Uni PotsdamFachbereich ChemieImpressum

(118)Karras, M.; Dąbrowski, M.; Pohl, R.; Rybáček, J.; Vacek, J.; Bednárová, L.; Grela, K.; Starý, I.*; Stará, I. G.*; Schmidt, B.* Helicenes as chirality inducing groups in transition metal catalysis: the first helically chiral olefin metathesis catalyst. Chem. Eur. J. 2018, 24, DOI
(117)Karras, M.; Holec, J.; Bednarova, L.; Pohl, R.; Schmidt, B.*; Stará, I. G.*; Stary, I.* Asymmetric Synthesis of Nonracemic 2-Amino[6]helicenes and Their Self-Assembly into Langmuir Films.  J. Org. Chem. 2018, 83, 5523-5538. DOI
(116)Paz, C.*; Heydenreich, M.; Schmidt, B., Vadra, N.; Baggio, R. Three new dihydro-agarofuran sesquiterpenes from the seeds of Maytenus boaria. Acta Cryst. C 2018, C74, 564-570. DOI
(115)Schultze, C.; Schmidt, B.* Prenylcoumarins in One or Two Steps by a Microwave-Promoted Tandem Claisen Rearrangement/Wittig Olefination/ Cyclization Sequence. J. Org. Chem. 2018, 83, 5210-5224. DOI
(114)Arias, H. R.; Feuerbach, D.; Schmidt, B.; Heydenreich, M., Paz, C.*; Ortells, M.O. Drimane Sesquiterpenoids Noncompetitively Inhibit Human alpha-4-beta-2 Nicotinic Acetylcholine Receptors with Higher Potency to Human alpha-3-beta-4 and alpha-7 Subtypes. J. Nat. Prod. 2018, 81, 811-817. DOI
(113)Schmidt, B.*; Petersen M. H.; Braun, D. Bidirectional Synthesis of 6-Acetoxy-5-hexadecanolide, the Mosquito Oviposition Pheromone of Culex quinquifasciatus, from a C2-symmetric Building Block unsing Olefin Metathesis Reactions. J. Org. Chem. 2018, 83, 1627-1633. DOI
(112)Schmidt, B.*; Schultze C. A one flask synthesis of pyranocoumarins through microwave promoted propargyl-Claisen rearrangement/Wittig-olefination. Eur. J. Org. Chem. 2018, 223-227. DOI
(111)Paz, C.*; Schmidt, B. Drimane Sesquiterpenes from Drimys winteri. In New Aspects in Medicinal Plants and Pharmacognosy; Tiezzi, A., Karpinski, T. M., Eds.; JB Books: Poznan, 2017, p 117-146. DOI
(110)Hermanns, J*. Schmidt, B. Zur Verwendung von QR-Codes in Uni-Seminaren- ein Baustein in den neu konzipierten Übungen zur Vorlesung "Organische Chemie für Studierende im Nebenfach" CHEMKON 2017, 24 DOI
(109)Schmidt, B.; Wolf, F. Synthesis of phenylpropanoids via Matsuda-Heck coupling of arene diazonium salts.  J. Org. Chem. 2017, 82, 4386-4395. DOI
(108)Schmidt, B.; Audörsch, S. Stereoselective total syntheses of polyacetylene plant metabolites via ester-tethered ring closing metathesis. J. Org. Chem. 2017, 82, 1743-1760. DOI
(107)Schmidt, B.; Riemer, M. Microwave-Promoted Pd-Catalyzed Synthesis of Dibenzofurans from Ortho-Arylphenols. J. Heterocycl. Chem. 2017, 53, 1287-1297. DOI
(106)Schmidt, B.*; Wolf, F.; Ehlert, C. Systematic Investigation into the Matsuda–Heck Reaction of α-Methylene Lactones: How Conformational Constraints Direct the β-H-Elimination Step. J. Org. Chem. 2016, 81, 11235-11249. DOI
(105)Schmidt, B.; Audörsch, S.; Kunz, O. Stereoselective Synthesis of 2Z,4E-Configured Dienoates through Tethered Ring Closing Metathesis. Synthesis 2016, 48,4509-4518. DOI
(104) Schmidt, B; Wolf, F.; Brunner, H. Styrylsufonates and -Sulfonamides through Pd-Catalysed Matsuda-Heck Reactions of Vinylsulfonic Acid Derivatives and Arenediazonium Salts. Eur. J. Org. Chem.  2016, 2972-2982. DOI
(103)Hermanns, J.; Riemer, M.; Schmidt, B. Die Magnolie - eine Heilpflanze?! Praxis der Naturwissenschaften - Chemie in der Schule, 201665(4), 32-35.
(102)Schmidt, B.; Audörsch, S. Stereoselective Total Synthesis of Atractylodemayne A, a Conjugated 2(E),8(Z),10(E)-Triene-4,6-diyne. Org.Lett. 2016, 18, 1162-1165.  DOI
(101)Schmidt, B.; Riemer, M. Microwave-Promoted Deprenylation: Prenyl Ether as a Thermolabile Phenol Protecting Group. Synthesis, 2016, 48, 1399-1406. DOI
(100)Göbel, R.; Stoltenberg, M.; Krehl, S.; Biolley, C.; Rothe, R.; Schmidt, B.; Hesemann, P.; Taubert, A.* A Modular Approach towards Mesoporous Silica Monoliths with Organically Modified Pore Walls: Nucleophillic Addition, Olefin Metathesis, and Cycloaddition. Eur. J. Inorg. Chem. 2016, 2088-2099. DOI
(99)Paz, C.*; Becerra, J.; Silvia, M.; Cabrera-Pardo, J.; Burgos, V.; Heydenreich, M.; Schmidt, B. (-)-8-Oxohobartine a New Indole Alkalod from Aristotelia chilensis (Mol.) Stuntz. Rec. Nat. Prod. 2016, 10, 68-73 DOI
(98)Schmidt, B.; Riemer, M.; Synthesis of Allyl- and Prenylcoumarins via Microwave-promoted Tandem Claisen-Rearrangement/Wittig-Olefination. Synthesis. 2016, 47, 141-149. DOI

