about
COSMO: a new approach to dielectric screening in solvents with explicit expressions for the screening energy and its gradientCharacterization of two polymorphic forms of tolfenamic acid, N-(2-methyl-3-chlorophenyl)anthranilic acid: their crystal structures and relative stabilitiesMechanistic studies on the reaction of nitro- and nitrosoarenes with vinyl Grignard reagentsRing size configuration effect and the transannular intrinsic rates in bislactam macrocyclesCorrelation of biological activity in β-lactam antibiotics with Woodward and Cohen structural parameters—a Cambridge database studyThe acid–base behaviour of hexamine and its N-acetyl derivativesThe mechanism of the metal ion promoted cleavage of RNA phosphodiester bonds involves a general acid catalysis by the metal aquo ion on the departure of the leaving groupThe conformational behaviour of thiacalix[4]arenes: the pinched cone–pinched cone transitionThe kinetics of hydrolysis of methyl and phenyl lsocyanatesPentazole chemistry: the mechanism of the reaction of aryldiazonium chlorides with azide ion at −80 °C: concerted versus stepwise formation of arylpentazoles, detection of a pentazene intermediate, a combined 1H and 15N NMR experimental and ab iPentazoles: proton and carbon-13 NMR spectra of some 1-arylpentazoles: kinetics and mechanism of degradation of the arylpentazole systemReaction of benzyne with [70]fullerene gives four monoadducts: formation of a triptycene homologue by 1,4-cycloaddition of a fullereneProtonation sequence of linear aliphatic polyamines by 13C NMR spectroscopyReactions of carbonyl compounds in basic solutions. Part 32.1 The Perkin rearrangementThe hydration and polymerisation of succinaldehyde, glutaraldehyde, and adipaldehydeCrystal structures of some acid salts of monobasic acids. Part XVII. Structure of sodium hydrogen diacetate, redetermined by neutron diffractionKinetics and mechanisms of the Bamberger rearrangement. Part 3. Rearrangement of phenylhydroxylamines to p-aminophenols in aqueous sulphuric acid solutionsKinetic substituent and isotope effects in the acid-catalysed rearrangement of N-phenylhydroxylamines. Are nitrenium lons involved?Conformation and intermolecular interactions of Meldrum's acid: an X-ray structural investigation of 2,2-dimethyl-1,3-dioxane-4,6-dioneSandmeyer reactions. Part 5. Estimation of the rates of 1,5-aryl/aryl radical translocation and cyclisation during Pschorr fluorenone synthesis with a comparative analysis of reaction energeticsSelective complexation of soft Pb2+ and Hg2+ by a novel allyl functionalized thioamide calix[4]arene in 1,3-alternate conformation: a UV-visible and 1H NMR spectroscopic investigationHeteroaromatic hydrogen exchange reactions. Part VIII. The ionisation of 1,3-dimethylindolin-2-oneKinetics of the hydrolysis and perhydrolysis of tetraacetylethylenediamine, a peroxide bleach activatorInsecticides. Part II. Crystal structures of 1,1-bis-(p-chlorophenyl)-2,2,2-trichloroethane (p,p′-DDT) and 1-(o-chlorophenyl)-1-(p-chlorophenyl)-2,2,2-trichloroethane (o,p′-DDT)Reactions of β-trimethylstannylcyclohexanones with peracids: investigations into the stannyl-directed Baeyer–Villiger reactionAromatic acylations catalysed by metal oxidesThe crystal structure of the ? form of quinolSpectroscopic studies on ranitidine—its structure and the influence of temperature and pHQuantitative measurement of proton dissociation and tautomeric constants of apigeninidinThermal isomerization of photochemically synthesized (Z)-9-styrylacridines. An unusually high enthalpy of Z→E conversion for stilbene-like compoundsMechanism of the periodate oxidation of ethane-1,2-diamine, NN′-dimethylethane-1,2-diamine, and 