Chemistry

Download Wiley Guide to Chemical Incompatibilities, 3rd Edition by Richard P. Pohanish, Stanley A. Greene PDF

By Richard P. Pohanish, Stanley A. Greene

"This ebook could be a required reference at the laboratory's security shelf as no the place else is quite a bit necessary details on hand in one volume."?Inside Laboratory administration, at the moment Edition"...a moveable reference on reactive components to steer all personnel...in cost of the dealing with, garage, and transportation of chemical materials."?Journal of the yankee Chemical Society, at the moment EditionThe authoritative source on risky chemical interactions now enlarged, revised, or even extra useful.The time period "incompatibilities" describes quite a lot of chemical reactions that produce bad leads to noncontrolled occasions: the iteration of poisonous gases, fireplace, explosions, corrosive job, polymerization, ruptured bins, construction of extra harmful compounds, and so forth. a transportable and easy-to-use reference on reactive elements as a rule present in trade, the Wiley advisor to Chemical Incompatibilities, 3rd variation compiles hard-to-find information on over 11,000 chemical substances, offering chemists, technicians, and engineers an intensive, lightning-quick source to exploit in the course of experimental training and within the occasion of an emergency.More than a revision of the former variation, this 3rd version has been rewritten and multiplied to develop insurance and enhance its usefulness. It includes approximately 9,000 chemical incompatibility profiles and approximately 250 new entries, masking flammability, violent and explosive binary reactions, incompatibilities, and reactions which can end result from actual switch. Alphabetical association offers concise incompatibility profiles for millions of typical advertisement chemical substances, permitting readers to appear up a given substance and immediately study if it is incompatible with universal fabrics, different chemical compounds, structural fabrics, or own protecting equipment.New for the 3rd version: chemical compounds that experience the capability to reason failures Chemical formulation and autoignition temperatures extra flash issues, in addition to molecular formulation, decrease and top explosive limits, autoignition temperatures, and NFPA?-type (Red) numerical fireplace codes protection reminders All entries keyed via CAS numbers to get rid of attainable confusion between synonyms Spanish-, French-, and German-language entries for overseas use Revised thesaurus is helping clients who is probably not chemists with common chemical phrases With millions of latest entries and easy-to-use association, the 3rd variation of the Wiley consultant to Chemical Incompatibilities continues to be a convenient source for all security, first-response, and plant administration execs chargeable for the dealing with, garage, and conveyance of chemical fabrics.

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Download The Alkaloids Chemistry and Physiology by R. H. F. Manske PDF

By R. H. F. Manske

The Alkaloids: Chemistry and body structure, quantity VI: complement to Volumes I and II updates the chemistry of the alkaloids by way of linking advancements to the content material of previous volumes. This booklet discusses the taxonomic place of the alkaloids in crops, exterior components governing alkaloid formation, pyrrolidine alkaloids, and constitution of the necines. The alkaloids of the pomegranate root bark, alkaloids of Sedum spp, constitution of dioscorine, and reactions of morphine and codeine also are elaborated. This e-book likewise covers the chemistry of colchicine, alkaloids derived from dibenzofuran, and organic results of the amaryllidaceae alkaloids. This quantity is an efficient reference for chemists and experts undertaking paintings on alkaloids.

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Download Opioid Analgesics: Chemistry and Receptors by Alan F. Casy, Robert T. Parfitt (auth.) PDF

By Alan F. Casy, Robert T. Parfitt (auth.)

The swiftly burgeoning learn of the prior twenty years on agonist-antagonist analgesics and opioid receptors makes this exhaustive evaluation of opioid anal­ gesics rather appropriate and well timed. After an introductory bankruptcy the extra 12 chapters start logically with morphine and congeners (4- epoxymorphinans) and finish with opioid receptors. All crucial chemical forms of centrally performing analgesics (including endogenous opioid-like ingredients) and their antagonists in addition to the combined agonist-antagonists are handled completely, even though no longer consistently (and for solid cause) in ancient (chrono­ logical) order. A bankruptcy on miscellaneous forms (atypical constructions for the main half) contains the benzimidazoles (etonitazene), aminotetralins (dezocine), tetrahydroisoquinolines (methopholine), etc. very important elements and correlations of chemistry, pharmacology, and biochemistry are mentioned extensive. Literature citations are a variety of. For educators, working towards laboratory scientists, and physicians, this scholarly overview through authors good of opioid analgesics versed within the chemistry, pharmacology, and biochemistry might be informative, stimulating, and thought-provoking. Everette L. may possibly scientific university of Virginia Richmond, VA 23298 v Preface The heritage of opium predates the written observe, even though wisdom of its materials dates again under two hundred years. Over the centuries its recognition for the comfort of ache has waxed and waned, till this present day the opiates are widely known as first-class analgesics yet with negative aspects that experience impaired their use heavily. there's a transparent want for a effective analgesic with minimum results at the respiration facilities and gastrointestinal tract and ideally without dependence liability.