(97)Schmidt, B.; Riemer, M.; Schilde, U. The Tandem Claisen Rearrangement/6-endo Cyclization Approach to Allylated and Prenylated Chromones Eur. J. Org. Chem. 2015, 7602-7611. DOI
(96)Paz, C.; Becerra, J.; Silva, M.; Burgos, V.; Heydenreich, M.; Schmidt, B.; Tran, T.; Vetter,I.; (-)-Pentylsedinine, a New Alkaloid from the Leaves of Lobelia tupa with Agonist Activity at Nicotinic Acetylcholine Receptor. Nat. Prod. Commun. 2015, 10, 1355-1357.
(95)Schmidt, B.; Elizarov, N.; Riemer, N.; Hölter, F. Acetamidoarenediazonium Salts: Opportunities for Multiple Arene Functionalizations Eur. J. Org. Chem. 2015, 5826-5841 DOI
(94)Schmidt, B.; Riemer, M.: Magnaldehydes B and E and Dictyobiphenyl B by Microwave-Promoted Cross-Coupling of Boronophenols Eur. J. Org. Chem. 2015, 3760-3766. DOI 
(93)Schmidt, B.; Elizarov, N.; Schilde, U.; Kelling, A. Dual Role of Acetanilides: Traceless Removal of a Directing Group through Deacetylation/Diazotation and Palladium-Catalyzed C-C Coupling Reaction. J. Org. Chem. 2015, 80, 4223-4234. DOI


