Abstract is: Albert Jakob Eschenmoser (born 5 August 1925) is a Swiss organic chemist, best known for his work on the synthesis of complex heterocyclic natural compounds, most notably vitamin B12. In addition to his significant contributions to the field of organic synthesis, Eschenmoser pioneered work in the Origins of Life (OoL) field with work on the synthetic pathways of artificial nucleic acids. Before retiring in 2009, Eschenmoser held tenured teaching positions at the ETH Zurich and The Skaggs Institute for Chemical Biology at The Scripps Research Institute in La Jolla, California as well as visiting professorships at the University of Chicago, Cambridge University, and Harvard.
human | Q5 |
P2381 | Academic Tree ID | 52747 |
P5463 | AE member ID | Eschenmoser_Albert |
P6231 | BDELIS ID | 77915 |
P13049 | DDB person (GND) ID | 123409071 |
P7902 | Deutsche Biographie (GND) ID | 123409071 |
P8168 | FactGrid item ID | Q886125 |
P2163 | FAST ID | 178163 |
P2070 | Fellow of the Royal Society ID | 11406 |
P646 | Freebase ID | /m/02w_6ml |
P2600 | Geni.com profile ID | 6000000040360761859 |
P227 | GND ID | 123409071 |
P902 | HDS ID | 044428 |
P269 | IdRef ID | 272480150 |
P213 | ISNI | 000000001260817X |
P8189 | J9U ID | 987007369016905171 |
P10299 | Leopoldina member ID (new) | albert-eschenmoser |
P3413 | Leopoldina member ID (superseded) | 173 |
P244 | Library of Congress authority ID | n86833322 |
P5587 | Libris-URI | ljx000d40sv041g |
P5380 | National Academy of Sciences member ID | 46714 |
P1006 | Nationale Thesaurus voor Auteursnamen ID | 129149179 |
P3360 | Nobel Prize People Nomination ID | 14002 |
P1015 | NORAF ID | 90281644 |
P1375 | NSK ID | 000194167 |
P1207 | NUKAT ID | n2012153022 |
P10283 | OpenAlex ID | A5088487447 |
P9640 | PAS member ID | ordinary/eschenmoser |
P3368 | Prabook ID | 487715 |
P1153 | Scopus author ID | 7007015211 |
P906 | SELIBR ID | 185644 |
P3987 | SHARE Catalogue author ID | 94359 |
P214 | VIAF ID | 64913917 |
P10832 | WorldCat Entities ID | E39PBJrckQVWBFjgXB8C47GGpP |
P485 | archives at | ETH Zurich University Archives | Q39934978 |
P166 | award received | Austrian Decoration for Science and Art | Q306590 |
Davy Medal | Q220842 | ||
Benjamin Franklin Medal | Q817496 | ||
Welch Award in Chemistry | Q1632244 | ||
Arthur C. Cope Award | Q2475932 | ||
Wolf Prize in Chemistry | Q968876 | ||
Cothenius Medal | Q1136626 | ||
Dannie Heineman Prize | Q1164466 | ||
Ernest Guenther Award | Q1256023 | ||
Marcel Benoist Prize | Q1307788 | ||
Oparin Medal | Q7095600 | ||
Foreign Member of the Royal Society | Q14906020 | ||
Pour le Mérite for Sciences and Arts order | Q15056034 | ||
August Wilhelm von Hofmann Medal | Q15116950 | ||
Roger Adams Award in Organic Chemistry | Q15842831 | ||
Inhoffen-Medaille | Q18412678 | ||
Grand Prize of the French Academy of Science | Q3114992 | ||
Centenary Prize | Q18560142 | ||
Robert Robinson Award | Q18560196 | ||
Sir Derek Barton Gold medal | Q18560200 | ||
Tetrahedron Prize | Q21061286 | ||
Nakanishi Prize | Q24255499 | ||
Paracelsus Prize | Q24321806 | ||
F. A. Cotton Medal | Q31836935 | ||
??? | Q126416239 | ||
P27 | country of citizenship | Switzerland | Q39 |
P184 | doctoral advisor | Leopold Ružička | Q122996 |