2-aminoethanolThe catalytic resting state of asymmetric homogeneous hydrogenation. Exchange processes delineated by nuclear magnetic resonance saturation-transfer (DANTE) techniquesTautomeric pyridines. Part XV. Pyridone–hydroxypyridine equilibria in solvents of differing polaritySynthesis and thermolysis of rhodium and iridium complexes of endo-6-vinylbicyclo[3.1.0]hex-2-ene. A metal-promoted vinylcyclopropane to cyclopentene rearrangementSynthesis and crystal structure of the bromide salt of the inside protonated form of the cage amine [(2.3)3]adamanzane, 1,4,8,12-tetraazatricyclo[6.6.3.24,12]nonadecane and synthesis of the bowl amine [(2.3)2.21]adamanzane, 1,5,9,12-tetraazabicyclo[7A theoretical conformational study of push–pull ethylenes. Part 1. Substituted methyleneimidazolidinesCrystal, molecular, and electronic structure of 13,13-difluoro-1,7-methano[12]annuleneCrown-containing styryl dyes: cation-induced self-assembly of multiphotochromic 15-crown-5 ethers into photoswitchable molecular devicesPhotoswitchable molecular pincers: synthesis, self-assembly into sandwich complexes and ion-selective intramolecular [2+2]-photocycloaddition of an unsaturated bis-15-crown-5 etherThe cyclization of N-butylpent-4-enylaminyl revisited: a combined theoretical and experimental study †
P1433
Q29011962-5F49615C-A7DC-45FE-BE39-8B093D1254F8Q29029207-4F8FDD27-AB83-437A-883C-B10E342E8D89Q29039259-2793775E-1A49-452C-A41C-7220289B05B3Q29400083-41D0D39D-CD2C-400F-851E-0C44F44E1826Q55889174-1E06F75A-D37B-4B0C-B360-6B28B7FAC8CAQ56018213-E653EFEB-1D5D-43C3-8AF3-41DDA88FF15FQ56060453-372150EF-8F8F-4E45-BAA6-DA0F9A9D55F8Q56084967-DC8EDC48-0FF0-471F-87A8-503DDCF834DFQ56112928-8973C9C7-3153-4189-9D82-0A8A97682270Q56421669-B8CB1049-7537-4F23-8982-2CBB074D9AE7Q56421831-E4A26A23-A72C-4205-ABA3-727685A9A426Q56421841-E0C9B774-227E-41E1-8FC1-F13535EA843BQ56456895-1681A800-6E63-4972-8F27-C3AD7D7A177BQ56502996-310B8580-7AD6-4329-A311-0F9140415DD6Q56531031-F009D971-53F9-43A0-AE99-E13DB2778708Q56531046-9FCE1E4E-4798-4369-B32D-52A06890E4E0Q56531066-C2BBF978-8F9A-481E-93D5-138C0A918632Q56531090-B12A93F9-56A6-473C-8778-F98E0469FFA8Q56531118-A260E668-1F4D-4A1F-ADD9-EBE7C5130C6DQ56535526-ADF5F390-09BA-41C4-8C04-F349DE03FF4FQ56535654-D10B1457-63F9-465E-B0FC-10015C4CEB3FQ56535764-AB54A9B9-EE8C-4EAD-9441-389A3EDD93E0Q56566129-98663BB4-A04E-4F01-96EE-1E57B43E2383Q56637631-C6FBF525-61FF-4FB8-AD52-46FF930B0C2CQ56656010-393A797F-9028-41B3-9173-32207E697A35Q56656516-4BC8DBBF-119B-4460-841D-F6DFB89200FAQ56657812-93C91648-E004-490B-A2A1-DE4D626B58A9Q56658263-DED3A6E5-5938-4769-B3DD-EEFD86FEF6A7Q56659274-FF7E60AF-73F0-4762-9423-5A66991982B6Q56680337-40BD427A-25BA-41CC-94D9-5D1450AE8791Q56807416-7AEF31F1-C783-4120-A856-80320C946F02Q56812951-BB1A2246-DEE4-4250-B721-B1884FD30386Q56864629-792F5BBD-4127-4A87-B1F4-15BB286B6DBCQ56866074-AD88AE8A-FE50-49B8-84FC-0E2A11C43E51Q56956418-FC9FF04E-9F42-4691-8432-8EA2A74347C3Q56979091-4E5159B4-A0EA-41D2-8BC4-FE3E3054F75DQ56979121-B3861AB4-4920-4EA0-AE63-294DEC01D4A2Q56983223-1A826C51-FCEB-4E46-B768-7798B52205F6Q56983232-63A51556-D0BC-4984-B9D5-0BE2B17C150CQ56983823-C58D025D-1A8A-409F-8AA2-F56E16B9958B
P1433
description
journal
@en
revista científica
@es
wetenschappelijk tijdschrift van Royal Society of Chemistry
@nl
wissenschaftliche Fachzeitschrift
@de
name
Perkin transactions II RSC
@ast
Perkin transactions II RSC
@en
Perkin transactions II RSC
@es
Perkin transactions II RSC
@nl
type
label
Perkin transactions II RSC
@ast
Perkin transactions II RSC
@en
Perkin transactions II RSC
@es
Perkin transactions II RSC
@nl
prefLabel
Perkin transactions II RSC
@ast
Perkin transactions II RSC
@en
Perkin transactions II RSC
@es
Perkin transactions II RSC
@nl
P1156
11000153777