Chemistry Olympiad in Cambridge Protein Folding
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Geoffrey Wilkinson
THE LONG SEARCH FOR STABLE TRANSITION METAL ALKYLS Nobel Lecture, December 11, 1973 by G EOFFREY W ILKINSON Imperial College of Science & Technology, London, England Chemical compounds in which there is a single bond between a saturated car- bon atom and a transition metal atom are of unusual importance. Quite aside from the significance and role in Nature of the cobalt to carbon bonds in the vitamin B 12 system and possible metal to carbon bonds in other biological systems, we need only consider that during the time taken to deliver this lec- ture, many thousands, if not tens of thousands of tons of chemical compounds are being transformed or synthesised industrially in processes which at some stage involve a transition metal to carbon bond. The nonchemist will pro- bably be most familiar with polyethylene or polypropylene in the form of do- mestic utensils, packaging materials, children’s toys and so on. These materials are made by Ziegler-Natta* or Philipps’ catalysis using titanium and chro- mium respectively. However, transition metal compounds are used as catalysts in the synthesis of synthetic rubbers and other polymers, and of a variety of simple compounds used as industrial solvents or intermediates. For example alcohols are made from olefins, carbon monoxide and hydrogen by use of cobalt or rhodium catalysts, acetic acid is made by carbonylation of methanol using rhodium catalysts and acrylonitrile is dimerised to adiponitrile (for nylon) by nickel catalysts. We should also not forget that the huge quantities of petroleum hydrocarbons processed by the oil and petrochemical industry are re-formed over platinum, platinum-rhenium or platinum-germanium sup- ported on alumina. -
Former Fellows Biographical Index Part
Former Fellows of The Royal Society of Edinburgh 1783 – 2002 Biographical Index Part Two ISBN 0 902198 84 X Published July 2006 © The Royal Society of Edinburgh 22-26 George Street, Edinburgh, EH2 2PQ BIOGRAPHICAL INDEX OF FORMER FELLOWS OF THE ROYAL SOCIETY OF EDINBURGH 1783 – 2002 PART II K-Z C D Waterston and A Macmillan Shearer This is a print-out of the biographical index of over 4000 former Fellows of the Royal Society of Edinburgh as held on the Society’s computer system in October 2005. It lists former Fellows from the foundation of the Society in 1783 to October 2002. Most are deceased Fellows up to and including the list given in the RSE Directory 2003 (Session 2002-3) but some former Fellows who left the Society by resignation or were removed from the roll are still living. HISTORY OF THE PROJECT Information on the Fellowship has been kept by the Society in many ways – unpublished sources include Council and Committee Minutes, Card Indices, and correspondence; published sources such as Transactions, Proceedings, Year Books, Billets, Candidates Lists, etc. All have been examined by the compilers, who have found the Minutes, particularly Committee Minutes, to be of variable quality, and it is to be regretted that the Society’s holdings of published billets and candidates lists are incomplete. The late Professor Neil Campbell prepared from these sources a loose-leaf list of some 1500 Ordinary Fellows elected during the Society’s first hundred years. He listed name and forenames, title where applicable and national honours, profession or discipline, position held, some information on membership of the other societies, dates of birth, election to the Society and death or resignation from the Society and reference to a printed biography. -
Charles Kemball Was One of the Most Distinguished British Chemists of His Generation
