@article {2159,
	title = {Improved procedure for the bimolecular oxidative amidation of phenols},
	journal = {Journal of Organic Chemistry},
	volume = {73},
	number = {11},
	year = {2008},
	note = {ISI Document Delivery No.: 307MRTimes Cited: 17Cited Reference Count: 24Liang, Huan Ciufolini, Marco A.},
	month = {Jun},
	pages = {4299-4301},
	type = {Article},
	abstract = {Trifluoroacetic acid (TFA) is an effective promoter of the bimolecular Ritter-like oxidative amidation of 4-substituted phenols induced by PhI(OAc)(2) in MeCN. This suppresses the need for fluoroalcohol cosolvents, increases the yields, and facilitates isolation/purification procedures.},
	keywords = {DERIVATIVES, ETHERS, FR901483, HYPERVALENT IODINE OXIDATION, lactones, REAGENTS, SPIROLEUCETTADINE},
	isbn = {0022-3263},
	url = {<Go to ISI>://000256323500050},
	author = {Liang, H. and Ciufolini,Marco A.}
}
@article {4368,
	title = {Chiral synthesis of tri-O-methylimbricatine, an etherified derivative of the starfish alkaloid imbricatine},
	journal = {Tetrahedron Letters},
	volume = {39},
	number = {33},
	year = {1998},
	note = {ISI Document Delivery No.: 104XFTimes Cited: 6Cited Reference Count: 14},
	month = {Aug},
	pages = {5999-6002},
	type = {Article},
	abstract = {A chiral synthesis of tri-O-methylimbricatine (2), the tri-O-methyl derivative of the unique benzyltetrahydroisoquinoline alkaloid imbricatine (1) isolated from the starfish Dermasterias imbricata, has been accomplished. As a result of the synthesis, the correctness of the structure and absolute stereochemistry proposed for imbricatine has been unequivocally confirmed. (C) 1998 Elsevier Science Ltd. All rights reserved.},
	keywords = {amino acids and derivatives, AMINO-ACIDS, DERMASTERIAS-IMBRICATA, imidazoles/imidazolines, isoquinolines, REAGENTS, thioethers},
	isbn = {0040-4039},
	url = {<Go to ISI>://000075041200034},
	author = {Ohba, M. and Nishimura, Y. and Imasho, M. and Fujii, T. and Kubanek, J. and Andersen, R. J.}
}
@article {3264,
	title = {THE ONE-STEP SYNTHESIS OF CHIRAL AMINO PHOSPHINO FERROCENES},
	journal = {Journal of Organometallic Chemistry},
	volume = {492},
	number = {2},
	year = {1995},
	note = {ISI Document Delivery No.: QV350Times Cited: 10Cited Reference Count: 24},
	month = {May},
	pages = {157-164},
	type = {Article},
	abstract = {Reaction of the chiral lithium reagent-2-lithio-(alpha-N,N-dimethyl)aminoethylbenzene with 1,1{\textquoteright}-ferrocenediylphenylphosphine gives chiral aminophosphinoferrocenes that contain both chiral carbon and phosphorus centres. Treatment of the ferroceno-phane with 2-lithio-N,N-dimethylaminomethylferrocene followed by hydrolysis gives the product ferrocenyl 2-(dimethylaminomethylferrocenyl) phenylphosphine as a pair of diastereomers. The single crystal structures of compound 3a PdCl2 and compound 4. PdCl2.2CH(2)Cl(2) have been determined. The compounds, 2-(ferrocenylphenylphosphino)-1-(alpha-N, N{\textquoteright}-dimethylaminoethylbenzene)ferrocene, 5 and 1-[2-(alpha-N,N{\textquoteright}-dimethyraminoethylbenzene)phenylphospphino]-1{\textquoteright}-diphenyl phosphinoferrocene, 6a, have also been prepared by minor modifications of the methodology developed.},
	keywords = {<1>FERROCENOPHANES, ASYMMETRIC-SYNTHESIS, CATALYST, chirality, crystal structure, FERROCENE, GRIGNARD, HALIDES, HYDROGENATION, iron, METAL-COMPLEXES, ORGANIC, palladium, PHOSPHORUS, PLANAR CHIRALITY, REAGENTS, SECONDARY},
	isbn = {0022-328X},
	url = {<Go to ISI>://A1995QV35000005},
	author = {Butler, I. R. and Cullen, W. R. and Rettig, S. J. and White, A. S. C.}
}