P185 | doctoral student | Andreas Pfaltz | Q15783334 |
Jakob Schreiber | Q116741243 | ||
P69 | educated at | ETH Zurich | Q11942 |
P108 | employer | ETH Zurich | Q11942 |
P734 | family name | Eschenmoser | Q76417743 |
Eschenmoser | Q76417743 | ||
Eschenmoser | Q76417743 | ||
P101 | field of work | organic chemistry | Q11351 |
vitamin B12 | Q187706 | ||
total synthesis | Q644785 | ||
P735 | given name | Albert | Q577011 |
Albert | Q577011 | ||
P1412 | languages spoken, written or signed | German | Q188 |
P463 | member of | Royal Society | Q123885 |
Göttingen Academy of Sciences | Q414188 | ||
American Academy of Arts and Sciences | Q463303 | ||
Academia Europaea | Q337234 | ||
National Academy of Sciences | Q270794 | ||
Pontifical Academy of Sciences | Q938622 | ||
German Academy of Sciences Leopoldina | Q543804 | ||
P1559 | name in native language | Albert Eschenmoser | |
P1411 | nominated for | Nobel Prize in Chemistry | Q44585 |
P106 | occupation | chemist | Q593644 |
university teacher | Q1622272 | ||
P21 | sex or gender | male | Q6581097 |
Q73488113 | 2,6-Diamino-5,8-diaza-7,9-dicarba-purine |
Q50201734 | 2,6-diaminopurine in TNA: effect on duplex stabilities and on the efficiency of template-controlled ligations |
Q56488908 | A Fragmentational Approach to Macrolides: (5-E, 8-Z)-6-methyl-5,8-undecadien-11-olide |
Q56488831 | A New Type of Corrin Synthesis |
Q56488785 | A Synthetic Route to Metal-free Corrins |
Q56488768 | A Synthetic Route to the Corrin System |
Q47177731 | A search for interstellar oxiranecarbonitrile (C3H3NO). |
Q56657260 | Albert Eschenmoser - List of Scientific Publications |
Q29300358 | Are Oxazolidinones Really Unproductive, Parasitic Species in Proline Catalysis? – Thoughts and Experiments Pointing to an Alternative View |
Q72505788 | B12: reminiscences and afterthoughts |
Q79455076 | Base-pairing systems related to TNA containing phosphoramidate linkages: synthesis of building blocks and pairing properties |
Q31048287 | Base-pairing systems related to TNA: alpha-threofuranosyl oligonucleotides containing phosphoramidate linkages |
Q73488117 | C-Nucleosidations with 2,6-diamino-5,8-diaza-7,9-dicarba-purine |
Q57482404 | CLAISEN'sche Umlagerungen bei Allyl- und Benzylalkoholen mit 1-Dimethylamino-1-methoxy-äthen |
Q56489535 | CLAISEN'sche Umlagerungen bei Allyl- und Benzylalkoholen mit Hilfe von Acetalen des N, N-Dimethylacetamids. Vorläufige Mitteilung |
Q56491991 | Centenary Lecture. (Delivered november 1969). Roads to corrins |
Q56499490 | Chemical Etiology of Nucleic Acid Structure: Comparing Pentopyranosyl-(2'→4') Oligonucleotides with RNA |
Q28137995 | Chemical etiology of nucleic acid structure: the alpha-threofuranosyl-(3'-->2') oligonucleotide system |
Q56489780 | Chemie der α-Aminonitrile 1. Mitteilung Einleitung und Wege zu Uroporphyrinogen-octanitrilen |
Q56489796 | Chemie von ?-Aminonitrilen. Aziridin-2-carbonitril photochemische Bildung aus 2-Aminopropennitril |
Q56489814 | Chemie von a-Aminonitrilen. Aldomerisierung von Glycolaldehyd-phosphat zu racemischen Hexose-2,4,6-triphosphaten und (in Gegenwart von Formaldehyd) racemischen Pentose-2,4-diphosphaten: rac-Allose-2,4,6-triphosphat und rac-Ribose-2,4-diphosphat sind |
