@article {2683,
	title = {Total Synthesis of Siphonazoles by the Use of a Conjunctive Oxazole Building Block},
	journal = {Organic Letters},
	volume = {11},
	number = {11},
	year = {2009},
	note = {ISI Document Delivery No.: 452NFTimes Cited: 6Cited Reference Count: 47Zhang, Jianmin Ciufolini, Marco A.},
	month = {Jun},
	pages = {2389-2392},
	type = {Article},
	abstract = {The preparation of 4-carbethoxy-5-methyl-2-(phenylsulfonyl)methyloxazole and its use in the elaboration of more complex oxazoles are described. A total synthesis of the unique natural products, siphonazoles A and 13, illustrates an application of the new building block.},
	keywords = {ACCESS, CARBONYL-COMPOUNDS, CONDENSATION, CYCLOISOMERIZATION, DOUBLE ELIMINATION PROTOCOL, GOLD CATALYSIS, INTRAMOLECULAR HYDROAMINATION, LITHIATION, PHORBOXAZOLES, VIRGINIAMYCIN-M2},
	isbn = {1523-7060},
	url = {<Go to ISI>://000266546300042},
	author = {Zhang, J. M. and Ciufolini,Marco A.}
}
@article {1412,
	title = {Nanoscopic liquid bridges between chemically patterned atomistic walls},
	journal = {Journal of Physical Chemistry B},
	volume = {110},
	number = {8},
	year = {2006},
	note = {ISI Document Delivery No.: 020WQTimes Cited: 6Cited Reference Count: 38},
	month = {Mar},
	pages = {3764-3772},
	type = {Article},
	abstract = {A binary liquid mixture, containing the Lennard-Jones molecules A and B, in equilibrium with a bulk liquid reservoir near the point of phase separation, confined between atomistic chemically patterned walls, is studied by grand canonical Monte Carlo simulations. In the bulk, the B-rich phase is stable and the A-rich phase is metastable. The walls bear patches attractive to A; when the walls are close, A-rich liquid bridges condense between the patches. The normal and lateral forces on the walls are measured as a function of the wall separation and of the lateral displacement between the patches on opposite walls. When there are one or two molecular layers in the bridge and the wall lattice constant is close to that of crystalline A, the normal and lateral forces depend strongly on the registry of the wall lattices, varying in an oscillatory manner.},
	keywords = {BEHAVIOR, capillary, CONDENSATION, FILMS, FLUIDS, FORCES, INDUCED PHASE-TRANSITIONS, MOLECULARLY THIN-LAYERS, PORES, SHEAR, STRUCTURED WALLS},
	isbn = {1520-6106},
	url = {<Go to ISI>://000235944300039},
	author = {Hemming, C. J. and Patey, G. N.}
}
@article {5042,
	title = {Inhibition of the G(2) DNA damage checkpoint and of protein kinases Chk1 and Chk2 by the marine sponge alkaloid debromohymenialdisine},
	journal = {Journal of Biological Chemistry},
	volume = {276},
	number = {21},
	year = {2001},
	note = {ISI Document Delivery No.: 435FJTimes Cited: 78Cited Reference Count: 61},
	month = {May},
	pages = {17914-17919},
	type = {Article},
	abstract = {Cells can respond to DNA damage by activating checkpoints that delay cell cycle progression and allow time for DNA repair. Chemical inhibitors of the G(2) phase DNA damage checkpoint may be used as tools to understand better how the checkpoint is regulated and may be used to sensitize cancer cells to DNA-damaging therapies. However, few inhibitors are known. We used a cell-based assay to screen natural extracts for G(2) checkpoint inhibitors and identified debromohymenialdisine (DBH) from a marine sponge. DBH is distinct structurally from previously known G(2) checkpoint inhibitors. It inhibited the G(2) checkpoint with an IC50 of 8 muM and showed moderate cytotoxicity (IC50 = 25 muM) toward MCF-7 cells. DBH inhibited the checkpoint kinases Chk1 (IC50 = 3 muM) and Chk2 (IC50 = 3.5 muM) but not ataxia-telangiectasia mutated (ATM), ATM-Rads-related protein, or DNA-dependent protein kinase in vitro, indicating that it blocks two major branches of the checkpoint pathway downstream of ATM. It did not cause the activation or inhibition of different signal transduction proteins, as determined by mobility shift analysis in Western blots, suggesting that it inhibits a narrow range of protein kinases in vivo.},
