| Year |
Citation |
Score |
| 2024 |
Sarkar R, Korell A, Schneider C. Organocatalytic enantioselective oxa-Piancatelli rearrangement. Chemical Communications (Cambridge, England). 60: 3063-3066. PMID 38385217 DOI: 10.1039/d4cc00708e |
0.434 |
|
| 2023 |
Dorsch C, Schneider C. Brønsted Acid Catalyzed Asymmetric Synthesis of cis-Tetrahydrocannabinoids*. Angewandte Chemie (International Ed. in English). e202302475. PMID 37057742 DOI: 10.1002/anie.202302475 |
0.376 |
|
| 2023 |
Gärtner CV, Schneider C. Enantioselective 1,6-Addition of β-Ketoester Enolates to Generated -Quinone Methides Enabled by Cooperative Palladium and Brønsted Acid Catalysis. Organic Letters. 25: 416-420. PMID 36625600 DOI: 10.1021/acs.orglett.2c04127 |
0.383 |
|
| 2022 |
Sarkar R, Kallweit I, Schneider C. Enantioselective [6 + 2]-Cycloaddition of Transient 3-Methide-3-pyrroles with 2-Vinylindoles under Chiral Brønsted Acid Catalysis. Organic Letters. 24: 6433-6437. PMID 36040102 DOI: 10.1021/acs.orglett.2c02548 |
0.493 |
|
| 2022 |
Gärtner CV, Schneider C. Enantioselective Annulation of α,β-Unsaturated -Acyliminium Ions with β-Keto Ester Enolates via Cooperative Palladium and Brønsted Acid Catalysis. Organic Letters. 24: 3560-3564. PMID 35544381 DOI: 10.1021/acs.orglett.2c01265 |
0.338 |
|
| 2022 |
Loui HJ, Schneider C. Cooperative Palladium/Brønsted Acid Catalysis toward the Highly Enantioselective Allenylation of β-Keto Esters. Organic Letters. 24: 1496-1501. PMID 35171616 DOI: 10.1021/acs.orglett.2c00179 |
0.33 |
|
| 2021 |
Sachse F, Schneider C. Cooperative Photoinduced/Brønsted Acid Catalyzed Cycloaddition of Transient Thioaldehydes and -Quinone Methides toward a Synthesis of Benzo[][1,3]oxathiines. Organic Letters. PMID 33733788 DOI: 10.1021/acs.orglett.1c00588 |
0.365 |
|
| 2021 |
Loui HJ, Suneja A, Schneider C. Cooperative Rh/Chiral Phosphoric Acid Catalysis toward the Highly Stereoselective (3 + 3)-Cycloannulation of Carbonyl Ylides and Indolyl-2-methides. Organic Letters. PMID 33721497 DOI: 10.1021/acs.orglett.1c00489 |
0.451 |
|
| 2020 |
Kallweit I, Laue M, Schneider C. Brønsted-Acid-Catalyzed (3+2)-Cycloannulation of In-Situ-Generated 3-Methide-3-pyrroles: Asymmetric Synthesis of Cyclopenta[]pyrroles. Organic Letters. PMID 33175541 DOI: 10.1021/acs.orglett.0c03452 |
0.447 |
|
| 2020 |
Tripathy M, Schneider C. Short Synthesis of Alkaloid (-)-205B. The Journal of Organic Chemistry. PMID 32880454 DOI: 10.1021/Acs.Joc.0C01885 |
0.511 |
|
| 2020 |
Göricke F, Haseloff S, Laue M, Schneider M, Brumme T, Schneider C. Phosphoric Acid-Catalyzed Formation of Hydrogen-Bonded ortho-Quinone Methides. Enantioselective Cycloaddition with β-Dicarbonyl Compounds toward Benzannulated Oxygen Heterocycles. The Journal of Organic Chemistry. PMID 32786622 DOI: 10.1021/Acs.Joc.0C01375 |
0.532 |
|
| 2020 |
Göricke F, Schneider C. Palladium-Catalyzed, Enantioselective (3 + 2)-Cycloannulation of β-Keto Esters with Alkylidene 2-Indoles toward Complex Indole-Based Heterocycles. Organic Letters. PMID 32677434 DOI: 10.1021/Acs.Orglett.0C02166 |
0.485 |
|
| 2020 |
Mayer M, Pahl M, Spanka M, Grellmann M, Sickert M, Schneider C, Asmis KR, Belder D. Unravelling the configuration of transient ortho-quinone methides by combining microfluidics with gas phase vibrational spectroscopy. Physical Chemistry Chemical Physics : Pccp. PMID 32051997 DOI: 10.1039/C9Cp06435D |
0.338 |
|
| 2020 |
Schneider C, Suneja A, Loui HJ. Cooperative Catalysis for the Highly Diastereo- and Enantioselective [4+3]-Cycloannulation of ortho-Quinone Methides and Carbonyl Ylides. Angewandte Chemie (International Ed. in English). PMID 31895488 DOI: 10.1002/Anie.201913603 |
0.526 |
|
| 2019 |
Ukis R, Schneider C. Brønsted Acid-Catalyzed, Diastereo- and Enantioselective, Intramolecular Oxa-Diels-Alder Reaction of ortho-Quinone Methides and Unactivated Dienophiles. The Journal of Organic Chemistry. PMID 31117571 DOI: 10.1021/Acs.Joc.9B00860 |
0.516 |
|
| 2019 |
Schlegel M, Schneider C. Iron(III)-Catalyzed (4 + 2)-Cycloannulation of 2-Hydroxy Ketoxime Ethers with Indol-2-ylamides: Synthesis of Indole-Fused 2-Piperidinones. The Journal of Organic Chemistry. PMID 30917274 DOI: 10.1021/Acs.Joc.9B00261 |
0.478 |
|
| 2019 |
Kallweit I, Schneider C. Brønsted Acid Catalyzed [6 + 2]-Cycloaddition of 2-Vinylindoles with in Situ Generated 2-Methide-2 H-pyrroles: Direct, Catalytic, and Enantioselective Synthesis of 2,3-Dihydro-1 H-pyrrolizines. Organic Letters. PMID 30620204 DOI: 10.1021/Acs.Orglett.8B03833 |
0.516 |
|
| 2019 |
Hoffmeyer P, Schneider C. Continuous Flow Synthesis of Highly Substituted Tetrahydrofurans European Journal of Organic Chemistry. 2019: 5326-5333. DOI: 10.1002/Ejoc.201900421 |
0.356 |
|
| 2018 |
Hoffmeyer P, Schneider C. Stereoselective Synthesis of 2,3,5-Trisubstituted Tetrahydrofurans Initiated by a Ti-BINOLate-Catalyzed Vinylogous Aldol Reaction. The Journal of Organic Chemistry. PMID 30575382 DOI: 10.1021/Acs.Joc.8B02828 |
0.572 |
|
| 2018 |
Suneja A, Schneider C. Phosphoric Acid Catalyzed [4 + 1]-Cycloannulation Reaction of ortho-Quinone Methides and Diazoketones: Catalytic, Enantioselective Access toward cis-2,3-Dihydrobenzofurans. Organic Letters. PMID 30407018 DOI: 10.1021/Acs.Orglett.8B03311 |