Q56491811 | Chemistry of corphinoids: structural properties of corphinoid nickel(II) complexes related to coenzyme F430 |
Q56491724 | Chemistry of corphinoids: synthesis of a nickel(II) complex containing the chromophore system of coenzyme F430 |
Q56490096 | Chemistry of potentially prebiological natural products |
Q56491669 | Chemistry of pyrrocorphins: C-methylations at the periphery of pyrrocorphins and related corphinoid ligand systems |
Q56489515 | Chromsäureester als Zwischenprodukte bei der Oxydation von Alkoholen. Geschwindigkeits-limitierende Veresterung eines sterisch Gehinderten Alkohols |
Q56488814 | Corphin, a Corrinoid-Porphinoid Ligand System |
Q56657258 | Corrin Syntheses. Part I |
Q56794550 | Crystal Structure of Homo-DNA and Nature's Choice of Pentose over Hexose in the Genetic System |
Q27639965 | Crystal structure of a B-form DNA duplex containing (L)-alpha-threofuranosyl (3'-->2') nucleosides: a four-carbon sugar is easily accommodated into the backbone of DNA |
Q56657263 | Curriculum Vitae - Albert Eschenmoser |
Q56489723 | Das Pyrrocorphin-Ligandsystem: Synthese des 2,2,7,7,12,12,17-Heptamethyl-2,3,7,8,12,13-hexahydroporphyrins. Kurzmitteilung |
Q56489702 | Der Einbau von Magnesium in Liganden der Chlorophyll-Reihe mit (2,6-Di-t-butyl-4-methylphenoxy)magnesiumjodid |
Q56489763 | Die Sattelkonformation der hydroporphinoiden Nickel(II)-Komplexe: Struktur, Ursprung und stereochemische Konsequenzen |
Q55932200 | Die Synthese von Acetylen‐carbonyl‐Verbindungen durch Fragmentierung von α, β‐Epoxy‐ketonen mit p‐Toluolsulfonylhydrazin. Vorläufige Mitteilung |
Q28277634 | Dihydrogen trioxide (HOOOH) is generated during the thermal reaction between hydrogen peroxide and ozone |
Q56488844 | Dimethyl(methylene)ammonium Iodide |
Q29026440 | Eine neuartige Fragmentierung cyclischer α, ß‐ungesättigter Carbonylsysteme; Synthese von Exalton und rac‐Muscon aus Cyclododecanon Vorläufige Mitteilung |
Q56489592 | EndocyclischeSN-Reaktionen am gesättigten Kohlenstoff? Vorläufige Mitteilung |
Q36781387 | Enhanced reactivity in dioxirane C-H oxidations via strain release: a computational and experimental study |
Q37967638 | Etiology of potentially primordial biomolecular structures: from vitamin B12 to the nucleic acids and an inquiry into the chemistry of life's origin: a retrospective |
Q29010427 | Evidence for Ozone Formation in Human Atherosclerotic Arteries |
Q33962509 | Evidence for antibody-catalyzed ozone formation in bacterial killing and inflammation |
Q34760451 | Evidence for the production of trioxygen species during antibody-catalyzed chemical modification of antigens |
Q28372127 | Formation of glycolaldehyde phosphate from glycolaldehyde in aqueous solution |
Q56489003 | Interconversion of the Chromophore Systems of Porphyrinogen and 2,3,7,8,12,13-Hexahydroporphyrin |
Q56657257 | Introductory Remarks on the Publication Series ‘Corrin Syntheses-Parts I-VI’ |
Q56489570 | Langsame Inversion am pyramidal gebundenen Stickstoff: Isolierung und Epimerisierung diastereomerer N-Methoxy-3,3-di-methoxycarbonyl-5-cyan-1, 2-oxazolidine. Vorläufige Mitteilung |
Q80831639 | Mannich-type C-nucleosidations in the 5,8-diaza-7,9-dicarba-purine family |
