reaction. Tetrahedron Lett. 1985, 26, 2065-2068.

[3] Maier, M.; Schmidt, R. R.: Funktionell substituierte 3,4 Dihydro 2H pyrane durch Hetero-Diels-Alder Reaktionen. Liebigs Ann. Chem. 1985, 2261.

[2] Schmidt, R. R.; Maier, M.: Hetero-Diels-Alder Reactions of a-Methoxymethylene substituted 1,3 Dicarbonyl Compounds with Enol and Enediol Ethers. Tetrahedron Lett. 1982, 23, 1789-1792.

[1] Schmidt, R. R.; Maier, M.: D-Biotin aus D-Arabinose. Synthesis 1982, 747.

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