0.529 |
|
| 2018 |
Schneider C, Göricke F. Palladium-Catalyzed Enantioselective Addition of Chiral Metal Enolates to In Situ Generated Ortho-Quinone Methides. Angewandte Chemie (International Ed. in English). PMID 30278112 DOI: 10.1002/Anie.201809692 |
0.51 |
|
| 2018 |
Schneider C, Hodik T. A Highly Enantio- and Diastereoselective Synthesis of Spirocyclic Dihydroquinolones via Domino Michael Addition-Lactamization of ortho-Quinone Methide Imines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30246893 DOI: 10.1002/Chem.201803886 |
0.554 |
|
| 2018 |
Schlegel M, Schneider C. Lewis acid-catalyzed Friedel-Crafts reactions toward highly versatile, α-quaternary oxime ethers. Chemical Communications (Cambridge, England). PMID 30221283 DOI: 10.1039/C8Cc06823B |
0.562 |
|
| 2018 |
Spanka M, Schneider C. Phosphoric Acid Catalyzed Aldehyde Addition to in Situ Generated o-Quinone Methides: An Enantio- and Diastereoselective Entry toward cis-3,4-Diaryl Dihydrocoumarins. Organic Letters. PMID 30074397 DOI: 10.1021/Acs.Orglett.8B01865 |
0.489 |
|
| 2018 |
Schneider C, Schlegel M, Coburger P. A Novel Sc(OTf)3-Catalyzed (2+2+1)-Cycloannulation/Aza-Friedel-Crafts Alkylation Sequence toward Multicyclic 2-Pyrrolines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29939442 DOI: 10.1002/Chem.201802478 |
0.506 |
|
| 2018 |
Schlegel M, Schneider C. Rapid Construction of Complex 2-Pyrrolines through Lewis Acid-Catalyzed, Sequential Three-Component Reactions via in Situ-Generated 1-Azaallyl Cations. Organic Letters. PMID 29741908 DOI: 10.1021/Acs.Orglett.8B01205 |
0.519 |
|
| 2018 |
Schneider C, Kretzschmar M, Hofmann F, Moock D. Intramolekulare Aza-Diels-Alder-Reaktionen von ortho-Chinonmethidiminen - ein schneller, katalytischer und enantioselektiver Aufbau benzoanellierter Chinolizidine. Angewandte Chemie (International Ed. in English). PMID 29488296 DOI: 10.1002/Anie.201800787 |
0.343 |
|
| 2018 |
Braunschweig H, Damme A, Dück K, Krummenacher I, Paprocki V, Radacki K, Ramler J, Schiller C, Schneider C. Boryl- and Silyl-Substituted Mixed Sandwich Compounds of Scandium. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29363206 DOI: 10.1002/Chem.201704908 |
0.4 |
|
| 2018 |
Appun J, Stolz F, Naumov S, Abel B, Schneider C. Modular Synthesis of Dipyrroloquinolines - A Combined Synthetic and Mechanistic Study. The Journal of Organic Chemistry. PMID 29355317 DOI: 10.1021/Acs.Joc.7B02466 |
0.532 |
|
| 2018 |
Braunschweig H, Brunecker C, Dewhurst RD, Schneider C. Does Lewis basicity correlate with catalytic performance in zerovalent group 8 complexes? Zeitschrift FüR Naturforschung B. 73: 149-153. DOI: 10.1515/Znb-2017-0193 |
0.341 |
|
| 2017 |
Stolz F, Appun J, Naumov S, Schneider C, Abel B. A Complex Catalytic Reaction Caught in the Act: Intermediates and Products Sampling Online by Liquid μ-Beam Mass Spectrometry and Theoretical Modeling. Chempluschem. 82: 233-240. PMID 31961544 DOI: 10.1002/Cplu.201600347 |
0.472 |
|
| 2017 |
Pfeiffer SA, Rudisch BM, Glaeser P, Spanka M, Nitschke F, Robitzki AA, Schneider C, Nagl S, Belder D. Continuous purification of reaction products by micro free-flow electrophoresis enabled by large area deep-UV fluorescence imaging. Analytical and Bioanalytical Chemistry. PMID 29085988 DOI: 10.1007/S00216-017-0697-8 |
0.343 |
|
| 2017 |
Gebauer K, Reuß F, Spanka M, Schneider C. Relay Catalysis: Manganese(III) Phosphate Catalyzed Asymmetric Addition of β-Dicarbonyls to ortho-Quinone Methides Generated by Catalytic Aerobic Oxidation. Organic Letters. PMID 28809505 DOI: 10.1021/Acs.Orglett.7B02185 |
0.492 |
|
| 2017 |
Schlegel M, Schneider C. Lewis Acid-Catalyzed Nucleophilic Addition of Indoles to in situ Generated 2-Amidoallyl Cations. The Journal of Organic Chemistry. PMID 28499088 DOI: 10.1021/Acs.Joc.7B00791 |
0.478 |
|
| 2017 |
Schulze S, Pahl M, Stolz F, Appun J, Abel B, Schneider C, Belder D. Liquid beam desorption mass spectrometry for the investigation of continuous flow reactions in microfluidic chips. Analytical Chemistry. PMID 28489359 DOI: 10.1021/Acs.Analchem.7B01026 |
0.302 |
|
| 2017 |
Appun J, Boomhoff M, Hoffmeyer P, Kallweit I, Pahl M, Belder D, Schneider C. A Highly Stereoselective Synthesis of Tetrahydrofurans. Angewandte Chemie (International Ed. in English). PMID 28485546 DOI: 10.1002/Anie.201700774 |
0.552 |
|
| 2017 |
Hodík T, Schneider C. Brønsted acid-catalyzed, enantioselective synthesis of 1,4-dihydroquinoline-3-carboxylates via in situ generated ortho-quinone methide imines. Organic & Biomolecular Chemistry. PMID 28402372 DOI: 10.1039/C7Ob00488E |
0.58 |
|
| 2017 |
Weilbeer C, Sickert M, Naumov S, Schneider C. Frontispiece: The Brønsted Acid-Catalyzed, Enantioselective Aza-Diels-Alder Reaction for the Direct Synthesis of Chiral Piperidones Chemistry - a European Journal. 23. DOI: 10.1002/Chem.201780362 |
0.568 |
|
| 2016 |
Braunschweig H, Krummenacher I, Lichtenberg C, Mattock JD, Schäfer M, Schmidt U, Schneider C, Steffenhagen T, Ullrich S, Vargas A. Dibora[2]ferrocenophane: A Carbene-Stabilized Diborene in a Strained cis-Configuration. Angewandte Chemie (International Ed. in English). PMID 27995698 DOI: 10.1002/Anie.201609601 |