Q79366717 | Mapping the landscape of potentially primordial informational oligomers: oligodipeptides and oligodipeptoids tagged with triazines as recognition elements |
Q79366719 | Mapping the landscape of potentially primordial informational oligomers: oligodipeptides tagged with 2,4-disubstituted 5-aminopyrimidines as recognition elements |
Q37414917 | Metabolite-initiated protein misfolding may trigger Alzheimer's disease |
Q56488872 | Metal-Free Derivatives of the Corphin Ligand System |
Q74461556 | Mineral induced formation of sugar phosphates |
Q56489918 | Naturstoff-Strukturen hinterfragen |
Q36196869 | New insights into the mechanism and an expanded scope of the Fe(III)-mediated vinblastine coupling reaction |
Q56489457 | Notiz über die Selektivität der Spaltung von Carbonsäuremethylestern mit Lithiumjodid |
Q47842451 | On a hypothetical generational relationship between HCN and constituents of the reductive citric acid cycle |
Q88520807 | Opposite Orientation of Backbone Inclination in Pyranosyl-RNA and Homo-DNA Correlates with Opposite Directionality of Duplex Properties |
Q34865370 | Ozone in biology |
Q56489686 | Photochemische und nicht-photochemische A/D-Secocorrin→Corrin-Cyclisierungen bei 19-Carboxy- und 19-Formyl-1-methyliden-1,19-secocorrinaten. Decarboxylierbarkeit und Deformylierbarkeit von Nickel (II)-19-carboxy- bzw. 19-formyl-corrinaten. Vorläuf |
Q36601327 | Probing the antibody-catalyzed water-oxidation pathway at atomic resolution |
Q56489875 | Pyranosyl-RNA (‘p-RNA’): NMR and Molecular-Dynamics Study of the Duplex Formed by Self-pairing of Ribopyranosyl-(C-G-A-A-T-T-C-G) |
Q47774134 | Question 1: commentary referring to the statement "the origin of life can be traced back to the origin of kinetic control" and the question "do you agree with this statement; and how would you envisage the prebiotic evolutionary bridge between therm |
Q64028608 | Reactions of the HCN-Tetramer with Aldehydes |
Q56489906 | Revisited after 50 Years: The ‘Stereochemical Interpretation of the Biogenetic Isoprene Rule for the Triterpenes’ |
Q56491898 | Robert Robinson Lecture. Post-B12 problems in corrin synthesis |
Q56488802 | Slow Inversion at Pyramidal Nitrogen: Isolation of Diastereomeric 7-Chloro-7-azabicyclo-[4.1.0]heptanes at Room Temperature |
Q60303858 | Some Aspects of Acid-Catalysed Cyclizations of Terpenoid Polyenes |
Q40832116 | Strain release in C-H bond activation? |
Q56489609 | Sulfidkontraktionviaalkylative Kupplung: Eine methode zur darstellung von β-dicarbonylderivaten. Über synthetische methoden, 1. Mitteilung |
Q55931878 | Synthese des Colchicins |
Q55931881 | Synthese des Colchicins |
Q34236290 | Synthesis and optical rotation of the (-)-cannabidiols |
Q56489889 | The -L-Threofuranosyl-(3′→2′)-oligonucleotide System (‘TNA'): Synthesis and Pairing Properties |
Q56489137 | The Chemistry of Pyrrocorphins: Stereoselectivity in the Porphyrinogen→Pyrrocorphin Tautomerization |
Q56489151 | The Chemistry of Pyrrocorphins:C-Methylation of Pyrrocorphinates at the Ligand Periphery |
Q55966717 | The Dihydrocorphinol→ Corrin Ring Contraction: A Potentially Biomimetic Mode of Formation of the Corrin Structure |
