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4 edition of The Chemistry of cyanates and their thio derivatives found in the catalog.

The Chemistry of cyanates and their thio derivatives

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Published by J. Wiley in Chichester [Eng.], New York .
Written in English

    Subjects:
  • Cyanates.,
  • Thiocyanates.

  • Edition Notes

    Statementedited by Saul Patai.
    SeriesThe Chemistry of functional groups
    ContributionsPatai, Saul.
    Classifications
    LC ClassificationsQD305.A2 C495
    The Physical Object
    Pagination2 v. :
    ID Numbers
    Open LibraryOL4281496M
    ISBN 100471994251
    LC Control Number78307688

    Thio-analogues of 5,6-dihydrouracil and its methyl derivatives (I) showed characteristic reactivities towards nucleophiles, yielding ureas (II), carbamates (IV), and dimethoxy-derivatives (VI), when treated with methoxide ion. These reactions are affected by the . Hammerich O, Parker VD. () The electrochemistry of cyanates and related compounds The Chemistry of Cyanates and Their Thio Derivatives: Part 1. Hao W, Parker VD. () Rapid formation and slow collapse of a carbocation - Anion pair to a neutral molecule Journal of Organic Chemistry. Parker VD.


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The Chemistry of cyanates and their thio derivatives Download PDF EPUB FB2

The most complete resource in functional group chemistryPatais Chemistry of Functional Groups is one of chemistrys landmark book series in organic chemistry. An indispensible resource for the organic chemist, this is the most comprehensive reference available in functional group : Saul Patai.

The Chemistry of Cyanates and Their Thio Derivatives Parts 1 & 2. (The Chemistry of Functional Groups) Hardcover – January 1, by Saul Patai (Author) See all formats and editions Hide other formats and editionsAuthor: Saul Patai.

The most complete resource in functional group chemistry Patai's Chemistry of Functional Groups is one of chemistry's landmark book series in organic chemistry. An indispensible resource for the organic chemist, this is the most comprehensive reference available in functional group : Saul Patai.

Electronic structure of the cyanato and thiocyanato groups: ground state and excited states \/ Klaus Wittel, James L.

Meeks and Se\u00E9n P. McGlynn -- Structural chemistry of the cyanates and their thio derivatives \/ Istv\u00E1n Hargittai and Iain C. Paul -- Stereochemical and conformational aspects of cyanates and related groups \/ George C.

Patai's Chemistry of Functional Groups is one of chemistry's landmark book series in organic chemistry.

An indispensible resource for the organic chemist, this is the most comprehensive reference available in functional group chemistry. Electronic books: Additional Physical Format: Print version: Chemistry of cyanates and their thio derivatives.

Part 1. Chichester: Wiley, (OCoLC) Material Type: Document, Internet resource: Document Type: Internet Resource, Computer File: All Authors / Contributors: Saul Patai. Structural chemistry of the cyanates and their thio derivatives. In The Chemistry of Cyanates and Their Thio Derivatives: Part 1 (pp.

John Wiley and Sons by: 5. Cyanates and Their Thio Derivatives: Volume 1 () In book: Cyanates and Their Thio Derivatives: Volume 1 (), pp - and their bands intensify dramatically in. A 'read' is counted each time someone views a publication summary (such as the title, abstract, and list of authors), clicks on a figure, or views or downloads the full-text.

Cyanates and Their Thio Derivatives: Volume 2 () of Cyanates with Nucleic Acids and Their ConstituentsAction of Cyanates at the Cellular LevelToxicology and Pharmacology of.

For more than 50 passages, Smithsonian Conservation Biology Institute verbs are undergone at the book of using new directions at the Zoo and in their Christian files.

not, they are worrying a right cyanates and their thio derivatives volume 1 of new earnest job, century, l, experiments, set, simulation same site(EEHV), and the students /5. Document Type: Book: ISBN: OCLC Number: Description: XIV Seiten, Seite Series Title.

Structural chemistry of the cyanates and their thio derivatives István Hargittai Central Research Institute of Chemistry of the Hungarian Academy of Sciences, H‐ Budapest, Puskin utca.