0.326 |
|
| 2016 |
Nikolaev VA, Medvedev JJ, Galkina OS, Azarova KV, Schneider C. Unusual reactions of diazocarbonyl compounds with α,β-unsaturated δ-amino esters: Rh(II)-catalyzed Wolff rearrangement and oxidative cleavage of N-H-insertion products. Beilstein Journal of Organic Chemistry. 12: 1904-1910. PMID 27829897 DOI: 10.3762/Bjoc.12.180 |
0.468 |
|
| 2016 |
Bera K, Schneider C. Brønsted Acid Catalyzed [3 + 2]-Cycloaddition of Cyclic Enamides with in Situ Generated 2-Methide-2H-indoles: Enantioselective Synthesis of Indolo[1,2-a]indoles. Organic Letters. PMID 27782406 DOI: 10.1021/Acs.Orglett.6B02898 |
0.779 |
|
| 2016 |
Weilbeer C, Sickert M, Naumov S, Schneider C. The Brønsted Acid-Catalyzed, Enantioselective Aza-Diels-Alder Reaction for the Direct Synthesis of Chiral Piperidones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27748978 DOI: 10.1002/Chem.201604356 |
0.586 |
|
| 2016 |
Gebauer K, Schneider C. The First Organocatalytic Cope Rearrangement. Angewandte Chemie (International Ed. in English). PMID 27717104 DOI: 10.1002/Anie.201608508 |
0.367 |
|
| 2016 |
Arrowsmith M, Böhnke J, Braunschweig H, Celik MA, Claes C, Ewing WC, Krummenacher I, Lubitz K, Schneider C. Neutral Diboron Analogues of Archetypal Aromatic Species by Spontaneous Cycloaddition. Angewandte Chemie (International Ed. in English). PMID 27374193 DOI: 10.1002/Anie.201602384 |
0.478 |
|
| 2016 |
Kretzschmar M, Hodík T, Schneider C. Brønsted Acid Catalyzed Addition of Enamides to ortho-Quinone Methide Imines-An Efficient and Highly Enantioselective Synthesis of Chiral Tetrahydroacridines. Angewandte Chemie (International Ed. in English). PMID 27356207 DOI: 10.1002/Anie.201604201 |
0.556 |
|
| 2016 |
Braunschweig H, Constantinidis P, Dellermann T, Ewing WC, Fischer I, Hess M, Knight FR, Rempel A, Schneider C, Ullrich S, Vargas A, Woollins JD. Highly Strained Heterocycles Constructed from Boron-Boron Multiple Bonds and Heavy Chalcogens. Angewandte Chemie (International Ed. in English). PMID 27027522 DOI: 10.1002/Anie.201601691 |
0.395 |
|
| 2016 |
Schneider C, Bera K. Brønsted Acid Catalyzed [3+2]-Cycloaddition of 2-Vinylindoles with In Situ Generated 2-Methide-2H-indoles - Highly Enantioselective Synthesis of Pyrrolo[1,2-a]indoles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26991961 DOI: 10.1002/Chem.201601020 |
0.773 |
|
| 2016 |
Alamsetti SK, Spanka M, Schneider C. Synergistic Rhodium/Phosphoric Acid Catalysis for the Enantioselective Addition of Oxonium Ylides to ortho-Quinone Methides. Angewandte Chemie (International Ed. in English). 55: 2392-6. PMID 26762542 DOI: 10.1002/Anie.201509247 |
0.504 |
|
| 2016 |
Bissert R, Braunschweig H, Dewhurst RD, Schneider C. Metal-Only Lewis Pairs Based on Zerovalent Osmium Organometallics. 35: 2567-2573. DOI: 10.1021/Acs.Organomet.6B00495 |
0.358 |
|
| 2016 |
Stolz F, Appun J, Naumov S, Schneider C, Abel B. Back Cover: A Complex Catalytic Reaction Caught in the Act: Intermediates and Products Sampling Online by Liquid μ-Beam Mass Spectrometry and Theoretical Modeling (ChemPlusChem 2/2017) Chempluschem. 82: 334-334. DOI: 10.1002/Cplu.201600600 |
0.343 |
|
| 2016 |
Arrowsmith M, Böhnke J, Braunschweig H, Celik MA, Claes C, Ewing WC, Krummenacher I, Lubitz K, Schneider C. Neutrale Dibor-Analoga von archetypischen aromatischen Verbindungen durch spontane Cycloaddition Angewandte Chemie. 128: 11441-11445. DOI: 10.1002/Ange.201602384 |
0.307 |
|
| 2015 |
Braunschweig H, Damme A, Dück K, Fuß M, Hörl C, Kramer T, Krummenacher I, Kupfer T, Paprocki V, Schneider C. Ansa-Complexes of [Mn(η(5) -C5 H5 )(η(6) -C6 H6 )]: Preparation, Characterization, and Reactivity of [n]Manganoarenophanes (n=1, 2, 3). Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 14797-803. PMID 26387512 DOI: 10.1002/Chem.201502161 |
0.315 |
|
| 2015 |
Bissinger P, Braunschweig H, Celik MA, Claes C, Dewhurst RD, Endres S, Kelch H, Kramer T, Krummenacher I, Schneider C. Synthesis of cyclic diborenes with unprecedented cis-configuration. Chemical Communications (Cambridge, England). 51: 15917-20. PMID 26360103 DOI: 10.1039/C5Cc07103H |
0.355 |
|
| 2015 |
Nareddy PR, Schneider C. A highly enantioselective, organocatalytic [3+2]-cycloannulation reaction towards the de novo-synthesis of 1-cyclopentenyl-α-keto esters. Chemical Communications (Cambridge, England). 51: 14797-800. PMID 26300444 DOI: 10.1039/C5Cc05967D |
0.505 |
|
| 2015 |
Boomhoff M, Ukis R, Schneider C. A Highly Stereocontrolled, One-Pot Approach toward Pyrrolobenzoxazinones and Pyrroloquinazolinones through a Lewis Acid-Catalyzed [3 + 2]-Cycloannulation Process. The Journal of Organic Chemistry. 80: 8236-44. PMID 26241849 DOI: 10.1021/Acs.Joc.5B01293 |
0.481 |
|
| 2015 |
Medvedev JJ, Meleshina MV, Panikorovskii TL, Schneider C, Nikolaev VA. Domino reactions of diazodicarbonyl compounds with α,β-unsaturated δ-amino esters: a convenient way towards 2-oxopiperidines, dihydropyridinones and isoquinolinediones. Organic and Biomolecular Chemistry. 13: 9107-9117. PMID 26222918 DOI: 10.1039/C5Ob01197C |
0.481 |
|
| 2015 |