(92)Buddrus, J.; Schmidt, B. "Grundlagen der Organischen Chemie, 5. Auflage" De Gruyter Verlag, Berlin, 2014.
(91)Schmidt, B.; Riemer, M.; Schilde, U. Chroman-4-ones via Microwave-Promoted Domino Claisen Rearrangement-Oxa-Michael Addition: Synthesis of Tabchromones A and B. Synlett, 2014, 25, 2943-2946 DOI.
Schmidt, B.; Hauke, S. Olefin cross methathesis based de novo synthesis of a partially protected L-amicetose and a fully protected L-cinerulose derivative. Beilstein J. Org. Chem. 2014, 10, 1023-1031. DOI
Riemer, M. Allyl Alkyl Carbonates. Synlett, 2014, 25, 1041-1042. DOI
Schmidt, B.; Riemer, M. Suzuki-Miyaura Coupling of Halophenols and Phenol Boronic Acids: Systematic Investigation of Positional Isomer Effects and Conclusions for the Synthesis of Phytoalexins from Pyrinae. J. Org. Chem. 2014, 79, 4104-4118 . DOI
Schmidt, B.; Hauke, S.; Mühlenberg, N. Imino Glycals via Ruthenium-Catalyzed RCM and Isomerization. Synthesis, 2014, 46, 1648-1658. DOI
(86) Schmidt, B.; Hauke, S.; Krehl, S.; Kunz, O. Ring Closing Metathesis. In Comprehensive Organic Synthesis II; Fürstner, A. (Vol. Ed.); Knochel, P., Molander, G. A., Eds.; Elsevier, 2014; Vol. 5, 1400- 1482. DOI
Schmidt, B.; Krehl, S. Domino- and tandem olefin metathesis reactions. In Olefin Metathesis―Theory and Practice; Grela, K., Ed.; Wiley: Chichester, 2014 (scheduled publication date: May 2014).
(84) Schmidt, B.; Hauke, S. Metathesis-based de-novo-synthesis of noviose. Eur. J. Org. Chem. 2014, 10, 1951-1960. DOI


Schmidt, B.; Kunz, O. Bidirectional cross metathesis and ring-closing metathesis/ring opening of a C2-symmetric building block: a strategy for the synthesis of decanolide natural products. Beilstein J. Org. Chem. 2013, 9, 2544-2555. DOI
Schmidt, B.; Kunz, O. Stereoselective Synthesis of Dienyl Phosphonates via Extended Tethered Ring-Closing Metathesis Org. Lett. 2013, 15, 4470–4473. DOI
Schmidt, B.; Riemer, M.; Karras, M. 2,2’-Biphenols via protecting group free thermal or microwave accelerated Suzuki-Miyaura coupling in water. J. Org. Chem. 2013, 78, 8680–8688. DOI
(Highlighted in Synfacts: DOI)

Schmidt, B.; Krehl, S.; Hauke, S. Assisted tandem catalytic cross metathesis-oxidation: in one flask from styrenes to 1,2-diketones and further to quinoxalines. J. Org. Chem. 2013, 78, 5427–5435. DOI
Schmidt, B.; Hauke, S. Cross metathesis of allyl alcohols: how to suppress and how to promote double bond isomerization. Org. Biomol. Chem. 2013, 11, 41944206. DOI
Schmidt, B.; Elizarov, N.; Berger, R.; Hölter, F. Scope and limitations of the Heck-coupling of phenol diazonium salts and styrenes: a protecting-group economic synthesis of phenolic stilbenes. Org. Biomol. Chem. 2013, 11, 36743691. DOI
Schmidt, B.; Elizarov, N.; Berger, R.; Petersen, M. H. From paracetamol to rolipram and derivatives: application of deacetylation-diazotation sequences and Pd-catalyzed Matsuda-Heck reaction. Synthesis 2013, 45, 11741180. DOI
Hermanns, J.; Schmidt, B. Marine Naturstoffe – ein Sachtext für die Sekundarstufe II. Praxis der Naturwissenschaften – Chemie in der Schule 2013, 62(2), 2931.
Schmidt, B.; Berger, R. A Deacetylation–Diazotation–Coupling Sequence: Palladium- Catalyzed C-C Bond Formation with Acetanilides as Formal Leaving Groups. Adv. Synth. Catal. 2013, 355, 463476. DOI