Get this from a library. The chemistry of cyanates and their thio derivatives / 1. The chemistry of the — NCS group. In book: Cyanates and Their Thio Derivatives: Volume 2 () (pp - ) Ľ.

The chemistry of 4,6-dialkylamino-1,3,5-triazines with bulky alkyl. The Chemistry of Functional Groups: The Chemistry of Cyanates and their Thio Derivatives Edited by Saul Patel. Pp in two volumes. John Wiley and Son, Chichester and New York.

In the series The Chemistry of Functional Groups. £ This is Cited by: 5. Today numerous alkyl and aryl cyanates are available and a series of review articles – provide an excellent overview of the chemistry of this class of compounds.

Several tables listing numerous cyanates and the yields from different preparative procedures can be found.Discussion of individual examples therefore seems to be. The chemistry of the quinonoid compounds (2 volumes, 4 parts) The chemistry of the thiol group (2 parts) The chemistry of the hydrazo, azo and azoxy groups (2 volumes, 3 parts) The chemistry of amidines and imidates (2 volumes) The chemistry of cyanates and their thio derivatives (2 parts) The chemistry of diazonium and diazo groups (2 parts).

iso(thio)cyanates, organophosphorus compounds. ABSTRACT The cytotoxic activity of Iso(thio)cyanate derivatives and some new organophosphorus compounds were determined, using MTT assay against human hepatocellular carcinoma (HepG2) and adenocarcinoma breast (MCF-7) in comparison with the reference drug 5-flurouracil.

related functional groups on which no separate volume is planned (e.g. a chapter on. ‘Thioketones’ is included in the volume The Chemistry of the Carbonyl Group, and a. chapter on ‘Ketenes’ is included in the volume The Chemistry of Alkenes). Download Citation | Supplement B: The Chemistry of Acid Derivatives: Part 2 | The series 'The Chemistry of Functional Groups' is planned to cover in each volume all aspects of the chemistry.

select article The chemistry of cyanates and their thio derivatives: Parts 1 and 2: Edited by Saul Patai. xxii + John Wiley, Chichester.

£ (Thio)acyl(iso)(thio)cyanates, and -fulminates (R = R′, R′O, R′S, R 2 ′N). During my work on cyanates ina surprising observation was the formation of a peak at m/z 91 (C 6 H 5 N •+) in the mass spectrum of phenyl cyanate, PhOCN, and this became the base peak in the mass spectrum of phenyl isocyanate, by: 1.

Two types of rearrangements have been investigated computationally at the B3LYP/+G(d,p) level. The activation barriers for rearrangement of acyl thiocyanates RCO–SCN to the corresponding isothiocyanates RCO–NCS are 30–31 kcal/mol in agreement with the observation that the thiocyanates are in some cases isolable albeit very sensitive compounds.

Alkoxycarbonyl- (alkylthio)carbonyl Cited by: 9. Thanks to their high reactivities, cyanates, thiocyanates, isocyanates and isothiocyanates have widespread uses in preparative chemistry1 and attract the interest of physical-organic and theoretical chemists as well.

These compounds can also undergo several fascinating rearrangements. A number of 1,2- 1,3- and 1,4-shifts of substituent groups of. The Chemistry of Cyanates and Their Thio Derivatives, Part 1 (Patai's Chemistry of Functional Groups) (Pt. 2 (PATAI?S Chemistry of Functional Groups) Saul Patai.

Published by Wiley-Blackwell () ISBN Fair. This is an ex-library book and may have the usual library/used-book markings book has hardback covers. An ab initio study of the geometries and relative stabilities of isocyanates and cyanates. New York, ) eh. 16, and references therein. [2] D.A.

Ben-Efraim, in: The chemistry of cyanates and their thio derivatives, ed. Patai (Wiley. New York, ) eh. 5, and references therein.

[3] The chemistry of cyanates and their thio Cited by: Abstract. Anhydrous FeCl 3 oxidizes potassium thiocyanate to the corresponding radical and promotes subsequent addition to nucleophilic olefins to produce dithiocyanate derivatives under mild conditions with high efficiency. Excellent yields and chemoselectivities together with the environmental-friendly nature of the Fe(III) chloride makes this method an attractive alternative to established Cited by: Organization of the book.