	keywords = {14-3-3 BINDING, BHK CELLS, CDC25, CELL-CYCLE CHECKPOINTS, CHROMOSOME, CONDENSATION, DEPENDENT KINASES, H3 PHOSPHORYLATION, INDUCED MITOTIC DELAY, MAMMALIAN-CELLS, PHOSPHATASE, RADIOSENSITIZING AGENT},
	isbn = {0021-9258},
	url = {<Go to ISI>://000168866500042},
	author = {Curman, D. and Cinel, B. and Williams, D. E. and Rundle, N. and Block, W. D. and Goodarzi, A. A. and Hutchins, J. R. and Clarke, P. R. and Zhou, B. B. and Lees-Miller, S. P. and Andersen, R. J. and Roberge, M.}
}
@article {5190,
	title = {Ion fragmentation in an electrospray ionization mass spectrometer interface with different gases},
	journal = {Rapid Communications in Mass Spectrometry},
	volume = {15},
	number = {4},
	year = {2001},
	note = {ISI Document Delivery No.: 405PTTimes Cited: 12Cited Reference Count: 43},
	pages = {249-257},
	type = {Article},
	abstract = {Nitrogen, argon, and krypton are used as curtain gases in an electrospray ionization mass spectrometer in an attempt to study the effect of these gases on the extent of ion fragmentation between the orifice and the skimmer of the interface region. A previously published collision model predicts that the degree of ion fragmentation increases with increasing mass of the curtain gas. However, the fragmentation yields are found to be the opposite to that expected. It is believed that the reversed trend with argon and krypton is caused by condensation of the gases within the free jet expansion between the orifice and the skimmer. A condensation parameter can be used to predict the degree of clustering of gases within a free jet expansion. When the condensation parameter is minimized, the predicted trend of fragmentation with mass is observed. Copyright (C) 2001 John Wiley \& Sons, Ltd.},
	keywords = {CONDENSATION, FREE-JET EXPANSIONS, INDUCED DISSOCIATION, LIQUID-HELIUM CLUSTERS, MYOGLOBIN, PERFORMANCE, PROTEIN IDENTIFICATION, SPECTROSCOPY, TECHNOLOGY, TEMPERATURE},
	isbn = {0951-4198},
	url = {<Go to ISI>://000167168800002},
	author = {Schneider, B. S. and Douglas, D. J. and Chan, D. D. Y.}
}
@article {4749,
	title = {Isotropic fluid phases of dipolar hard spheres},
	journal = {Physical Review Letters},
	volume = {84},
	number = {1},
	year = {2000},
	note = {ISI Document Delivery No.: 271HJTimes Cited: 86Cited Reference Count: 28},
	month = {Jan},
	pages = {115-118},
	type = {Article},
	abstract = {Monte Carlo simulations are used to calculate the equation of state and free energy-of dipolar hard sphere fluids at low temperatures and densities. Evidence for the existence of isotropic-fluid-isotropic-fluid phase transitions is presented and discussed. Condensation in the dipolar hard sphere fluid is unusual in that it is not accompanied by large energy or entropy changes. An explanation of this behavior is put forward.},
	keywords = {CLUSTERS, COMPUTER-SIMULATION, CONDENSATION, LIQUID, orientational order, SYSTEMS},
	isbn = {0031-9007},
	url = {<Go to ISI>://000084587900029},
	author = {Camp, P. J. and Shelley, J. C. and Patey, G. N.}
}