Q47346359 | The TNA-family of nucleic acid systems: properties and prospects |
Q56490408 | The search for the chemistry of life's origin |
Q46312041 | The structure of a TNA-TNA complex in solution: NMR study of the octamer duplex derived from alpha-(L)-threofuranosyl-(3'-2')-CGAATTCG. |
Q46792853 | Theoretical exploration of the mechanism of riboflavin formation from 6,7-dimethyl-8-ribityllumazine: nucleophilic catalysis, hydride transfer, hydrogen atom transfer, or nucleophilic addition? |
Q48500961 | Towards a chemical etiology of nucleic acid structure |
Q55952055 | Vitamin B12: Experiments Concerning the Origin of Its Molecular Structure |
Q47481890 | Vladimir Prelog. 23 July 1906--7 January 1998: Elected For.Mem.R.S. 1962 |
Q56489938 | Warum Pentose- und nicht Hexose-Nucleinsäuren? |
Q56489834 | Warum pentose-und nicht hexose-nucleinsäuren? Teil III. Oligo(2′,3′-dideoxy-β-D-glucopyranosyl) nucleotide (‘homo-DNS’): Paarungesigenschaften |
Q56489851 | Why Pentose- and Not Hexose-Nucleic Acids??. Part VII. Pyranosyl-RNA (?p-RNA?). Preliminary communication |
Q27642786 | Why does TNA cross-pair more strongly with RNA than with DNA? an answer from X-ray analysis |
Q29544463 | Zur Kenntnis der Triterpene. 190. Mitteilung. Eine stereochemische Interpretation der biogenetischen Isoprenregel bei den Triterpenen |
Q55966716 | Zur Kenntnis des Faktors F430 aus methanogenen Bakterien: Struktur des porphinoiden Ligandsystems |
Q52348130 | [Moments of success are exceptionally joyful. Interview with Albert Eschenmoser by L. Weber]. |
Q56489262 | Über den sterischen Verlauf der säurekatalysierten Cyclisation in der Terpenreihe. Cyclisation der cis-7-Methyl-octadien-(2,6)-säure-(1) |
Q56489232 | Über die Spaltung des Mesylesters von 2-Methyl-2-oxymethyl-cyclopentanon mit Basen |
Q56489289 | Über die relative Geschwindigkeit der Chromosäureoxydation sekundärer, alicyclischer Alkohole. Vorläufige Mitteilung |
Q56489380 | Über eine neue Bildungsweise des Troponsystems. Vorläufige Mitteilung |
Q56437898 | α, β‐Epoxyketon → Alkinon‐Fragmentierung I: Synthese von exalton und rac ‐ muscon aus cyclododecanon über synthetische methoden, 3. Mitteilung |
Q56489628 | α,β-Epoxyketon → Alkinon-Fragmentierung II: Pyrolytischer Zerfall der Hydrazone aus α,β-Epoxyketonen und N-Amino-aziridinen. Über synthetische Methoden, 4. Mitteilung |
Q56489670 | α‐Chlor‐nitrone I: Darstellung und Ag+‐induzierte Reaktion mit Olefinen. Über synthetische Methoden, 5. (vorläufige) Mitteilung |
Q122996 | Leopold Ružička | doctoral student | P185 |
Category:Albert Eschenmoser | wikimedia | |
Arabic (ar / Q13955) | ألبرت إيشنموسر | wikipedia |
Egyptian Arabic (arz / Q29919) | البرت ايشنموسر | wikipedia |
Альберт Эшэнмозер | wikipedia | |
Albert Eschenmoser | wikipedia | |
Albert Eschenmoser | wikipedia | |
Albert Eschenmoser | wikipedia | |
Persian (fa / Q9168) | آلبرت اشنموزر | wikipedia |
Albert Eschenmoser | wikipedia | |
アルバート・エッシェンモーザー | wikipedia | |
알버트 에센모저 | wikipedia | |
Albert Eschenmoser | wikipedia | |
Albert Eschenmoser | wikipedia | |
Эшенмозер, Альберт | wikipedia | |
Albert Eschenmoser | wikipedia | |
Albert Eschenmoser | wikipedia | |
阿尔伯特·艾申莫瑟 | wikipedia |
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