@article { ISI:000242759500013,
	title = {Efficient N-arylation of amines catalyzed by Cu-Fe-hydrotalcite},
	journal = {Catalysis Communications},
	volume = {8},
	number = {1},
	year = {2007},
	month = {JAN},
	pages = {65-68},
	publisher = {ELSEVIER SCIENCE BV},
	type = {Article},
	address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS},
	abstract = {<p>An efficient N-arylation of amines with aryl halides in presence of heterogeneous recyclable Cu-Fe-hydrotalcite catalyst has been developed. (c) 2006 Elsevier B.V. All rights reserved.</p>},
	keywords = {amines, Aryl halides, Cu-Fe-hydrotalcite, heterogeneous catalyst, N-arylation},
	issn = {1566-7367},
	doi = {10.1016/j.catcom.2006.05.030},
	author = {Jadhav, Vinod H. and Dumbre, Deepa K. and Phapale, Vilas B. and Borate, Hanumant B. and Wakharkar, Radhika D.}
}
@article { ISI:000243492800021,
	title = {Enantiomeric separation of novel anticancer agent 5-hydroxy-3-(4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-cyclopent-2-en- 1-one},
	journal = {Journal of Chromatography A},
	volume = {1138},
	number = {1-2},
	year = {2007},
	month = {JAN},
	pages = {184-189},
	publisher = {ELSEVIER SCIENCE BV},
	type = {Article},
	address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS},
	abstract = {<p>The enantiomers of 5-hydroxy-3-(4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-cyclopent-2-en- 1-one, a novel anticancer agent, were separated by derivatisation with caronaldehyde, separation of the resulting diastereoisomers of the corresponding esters by silica gel column chromatography and regeneration of alcohols (S)-5-hydroxy-3-(4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-cyclopent-2 -en-1-one and (R)5-hydroxy-3-(4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-cyclopent-2- en- 1-one under aqueous conditions. The absolute configuration of the enantiomers was determined by H-1 NMR studies of the corresponding Mosher esters. Alternatively, the enantiomers were separated by preparative HPLC to collect the (S)- and (R)-5-hydroxy-3-(4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-cyclopent-2 -en-1-ones with high purity which was comparable with that obtained by the chemical method. The details of these methods have been presented herein. (c) 2006 Elsevier B.V. All rights reserved.</p>},
	keywords = {Anticancer, column chromatography, diaryl cyclopentenone, diastereoisomers, enantioseparation, HPLC, Resolution},
	issn = {0021-9673},
	doi = {10.1016/j.chroma.2006.10.076},
	author = {Shinde, Popat D. and Jadhav, Vinod H. and Borate, Hanumant B. and Bhide, Sunil R. and Sonawane, Kiran B. and Wakharkar, Radhika D.}
}