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Download Biocompatible Polymeric Materials and Tourniquets for Wounds by Jan W. Gooch PDF

By Jan W. Gooch

In contemporary years biocompatible polymers for accidents and wounds have visible advances and suggestions that experience outpaced the becoming field's literature. during this e-book, Dr. Jan W. Gooch, a countrywide examine Council examine Associateship Award recipient, finds how cutting edge polymer know-how might be utilized to the typical strive against and trauma wounds linked to broken tender tissue and bleeding. The scope of his research, that is adapted to biomaterial scientists, polymer scientists, and biomedical engineers, spans 4 distinctive units for wounds: • Liquid and particulate barrier dressings for gentle tissue wounds • Sutureless tissue adhesives • Antibacterial nanoemulsions • One-hand operated and automated tourniquets for the battlefield

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Download The Third Component of Complement: Chemistry and Biology by J. E. Volanakis (auth.), John D. Lambris Ph. D. (eds.) PDF

By J. E. Volanakis (auth.), John D. Lambris Ph. D. (eds.)

The 3rd element of supplement, C3, is among the such a lot flexible proteins and an incredible player in immune surveillance and immune reaction pathways. Its multifunctio­ nality relies on its skill to engage in particular with a number of serum supplement proteins, cellphone floor receptors, and mem­ brant;-associated regulatory proteins. one in every of its so much fascinating recommendations of interplay with mobilephone surfaces is the covalent binding of activated C3 in the course of the inner thioester. the sphere has accelerated over the last 10 years and a wealth of data has accrued. C3 from quite a few species and plenty of of the human C3 binding proteins were cloned and expressed. quite a few mobile responses mediated by means of the diffe­ lease fragments of C3 were defined. The findings that C3 interacts in a ligand-receptor-like type with proteins of nonself beginning corresponding to the gC of herpes simplex virus, a 70-kDa protein from Candida albicans, proteins from Epstein-Barr virus, and so forth. has opened a brand new box of research. The papers assembled during this quantity summarize the wealth of information at the a number of elements of the C3 interactions; jointly they create to the reader new info at the chemistry, molecular gene­ tics, biology, and pathophysiology of C3 and C3-binding proteins. Emphasis is given to structural good points as they relate to capabilities. Spring 1989 JOHN D. LAMBRIS, HANS J. MULLER-EBERHARD desk of Contents J. E. VOLANAKIS: Participation of C3 and Its Ligands in supplement Activation . . . . . . . . . . . 1 S. R. BARNUM, G. FEY, and B. F. TACK: Biosynthesis and Genetics of C3 . . . . . . . . . . . . .

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Download Spectrometric Titrations volume Analytical Chemistry by Jürgen Polster, H. Lachmann PDF

By Jürgen Polster, H. Lachmann

Lately built equipment for the spectroscopic research of chemical equilibria are summarized sincerely and concisely during this ebook. The equipment themselves are acceptable to almost any spectroscopic method that produces an output sign linearly established upon the focus of answer elements, a criterion met via UV/vis, IR, fluorescence, CD, ORD, NMR, and ESR. tools of review appropriate to every of those sorts of spectroscopy also are handled within the textual content. An appendix directory the pc courses EDIA and TIFIT, which helped the authors to interpret their information, rounds off the publication. on account that equilibria play a basic function in a big selection of difficulties in either chemistry and biochemistry, this publication can be worthy not just to chemists and biochemists but additionally to biologists, pharmacologists and toxicologists.