Symbols used. Volumes and chapters of the series () 5. The chemistry of cyanates and their thio derivatives() The chemistry of diazonium and diazo groups() nitroso and nitro compounds and their derivatives() The chemistry of the metal-carbon bond.

Volume 1. The. This chapter discusses the chemistry and developments of N-thiocarbonyl carbohydrate N-thiocarbonyl compounds, conjugation of the π-system of the C=S group and the lone pair of nitrogen can take electron-donation effect of N-substituents at thiocarbonyl groups is quite important and stabilizing, more than in the related N-carbonyl by: Ben-Efraim DA () Detection and determination of cyanates, isocyanates isothiocyanates and thiocyanates.

In: Patai S (Ed) The Chemistry of Cyanates and their Thio Derivatives. Wiley, Chichester (vol 1, pp –) Google ScholarCited by: According to first-principles calculations, it should be possible to grow two-dimensional (2D) forms of copper thio-cyanate (CuSCN) and copper seleno-cyanate (CuSeCN) since their energies are only marginally higher than those of their most stable three-dimensional (3D) wurtzite structures.

Here we Cited by: 9. Other derivatives, usually prepared in situ, have been demonstrated to perform interesting reactions by a simple and efficient methodology.2 Continuing our studies on the chemistry of iodine (III) reagents,3 we describe here the reactivity of [bis(acetoxy)iodo]benzene (BAIB) with trimethylsilyl isothiocyanate (TMSNCS), as reagent combination Cited by: The chemistry of the carbon-halogen bond (2 parts) The chemistry of the quinonoid compounds (2 volumes 4 parts) The chemistry of the thiol group (2 parts) The chemistry of the hydrazo azo and azoxy groups (2 parts) The chemistry of amidines and imidates The chemistry of cyanates and their thio derivatives (2 parts).

Shaw, R., in “The Chemistry of Cyanates and their Thio Derivatives”, Part 1, Patai, S., Ed.; John Wiley and Sons: New York, Google Scholar. Drobnica L, Kristian P and Augustin J, ‘The Chemistry of cyanates and their thio-derivatives’ Part 2, Ed Patai S, New York, John Wiley and Sons, ; PUBLICATION SERVICES JournalsAuthor: Gunanka Hazarika, Pradeep K.

Tripathy. Part of the NATO ASI Series book series (ASIC, volume ) Abstract There are unambiguously linear and unambiguously bent molecules, and in between, there are also molecules that possess a flat potential energy minimum in the vicinity of the linear configuration and can Cited by: 2.

Thieme E-Books & E-Journals. DE EN; Home Products. Journals Books amino acid derivatives - thiocyanates - selenocyanates - [2+3] cycloaddition In The Chemistry of Cyanates and Their Thio Derivatives Part 2: Cited by: The chemistry of functional groups: The chemistry of cyanates and their thio derivatives Edited by Saul Patel.

Pp in two volumes. John Wiley and Son, Chichester and New York. in the series the chemistry of functional groups. £ Peter Sykes. Fragmentation: Larger alkyl fragments (with C n>4) are chiefly formed by direct dehydrogenate and undergo substantial H and skeleton rearrangements.

Smaller alkyl fragments (C 2 to C 4) are mainly formed by secondary decomposition of higher alkyl ations of groups from within the chain (and recombination of its ends) also occur.

John wiley sons the chemistry of organic derivatives of gold and silver patai   Rodd’s Chemistry of Carbon Compounds, Second Edition, Volume I, Part D: Dihydric Alcohols: Their Oxidation Products and Derivatives describes acyclic compounds containing two functional groups on different carbon atoms.

This volume is composed of six chapters, and begins with a description of dihydric alcohols and their Edition: 2.Thieme E-Books & E-Journals. DE EN; Home Products. Journals Books Division of Organic Chemistry, Indian Institute of Chemical Technology, HyderabadIndia Fax: 40 ; The Chemistry of Cyanates and their Thio Derivatives Part 2: Cited by: