William D. Morton

ORCID: 0000-0003-2269-6451
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About
Contact & Profiles
Research Areas
  • Fluorine in Organic Chemistry
  • Synthesis and Reactions of Organic Compounds
  • Inorganic Fluorides and Related Compounds
  • Chemical Reactions and Mechanisms
  • Chemical Synthesis and Reactions
  • Synthesis and properties of polymers
  • Anesthesia and Sedative Agents
  • Renal function and acid-base balance
  • Inorganic and Organometallic Chemistry
  • Per- and polyfluoroalkyl substances research
  • Non-Invasive Vital Sign Monitoring
  • Porphyrin and Phthalocyanine Chemistry
  • Renin-Angiotensin System Studies
  • 3D Printing in Biomedical Research
  • Hemodynamic Monitoring and Therapy
  • Synthesis and Catalytic Reactions
  • Complement system in diseases
  • Nausea and vomiting management
  • Physiological and biochemical adaptations
  • Carbon dioxide utilization in catalysis
  • Cyclopropane Reaction Mechanisms
  • Catalysis and Oxidation Reactions
  • History and advancements in chemistry
  • Chemical Reaction Mechanisms
  • Anesthesia and Pain Management

Confluence Life Sciences (United States)
2022-2024

McMaster University
1989-1997

University of Manchester
1980-1989

SickKids Foundation
1987-1988

University of Toronto
1987-1988

Hospital for Sick Children
1987-1988

Institute of Science and Technology
1980

Queen's University
1978

Occidental College
1964

Planaria which have cannibalized untrained planaria exposed to photic stimuli only, handling or previous conditioning, all require significantly fewer trials in a conditioning situation than naive planaria.

10.1126/science.146.3641.274 article EN Science 1964-10-09

The epidermis is a barrier that prevents water loss while keeping harmful substances from penetrating the host. impermeable cornified layer of stratum corneum maintained by balancing continuous turnover driven epidermal basal cell proliferation, suprabasal differentiation, and corneal shedding. desquamation process tightly regulated balance activities serine proteases Kallikrein-related peptidases (KLK) family their cognate inhibitor lymphoepithelial Kazal type-related (LEKTI), which encoded...

10.1126/scitranslmed.abp9159 article EN Science Translational Medicine 2022-12-14

N-Fluoroquinuclidinium fluoride, prepared in high yield by treatment of a cold, dilute solution quinuclidine trichlorofluoromethane with fluorine at low pressure specially designed, virtually all glass vacuum system, acts as site-selective electrophilic fluorinating agent towards carbanionic substrates [PhCNa(CO2Et)2→ PhCF(CO2Et)2; Me2CLiNO2→ Me2CFNO2; RMgX → RF (R = Ph, X Br; R c-C6H11, Cl); [graphic omitted]H2→ omitted]HF; PhSiCl3/F–(in situ)→ PhF].

10.1039/p19880002805 article EN Journal of the Chemical Society. Perkin transactions I/Journal of the Chemical Society. Perkin transactions. I 1988-01-01

10.1007/bf03014455 article EN Canadian Journal of Anesthesia/Journal canadien d anesthésie 1997-04-01

Perfluorovinylsulphur pentafluoride is attacked by sodium methoxide in methanol to give 1,2,2-trifluoro-2-methoxyethylsulphur pentafluoride, and bromine (→ SF5·CFBr·CF2Br), hydrogen bromide SF5·CHF·CF2Br), trifluoroiodomethane SF5·CFl·C2F5) under photochemical conditions monochloride SF5·CFCl·CF2Br, SF5·CFBr·CF2Cl) thermal yield the corresponding 1 : adducts by-products derived from C–S bond fission. Hexafluoro-1,1-di-iodopropane, a by-product of reaction between olefin trifluoroiodomethane,...

10.1039/p19740001266 article EN Journal of the Chemical Society. Perkin transactions I/Journal of the Chemical Society. Perkin transactions. I 1974-01-01

10.1007/bf03007694 article EN Canadian Journal of Anesthesia/Journal canadien d anesthésie 1987-01-01

1. The rate of smooth muscle cell proliferation in age-matched 1-4-week-old spontaneously hypertensive (SHR) and normotensive Wistar-Kyoto (WKY) rats was compared using autoradiography. 2. Labelling index, defined as labelled cells/sum unlabelled cells × 1000, obtained from perfusion-fixed superior mesenteric large arteries. 3. In the arteries, labelling indices were similar between SHR WKY at all age groups, except 1 week when index higher SHR. 4. rat strains groups. 5. We conclude that,...

10.1042/cs0760475 article EN Clinical Science 1989-05-01

U.v. irradiation of a mixture sulphur chloride pentafluoride and trifluoroethylene yields (ca. 7 : 3) 2-chloro-1,2,2-trifluoroethylsulphur (I) 2-chloro-1,1,2-trifluoroethylsulphur (II). Both (II) give, inter alia, chlorotrifluoroethylene when pyrolysed. Isomer perfluorovinylsulphur treated with potassium hydroxide, but isomer appears to be completely destroyed by this reagent.

