Moffat

Moffat T P, Fan FRF and Bard A 1991 Electrochemical and scanning tunneling microscopic study of dealloying of CUjAu J. Electrochem. Soc. 138 3224... 

W. G. Moffat, Handbook of Binary Phase Diagrams, General Electric Co., Schenectady, N.Y., 1976. 

K Moffat, R Flenderson. Curr Opin Stiaict Biol 5 656, 1995. 

This objection is supported by recent results of Moffat ef al. (109, 110), who observed severe interphase mass transfer limitations for the same system, in spite of calculations which predicted the mass transfer rate to be several orders of magnitude greater than the observed rate. As... 

The general procedure described here was originally published by the submitters,3 who have used this insoluble reagent to prepare aldehydes and ketones under Moffat oxidation conditions.4 A polymeric reagent offers two advantages (a) when an oxidation is complete, the urea... 

POLYMERIC CARBODIIMIDE. II. MOFFAT OXIDATION 4-tert-BUTYLCYCLOHEXANONE... 

The general procedure described here was originally published by the submitters.3 Both ketones and aldehydes may be prepared, and this method is particularly effective when the mild conditions of the Moffat oxidation are required, but the dicyclohexylurea by-product formed with the usual reagents causes purification problems. 

Mesitylene [Benzene, 1,3,5-tnmethyl-], 86 Z Met Gly Gly OEt [Gly cine,V-[Ar-[A-[(phenylmethoxy)carbonyl] -L-methionyl] glycyl] -, ethyl ester], 9 3 Methane, iodo-, hazard note 127 Methyl chlonde polystyrene [Benzene, diethenyl-, polymer with ethenyl-benzene, chloromcthylatcd], 96 Methyl iodide [Methane, iodo-], 79 Methyl mercaptan [Methanethiol], 73 Moffat oxidation, 99... 

The Oxidation of Some Carbohydrate Derivatives using Acetic Anhydride - Methyl Sulphoxide Mixtures and the Pfitzner-Moffat Reagent. Facile Synthesis of 3-Acetamido-3-deoxy-D-glucose and 3-Amino-3-deoxy-D-xylose, J. S. Brimacombe, J. G. H. Bryan, A. Husain, M. Stacey, and M. S. 

Table 2.1 HPLC capacity factors for secbuto-barbitone and vinbarbitone with an octadecyl silyl stationary phase and mobile phases of methanoiyO.l M sodium dihydrogen phosphate (40 60) at (a) pH 3.5, and (b) pH 8.5. From Moffat, A.C. (Ed.), Clarke s Isolation and Identification of Drugs, 2nd Edn, The Pharmaceutical Press, London, 1986. Reproduced by permission of The Royal Pharmaceutical Society...

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