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Download Chemistry and Metallurgy. Second Revised and Enlarged by A. Sherry, J. S. Beck, A. E. Cruddace PDF

By A. Sherry, J. S. Beck, A. E. Cruddace

Smooth strength Station perform, quantity five: Chemistry and Metallurgy makes a speciality of energy station chemistry and metallurgy.
The publication first deals info on strength station chemistry, together with the use, training, sampling, garage, and shipping of coal to strength stations. different issues comprise the industrial use of ash, research and trying out of coal and coke, gas-side cleansing of boilers, oil firing, burner fuels, trying out of gasoline oils and gases, and pollution.
The textual content additionally reports water remedy relative to the operation of boilers. The corrosion of metals; sampling and research of feed water, boiler water, and steam; instrumentation for qc; and on-load corrosion of boilers are mentioned. The booklet additionally appears at cooling water platforms in water remedy crops. subject matters contain water softening, evaporators, assets and caliber of uncooked water, demineralization, and boiler feed water composition.
The textual content additionally provides emphasis to plant cleansing and inspection and metallurgy and welding.
The publication is a worthwhile reference for readers attracted to strength station chemistry and metallurgy.

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Download Phosphorus Chemistry. Proceedings of the 1981 International by Louis D., & John G. Verkade, eds. Quin PDF