Schmidt, B.; Kunz, O.; Petersen, M. H. Total Syntheses of Naturally Occurring Seimatopolide A and Its Enantiomer from Chiral Pool Starting Materials Using a Bidirectional Strategy. J. Org. Chem. 2012, 77, 1089710906. DOI
Paz, C.; Peter, M. G.; Schmidt, B.; Becerra, J.; Gutierrez, M.; Astudillo, L.; Silva, M. Synthesis and AChE inhibiting activity of 2,4-substituted-6-phenylpyrimidines. J. Chil. Chem. Soc. 2012, 57, 12921294. DOI
Schmidt, B.; Krehl, S.; Jablowski, E. Assisted tandem catalytic RCM-aromatization in the synthesis of pyrroles and furans. Org. Biomol. Chem. 2012, 10, 51195130. DOI
Schmidt, B.; Krehl, S.; Sotelo-Meza, V. Synthesis of Chromanes through RCM-Transfer Hydrogenation. Synthesis 2012, 44, 16031613. (feature article) DOI
Schmidt, B.; Kunz, O. α,β-Unsaturated δ-Valerolactones through RCM-Isomerization Sequence. Synlett 2012, 23, 851854. DOI
Schmidt, B.; Elizarov, N. Selective arene functionalization through sequential oxidative and non-oxidative Heck reactions. Chem. Commun. 2012, 48, 43504352. DOI
Schmidt, B.; Krehl, S.; Kelling, A.; Schilde, U. Synthesis of 8-arylsubstituted coumarins based on ring closing metathesis and Suzuki-Miyaura coupling: synthesis of a furyl coumarin natural product from Galipea panamensis. J. Org. Chem. 2012, 77, 23602367. DOI
Schmidt, B.; Kunz, O. One-Flask Tethered Ring Closing Metathesis–Electrocyclic Ring Opening for the Highly Stereoselective Synthesis of Conjugated Z/E-Dienes. Eur. J. Org. Chem. 2012, 1008–1018. DOI


Duvinage, B.; Schmidt, B.; Kabutz, K. Kein Opium für die Feier, denn... Praxis der Naturwissenschaften – Chemie in der Schule 2011, 60(7), 36-41.
Schmidt, B.; Geißler, D. Olefin-Metathesis-Based Synthesis of Furans by an RCM/Deprotonation/Phosphorylation Sequence and Their Diels–Alder Reactions. Eur. J. Org. Chem. 2011, 7140–7147DOI
(64)Schmidt, B.; Geißler, D. Ru- and Pd-Catalysed Synthesis of 2-Arylfurans by One-Flask Heck Arylation/Oxidation. Eur. J. Org. Chem. 20114814–4822. DOI
(63)Schmidt, B.; Krehl, S. A single precatalyst Tandem RCM-allylic oxidation sequence. Chem. Commun. 2011, 58795881. DOI
(62)Schmidt, B.; Hölter, F. Suzuki-Miyaura coupling reactions with Phenol diazonium salts. Org. Biomol. Chem. 2011, 9, 49194920DOI
(61)Schmidt, B.; Hölter, F.; Kelling, A.; Schilde, U. Pd-catalyzed arylation reactions with phenol diazonium salts: application in the synthesis of diarylheptanoids J. Org. Chem. 2011, 76, 33573365. DOI
(60)Schmidt, B.; Berger, R.; Kelling, A.; Schilde, U. Pd-catalyzed [2+2+1] coupling of alkynes and arenes: phenol diazonium salts as mechanistic trapdoors. Chem. Eur. J. 2011, 17, 70327040. DOI
(59) Schmidt, B.; Staude, L. Desymmetrization of (R,R)-Hexa-1,5-diene-3,4-diol via Monofunctionalization and Rhodium-Catalyzed Allylic Substitution  J. Org. Chem. 2011, 76, 2220–2226. DOI
(58)Buddrus, J.; unter Mitarbeit von Schmidt, B. „Grundlagen der Organischen Chemie“ de Gruyter Verlag, Berlin, 2011.
(57)Schmidt, B.; Schanzenbach, D. Allyl ether (2011), Encyclopedia of Reagents for Organic Synthesis (Online), John Wiley & Sons Ltd., www.mrw.interscience.wiley.com/eros/, [March 18th 2011].
(56)Schmidt, B.; Staude, L.; Kelling, A.; Schilde, U. A Cross-Metathesis-Conjugate Addition Route to Enantiopure γ-Butyrolactams and γ-Lactones from a C2-Symmetric Precursor. Eur. J. Org. Chem. 2011, 1721–1727. DOI
(55)Reznichenko, A.; Emge, T.; Audörsch, S.; Klauber, E.; Hultzsch, K.; Schmidt, B.  Group 5 Metal Binaphtholate Complexes for Catalytic Asymmetric Hydroaminoalkylation and Hydroamination/Cyclization. Organometallics 201130 , 921–924. DOI


(54)Krehl, S.; Geißler, D.; Hauke S.; Kunz, O.; Staude, L.; Schmidt, B. The catalytic performance of Ru-NHC alkylidene complexes: PCy3 versus pyridine as the dissociating ligand. Beilstein J. Org. Chem. 2010, 6, 1188–1198. DOI
(53)Schmidt, B.; Hölter, F.; Berger, R. Mizoroki-Heck Reactions with 4-Phenoldiazonium Salts. Adv. Synth. Catal. 2010, 352, 2463–2473. DOI

