253 results on '"Baker, John W."'
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52. Integrated DGPS/acoustic system for underwater positioning.
53. In reply
54. Injury surveillance: A method for recording E codes for injured emergency department patients
55. Comparison of Premorbid and Postinjury MMPI-2 Profiles in Late PostconcussionClaimants.
56. Business management; communicating for stronger productivity
57. REPAIR OF MAJOR DEFECTS OF THE CHEST WALL AND SPINE WITH THE LATISSIMUS DORSI MYOCUTANEOUS FLAP.
58. Combined treatment of advanced cancer of the laryngopharynx and cervical esophagus.
59. Making the Case for Army Data Scientists.
60. 935. The mechanism of the reaction of aryl isocyanates with alcohols and amines. Part VII. The “spontaneous” reaction with amines.
61. 936. The mechanism of the reaction of aryl isocyanates with alcohols and amines. Part VIII. The base-catalysed reaction with amines.
62. 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.
63. Hydrolytic decomposition of esters of nitric acid. Part III. Kinetic evidence for ion exchange between anionic reagents and the solvent in the carbonyl elimination reaction (ECO2).
64. 218. Hydrolytic decomposition of esters of nitric acid. Part II. The effects of structural and solvent changes on the substitution and elimination reactions which occur in the hydrolysis of primary, secondary, and tertiary alkyl nitrates.
65. 217. Hydrolytic decomposition of esters of nitric acid. Part I. General experimental techniques. Alkaline hydrolysis and neutral solvolysis of methyl, ethyl, isopropyl, and tert.-butyl nitrates in aqueous alcohol.
66. 536. Mechanism of aromatic side-chain reactions, with special reference to the polar effects of substituents. Part XV. Mesomeric effects of elements of the oxygen group.
67. Notes.
68. 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.
69. 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.
70. 3. The mechanism of the reaction of aryl isocyanates with alcohols and amines. Part II. The base-catalysed reaction of phenyl isocyanate with alcohols.
71. 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
72. 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.
73. 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.
74. 21. α-Methylenic reactivity in olefinie systems. Part III. The Prins reaction with ethylene and α-methylstyrene.
75. Notes.
76. 135. The mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part XIII. Kinetic examination of the reaction of aryl isocyanates with methyl alcohol.
77. 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.
78. 78. α-Methylenic reactivity in olefinic systems. Part I. The Prins reaction with propylene.
79. 33. Mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part XI. The aldehydecyanohydrin reaction: evidence for the mesomeric effects of alkyl groups.
80. 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
81. 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.
82. 252. The polar effects of alkyl groups.
83. 272. Condensation of methyl pyruvate with methyl malonate in the presence of anhydrous zinc chloride.
84. 371. The dissociation constants of alkyl-substituted benzoic and phenylacetic acids.
85. 51. The mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part VII. Attack at a saturated carbon atom by a charged ion.
86. 313. The mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part VIII. The polar effects of halogens.
87. 43. Reactions of methyl Δβ-propene-ααβ-tricarboxylate. An example of three-carbon ring-chain prototropy involving a simple cyclopropane ring.
88. 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
89. 428. The mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part IV. The mechanism of quaternary salt formation.
90. 429. The mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part V. The polar effects of alkyl groups.
91. 205. The mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part II. Kinetic studies of the interaction of benzyl bromides with (1) pyridine, (2) aqueous alcohol, and (3) silver nitrate.
92. 198. Synthesis of substances analogous to bile acid degradation products. Part II. Synthesis of some straight-chain polycarboxylic esters.
93. 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.
94. 267. Anomalies in the reactivities of side-chain halogens with special reference to reaction mechanism.
95. 392. Reactions of ̉-substituted acetophenone derivatives. Part III. Comparison of the mechanism of interaction of ̉-halogenoacetophenones and of benzyl halides with primary and tertiary bases.
96. 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.
97. 447. The salt-forming characteristics of doubly- and singly-linked elements of the oxygen group. Part V. The rotation of camphor in strong mineral acids.
98. Functional Evaluation of Pharyngoesophageal Reconstructive Techniques
99. REPAIR OF MAJOR DEFECTS OF THE CHEST WALL AND SPINE WITH THE LATISSIMUS DORSIMYOCUTANEOUS FLAP
100. Serial changes in pulmonary blood flow occurring during acute rejection of a lung allograft
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