10.1039/j39690001947 article EN Journal of the Chemical Society C Organic 1969-01-01

Photochemical isomerization of 1-ethoxycarbonyl-, 1-cyano-, or 1-amido-hexafluoro-1H-azepine yields the respective 2-substituted hexafluoro-2-azabicyclo[3.2.0]hepta-3,6-diene (92–98%).The 2-ethoxycarbonylheptadiene undergoes Diels–Alder addition cyclopentadiene, to give four adducts by exo-attack at CFCF bonds, and furan, three analogous (attack CFCFN bond is preferred), adds phenyl azide reluctantly a 15 : 2 1 mixture adducts, where predominates, gives 3 trans- cis-exo-3,4-dibromides,...

10.1039/p19820002105 article EN Journal of the Chemical Society. Perkin transactions I/Journal of the Chemical Society. Perkin transactions. I 1982-01-01

Hexafluorobicyclo[2,2,0]hexa-2,5-diene reacts with chlorine or bromine in the dark to give a mixture of corresponding exo,exo- and trans-5,6-dihalogenohexafluorobicyclo[2,2,0]hex-2-enes; further, photochemical reaction halogen gives all-exo- exo,exo,exo,endo-2,3,5,6-tetrahalogenohexafluoro[2,2,0]hexanes. Catalytic hydrogenation diene at –50° exo-5H,6H/-hexafluorobicyclo[2,2,0]hex-2-ene. Hydrogen bromide adds photochemically mainly bicyclohexene arising from cis,exo-addition; cis,exo-addition...

10.1039/p19720002170 article EN Journal of the Chemical Society. Perkin transactions I/Journal of the Chemical Society. Perkin transactions. I 1972-01-01

Hexafluorobicyclo[2.2.0]hexa-2,5-diene is an active dipolarophile, reacting with the representative 1,3-dipoles phenyl azide. diazomethane, 2,2,2-trifluorodiazoethane. 2,4,6-trimethylbenzonitrile oxide, and benzonitrile N-phenylimide to give 1 : adducts, mixtures of 2 adducts. Related compounds are similarly reactive, addition CF:CF double bond 2-methoxypentafluorobicyclo [2.2.0]hexa-2,5-diene, exo-5,6-dibromohexa-fluorobicyclo [2.2.0]hex-2-ene, occurring azide respectively. 19F N.m.r....

10.1039/p19730001798 article EN Journal of the Chemical Society. Perkin transactions I/Journal of the Chemical Society. Perkin transactions. I 1973-01-01

The hexafluoro-Dewar-benzene adduct of phenyl azide yields hexafluoro-1-phenyl-1H-azepine on pyrolysis. Reaction ethyl azidoformate with hexafluorobenzene hexafluoro-1H-azepine-1-carboxylate (21%), octafluoronaphthalene 1,2-(ethoxycarbonylimino)-1,2,3,4,5,6,7,8-octafluoro-1,2-dihydronaphthalene (23%), and 1,2,3,4-tetrafluoronaphthalene 1,2-(ethoxycarbonylimino)-1,2,3,4-tetrafluoro-1-1,2-dihydronaphthalene (18%) 5,6,7,8-tetrafluoro-1-naphthylcarbamate (48%). No azepines were obtained from the...

10.1039/p19820002101 article EN Journal of the Chemical Society. Perkin transactions I/Journal of the Chemical Society. Perkin transactions. I 1982-01-01

Hexafluoropropene reacts with pentafluorobenzonitrile in the presence of caesium fluoride to give two mono-(2- and 4-), di-(2,4- 2,5-), tri-(2,4,5- 2,4,6-)(perfluoroisopropyl) derivatives; no solvent is necessary. The 2,4,5-derivative rearranges less sterically hindered 2,4,6-derivative when heated ion. ring fluorine atoms perfluoroisopropyl derivatives are highly susceptible nucleophilic displacement; cyano-group resists hydrolysis.

10.1039/p19750001035 article EN Journal of the Chemical Society. Perkin transactions I/Journal of the Chemical Society. Perkin transactions. I 1975-01-01

In this study, the cardiac output of 11 children (5 days to 18 yr age) was measured following cardiopulmonary bypass. Standard dye dilution outputs and an indirect Fick-CO2 technique were simultaneously determined. A rebreathing maneuver is described estimate oxygenated mixed venous PCO2 (PvCO2). This PvCO2 combined with end tidal CO2 production give a non-invasive Fick output. Non-invasive correlated well those by dye-dilution (r2 = 0.94) over range from 490-7280 ml/min. All determinations...

10.1097/00000542-198808000-00011 article EN Anesthesiology 1988-08-01

Abstract Die Titelverbindung (I) addiert Chlor unter Bildung der Isomeren (IIa) und (IIIa) (bei äquimolarer Chlor‐Menge im Dunkeln bei Raumtemperatur) bzw. (IVa) (Va) Chlorüberschuß Licht).

10.1002/chin.197248238 article DE Chemischer Informationsdienst 1972-11-28

Abstract Die bereits ohne Lösungsmittel in Gegenwart von CsF ablaufende Reaktion zwischen den Titelverbindungen (I) und (II) [Bildung der Produkte (III)‐(VI) Reaktionsbedingungen abhängiger Verteilung] wird untersucht.

10.1002/chin.197538111 article DE Chemischer Informationsdienst 1975-09-23

Abstract Die Titelverbindung reagiert mit den entsprechenden 1,3‐dipolaren Verbindungen zu 1:1‐Addukten (I) bzw. (II).

10.1002/chin.197346110 article DE Chemischer Informationsdienst 1973-11-13
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