(one of the most accessed articles in 2011)
(52) Schmidt, B.; Werner, F.; Kelling, A.; Schilde, U. The reaction of 3,4-dihydro-2H-pyran with oxalyl chloride: formation and crystal structure analysis of an unexpected bicyclic product. J. Heterocyclic Chem. 2010, 47, 1171–1175. DOI
(51) Schmidt, B.; Kunz, O.; Biernat, A. Total Synthesis of (–)-Cleistenolide. J. Org. Chem. 2010, 75, 2389–2394. DOI

(one of the most downloaded articles in 2010)
(50) Schmidt, B.; Geißler, D. Ring-Closing Metathesis of Acrylates: A Comparative Study. ChemCatChem 2010, 2, 423–429. DOI
(49) Schmidt, B.; Berger, R.; Hölter, F. Functionalized alkoxy arene diazonium salts from paracetamol. Org. Biomol. Chem. 2010, 8, 1406–1414. DOI


(48)Schmidt, B.; Berger, R.; Hölter, F.; Böge, N.; Kreipl, A. Process for production and applications of phenolic diazonium salts. Eur. Patent Appl. EP09158489, 2009.
(47) Schmidt, B.; Staude, L. Ring-Size-Selective Enyne Metathesis as a Tool for Desymmetrization of an Enantiopure C2-Symmetric Building Block. J. Org. Chem. 2009, 74, 9237–9240. DOI
(46) Schmidt, B.; Hölter, F. A stereodivergent synthesis of all stereoisomers of centrolobine: control of selectivity by a protecting group manipulation. Chem. Eur. J. 2009, 15, 11948–11953. DOI


(45) Schmidt, B.; Biernat A. Synthesis of 3-Deoxy Glycals via Tandem Metathesis Sequences and Their Use in an Intermolecular Heck Arylation. Eur. J. Org. Chem. 2008, 5764–5769. DOI
(44) Schmidt, B.; Hölter, F. Process for preparing aromatic diazonium salts from aromatic amides. WO 2008055927, 2008.
(43) Schmidt, B.; Biernat, A. The Tandem Ring-Closing Metathesis-Isomerization Approach to 6-Deoxyglycals. Chem. Eur. J. 2008, 14, 6135–6141. DOI
(42) Schmidt, B; Biernat, A. Tandem RCM-isomerization approach to glycals of desoxyheptoses from a common precursor. Org. Lett. 2008, 10, 105108. DOI


(41)     Schmidt, B.; Biernat, A. Synthesis of enantiomerically pure dihydrofurans and dihydropyrans from common precursors using RCM and Tandem RCM-isomerization. Synlett  2007, 2375–2378. DOI
Schmidt, B.; Nave, S. Synthesis of Dihydrofurans and Dihydropyrans with Unsaturated Side Chains Based on Ring Size-Selective Ring-Closing Metathesis. Adv. Synth. Catal. 2007, 349, 215–230. (Special issue on olefin metathesis, Fürstner, A.; Grubbs R. H.; Schrock, R. R., eds.) DOI


(39) Schmidt, B.; Staude, L. Unexpected hydrogen transfer in the course of olefin metathesis-isomerization based syntheses of chiral 2,3-dihydropyrans. J. Organomet. Chem. 2006, 690, 5218–5221. DOI

Schmidt, B.; Nave, S. Stereoselective syntheses of enantiomerically pure 2,5-disubstituted dihydropyrans based on olefin metathesis. J. Org. Chem. 2006, 71, 7364–7369. DOI

(37) Schmidt, B.; Nave, S. Control of Ring Size Selectivity by Substrate directable RCM. Chem. Commun. 2006, 2489-2491. highlighted in: Nachr. Chemie 2006, 54, 1184. DOI
(36) Schmidt, B.; Hermanns, J. Ring closing metathesis of substrates containing more than two C-C-double bonds: rapid access to functionalized heterocycles. Curr. Org. Chem. 2006, 10, 13631396 (Review). DOI
(35) Schmidt, B. Olefin metathesis and isomerization: From undesired side reactions to useful synthetic methodology. J. Mol. Catal. A 2006, 254, 5357. DOI
(34) Schmidt, B. Connecting catalytic cycles by organometallic transformations in situ: Novel perspectives in the olefin metathesis field. Pure Appl. Chem. 2006, 78, 469–476. DOI
(33) Schmidt, B.; Nave S. Palladium-Catalyzed O-Allylation of α-Hydroxy Carbonyl Compounds. Adv. Synth. Catal. 2006, 348, 531–537. DOI

