@article {87,
	title = {The promise of genomics for a {\textquoteright}Next generation{\textquoteright} of advances in higher-level legume molecular systematics},
	journal = {South African Journal of BotanySouth African Journal of Botany},
	volume = {89},
	year = {2013},
	note = {0254-6299},
	pages = {10-18},
	keywords = {Legumes, Leguminosae, Next-generation sequencing, phylogeny},
	author = {Doyle, Jeff J.}
}
@article {98,
	title = {Reconstructing the deep-branching relationships of the papilionoid legumes},
	journal = {South African Journal of BotanySouth African Journal of Botany},
	volume = {89},
	year = {2013},
	note = {0254-6299},
	pages = {58-75},
	keywords = {Leguminosae, matK, Papilionoideae, Phylogenetic classification, Sophoreae, Swartzieae},
	author = {Cardoso, D. and Pennington, R. T. and de Queiroz, L. P. and Boatwright, J. S. and Van Wyk, B. E. and Wojciechowski, M. F. and Lavin, M.}
}
@article {44,
	title = {6-Deoxyclitoriacetal from Clitoria macrophylla},
	journal = {PhytochemistryPhytochemistry},
	volume = {31},
	number = {12},
	year = {1992},
	note = {0031-9422},
	pages = {4329-4331},
	abstract = {A new rotenoid, 6-deoxyclitoriacetal, was isolated from the roots of Clitoria macrophylla and its structural assignment was established unambiguously by a series of HETCOR, COLOC and NOE difference experiments. In vitro tests showed that this compound possessed strong cytotoxic activity against cultured P-388 lymphocytic leukemia cells, but was not active with cultured KB cells. However, marginal activity was observed with vinblastine-resistant KB-V1 cells, and this was enhanced by the addition of vinblastine. This rotenoid may, therefore, interact with P-glycoprotein.},
	keywords = {12a-hydroxyrotenoid, 6-deoxyclitoriacetal, Clitoria macrophylla, COLOC NMR spectroscopy, cytotoxic activity., Leguminosae, roots},
	author = {Lin, Lee-Juian and Ruangrungsi, Nijsiri and Cordell, Geoffrey A. and Shieh, Hui-Ling and You, Min and Pezzuto, John M.}
}