Braunschweig H, Dellermann T, Ewing WC, Kramer T, Schneider C, Ullrich S. Reductive Insertion of Elemental Chalcogens into Boron-Boron Multiple Bonds. Angewandte Chemie (International Ed. in English). 54: 10271-5. PMID 26118498 DOI: 10.1002/Anie.201503398 |
0.316 |
|
| 2015 |
Saha S, Schneider C. Directing group assisted nucleophilic substitution of propargylic alcohols via o-quinone methide intermediates: Brønsted acid catalyzed, highly enantio- and diastereoselective synthesis of 7-alkynyl-12a-acetamido-substituted benzoxanthenes. Organic Letters. 17: 648-51. PMID 25611975 DOI: 10.1021/Ol503662G |
0.503 |
|
| 2015 |
Medvedev JJ, Galkina OS, Klinkova AA, Giera DS, Hennig L, Schneider C, Nikolaev VA. Domino [4 + 1]-annulation of α,β-unsaturated δ-amino esters with Rh(II)–carbenoids – a new approach towards multi-functionalized N-aryl pyrrolidines Organic and Biomolecular Chemistry. 13: 2640-2651. PMID 25582707 DOI: 10.1039/C4Ob02454K |
0.442 |
|
| 2015 |
Saha S, Alamsetti SK, Schneider C. Chiral Brønsted acid-catalyzed Friedel-Crafts alkylation of electron-rich arenes with in situ-generated ortho-quinone methides: highly enantioselective synthesis of diarylindolylmethanes and triarylmethanes. Chemical Communications (Cambridge, England). 51: 1461-4. PMID 25493449 DOI: 10.1039/C4Cc08559K |
0.513 |
|
| 2015 |
Saha S, Schneider C. Brønsted acid-catalyzed, highly enantioselective addition of enamides to in situ-generated ortho-quinone methides: a domino approach to complex acetamidotetrahydroxanthenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 2348-52. PMID 25488376 DOI: 10.1002/Chem.201406044 |
0.504 |
|
| 2015 |
Lindemann C, Schneider C. Quinolizidine-Based Alkaloids: A General Catalytic, Highly Enantio- and Diastereoselective Synthetic Approach Synthesis (Germany). DOI: 10.1055/S-0035-1561289 |
0.556 |
|
| 2014 |
Boomhoff M, Yadav AK, Appun J, Schneider C. Modular, flexible, and stereoselective synthesis of pyrroloquinolines: rapid assembly of complex heterocyclic scaffolds. Organic Letters. 16: 6236-9. PMID 25415061 DOI: 10.1021/Ol503167H |
0.465 |
|
| 2014 |
Henry L, Schneider C, Mützel B, Simpson PV, Nagel C, Fucke K, Schatzschneider U. Amino acid bioconjugation via iClick reaction of an oxanorbornadiene-masked alkyne with a Mn(I)(bpy)(CO)3-coordinated azide. Chemical Communications (Cambridge, England). 50: 15692-5. PMID 25370120 DOI: 10.1039/C4Cc07892F |
0.447 |
|
| 2014 |
Pischl MC, Weise CF, Haseloff S, Müller MA, Pfaltz A, Schneider C. A highly stereoselective and flexible strategy for the convergent synthesis of long-chain polydeoxypropionates: application towards the synthesis of the glycolipid membrane components hydroxyphthioceranic and phthioceranic acid. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 17360-74. PMID 25351748 DOI: 10.1002/Chem.201404034 |
0.465 |
|
| 2014 |
El-Sepelgy O, Haseloff S, Alamsetti SK, Schneider C. Brønsted acid catalyzed, conjugate addition of β-dicarbonyls to in situ generated ortho-quinone methides--enantioselective synthesis of 4-aryl-4H-chromenes. Angewandte Chemie (International Ed. in English). 53: 7923-7. PMID 24938645 DOI: 10.1002/Anie.201403573 |
0.788 |
|
| 2014 |
Schneider C, Abels F. Catalytic, enantioselective vinylogous Michael reactions. Organic & Biomolecular Chemistry. 12: 3531-43. PMID 24760480 DOI: 10.1039/C4Ob00332B |
0.487 |
|
| 2014 |
Abels F, Lindemann C, Schneider C. A general strategy for the catalytic, highly enantio- and diastereoselective synthesis of indolizidine-based alkaloids Chemistry - a European Journal. 20: 1964-1979. PMID 24436076 DOI: 10.1002/Chem.201304086 |
0.538 |
|
| 2014 |
Basu S, Gupta V, Nickel J, Schneider C. Organocatalytic enantioselective vinylogous Michael reaction of vinylketene silyl-N,O-acetals. Organic Letters. 16: 274-7. PMID 24341388 DOI: 10.1021/Ol403275K |
0.772 |
|
| 2014 |
El-Sepelgy O, Haseloff S, Alamsetti SK, Schneider C. Brønsted-Säure-katalysierte konjugierte Addition von β-Dicarbonylverbindungen an in situ erzeugteortho-Chinomethide - enantioselektive Synthese von 4-Aryl-4H-chromenen Angewandte Chemie. 126: 8057-8061. DOI: 10.1002/Ange.201403573 |
0.736 |
|
| 2013 |
Pischl MC, Weise CF, Müller MA, Pfaltz A, Schneider C. A convergent and stereoselective synthesis of the glycolipid components phthioceranic acid and hydroxyphthioceranic acid Angewandte Chemie - International Edition. 52: 8968-8972. PMID 23843294 DOI: 10.1002/Anie.201303776 |
0.47 |
|
| 2013 |
Peruncheralathan S, Aurich S, Teller H, Schneider C. The Ti-BINOLate-catalyzed, enantioselective ring-opening of meso-aziridines with amines. Organic & Biomolecular Chemistry. 11: 2787-803. PMID 23515632 DOI: 10.1039/C3Ob40222C |
0.515 |
|
| 2013 |
Pischl MC, Weise CF, Müller M, Pfaltz A, Schneider C. Eine konvergente und stereoselektive Synthese der Glycolipidkomponenten Phthioceransäure und Hydroxyphthioceransäure Angewandte Chemie. 125: 9138-9142. DOI: 10.1002/Ange.201303776 |
0.334 |
|
| 2012 |
Abels F, Lindemann C, Koch E, Schneider C. A general organocatalytic approach toward the enantioselective total synthesis of indolizidine based alkaloids Organic Letters. 14: 5972-5975. PMID 23163802 DOI: 10.1021/Ol302871U |