bis 2005

(32) Schmidt, B.; Pohler, M. Ruthenium-catalyzed tandem ring closing metathesis (RCM)-atom transfer radical cyclization (ATRC) sequences. J. Organomet. Chem. 2005, 690, 5552–5555. highlighted in: Nachr. Chemie 2006, 54, 98. DOI
(31) Schmidt, B. Ruthenium-Catalyzed Olefin Metathesis Double-Bond Isomerization Sequence. J. Org. Chem. 2004, 69, 7672–7687. DOI
(30) Schmidt, B.; Hermanns J. Olefin Metathesis directed toward Organic Synthesis: Principles and Applications. Top. Organomet. Chem. 2004, 13, 223–267 (Invited review). DOI
(29) Schmidt, B. Tandem Isomerization/Claisen Rearrangement of Diallyl- and Allylhomoallylethers: In Situ Conversion of Grubbs’ catalyst to a Ru-H Species. Synlett  2004, 1541–1544. DOI
(28) Schmidt B. In situ conversion of a Ru metathesis catalyst to an isomerization catalyst. Chem. Commun. 2004, 742-743. highlighted  in: Green Chemistry 2004, 6, G58. DOI
(27) Schmidt, B. Catalysis at the interface of ruthenium-carbene and ruthenium-hydride chemistry: organometallic aspects and applications to organic synthesis. Eur. J. Org. Chem. 2004, 1865–1881 (Review). DOI
(26) Schmidt, B.; Pohler, M.; Costisella, B. Ring closing olefin metathesis and radical cyclization as competing pathways. J. Org. Chem. 2004, 69, 1421–1424. DOI
(25) Schmidt, B. Rutheniumkatalysierte Cyclisierungen: mehr als "nur" Olefinmetathese! Angew. Chem. 2003, 115, 5146-5149; Ruthenium-catalysed cyclizations: More than just olefin metathesis! Angew. Chem. Int. Ed. 2003, 42, 4996–4999. ("Highlight") DOI
(24) Schmidt, B; Pohler, M. Tandem olefin metathesis-hydrogenation at ambient temperature: Activation of Ruthenium carbene complexes by addition of hydrides. Org. Biomol. Chem. 2003, 1, 2512–2517. DOI
(23) Schmidt, B. Heck arylation of cyclic enol ethers with aryldiazonium salts: Regio- and stereoselective synthesis of arylated oxacycles. Chem. Commun. 2003, 1656–1657. DOI


Schmidt, B. An olefin metathesis/double bond isomerization sequence catalyzed by in situ generated ruthenium–hydride species. Eur. J. Org. Chem. 2003, 816–819. DOI


Wildemann, H.; Dünkelmann, P.; Müller, M.; Schmidt, B. A short olefin metathesis- based route to enantiomerically pure arylated dihydropyrans and a,b-unsaturated d- valero lactones. J. Org. Chem. 2003, 68, 799–804. DOI

(20)Schmidt, B.; Pohler, M.; Costisella, B.; Di- and tetrahydropyrans with orthogonally protected hydroxymethyl side chains. A synthetic route and the structure elucidation of an unexpected acetal cleavage product. Tetrahedron 2002, 58, 7951–7958. DOI


Schmidt, B.; Wildemann, H. Synthesis of enantiomerically pure divinyl- and diallylcarbinols. J. Chem. Soc.-Perkin Trans. 1 2002, 1050–1060. DOI


Schmidt, B.; Costisella, B.; Roggenbuck, R.; Westhus, M.; Wildemann, H.; Eilbracht, P. Combining ring-closing metathesis and hydroformylation strategies: A novel approach to spirocyclic g-butyrolactones. J. Org. Chem. 2001, 66, 7658–7665. DOI


Schmidt, B. A de novo synthesis of 2,6-dideoxy-C-aryl glycosides based on ring closing metathesis and diastereoselective epoxide cleavage/anomerization reactions. Org. Lett. 2000, 2, 791–794. DOI


Schmidt, B.; Westhus, M. Diastereoselectivity in a ring closing metathesis reaction with a remote stereogenic centre leading to quaternary dihydropyrans. Tetrahedron 2000, 56, 2421–2426. DOI


Schmidt, B.; Wildemann, H. Single and double ring closing metathesis in the formation of dihydropyrans and bisoxacyclic systems with a quaternary centre. J. Chem. Soc.-Perkin Trans. 1 2000, 2916–2925. DOI


Schmidt, B.; Wildemann, H. Diastereoselective ring-closing metathesis in the synthesis of dihydropyrans. J. Org. Chem. 2000, 65, 5817–5822. DOI


Schmidt, B.; Wildemann, H. A synthesis of densely functionalized 2,3-dihydropyrans using ring-closing metathesis and base-induced rearrangements of dihydropyran oxides. Eur. J. Org. Chem. 2000, 3145–3163. DOI


Schmidt, B. Base-induced rearrangement of dihydropyran oxides: A novel synthesis of cyclic enol ethers with a hydroxy-function in the allylic position. Tetrahedron Lett. 1999, 40, 4319–4320. DOI


Schmidt, B. Epoxide opening reactions of aryl substituted dihydropyran oxides: regio- and stereochemical studies directed towards deoxy-aryl-C-glycosides. J. Chem. Soc.-Perkin Trans. 1 1999, 2627–2637. DOI


Schmidt, B.; Wildemann, H. Synthesis of functionalized 2,3- and 3,4-dihydropyrans starting from a-hydroxycarboxylic esters via RCM. Synlett 1999, 1591–1593. DOI


Hermanns, J.; Schmidt, B. Five- and six-membered silicon-carbon heterocycles. Part 2. Synthetic modifications and applications of silacycles. J. Chem. Soc.-Perkin Trans. 1 1999, 81–102 (Review). DOI


Kocienski, P. J.; Brown, R. C. D.; Pommier, A.; Procter, M.; Schmidt, B. Synthesis of Salinomycin. J. Chem. Soc.-Perkin Trans. 1 1998, 9–39. DOI


Hermanns, J.; Schmidt, B. Five- and six-membered silicon-carbon heterocycles. Part 1. Synthetic methods for the construction of silacycles. J. Chem. Soc.-Perkin Trans. 1 1998, 2209–2230 (Review). DOI


Schmidt, B.; Sattelkau, T. Ring closing metathesis as the key step in the synthesis of furan-substituted C-aryl glycosides. Tetrahedron 1997, 53, 12991–13000. DOI


Herberich, G. E.; Schmidt, B.; Schmitz, A.; Fischer, A.; Riedel, M.; Herrmann, H.-F.; Özdemir, D. Preparation of transition metal compounds with boratabenzene ligands as olefin polymerization catalysts. (Hoechst AG), GE 19, 624,466, 1996; Chem. Abstr. 1997, 127, P136151y.


Herberich, G. E.; Rosenplänter, J.; Schmidt, B.; Englert, U. Borabenzene derivatives .24. From lithium 1-methylboratabenzene to 2-mono- and 2,2-disubstituted 1-methyl- 1,2-dihydroborinines with Me3Si, Me3Ge, Me3Sn, and Me3Pb substituents. Degenerate sigmatropic rearrangements with exceptionally low barriers and the structure of 2-(Me3Sn)C5H5BMe. Organometallics 1997, 16, 926–931. DOI


Schmidt, B.; Kocienski, P.; Reid, G. A synthesis of oxolenes and furans via oxacyclopentylidene chromium and molybdenum complexes. Tetrahedron 1996, 52, 1617–1630. DOI


Herberich, G. E.; Schmidt, B.; Englert, U. Borabenzene Derivatives .22. Synthesis of Boratabenzene Salts from 2,4-Pentadienylboranes - Structure of [NMe3Ph][C5H5BMe]. Organometallics 1995, 14, 471–480. DOI


Herberich, G. E.; Schmidt, B.; Englert, U.; Wagner, T. Borabenzene Derivatives .21. 2,4-Pentadienylboranes as Key Intermediates of a Novel Route to Boracyclohexadienes and Boratabenzenes - Structure of [Li(Tmpda)](C5H5BNMe2). Organometallics 1993, 12, 2891–2893. DOI