@article {1034,
	title = {A convenient method for the conversion of hindered carboxylic acids to N-methoxy-N-methyl (Weinreb) amides},
	journal = {Journal of Organic Chemistry},
	volume = {69},
	number = {25},
	year = {2004},
	note = {ISI Document Delivery No.: 877EJTimes Cited: 14Cited Reference Count: 35},
	month = {Dec},
	pages = {8984-8986},
	type = {Article},
	abstract = {The conversion of sterically hindered carboxylic acids to N-methoxy-N-methyl amides can be efficiently carried out with 1.1 equiv of methanesulfonyl chloride, 3 equiv of triethylamine, and 1.1 equiv of N-methoxy-N-methylamine. Yields for this process range from 59\% to 88\%. The major byproduct in these reactions, N-methoxy-N-methylmethanesulfonamide, can be removed by placing the product mixture under vacuum for 14-24 h.},
	keywords = {CHEMISTRY, CHLORIDE, ESTERIFICATION, ESTERS, GROUP ACTIVATION, lactones, MILD, REAGENT},
	isbn = {0022-3263},
	url = {<Go to ISI>://000225550300061},
	author = {Woo, J. C. S. and Fenster, E. and Dake, G. R.}
}
@article {4732,
	title = {Colloid-catalysed arene hydrogenation in aqueous/supercritical fluid biphasic media},
	journal = {Chemical Communications},
	number = {11},
	year = {2000},
	note = {ISI Document Delivery No.: 316JJTimes Cited: 59Cited Reference Count: 24},
	pages = {941-942},
	type = {Article},
	abstract = {Hydrogenation of arenes, including the lignin model compound 2-methoxy-4-propylphenol, has been effected using a Rh colloid in biphasic aqueous/supercritical ethane reaction media; this is the first successful example of an unsupported colloid-catalysed hydrogenation of a substrate in a supercritical fluid; the same reaction does not proceed in aqueous/supercritical carbon dioxide or ionic liquid/supercritical fluid media.},
	keywords = {CO2, micelles, MILD, model compounds, PRESSURES, rhodium, SOLUBLE METAL-COMPLEXES, SPECTROSCOPY, SUPERCRITICAL CARBON-DIOXIDE, SYSTEMS},
	isbn = {1359-7345},
	url = {<Go to ISI>://000087163600026},
	author = {Bonilla, R. J. and James, Brian R. and Jessop, P. G.}
}
@article {4048,
	title = {Trapping of Cp*W(NO)(eta(2)-PhC CH), the key intermediate in the C-H activation of alkanes by Cp*W(NO)(CH2SiMe3)(CPh=CH2)},
	journal = {Organometallics},
	volume = {16},
	number = {9},
	year = {1997},
	note = {ISI Document Delivery No.: WX030Times Cited: 17Cited Reference Count: 21},
	month = {Apr},
	pages = {1825-1827},
	type = {Article},
	abstract = {Thermolysis of the vinyl nitrosyl complex Cp*W(NO)(CH2SiMe3)(CPh=CH2) (1) in ethyl acetate or acetonitrile affords the oxa- or azametallacycles Cp*W(NO)(eta(2)-OC(Me)(OEt)CH=CPh) (2) or Cp*W(NO)(eta(3)-HNC(Me)=NC(=CH2)CH=CPh) (3) and Cp*W(NO)(OH)(eta(2)-HN=C(Me)CH=CPh) (4), respectively. Kinetic and mechanistic studies provide compelling evidence for a pathway involving initial rate-limiting unimolecular elimination of SiMe4 from 1 with concomitant formation of Cp*W(NO)(eta(2)-CPh=CH), (A).},
	keywords = {HYDROXO COMPLEXES, MILD, REACTIVITY},
	isbn = {0276-7333},
	url = {<Go to ISI>://A1997WX03000005},
	author = {Legzdins,Peter and Lumb, S. A.}
}