0.546 |
|
| 2012 |
Gupta V, Sudhir V S, Mandal T, Schneider C. Organocatalytic, highly enantioselective vinylogous Mukaiyama-Michael reaction of acyclic dienol silyl ethers. Angewandte Chemie (International Ed. in English). 51: 12609-12. PMID 23132650 DOI: 10.1002/Anie.201207058 |
0.796 |
|
| 2012 |
Boomhoff M, Schneider C. A novel three-component [3+2] cycloannulation process for the rapid and highly stereoselective synthesis of pyrrolobenzoxazoles. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 4185-9. PMID 22407697 DOI: 10.1002/Chem.201200405 |
0.383 |
|
| 2012 |
Weise CF, Pischl MC, Pfaltz A, Schneider C. A general, asymmetric, and noniterative synthesis of trideoxypropionates. Straightforward syntheses of the pheromones (+)-vittatalactone and (+)-norvittatalactone Journal of Organic Chemistry. 77: 1477-1488. PMID 22188256 DOI: 10.1021/Jo202330B |
0.444 |
|
| 2012 |
Ohla S, Beyreiss R, Fritzsche S, Glaser P, Nagl S, Stockhausen K, Schneider C, Belder D. Monitoring on-chip Pictet-Spengler reactions by integrated analytical separation and label-free time-resolved fluorescence. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 1240-6. PMID 22179940 DOI: 10.1002/Chem.201101768 |
0.432 |
|
| 2012 |
Marti A, Peruncheralathan S, Schneider C. Cationic Late-Transition-MetalComplexes Catalyze the Ring Opening of Aziridines withAmines Synthesis. 44: 27-36. DOI: 10.1055/S-0031-1289611 |
0.331 |
|
| 2012 |
Weise CF, Immel S, Richter F, Schneider C. The oxy-cope rearrangement of aldol products. a combined experimental and theoretical study European Journal of Organic Chemistry. 1520-1529. DOI: 10.1002/Ejoc.201101690 |
0.324 |
|
| 2012 |
Gupta V, Sudhir VS, Mandal T, Schneider C. Organokatalytische, hochenantioselektive vinyloge Mukaiyama‐ Michael‐Reaktion acyclischer Dienolsilylether Angewandte Chemie. 124: 12778-12781. DOI: 10.1002/Ange.201207058 |
0.743 |
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| 2011 |
Weise CF, Pischl M, Pfaltz A, Schneider C. A non-iterative, flexible, and highly stereoselective synthesis of polydeoxypropionates-synthesis of (+)-vittatalactone Chemical Communications. 47: 3248-3250. PMID 21279191 DOI: 10.1039/C0Cc05215A |
0.454 |
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| 2011 |
Abels F, Schneider C. A Modified and Highly UsefulProtocol for the Brønsted Acid Catalyzed, Enantioselective,Vinylogous Mannich Reaction with Aliphatic Aldimines Synthesis. 2011: 4050-4058. DOI: 10.1055/S-0031-1289303 |
0.515 |
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| 2011 |
Marti A, Richter L, Schneider C. Iron-Catalyzed Ring-Openingof meso-Aziridines with Amines Synlett. 2011: 2513-2516. DOI: 10.1055/S-0030-1260338 |
0.322 |
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| 2011 |
Ruff BM, Zhong S, Nieger M, Sickert M, Schneider C, Bräse S. A Combined Vinylogous Mannich/Diels-Alder Approach for the Stereoselective Synthesis of Highly Functionalized Hexahydroindoles European Journal of Organic Chemistry. 2011: 6558-6566. DOI: 10.1002/Ejoc.201100996 |
0.532 |
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| 2010 |
Giera DS, Schneider C. InCl3-catalyzed allylic Friedel-Crafts reactions toward the stereocontrolled synthesis of 1,2,3,4-tetrahydroquinolines. Organic Letters. 12: 4884-7. PMID 20879793 DOI: 10.1021/Ol102023Z |
0.56 |
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| 2010 |
Sickert M, Abels F, Lang M, Sieler J, Birkemeyer C, Schneider C. The Brønsted acid catalyzed, enantioselective vinylogous Mannich reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 2806-18. PMID 20099284 DOI: 10.1002/Chem.200902537 |
0.518 |
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| 2010 |
Ghosh S, Nandakumar MV, Krautscheid H, Schneider C. Copper–bipyridine-catalyzed enantioselective α-amination of β-keto esters Tetrahedron Letters. 51: 1860-1862. DOI: 10.1016/J.Tetlet.2010.02.007 |
0.544 |
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| 2010 |
Schönherr H, Mollitor J, Schneider C. A Chemoenzymatic Approach to the Stereocontrolled Synthesis of the C1-C11 fragment of (+)-Peloruside A European Journal of Organic Chemistry. 2010: 3908-3918. DOI: 10.1002/Ejoc.201000369 |
0.344 |
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| 2010 |
TIETZE LF, SCHNEIDER C, MONTENBRUCK A. ChemInform Abstract: Inter- and Intramolecular Hetero-Diels-Alder Reactions. Part 47. Asymmetric 1,6-Induction in Hetero-Diels-Alder Reactions of Chiral Oxa- butadienes for a De-Novo Synthesis of Enantiomerically Pure Carbohydrates: Lewis Acid Dependent R Cheminform. 25: no-no. DOI: 10.1002/chin.199435048 |
0.592 |
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| 2009 |
Peruncheralathan S, Teller H, Schneider C. Titanium binolate catalyzed aminolysis of meso aziridines: a highly enantioselective and direct access to 1,2-diamines. Angewandte Chemie (International Ed. in English). 48: 4849-52. PMID 19475599 DOI: 10.1002/Anie.200901110 |
0.427 |
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| 2009 |
Schneider C. Catalytic, enantioselective ring opening of aziridines. Angewandte Chemie (International Ed. in English). 48: 2082-4. PMID 19173352 DOI: 10.1002/Anie.200805542 |
0.474 |
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| 2009 |
Schneider C, Giera D, Sickert M. A Straightforward Synthesis of (S)-Anabasine via the Catalytic, Enantioselective Vinylogous Mukaiyama-Mannich Reaction Synthesis. 2009: 3797-3802. DOI: 10.1055/S-0029-1217026 |
0.521 |
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| 2009 |
Nandakumar MV, Ghosh S, Schneider C. Enantioselective Synthesis of a Novel Chiral 2,9-Disubstituted 1,10-Phenanthroline and First Applications in Asymmetric Catalysis European Journal of Organic Chemistry. 2009: 6393-6398. DOI: 10.1002/Ejoc.200901038 |
0.667 |
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| 2009 |
Enkisch C, Schneider C. Sequential Mannich-Aza-Michael Reactions for the Stereodivergent Synthesis of Highly Substituted Pyrrolidines European Journal of Organic Chemistry. 2009: 5549-5564. DOI: 10.1002/Ejoc.200900787 |
0.523 |
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| 2008 |
Giera DS, Sickert M, Schneider C. Brønsted acid-catalyzed, enantioselective, vinylogous Mannich reaction of vinylketene silyl N,O-acetals. Organic Letters. 10: 4259-62. PMID 18754625 DOI: 10.1021/Ol8017374 |
0.533 |
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| 2008 |
Sickert M, Schneider C. The enantioselective, Brønsted acid catalyzed, vinylogous Mannich reaction. Angewandte Chemie (International Ed. in English). 47: 3631-4. PMID 18386272 DOI: 10.1002/Anie.200800103 |
0.503 |
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| 2008 |
Mai E, Schneider C. Catalytic, enantioselective synthesis of Boc-protected 1,2-amino alcohols through aminolysis of meso-epoxides with benzophenone imine Arkivoc. 2008. DOI: 10.3998/Ark.5550190.0009.G20 |
0.449 |
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| 2008 |
Schneider C, Sickert M. Brønsted Acid Catalyzed Vinylogous Mannich Reaction Synfacts. 2008: 0756-0756. DOI: 10.1055/s-2008-1077816 |
0.369 |
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| 2008 |
Khaliel S, Nandakumar MV, Krautscheid H, Schneider C. Organocatalytic Domino MannichAza-Michael Reactions towards the Stereoselective Synthesisof Highly Substituted Pipecolic Esters Synlett. 2008: 2705-2707. DOI: 10.1055/S-0028-1083377 |
0.576 |
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| 2008 |
Tschöp A, Nandakumar MV, Pavlyuk O, Schneider C. Scandium–bipyridine-catalyzed, enantioselective selenol addition to aromatic meso-epoxides Tetrahedron Letters. 49: 1030-1033. DOI: 10.1016/J.Tetlet.2007.12.006 |
0.523 |
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| 2008 |
Sickert M, Schneider C. Enantioselektive, Brønsted‐Säure‐katalysierte, vinyloge Mannich‐ Reaktion Angewandte Chemie. 120: 3687-3690. DOI: 10.1002/Ange.200800103 |
0.414 |
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| 2007 |
Nandakumar MV, Tschöp A, Krautscheid H, Schneider C. Indium-bipyridine-catalyzed, enantioselective thiolysis of meso-epoxides. Chemical Communications (Cambridge, England). 2756-8. PMID 17594044 DOI: 10.1039/B703625F |
0.476 |
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| 2007 |
Mai E, Schneider C. Scandium-bipyridine-catalyzed enantioselective aminolysis of meso-epoxides. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 2729-41. PMID 17163566 DOI: 10.1002/Chem.200601307 |
0.458 |
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| 2007 |
Peruncheralathan S, Henze M, Schneider C. Scandium triflate catalyzed aminolysis of meso-aziridines Synlett. 2289-2291. DOI: 10.1055/S-2007-984920 |
0.477 |
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| 2007 |
Mai E, Schneider C. Indium-Bipyridine Catalyzed, Enantioselective Aminolysis of meso-Epoxides Synlett. 2007: 2136-2138. DOI: 10.1055/S-2007-984902 |
0.468 |
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| 2007 |
Remme N, Koschek K, Schneider C. Scandium triflate catalyzed transesterification of carboxylic esters Synlett. 2007: 491-493. DOI: 10.1055/S-2007-967936 |
0.484 |
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| 2007 |
Peruncheralathan S, Henze M, Schneider C. Indium(III) chloride-catalyzed thiolysis of meso-aziridines Tetrahedron Letters. 48: 6743-6746. DOI: 10.1016/J.Tetlet.2007.07.082 |
0.414 |
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| 2007 |
Jakob F, Schneider C. Enzyme-Catalyzed Kinetic Resolution of 1,3-anti-Diol Monoesters – Efficient Preparation of Enantiomerically Highly Enriched and Unsymmetrically Substituted 1,3-anti-Diols European Journal of Organic Chemistry. 2007: 2958-2963. DOI: 10.1002/Ejoc.200700096 |
0.48 |
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| 2007 |
Tschöp A, Marx A, Sreekanth AR, Schneider C. Scandium-Bipyridine-Catalyzed, Enantioselective Alcoholysis ofmeso-Epoxides European Journal of Organic Chemistry. 2007: 2318-2327. DOI: 10.1002/Ejoc.200601101 |
0.467 |
|
| 2006 |
Schneider C. Synthesis of 1,2-Difunctionalized Fine Chemicals through Catalytic, Enantioselective Ring-Opening Reactions of Epoxides Synthesis. 2006: 3919-3944. DOI: 10.1055/S-2006-950348 |
0.506 |
