67 results on '"John W. Baker"'
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2. CCXXIV.—The formation and stability of spiro-compounds. Part XII. Further evidence for the multiplanar configuration of the cycloheptane ring
3. CCXXV.—The nature of the alternating effect in carbon chains. Part XXXIII. The nitration of some aromatic sulphonium and selenonium salts
4. CCVI.—The mechanism of tautomeric interchange and the effect of structure on mobility and equilibrium. Part II. Ring-chain tautomerism in its relation to the mutarotation of the sugars
5. 4. The mechanism of the reaction of aryl isocyanates with alcohols and amines. Part III. The 'spontaneous' reaction of phenyl isocyanate with various alcohols. Further evidence relating to the anomalous effect of dialkylanilines in the base-catalysed reaction
6. CXXII.—The nature of the alternating effect in carbon chains. Part XVII. The directive action of the groups ·CH2·CH2·NO2, ·CH:CH·NO2and ·C(NO2):CHR in aromatic substitution
7. 81. Mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part XVI. Hyperconjugation of groups of the type CH2X in the benzaldehyde–cyanohydrin equilibria
8. XXXVI.—Ring-chain tautomerism. Part IX. The mutarotation of the sugars
9. 141. Mechanism of aromatic side-chain reactions, with special reference to the polar effects of substituents. Part X. Physical and chemical evidence relating to the polar effect of o-methyl substituents in derivatives of the type C6H2Me3·CO·CH2R
10. 232. Mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part XIV. The aldehyde–cyanohydrin reaction with halogeno-benzaldehydes: polar effects of halogen substituents
11. 43. Reactions of methyl Δβ-propene-ααβ-tricarboxylate. An example of three-carbon ring-chain prototropy involving a simple cyclopropane ring
12. 5. The mechanism of the reaction of aryl isocyanates with alcohols and amines. Part IV. The evidence of infra-red absorption spectra regarding alcohol–amine association in the base-catalysed reaction of phenyl isocyanate with alcohols
13. CCLIX.—The mechanism of tautomeric interchange and the effect of structure on mobility and equilibrium. Part III. The function of alkaline and acid catalysts in the mutarotation of some derivatives of tetramethyl glucose
14. CLX.—The mechanism of tautomeric interchange and the effect of structure on mobility and equilibrium. Part IV. Further evidence relating to the mechanism of acid catalysis in the mutarotation of nitrogen derivatives of tetra-acetylglucose
15. 118. The mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part III. The effect of unipolar substituents on the critical energy and probability factors in the interaction of benzyl bromide with pyridine and α-picoline in various solvents
16. LVIII.—The nature of the alternating effect in carbon chains. Part XXIV. The directive action in aromatic substitution of certain groups containing triple linkings
17. LXII.—The nature of the alternating effect in carbon chains. Part XXX. The nitration of phenylbromocyanonitromethane, with special reference to an alleged example of intramolecular meta-rearrangement
18. 78. α-Methylenic reactivity in olefinic systems. Part I. The Prins reaction with propylene
19. 264. α-Methylenic reactivity in olefinic systems. Part IV. The structure of the dimeride formed by the stannic chloride-catalysed polymerisation of trimethylethylene. Synthesis and characterisation of isomeric methyl hexyl ketones
20. CCXCII.—The nature of the alternating effect in carbon chains. Part XXXI. The directive influence of ψ-acid systems in aromatic substitution. Nitration of ψ-acidic phenylnitromethanes and their salts
21. 392. Reactions of ω-substituted acetophenone derivatives. Part III. Comparison of the mechanism of interaction of ω-halogenoacetophenones and of benzyl halides with primary and tertiary bases
22. CCXIII.—Synthesis of substances analogous to bile acid degradation products. Part I. Preliminary investigation of methods of attachment of carboxylated side chains to the cyclopentane nucleus
23. 149. Reactions of ω-substituted acetophenone derivatives. Part II. The mechanism of the interaction of ω-halogenoacetophenones with primary and tertiary bases
24. 446. The salt-forming characteristics of doubly- and singly-linked elements of the oxygen group. Part IV. Oxonium phosphates of the carbonyl group, and investigations with derivatives of the type CH2Ph·COR
25. 21. α-Methylenic reactivity in olefinie systems. Part III. The Prins reaction with ethylene and α-methylstyrene
26. LXXXV.—Nature of the alternating effect in carbon chains. Part XII. Nitration of some derivatives of methyl benzylaminoformate
27. XV.—The formation and stability of spiro-compounds. Part X. spiro-Compounds derived from cyclo-heptane
28. 189. α-Methylenic reactivity in olefinic systems. Part II. The reaction between olefins and phenyl isocyanate : evidence relating to the catalytic action of stannic chloride
29. XLII.—The salt-forming characteristics of doubly- and singly-linked elements of the oxygen group. Part II. Nitration of benzaldehyde and acetophenone in sulphuric acid solution
30. CCCXXIX.—Reactions of ω-substituted acetophenone derivatives. Part I. ω-Halogeno-derivatives of ωm-and ωp-dinitroacetophenone
31. LIX.—The nature of the alternating effect in carbon chains. Part XXXII. The directive influence of ψ-basic systems in aromatic substitution. Nitration of benzylidene-m-nitroaniline
32. CXXXIV.—Ring-chain tautomerism. Part XIII. Three-carbon ring-chain tautomerism in a bridged ring system
33. Notes
34. XLI.—The salt-forming characteristics of doubly- and singly-linked elements of the oxygen group. Part I. The carbonyl group in benzaldehyde and acetophenone
35. 97. Synthesis of methyl α-methoxyacrylate and α-methoxyacrylonitrile: characterisation of methoxy-derivatives of propionic acid
36. 88. Syntheses in the indole series. Part II. Derivatives of β-keto-β-3-indolylpropionic acid
37. 272. Condensation of methyl pyruvate with methyl malonate in the presence of anhydrous zinc chloride
38. 199. Synthesis of substances analogous to bile acid degradation products. Part III. The attempted use of diallyl as an agent to introduce the requisite side chain in the synthesis of the acid C13H20O6
39. Notes
40. 934. The mechanism of the reaction of aryl isocyanates with alcohols and amines. Part VI. Preliminary investigations with amines: complex-formation by amines and ureas in benzene solution
41. 100. Syntheses in the indole series. Part I. Synthesis of indolyl-3-glyoxylic acid and of r-3-indolylglycine
42. 430. The mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part VI. The effects of p-alkyl substituents on prototropy in the methyleneazomethine system
43. 252. The polar effects of alkyl groups
44. 836. Reactions between trimethylethylene and formaldehyde catalysed by stannic chloride
45. 3. The mechanism of the reaction of aryl isocyanates with alcohols and amines. Part II. The base-catalysed reaction of phenyl isocyanate with alcohols
46. Hydrolytic decomposition of esters of nitric acid. Part IV. Acid hydrolysis, and the effects of change in the nucleophilic reagent on the S N and E co reactions
47. 267. Anomalies in the reactivities of side-chain halogens with special reference to reaction mechanism
48. 6. The mechanism of the reaction of aryl isocyanates with alcohols and amines. Part V. Kinetic investigations of the reaction between phenyl isocyanate and methyl and ethyl alcohols in benzene solution
49. 130. Mechanism of aromatic side-chain reactions, with special reference to the polar effects of substituents. Part X. Depolarisation potentials of p-substituted benzaldehydes in acid, neutral, and alkaline media at the dropping-mercury cathode
50. 313. The mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part VIII. The polar effects of halogens
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