[go: up one dir, main page]

Buckingham et al., 1970 - Google Patents

Cobalt (III)-promoted lysis at saturated carbon. Examples of internalucleophilic displacement

Buckingham et al., 1970

Document ID
4144443076045716923
Author
Buckingham D
Davis C
Sargeson A
Publication year
Publication venue
Journal of the American Chemical Society

External Links

Snippet

of Internal Nucleophilic Displacement Page 1 6159 Cobalt (III)-Promoted Lysis at Saturated Carbon. Examples of Internal Nucleophilic Displacement DA Buckingham, C. E. Davis, and A. M. Sargeson Contribution from the Research School of Chemistry, Australian National …
Continue reading at pubs.acs.org (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with heteroatoms or with carbon atoms having three bonds to hetero atoms, with at the most one to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/20—Carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/12—Oxygen or sulfur atoms

Similar Documents

Publication Publication Date Title
Buckingham et al. Stereochemistry and rearrangement in some triethylenetetramine disubstituted cobalt (III) ions
Buckingham et al. Cobalt (III)-promoted lysis at saturated carbon. Examples of internalucleophilic displacement
Weyh et al. Iminodiacetato, methyliminodiacetato, and 1, 3-propanediaminetetraacetato complexes of chromium (III)
Gore et al. Infrared absorption of aqueous solutions of organic acids and their salts
Shibahara et al. Preparation of trinuclear molybdenum (IV) ion, Mo3S4+ 4, and x-ray structure of Ca [Mo3S4 {HN (CH2CO2) 2} 3]· 11.5 H2O
Nakahara The Preparation and Properties of N-Salicylideneglycinato-aquo-copper (II), Sodium N-Salicylideneglycylglycinato-cuprate (II) and Related Compounds
Nakahara et al. The stability of fused rings in metal chelates. II. Copper (II) complexes of Schiff bases derived from pyruvic acid and amino acids or diamines
Gahan et al. Branched cyclononane macrocycles with pentaamine and tetraamine-thioether donors. Preparation and base hydrolysis of chlorocobalt (III) complexes
Buckingham et al. Labile (sulfonato) pentaamminecobalt (III) complexes: synthesis and kinetics and mechanism of acid and base hydrolysis
Isbell et al. Mechanisms for the mutarotation and hydrolysis of the glycosylamines and the mutarotation of the sugars
Kothari et al. Cobalt (III) complexes of cysteine and cysteine derivatives
Slebocka-Tilk et al. Effect of distortion on the hydrolytic reactivity of amides. 2. N-Pyramidalization: decomposition of N-benzoylaziridines in aqueous media
Buckingham et al. Cobalt (III)-promoted hydrolysis of chelated glycine esters. Kinetics, anion competition, and oxygen-18 exchange studies
Piper The Reaction of Tetrasulfurtetranitride with Nickel Chloride
Wieghardt et al. Synthesis and kinetics of the decarboxylation of two carbonate-bridged complexes of chromium (III) and rhodium (III). Crystal structure of. mu.-carbonato-di-. mu.-hydroxo-bis [(1, 4, 7-triazacyclononane) chromium (III)] diiodide hydrate
Buckingham et al. Intramolecular hydration of nitriles coordinated to cobalt (III). Formation of five-and six-membered chelated amides
Maley et al. Catalytic reactions involving azomethines. X. Transamination of 1-methyl-4-formylpyridinium iodide
Parker et al. Synthesis and characterization of stable rhenium (V) dioxo complexes with acyclic tetraamine ligands,[LReO2]+
Curtis et al. Synthesis, linkage isomerism, and ligand reactivity of (urea) pentaamminerhodium (III) complexes
US4060551A (en) Method of producing pantethine
Murakami et al. Catalysis of the. beta.-elimination of O-phosphothreonine by pyridoxal and metal ions
Fairlie et al. Cobalt-induced facile degradation of phenylurea to ammonia, carbon dioxide, and anilinium ion and other reactions of linkage isomeric cobalt (III) complexes of phenylurea
Buckingham et al. Cobalt (III)-promoted hydrolysis of glycine ethyl ester. Hg2+-induced acid hydrolysis and base hydrolysis of the. beta. 2-Co (trien) Cl (Gly-oet) 2+ ion
Francis et al. Kinetic study of the carbonate chelate ring opening of carbonatobisethylenediaminecobalt (III)(en) 2CoCO+ in alkaline solution
Vuletić et al. Co-ordination complexes of niobium and tantalum XVII. diperoxotetrafluoro-niobates (V) and tantalates (V)