CHARLES KEMBALL CBE, MA, ScD(Cantab), DSc(H-W,QUB), C Chem, FRSC, MRIA, FRS Charles Kemball was one of the most distinguished British chemists of his generation. He was born in Edinburgh in 1923, the only son of a distinguished dental surgeon, Charles Henry Kemball FRSE , and was educated at Edinburgh Academy. It was clear from an early age that he was very talented and even in the preparatory school at Edinburgh Academy his teacher found his speed at mental arithmetic rather disconcerting. Bright pupils were encouraged towards the Classics and it was only after the School Certificate Examination that a perceptive teacher persuaded him to move to the Sciences. He had an aptitude at shooting and was a member of the shooting VIII which won the Kinder Cup at Bisley in 1939. Subsequently he was captain of shooting and won the shooting cup in his final two years at the Academy. Despite his late move to sciences he won an Entrance Exhibition in Natural Sciences and went up to Trinity College Cambridge in 1940. At this time his interests lay more with Mathematics and Physics but he later moved to Chemistry and gained First Class Honours in Parts I and II of the Tripos. He went on to do research in the Department of Colloid Science under the direction of Professor E K Rideal, financed by a grant from the Ministry of Aircraft Production, to investigate problems in adhesion. In addition to some direct investigations into the strength of various adhesives for metals, the main work undertaken was a detailed study of the adsorption of vapours on the surface of mercury, to determine the magnitude of the forces attracting the molecules to the metal. -
Robert Burns Woodward
The Life and Achievements of Robert Burns Woodward Long Literature Seminar July 13, 2009 Erika A. Crane “The structure known, but not yet accessible by synthesis, is to the chemist what the unclimbed mountain, the uncharted sea, the untilled field, the unreached planet, are to other men. The achievement of the objective in itself cannot but thrill all chemists, who even before they know the details of the journey can apprehend from their own experience the joys and elations, the disappointments and false hopes, the obstacles overcome, the frustrations subdued, which they experienced who traversed a road to the goal. The unique challenge which chemical synthesis provides for the creative imagination and the skilled hand ensures that it will endure as long as men write books, paint pictures, and fashion things which are beautiful, or practical, or both.” “Art and Science in the Synthesis of Organic Compounds: Retrospect and Prospect,” in Pointers and Pathways in Research (Bombay:CIBA of India, 1963). Robert Burns Woodward • Graduated from MIT with his Ph.D. in chemistry at the age of 20 Woodward taught by example and captivated • A tenured professor at Harvard by the age of 29 the young... “Woodward largely taught principles and values. He showed us by • Published 196 papers before his death at age example and precept that if anything is worth 62 doing, it should be done intelligently, intensely • Received 24 honorary degrees and passionately.” • Received 26 medals & awards including the -Daniel Kemp National Medal of Science in 1964, the Nobel Prize in 1965, and he was one of the first recipients of the Arthur C. -
Young Career Focus: Dr. Stephen Thomas (University of Edinburgh, UK)
A166 Synform Young Career Focus Young Career Focus: Dr. Stephen Thomas (University of Edinburgh, UK) Background and Purpose. SYNFORM regularly meets young up-and-coming researchers who are performing exceptionally well in the arena of organic chemistry and related fields of research, in order to introduce them to the readership. This Young Career Focus presents Dr. Stephen Thomas (University of Edinburgh, UK). Biographical Sketch INTERVIEW Stephen Thomas was born in SYNFORM What is the focus of your current research Toronto, Canada, and moved to activity? Somerset (UK) at a young age where he completed his secondary Dr. S. Thomas We are interested in developing and under- school education at Court Fields standing sustainable catalytic methods. Our focus has been Com munity School and Richard on the application and use of the most abundant elements in Huish College. After gaining his the earth’s crust as catalysts the reductive functionalisation undergraduate degree from Cardiff of unsaturated groups. A key driver for us is understanding University (UK), Stephen complet- the methods we develop and how the unique reactivities of ed his PhD with Dr Stuart Warren at first-row transition metals and main group elements can be Dr. Stephen Thomas the University of Cambridge (UK). applied in new ways. Following post-doctoral research with Prof. Andreas Pfaltz at the University of Basel (Switzer- SYNFORM When did you get interested in synthesis? land), Stephen was appointed to a fixed-term lectureship at the University of Bristol (UK) associated with Prof. Varinder Dr. S. Thomas As an undergraduate I was lucky enough to Aggarwal FRS, allowing him to begin his independent join Prof. -
Los Premios Nobel De Química
Los premios Nobel de Química MATERIAL RECOPILADO POR: DULCE MARÍA DE ANDRÉS CABRERIZO Los premios Nobel de Química El campo de la Química que más premios ha recibido es el de la Quí- mica Orgánica. Frederick Sanger es el único laurea- do que ganó el premio en dos oca- siones, en 1958 y 1980. Otros dos también ganaron premios Nobel en otros campos: Marie Curie (física en El Premio Nobel de Química es entregado anual- 1903, química en 1911) y Linus Carl mente por la Academia Sueca a científicos que so- bresalen por sus contribuciones en el campo de la Pauling (química en 1954, paz en Física. 1962). Seis mujeres han ganado el Es uno de los cinco premios Nobel establecidos en premio: Marie Curie, Irène Joliot- el testamento de Alfred Nobel, en 1895, y que son dados a todos aquellos individuos que realizan Curie (1935), Dorothy Crowfoot Ho- contribuciones notables en la Química, la Física, la dgkin (1964), Ada Yonath (2009) y Literatura, la Paz y la Fisiología o Medicina. Emmanuelle Charpentier y Jennifer Según el testamento de Nobel, este reconocimien- to es administrado directamente por la Fundación Doudna (2020) Nobel y concedido por un comité conformado por Ha habido ocho años en los que no cinco miembros que son elegidos por la Real Aca- demia Sueca de las Ciencias. se entregó el premio Nobel de Quí- El primer Premio Nobel de Química fue otorgado mica, en algunas ocasiones por de- en 1901 al holandés Jacobus Henricus van't Hoff. clararse desierto y en otras por la Cada destinatario recibe una medalla, un diploma y situación de guerra mundial y el exi- un premio económico que ha variado a lo largo de los años. -
Cv Mlhg 2015
CURRICULUM VITAE Name: GREEN, Malcolm Leslie Hodder Address: St Catherine's College, Oxford or Inorganic Chemistry Laboratory South Parks Road OXFORD, OX1 3QR Date of Birth: 16/4/36, Eastleigh, Hampshire Nationality: British Marital Status: Married. Three children Degrees: B.Sc.(Hons), London; D.I.C., M.A.(Cantab), M.A.(Oxon), C.Chem., F.R.S.C., Ph.D., F.R.S. ACADEMIC CAREER 1953-56 Acton Technical College, University of London, B.Sc Hons. Chemistry 1956-59 Imperial College of Science and Technology, London; D.I.C. Ph.D. in chemistry. Supervisor Professor Sir G. Wilkinson 1959-60 Post-doctoral Research Associates Fellow. Imperial College of Science and Technology 1960-63 Assistant Lecturer in Inorganic Chemistry at Cambridge University 1961 Fellow of Corpus Christi College, Cambridge 1963 Sepcentenary Fellow of Inorganic Chemistry, Balliol College, Oxford and Departmental Demonstrator, University of Oxford 1965 University Lecturer, University of Oxford 1971 Visiting Professor, University of Western Ontario (Spring Term) 1972 Visiting Professor, Ecole de Chimie and Institute des Substances Naturelles, Paris (six months) 1973 A.P. Sloan Visiting Professor, Harvard University, (Spring Semester) 1979-84 Appointed to the British Gas Royal Society Senior Research Fellowship 1981 Sherman Fairchild Visiting Scholar at the California Institute of Technology(4 months) 1984 Re-appointed British Gas Royal Society Senior Research Fellow (1984-6) 1987 Vice-master, Balliol College, Oxford (T.T.) 1989 Appointed Professor of Inorganic Chemistry and Head of Department, Oxford University Fellow of St Catherine's College, Oxford 2004- present Emeritus Research Professor in the Inorganic Chemistry Laboratory, Oxford University Emeritus Fellow of Balliol College and St Catherine’s College Publications Two text books, 646 refereed papers and 8 patents. -
Lithiation-Borylation Methodology and Its Application in Synthesis
Lithiation-Borylation Methodology and Its Application in Synthesis Literature Seminar 2018/06/23 Hongyu CHEN (M1) Contents • Introduction • Part 1 : Factors responsible for the 1,2-migration • Part 2 : Factors responsible for stereocontrol • Part 3 : Application of lithiation-borylation reaction in synthesis • Summary Contents • Introduction • Part 1 : Factors responsible for the 1,2-migration • Part 2 : Factors responsible for stereocontrol • Part 3 : Application of lithiation-borylation reaction in synthesis • Summary Anatomy of The Lithiation-Borylation Reaction R3 B(OR)2 Stereoretentive B(OR)2 R2 R Borylation 2 1,2-Metallate R3 OLG R1 R1 Rearrangement R Homologated X Li 3 Boronate complex B(OR)2 product R2 R2 OLG Lithiation OLG R1 R1 OLG = OCb or OTIB Lithium carbenoid R2 X = H or SnR OLG R2 3 Stereoinvertive R 1 R3 R1 Borylation B(OR)2 1,2-Metallate R B(OR)2 3 Rearrangement Boronate complex Homologated product ・ R1, R2 and R3 = Alkyl, Alkenyl or Aryl ・ Reagent Control ・ Complete Stereospecificity Arylation ・ Contiguous Stereocenters Alkynylation ・ Quaternary Stereocenters Oxidation Fluorination ・ Natural Product Synthesis Assembly-Line Synthesis ・ Assembly-Line Synthesis http://www.chm.bris.ac.uk/org/aggarwal/research.php#li-b The First Nonenzymatic Asymmetric Synthesis (H. C. Brown, 1961) DG )2BH [O] + BH3 )2B 0 ℃ H HO H 90% yield, 87% ee cis, cis; cis, trans; trans, trans etc. R*CHCHCHCHR’ R*OH R* R' R*CO2H R* R’ R' R*D R*CHO General Asymmetric Synthesis R* R* R' R*CH OH via Chiral Organoboranes 2 R*NH2 R*CH2CHCH2 R* B R*R’NH R*R’CHNH2 R*CCR’ R*CCH R*COR’ R*CH2COR’ R*R’CHOH R*CH2CN R*COCCR’ R*CH2CO2Et R*R ’COH Brown, H. -
Guidelines and Suggested Title List for Undergraduate Chemistry Libraries, Serial Publication Number 44
DOCUMENT RESUME ED 040 037 SE 008 009 AUTHOR Marquardt, D. N., Ed. TITLE Guidelines and Suggested Title List for Undergraduate Chemistry Libraries, Serial Publication Number 44. INSTITUTION Advisory Council on Coll, Chemistry. PUB DATE Sep 69 NOTE 44p. AVAILABLE FROM Advisory Council on College Chemistry, Dept. of Chemistry, Stanford Univ., Stanford,California 94305 (free) EDRS PRICE EDRS P-: ice MF.40.25 HC-$2.30 DESCRIPTORS Advisory Committees, *Bibliographies,Booklists, *Chemistry, *College Science, *LibraryGuides, Research Reviews (Publications): *Resource Materials, Scholarly Journals IDENTIFIERS Advisory Council on College Chemistry ABSTRACT Contained are guidelines and an extensivelist of books and journals suitable for anundergraduate chemistry library. The guidelines are concerned with theorganization and acquisition policy of chemistry libraries, and withinter-library loan and photoduplication services. Various sections of the reportdeal with journals and abstracts, review serials,foreign language titles, U.S. Government publications and a suggestedtitles list. The books in the titles list are in the areas of analytical,biological, inorganic, organic and physical chemistry. Ingeneral, introductory texts have not been included. The list isarranged alphabetically with entries by author or editor unless the workis better known by title. The library of Congress classification numberand the Dewey Decimal classification number, when available, aregiven for each entry. Book prices are also given. The reportconcludes with a directory of publishers and dealers. This report shouldbe most useful for college libraries, science teachers, and students. (LC) 0 GUIDELINES AND SUGGESTEDTITLE LIST for t...UNDERGRADUATE CHEMISTRY LIBRARIES M CI Revised 1969 Co Co A Report Authorized by the ADVISORY COUNCIL ON COLLEGE CHEMISTRY Edited by D. -
Chemical Lecture Demonstrations: an Opportunity for Engagement Through Collections, Instruction, and Reference
This is an Accepted Manuscript of an article published by Taylor & Francis Group in Science & Technology Libraries on 11/21/2017, available online: https://www.tandfonline.com/doi/abs/10.1080/0194262X.2017.1389667 Chemical Lecture Demonstrations: An Opportunity for Engagement through Collections, Instruction, and Reference David E. Hubbard Science & Engineering Librarian and Associate Professor Texas A&M University Libraries College Station, TX 77843 Abstract: Chemical lecture demonstrations have been used as a pedagogical tool since at least the founding of chemistry as a discipline in the 1600s. This paper describes how science librarians can engage chemistry faculty and students through chemical lecture demonstrations. This paper describes chemical lecture demonstrations – including history and efficacy – and discusses how science librarians can engage chemistry faculty and students through collections, instruction, and reference in support of this pedagogy. In addition to outlining a research guide and lesson plan for chemical lecture demonstrations, this paper identifies chemical lecture demonstration monographs found in WorldCat® and analyzes the holdings of those monographs within the thirty- six-member Greater Western Library Alliance (GWLA) consortium. Introduction Chemical lecture demonstrations, which are lively displays of chemical principles to an audience of students or the general public, are an important pedagogical tool used to educate and engage. Monographs have been one of the major means to educate others on how to conduct these demonstrations. The purpose of this bibliographical investigation is to identify and examine chemical lecture demonstration monograph holdings within the thirty-six-member Greater Western Library Alliance (GWLA) consortium (Greater Western Library Alliance n.d.), and to describe local support for chemical lecture demonstrations through collections, instruction, and reference. -
Former Fellows Biographical Index Part
Former Fellows of The Royal Society of Edinburgh 1783 – 2002 Biographical Index Part One ISBN 0 902 198 84 X Published July 2006 © The Royal Society of Edinburgh 22-26 George Street, Edinburgh, EH2 2PQ BIOGRAPHICAL INDEX OF FORMER FELLOWS OF THE ROYAL SOCIETY OF EDINBURGH 1783 – 2002 PART I A-J C D Waterston and A Macmillan Shearer This is a print-out of the biographical index of over 4000 former Fellows of the Royal Society of Edinburgh as held on the Society’s computer system in October 2005. It lists former Fellows from the foundation of the Society in 1783 to October 2002. Most are deceased Fellows up to and including the list given in the RSE Directory 2003 (Session 2002-3) but some former Fellows who left the Society by resignation or were removed from the roll are still living. HISTORY OF THE PROJECT Information on the Fellowship has been kept by the Society in many ways – unpublished sources include Council and Committee Minutes, Card Indices, and correspondence; published sources such as Transactions, Proceedings, Year Books, Billets, Candidates Lists, etc. All have been examined by the compilers, who have found the Minutes, particularly Committee Minutes, to be of variable quality, and it is to be regretted that the Society’s holdings of published billets and candidates lists are incomplete. The late Professor Neil Campbell prepared from these sources a loose-leaf list of some 1500 Ordinary Fellows elected during the Society’s first hundred years. He listed name and forenames, title where applicable and national honours, profession or discipline, position held, some information on membership of the other societies, dates of birth, election to the Society and death or resignation from the Society and reference to a printed biography. -
Prostaglandin Total Synthesis Enabled by the Organocatalytic Dimerization of Succinaldehyde
Bennett, S. H., Coulthard, G., & Aggarwal, V. K. (2020). Prostaglandin Total Synthesis Enabled by the Organocatalytic Dimerization of Succinaldehyde. Chemical Record. https://doi.org/10.1002/tcr.202000054 Publisher's PDF, also known as Version of record License (if available): CC BY Link to published version (if available): 10.1002/tcr.202000054 Link to publication record in Explore Bristol Research PDF-document This is the final published version of the article (version of record). It first appeared online via Wiley at https://onlinelibrary.wiley.com/doi/full/10.1002/tcr.202000054 . Please refer to any applicable terms of use of the publisher. University of Bristol - Explore Bristol Research General rights This document is made available in accordance with publisher policies. Please cite only the published version using the reference above. Full terms of use are available: http://www.bristol.ac.uk/pure/user-guides/explore-bristol-research/ebr-terms/ Personal Account DOI: 10.1002/tcr.202000054 Prostaglandin Total Synthesis Enabled by THE the Organocatalytic Dimerization of CHEMICAL RECORD Succinaldehyde Steven H. Bennett,[a] Graeme Coulthard,[b] and Varinder K. Aggarwal*[a] In memory of Stuart Warren: a gentleman, a scholar, and a dedicated teacher of chemistry. Chem. Rec. 2020, 20, 1–13 © 2020 The Authors. Published by The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA 1 Personal Account THE CHEMICAL RECORD Abstract: Prostaglandins have been attractive targets in total synthesis for over 50 years, resulting in the development of new synthetic strategies and methodologies that have served the broader chemical community. However, these molecules are not just of academic interest, a number of prostaglandin analogues are used in the clinic, and some are even on the WHO list of essential medicines.