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| 2006 |
Schneider C, Khaliel S. Microwave-Assisted Silyloxy-Cope Rearrangement of syn-Aldol Products in DMF: Enhancement of Rate and Diastereoselectivity Synlett. 2006: 1413-1415. DOI: 10.1055/S-2006-939729 |
0.438 |
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| 2006 |
Schneider C, Hansch M, Sreekumar P. Zirconium–BINOLate-catalyzed, enantioselective aldol-Tishchenko reactions of aromatic ketone aldols Tetrahedron: Asymmetry. 17: 2738-2742. DOI: 10.1016/J.Tetasy.2006.10.019 |
0.563 |
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| 2005 |
Schneider C, Hansch M, Weide T. The zirconium alkoxide-catalyzed aldol-Tishchenko reaction of ketone aldols. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 3010-21. PMID 15770713 DOI: 10.1002/Chem.200400951 |
0.532 |
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| 2004 |
Schneider C, Sreekanth AR, Mai E. Scandium-bipyridine-catalyzed enantioselective addition of alcohols and amines to meso-epoxides. Angewandte Chemie (International Ed. in English). 43: 5691-4. PMID 15495155 DOI: 10.1002/Anie.200460786 |
0.361 |
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| 2004 |
Schneider C, Klapa K, Hansch M. Zr(Ot-Bu)4-catalyzed Tishchenko reduction of β-hydroxy ketones Synlett. 2005: 91-94. DOI: 10.1055/S-2004-836056 |
0.436 |
|
| 2004 |
Schneider C, Sreekanth AR, Mai E. Scandium-Bipyridin-katalysierte, enantioselektive Addition von Alkoholen und Aminen anmeso-Epoxide Angewandte Chemie. 116: 5809-5812. DOI: 10.1002/Ange.200460786 |
0.431 |
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| 2003 |
Schneider C, Hansch M. First Catalytic, Enantioselective Aldol—Tishchenko Reactions with Ketone Aldols as Enol Equivalents. Cheminform. 34. DOI: 10.1055/S-2003-38741 |
0.528 |
|
| 2002 |
Schneider C. Catalytic, enantioselective syntheses of beta-lactones--versatile synthetic building blocks in organic chemistry. Angewandte Chemie (International Ed. in English). 41: 744-6. PMID 12491322 DOI: 10.1002/1521-3773(20020301)41:5<744::Aid-Anie744>3.0.Co;2-V |
0.332 |
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| 2002 |
Schneider C. First de novo synthesis of the bisindole alkaloid vinblastine. Angewandte Chemie (International Ed. in English). 41: 4217-9. PMID 12434344 DOI: 10.1002/1521-3773(20021115)41:22<4217::Aid-Anie4217>3.0.Co;2-U |
0.427 |
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| 2002 |
Schneider C, Reese O. Highly stereoselective and efficient synthesis of functionalized cyclohexanes with multiple stereocenters. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 2585-94. PMID 12180338 DOI: 10.1002/1521-3765(20020603)8:11<2585::Aid-Chem2585>3.0.Co;2-C |
0.54 |
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| 2002 |
Schneider C, Tolksdorf F, Rehfeuter M. Asymmetric Synthesis of the Polyol Portion of the Polyene Macrolide Antibiotic RK-397 Synlett. 2002: 2098-2100. DOI: 10.1055/S-2002-35584 |
0.419 |
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| 2001 |
Schneider C, Hansch M. Zr(OtBu)4-catalysed synthesis ofacetone aldol adducts and domino aldol-Tishchenko reactions with diacetonealcohol as enol equivalent Chemical Communications. 1218-1219. DOI: 10.1039/B102941J |
0.519 |
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| 2001 |
Schneider C, Brauner J. Lewis Base-Catalyzed Addition of Trialkylaluminum Compounds to Epoxides European Journal of Organic Chemistry. 2001: 4445-4450. DOI: 10.1002/1099-0690(200112)2001:23<4445::Aid-Ejoc4445>3.0.Co;2-U |
0.511 |
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| 2000 |
Schneider C, Reese O. Domino Michael Aldol and Domino Michael Mannich Reactions: Highly Stereoselective Synthesis of Functionalized Cyclohexanes Angewandte Chemie. 39: 2948-2950. PMID 11028020 DOI: 10.1002/1521-3773(20000818)39:16<2948::Aid-Anie2948>3.0.Co;2-P |
0.517 |
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| 2000 |
Schneider C. Quaternary Ammonium Salt Catalyzed Azidolysis of Epoxides with Trimethylsilyl Azide Synlett. 2000: 1840-1842. DOI: 10.1055/S-2000-8687 |
0.49 |
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| 2000 |
Schneider C, Reese O. Diastereoselective Conjugate Additions to t-Leucine-Derived N-Enoyl 1,3-Oxazolidin-2-ones Synthesis. 2000: 1689-1694. DOI: 10.1055/S-2000-8199 |
0.39 |
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| 2000 |
Schneider C, Brauner J. Lewis base-catalyzed addition of triethylaluminum to epoxides Tetrahedron Letters. 41: 3043-3046. DOI: 10.1016/S0040-4039(00)00332-4 |
0.412 |
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| 2000 |
Schneider C, Reese O. Domino-Michael-Aldol- und Domino-Michael-Mannich-Reaktionen: Hochdiastereoselektive Synthese funktionalisierter Cyclohexane Angewandte Chemie. 112: 3074-3076. DOI: 10.1002/1521-3757(20000818)112:16<3074::Aid-Ange3074>3.0.Co;2-B |
0.526 |
|
| 2000 |
Schneider C, Schuffenhauer A. Stereodivergent Synthesis of Highly Substituted Tetrahydropyrans European Journal of Organic Chemistry. 2000: 73-82. DOI: 10.1002/(Sici)1099-0690(200001)2000:1<73::Aid-Ejoc73>3.0.Co;2-4 |
0.542 |