By Louis D., & John G. Verkade, eds. Quin

content material: Phosphorus-carbon compounds with p[pi]-p[pi] bonds / R. Appel --
Selective bond formation of organophosphorus acids with practical teams of organic significance / L. Horner, R. Gehring, and H.-W. Flemming --
Chemical synthesis and organic homes of the 5'-terminus of eukaryotic messenger ribonucleic acids (mRNA) / Tsujiaki Hata, Mitsuo Sekine, Iwao Nakagawa, Kazuo Yamaguchi, Shinkichi Honda, Takashi Kamimura, Kazuko Yamaguchi, and Kin-Ichiro Miura --
Triphenylphosphane-diethylazodicarboxylate : an invaluable process for directed structural version of carbohydrates / E. Zbiral, H.H. Brandstetter, and E. Mark --
man made software of aspect natural substituted phosphorus ylides / H.J. Bestmann --
Mono-, di-, and multi-ylides in organometallic chemistry / Hubert Schmidbaur --
man made and spectroscopic investigations related to [alpha]-heterosubstituted phosphonate carbanions / Hans Zimmer --
a brand new method of activation of hydroxy compounds utilizing pentacoordinated spirophosphoranes / J.I.G. Cadogan, I. Gosney, D. Randles, and S. Yaslak --
man made functions of [alpha]-amino substituted phosphine oxides / A. Van Der Gen and N.L.J.M. Broekhof --
Reactions of aziridines, 4-oxazolines, and their derivatives with alkylidene phosphoranes and phosphorus(III) nucleophiles / M. Vaultier and R. Carrié --
Phosphonates containing sulfur and selenium : synthesis, reactions, and new purposes / M. Mikołajczyk, S. Grzejszczak, W. Midura, M. Popielarczyk, and J. Omelańczuk --
Umpolung of [alpha], [beta]-ethylenic ketones and aldehydes through phosphorus teams / H.J. Cristau, J.P. Vors, Y. Beziat, C. Niangoran, and H. Christol --
Monomeric metaphosphates in enzymic and in enzyme-model structures / F.H. Westheimer --
Stereoelectronic results in phosphate esters / D.G. Gorenstein, R. Rowell, and okay. Taira --
Stereospecific synthesis and project of absolute configuration at phosphorus in nucleoside 3'- and 5'-O-arylphosphorothioates and nucleoside cyclic 3',5'-phosphorothioates / J. Baraniak, Z.J. Leśnikowski, W. Niewiarowski, W.S. Zieliński, and W.J. Stec --
The stereochemistry of chiral cyclic phosphorus esters : do theories of bond-forming and bond-breaking approaches healthy the proof? / Thomas D. Inch and C. Richard corridor --
The stereochemical process the alkaline hydrolysis of 1,3,2-oxazaphospholidine-2-thiones / C. Richard corridor and Thomas D. Inch --
Hydrolysis of adenosine 5'-triphosphate : an isotope-labeling examine / Seymour Meyerson, Eugene S. Kuhn, Fausto Ramirez, and James F. Marecek --
Nucleoside phosphorothioates for the learn of enzyme mechanisms / F. Eckstein --
Chiral [¹⁶O, ¹⁷O, ¹⁸O] phosphate monoesters for selecting the stereochemical process phosphokinases / Gordon Lowe, Paul M. Cullis, Richard L. Jarvest, and Barry V.L. Potter --
Syntheses and configurational assignments of thymidine 3'- and 5'-(4-nitrophenyl [¹⁷O, ¹⁸O] phosphates) / Shujaath Mehdi, Jeffrey A. Coderre, and John A. Gerlt --
The mechanism of aldehyde-induced ATPase actions of kinases / W.W. Cleland and Alan R. Rendina --
Kinetic and thermodynamic reviews of yeast inorganic pyrophosphatase / Barry S. Cooperman --
The position of histidine residues and the conformation of sure ATP on ATP-utilizing enzymes / P.R. Rosevear, G.M. Smith, S. Meshitsuka, A.S. Mildvan, P. Desmeules, and G.L. Kenyon --
[¹⁸O/[¹⁶O]³¹P-NMR stories of phosphoryl move enzymes / J.J. Villafranca, F.M. Raushel, R.P. Pillai, M.S. Balakrishnan, C. Debrosse, and T.D. Meek --
capability antiviral nucleotides / D.W. Hutchinson --
Phosphinomethanes : synthesis and reactivity / H.H. Karsch --
instruction and artificial reactions of [alpha]- alkoxyallyl phosphorus ylides / M. Maleki, J.A. Miller, and O.W. Lever, Jr. --
[Alpha]-phosphorylated carbanions : man made beneficial properties / G. Sturtz, B. Corbel, M. Baboulène, and J.J. Yaouanc --
a brand new synthesis of indoles / M. Le Corre, A. Hercouet, and H. Le Baron --
Alkylation when it comes to monomeric and polymeric alkoxyphosphonium salts / Donald W. Hamp and Edward S. Lewis --
a few preparative and mechanistic features of the chemistry of phosphoric acid and thiophosphoric acid chloride betaines / M. Meisel, C. Donath, and H. Grunze --
"Activated" phosphoranes for the cyclodehydration and chlorination of easy diols / S. Woody Bass, Carey N. Barry, Philip L. Robinson, and Slayton A. Evans, Jr. --
N-alkylation of organophosphorus amides : a brand new, handy path to fundamental and secondary amines / A. Zwierzak --
Phosphoric amide reagents / Erik B. Pedersen --
Reversible protecting of acetylcholinesterase via covalent phosphorylation within the presence of a unique cyclic phosphate ester / H. chief, L. Raveh, R. Brukstein, M. Spiegelstein, and Y. Ashani --
[Alpha]-aminophosphonous acids: a brand new category of biologically lively amino acid analogs / E.K. Baylis, C.D. Campbell, J.G. Dingwall, and W. Pickles --
Phosphonodipeptides / Lidia Kupczyk-Subotkowska, Pawel Kafarski, Janusz Kowalik, Barbara Lejczak, Przemyslaw Mastalerz, Józef Oleksyszyn, and Jerzy Szewczyk --
a few points of the chemical synthesis of oligodeoxyribonucleotides / Colin B. Reese and Lydia Valente --
Coupling of fatty diazomethylketones with organophosphorus acids : an method of glycerophospholipid analog synthesis / David A. Marsh and Joseph G. Turcotte --
layout of organophosphorus reagents for peptide synthesis / R. Ramage, B. Atrash, and M.J. Parrott --
the character of the power transduction hyperlinks in mitochondrial oxidative phosphorylation / Fausto Ramirez, Shu-I Tu, Prabha R. Chatterji, Hiroshi Okazaki, James F. Marecek, and Brian McKeever --
ADP hydrolysis promoted by means of cobalt(III) / Markus Hediger and Ronald M. Milburn --
PMR measurements of chair-twist conformational equilibria for diastereomeric P-derivatives of thymidine cyclic 3',5'-monophosphate : attainable implications for certainly happening cyclic nucleotides / Alan E. Sopchik, Gurdip S. Bajwa, Keith A. Nelson, and Wesley G. Bentrude --
Phosphonate inhibitors of carboxypeptidase A / Neil E. Jacobsen and Paul A. Bartlett --
"Illicit shipping" structures for organophosphorus antimetabolites / Maqsood Sheikh, Barry Gotlinsky, Burton E. Tropp, Robert Engel, and Thomas Parker --
The training of phosphorus esters and thioesters from white phosphorus / Charles Brown, Robert F. Hudson, Gary A. Wartew, and Harold Coates --
Thermal rearrangement and condensation of O, O-dimethyl-O-phenylphosphorothionate / Herbert Teichmann and Gerhard Schramm --
Synthesis and reactivity of (silylamino)phosphines / Robert H. Neilson, Patty Wisian-Neilson, David W. Morton, and H. Randy O'Neal --
Addition of lithium dialkylcuprates to [alpha], [beta]-unsaturated phosphoryl compounds : nucleophilic homes of adducts / R. Bodalski, T. Michalski, J. Monkiewicz, and K.M. Pietrusiewicz --
Phosphorylated ketenes / O.I. Kolodyazhnyi, V.I. Yakovlev, and V.P. Kukhar --
coaching and homes of N-(Hydroxycarbonylmethyl)aminomethyl alkyl- and arylphosphinic acids and derivatives / Ludwig Maier --
a few elements of aminoalkylphosphonic acids synthesis via the reductive amination strategy / P. Savignac and N. Collignon --
fresh effects on open-chain and cyclic phosphanes and organylphosphanes / Marianne Baudler --
Formation of phosphorus oxoacids with P-P-P-P-P-P and P-P-P-P-P frameworks and similar compounds / Toshio Nakashima, Hirohiko Waki, and Shigeru Ohashi --
NMR characterization of homologous cyclic phosphoramides / Jack E. Richman, Robert B. Flay, and O.D. Gupta --
Synthesis and chemical habit of a few bicyclophosphanes / C. Bonningue, O. Diallo, D. Houalla, A. Klaebe, and R. Wolf --
Reactions of 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide / Sven-Olov Lawesson --
Small jewelry with tervalent phosphorus / Ekkehard Fluck and Horst Richter --
The unforeseen formation of 1,2-oxaphosphol-3-ene 2-oxides within the response of diacetone alcohol with phosphonous dihalides / Kurt Moedritzer and Raymond E. Miller --
Dihydrophenophosphazines through the interplay of diarylamines and phosphorus trichloride : purposes and obstacles / Harold S. Freeman and Leon D. Freedman --
Contributions to the chemistry of N-phosphoryl phosphazenes / L. Riesel, E. Herrmann, A. Pfützner, J. Steinbach, and B. Thomas --
Conjugation in phosphazenes: pyrrylphosphazenes and phosphazenyl carbanions / K.D. Gallicano, R.T. Oakley, R.D. Sharma, and N.L. Paddock --
constitution, conformation, and basicity in cyclophosphazenes and comparable compounds / R.A. Shaw and S.N. Nabi --
Phosphazene jewelry and excessive polymers associated with transition metals or biologically energetic natural species / H.R. Allcock --
Polymerization of hexachlorocyclotriphosphazene / John W. Fieldhouse and Daniel F. Graves --
Alkenylfluorocyclotriphosphazenes / Christopher W. Allen, Randall P. vibrant, and Kolikkara Ramachandran --
The reactions of halophosphazenes with organometallic reagents / Paul J. Harris and Harry R. Allcock --
1,2-bis(dichlorophosphino)alkanes / E.H. Uhing and A.D.F. Toy --
items of peracid oxidation of S-alkyl phosphorothiolate insecticides / Yoffi Segall and John E. Casida --
learn on organophosphorus pesticides, synthesis of O-alkyl O-substituted phenyl alkylphosphonothioates / Wu Kiun-Houo, solar Yung-Min, and Wang Sing-Min --
creation of phosphorus into the polyethyleneterephthalate molecule / G. Borisov, ok. Troev, and A. Grozeva --
chosen novel trivalent organophosphorus processing stabilizers for polyolefins / J.D. Spivack, A. Patel, and L.P. Steinhuebel --
Oligomeric phosphorus esters with flame retardant application / Edward D. Weil, Ralph B. Fearing, and Fred Jaffe. Crystalline calcium polyphosphate fibers / E.J. Griffith --
Fluorination of phosphoapatites : attainable adjustments in their constitution / G. Montel, G. Bonel, J.C. Heughebaert, M. Vignoles, M. Hamad, and G. Bacquet --
photograph- and thermo-coloring of diminished phosphate glasses / Y. Abe, R. Ebisawa, D.E. Clark, and L.L. Hench --
A gel chromatographic learn at the interactions of long-chain polyphosphate anions with magnesium ions / Tohru Miyajima, Toshimitsu Onaka, and Shigeru Ohashi --
Phosphaalkenes, R₂C=PR', and phosphaalkynes, RC:::P / H.W. Kroto and J.F. Nixon --
fresh advancements within the chemistry of dicoordinated phosphorus radicals and cations / S.G. Baxter, A.H. Cowley, R.A. Kemp, S.K. Mehrotra, and J.C. Wilburn --
³¹P NMR investigations on dicoordinated phosphorus compounds in P(II) = C-P(III) structures / R. Appel, V. Barth, H. Kunze, B. Laubach, V. Paulen, and F. Knoll --
Synthesis and houses of phosphaalkenes / T.A. Van Der Knaap, T.C. Klebach, F. Visser, R. Lourens, and F. Bickelhaupt --
Routes to dicoordinated phosphorus compounds / okay. Issleib, H. Oehme, H. Schmidt, and G.-R. Vollmer --
Reactions of 2,4,6-tri(t-butyl)phenyllithium with phosphorus halides / Masaaki Yoshifuji, Ichiro Shima, and Naoki Inamoto --
Synthesis of recent dicoordinated phosphorus compounds with a P(III)=N bond / C. Malavaud, L. Lopez, T. N'gando M'pondo, M.T. Boisdon, Y. Charbonnel, and J. Barrans --Cyano anions of dicoordinated, tricoordinated, tetracoordinated, pentacoordinated, and hexacoordinated phosphorus / Alfred Schmidpeter, Franz Zwaschka, and William S. Sheldrick --
coaching, reactions, and buildings of a few N, N'-dimethylurea-bridged phosphorus compounds / Norbert Weferling and Reinhard Schmutzler --
A strong monocyclic triarylalkoxyhydridophosphorane / A 10-P-5 species with an apical P-H bond --
Michael R. Ross and J.C. Martin --
Monocyclic phosphoranide and phosphoranoxide anions : P(V) oxyphosphorane carbanion --
P(IV) ylide alkoxide tautomerism / Itshak Granoth, Rivka Alkabets, Ezra Shirin, Yair Margalit, and Peter Bell --
Selectivity in reactions of tricyclic phosphatranes / D. Van Aken, I.I. Merkelbach, J.H.H. Hamerlinck, P. Schipper, and H.M. greenback --
The perfluoropinacolyl crew : a stabilizing substituent for strange phosphites and phosphoranes / Gerd-Volker Röschenthaler, Rainer Bohlen, and Werner Storzer --
Tartaric acid in phosphorus chemistry : phosphor emetics and oligomers / A. Munoz, L. Lamandé, M. Koenig, and R. Wolf --
Nucleophilic substitution at pentacoordinated phosphorus : addition-elimination mechanism / A. Skowrońska, J. Stanek-Gwara, and M. Nowakowski --
steel chelates of aminoalkylphosphonic acids : stabilities, homes, and reactions / Arthur E. Martell --
Transition VIB steel [pi]-complexes of [lambda]³- and [lambda]⁵-phosphorins and a few in their reactions / okay. Dimroth --
Synthesis of transition steel phosphoranides : conversion of bicyclic phosphoranes into phosphoranides and phosphane adducts with transition steel derivatives / J.G. Riess, F. Jeanneaux, P. Vierling, J. Wachter, and A. Grand --
Secondary phosphino macrocyclic ligands / Evan P. Kyba and Heinz H. Heumüller --
Dicoordinated and tricoordinated acyclic phosphazenes as complicated ligands / O.J. Scherer, H. Jungmann, and R. Konrad --
steel complexes of amino(cyclophosphazenes) / V. Chandrasekhar, S.S. Krishnamurthy, and M. Woods --
Structural and magnetic research on transition steel complexes with tripodal polytertiary phosphines / L. Sacconi --
using alkylaminobis(difluorophosphines) as ligands to stabilize novel binuclear complexes / J.H. Kim, K.S. Raghuveer, T.W. Lee, L. Norskov-Lauritzen, V. Kumar, M.G. Newton, and R.B. King --
New elements of the coordination chemistry of carbonyl phosphines / Edith F. Landvatter and Thomas B. Rauchfuss --
New chiral aminophosphine ligands : program to catalytic uneven C-C bond formation / Gérard Buono, Christian Triantaphylides, Gilbert Peiffer, André Mortreux, and Francis Petit --
31P NMR reviews of catalytic intermediates in triphenylphosphine rhodium advanced hydroformylation structures / Alexis A. Oswald, Joseph S. Merola, Edmund J. Mozeleski, Rodney V. Kastrup, and John C. Reisch --
New facts at the mechanism of the Perkow-Arbuzov response / László Tőke, Imre Petneházy, Győngyi Szakál, Harry R. Hudson, Luba Powroznyk, and Christopher J. Cooksey --
constitution and reactivity of quasiphosphonium intermediates / H.R. Hudson, A.T.C. Kow, and ok. Henrick --
Reactions of triorganosilyl halides with esters of tricoordinated and tetracoordinated phosphorus / J. Chojnowski, M. Cypryk, J. Michalski, and L. Wozniak --
Halogenolysis of the phosphorus-sulfur bond in thioloesters of natural phosphorus thioacids / B. Krawiecka, J. Michalski, and E. Tadeusiak --
Isotope results in amination reactions of chlorocyclophosphazenes / J.M.E. Goldschmidt, R. Halevi, and E. Licht --
Zwitterionic [sigma]-complexes : their function as intermediates in phosphorylation of aromatics through phosphorus compounds / Y. Gololobov and P. Onys'ko --
Use of X-ray structural effects on phosphorus compounds in modeling response mechanisms / Robert R. Holmes, Judith C. Gallucci, and Joan A. Deiters --
Ligand results at the response of alkoxide ions with organophosphorus derivatives containing a number of leaving teams / Kenneth E. Debruin, Charles E. Ebersole, Morgan M. Hughes, and David M. Johnson --
Methanolysis of a phosphate ester / William S. Wadsworth, Jr. --
Reactivity of tricoordinated phosphorus compounds : a mechanistic examine with numerous substrates / C. Dennis corridor, Robert C. Edwards, John R. Lloyd, Paul D. Beer, Philip J. Hammond, Alberto O. D'amorim, and Melvin P. Melrose --
a brand new stereospecific synthesis of a P(III) organophosphorus ester / Leonard J. Szafraniec, Linda L. Szafraniec, and Herbert S. Aaron --
A unmarried crystal X-ray diffraction research of (1R,1'S)-1,1'-ethylenebis(1,2,3,4-tetrahydro-4,4-dimethyl-1-phenylphosphinolinium) diperchlorate / Narayanasamy Gurusamy, ok. Darrell Berlin, Dick Van Der Helm, and M. Bilayet Hossain --
Stereochemical research of chiral onium hexaarylphosphates / G.P. Schiemenz and J. Pistor --
Spectroscopy of phosphorus compounds : d[pi]-p[pi] bonding results at the 31P NMR chemical shifts of N-aryliminophosphoranes / Philip C. Murphy and John C. Tebby --
¹H, ¹⁹F, ³¹P, and ¹³C NMR research of diphosphanes and triphosphanes / J.P. Albrand and C. Taïeb --
crucial ³¹P chemical shift tensor elements as decided by way of reliable country NMR / J.P. Dutasta, J.B. Robert, and L. Wiesenfeld --
software of the ¹⁸O shift at the ³¹P NMR spectrum to the elucidation of biochemical phosphate move mechanisms / Frank Jordan, Salvatore J. Salamone, and Alice L. Wang --
Phospholipase A2 hydrolysis of phospholipids : use of ³¹P NMR to review the hydrolysis, acyl migration, regiospecific synthesis, and solubilization of phospholipids / Andreas Plũckthun and Edward A. Dennis --
Photolytic rearrangement of phosphorus, germanium, and silicon azides : proof for brand spanking new hybridized species / J.P. Majoral, G. Bertrand, A. Baceiredo, and P. Mazerolles --
Diphenylphosphinous acid through UV irradiation of aroyl diphenyl phosphines / okay. Praefcke and M. Dankowski --
Chemical version displaying 3 phenomena : phosphorane [yields] ylide, ylide [yields] phosphorane, and phosphorane [equilibrium] ylide / Ramon Burgada, Yves Leroux, and Y.O. El Khoshnieh --
Base-catalyzed reactions of phosphonomethylphosphinates, bis(phosphonomethyl)phosphinates, and bis(phosphonomethyl)phosphinic amides with aldehydes / W. Franklin Gilmore and Joon Sup Park --
Structure-reactivity stories on oxygen-containing phosphorus-based ligands / Yuan Chengye, Ye Weizhen, Zhou Chengming, and Hui Yongzheng --
Phosphoric and carboxylic amides : comparability of bonding and reactivity / Tomasz A. Modro.

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