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| 1999 |
Hiort J, Chaidir, Bohnenstengel FI, Nugroho BW, Schneider C, Wray V, Witte L, Hung PD, Kiet LC, Proksch P. New Insecticidal Rocaglamide Derivatives from the Roots of Aglaia duperreana Journal of Natural Products. 62: 1632-1635. DOI: 10.1021/Np990242G |
0.308 |
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| 1999 |
Schneider C, Rehfeuter M. General and Asymmetric Synthesis of Protected 1,3,5‐Triols with Pendant Functional Groups Chemistry: a European Journal. 5: 2850-2858. DOI: 10.1002/(Sici)1521-3765(19991001)5:10<2850::Aid-Chem2850>3.0.Co;2-7 |
0.465 |
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| 1999 |
Schneider C, Börner C, Schuffenhauer A. Stereoselective Synthesis of Highly Substituted Piperidines European Journal of Organic Chemistry. 1999: 3353-3362. DOI: 10.1002/(Sici)1099-0690(199912)1999:12<3353::Aid-Ejoc3353>3.0.Co;2-Q |
0.546 |
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| 1998 |
Schneider C. New Polyol Syntheses. Angewandte Chemie (International Ed. in English). 37: 1375-1378. PMID 29710909 DOI: 10.1002/(Sici)1521-3773(19980605)37:10<1375::Aid-Anie1375>3.0.Co;2-H |
0.398 |
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| 1998 |
Schneider C, Börner C. Novel and Stereocontrolled Synthesis of Enantiopure and Polyalkyl Substituted Piperidines Synlett. 1998: 652-654. DOI: 10.1055/S-1998-1725 |
0.476 |
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| 1998 |
Schneider C, Rehfeuter M. Enantioselective Polyol Synthesis via the Cope Rearrangement of Chiral Aldol Products. A Synthesis of the C1-C10-Fragment of Nystatin A1 Tetrahedron Letters. 39: 9-12. DOI: 10.1016/S0040-4039(97)10455-5 |
0.423 |
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| 1998 |
Schneider C. Application of the Silyloxy Cope Rearrangement of Chiral Aldol Products Towards a Synthesis of (+)‐Lasiol European Journal of Organic Chemistry. 1998: 1661-1663. DOI: 10.1002/(Sici)1099-0690(199808)1998:8<1661::Aid-Ejoc1661>3.0.Co;2-0 |
0.448 |
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| 1997 |
Schneider C. Stereodivergent Synthesis of Enantiopure Tetrahydropyrans via the Silyloxy-Cope Rearrangement of Chiral Aldol Products Synlett. 1997: 815-817. DOI: 10.1055/S-1997-5748 |
0.465 |
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| 1997 |
Schneider C, Rehfeuter M. Highly stereoselectively cope rearrangements of enantiomerically pure, silylated syn-aldols Tetrahedron. 53: 133-144. DOI: 10.1016/S0040-4020(96)00958-1 |
0.453 |
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| 1996 |
Schneider C, Rehfeuter M. Stereoselective Cope Rearrangements of Syn- and Anti-Aldol Products Synlett. 1996: 212-214. DOI: 10.1055/S-1996-5369 |
0.338 |
|
| 1996 |
Tietze LF, Schneider C, Grote A. Stereodivergent Hetero-Diels-Alder Reactions of Chiral 1-Oxa-1,3-butadienes through a Conformational Switch Induced by Lewis Acids Chemistry - a European Journal. 2: 139-148. DOI: 10.1002/Chem.19960020205 |
0.662 |
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| 1994 |
Tietze LF, Montenbruck A, Schneider C. Inter- and Intramolecular Hetero-Diels-Alder Reactions, Part 48.1
De-NovoSynthesis of Enantiopure Carbohydrates: Preparation of Ethyl β-D- and β-L-Mannopyranosides by an Asymmetrically Induced Hetero Diels-Alder Reaction Synlett. 1994: 509-510. DOI: 10.1055/S-1994-22907 |
0.559 |
|
| 1994 |
Tietze LF, Schneider C, Montenbruck A. Asymmetric 1,6-Induction in Hetero-Diels–Alder Reactions of Chiral Oxabutadienes for a De Novo Synthesis of Enantiomerically Pure Carbohydrates: Lewis Acid Dependent Reversal of Facial Selectivity Angewandte Chemie International Edition in English. 33: 980-982. DOI: 10.1002/Anie.199409801 |
0.636 |
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| 1994 |
Tietze LF, Schneider C, Montenbruck A. Asymmetrisch 1,6-induzierte Hetero-Diels-Alder-Reaktion chiraler Oxabutadiene zur De-novo-Synthese enantiomerenreiner Kohlenhydrate: Umkehr der Seitendifferenzierung durch Variation des Lewis-Säure-Initiators Angewandte Chemie. 106: 1031-1032. DOI: 10.1002/Ange.19941060915 |
0.567 |
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| 1993 |
Pohl E, Herbst-Irmer R, Noltemeyer M, Schneider C, Tietze LF. Structures of endo- and exo-3-acetoxy-2,4-diethoxy-6-(2-oxo-1,3-oxazolidin-3-ylcarbonyl)-3,4-dihydro-2H-pyran Acta Crystallographica Section C Crystal Structure Communications. 49: 1850-1852. DOI: 10.1107/S0108270193004202 |
0.379 |
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| 1992 |
Tietze LF, Schneider C. Efficient Control of theendo/exo-Selectivity in Intermolecular Hetero Diels-Alder Reactions of a New 1-Oxa-1,3-butadiene with Different Lewis Acids1 Synlett. 1992: 755-756. DOI: 10.1055/S-1992-21483 |
0.56 |
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| 1991 |
Tietze LF, Schneider C. Intra- and intermolecular hetero-Diels-Alder reactions. 34. Enantioselective total synthesis of the mycotoxin (-)-talaromycin B by a hetero Diels-Alder reaction The Journal of Organic Chemistry. 56: 2476-2481. DOI: 10.1021/Jo00007A040 |
0.598 |
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