Developing an outcome-based assessment for family therapy training: the Rochester Objective Structured Clinical Evaluation (ROSCE).

This paper addresses a growing need for cost-effective, outcome-based assessment in family therapy training. We describe the ROSCE, a structured, evidence-informed, learner-centered approach to the assessment of clinical skills developed at the University of Rochester Medical Center. The ROSCE emphasizes direct observation of trainees demonstrating clinical competencies.

Ligand substitution behavior of Ru(6)(mu(6)-C)(CO)(17) with unsaturated diphosphines: facile capping of a polyhedral face and photochemically promoted P-C bond cleavage in the cluster Ru(6)(mu(6)-C)(CO)(14)(mu(3)-bpcd).

The ligand substitution chemistry of the hexaruthenium cluster Ru(6)(mu(6)-C)(CO)(17) () with several unsaturated diphosphine ligands has been investigated. Thermolysis of with (Z)-Ph(2)PCH[double bond, length as m-dash]CHPPh(2) (dppen) furnishes the new cluster compounds Ru(5)(mu(5)-C)(CO)(12)(mu(3)-dppen) (), Ru(6)(mu(6)-C)(CO)(14)(mu(3)-dppen) (), and Ru(6)(mu(6)-C)(CO)(12)(mu(3)-dppen)(mu-dppen) (). Clusters and are also obtained when a mixture of and dppen is treated with the oxidative-decarbonylation reagent Me(3)NO.

Bismuth aryloxides.

The synthesis and full characterization (mp, NMR, UV/vis, FTIR, and elemental analysis) of 13 bismuth aryloxides are reported. We have prepared bismuth aryloxides with alkyl, aryl, and allylic substituents on the aryl rings. Eleven of these bismuth aryloxides have been characterized with single crystal X-ray diffraction methods.

Unusual manganese(III)-mediated oxidative free radical additions of 1,3-dicarbonyl compounds to benzonorbornadiene and 7-heterobenzonorbornadienes: mechanistic studies.

Benzonorbornadiene and heterobenzonorbornadiene were reacted with dimedone/acetylacetone and Mn(OAc)3 in the presence and absence of Cu(OAc)2. The reaction of benzonorbornadiene with dimedone gave mainly the dihydrofuran addition product, whereas the reaction with acetylacetone produced a rearranged product in addition to the dihydrofuran derivative. On the other hand, oxanorbornadiene gave unusual products such as the cycloproponated compound and a product arising from the incorporation of 2 mol of dimedone.

Structure elucidation of an unexpected product from dehydration of a beta-hydroxyketone.

The structure of an unexpected compound from the dehydration of an aldol addition product has been determined using 1-D and 2-D NMR techniques. This reaction is the last step in a new synthetic approach to the galanthan ring system. Complete 1H and 13C NMR assignments for two synthetic precursors are also reported.

Molybdocalixarene structure control via rim deprotonation. synthesis, characterization, and crystal structures of calix[4]arene Mo(VI) monooxo complexes and calix[4]arene alkali metal/Mo(VI) dioxo complexes.

We report a series of calix[4]arene Mo(VI) dioxo complexes M2RC4MoO2 (M = alkali metal, R = H or Bu(t)) that were fully characterized by NMR, X-ray, IR, UV/vis, and elemental analysis. Molybdocalix[4]arene structures can be controlled via lower rim deprotonation, groups at para positions of calix[4]arene, and alkali metal counterions. Mono deprotonation at the lower rim leads to calix[4]arene Mo(VI) monooxo complexes RC4MoO (R = H, Bu(t), or allyl), and full deprotonation gives rise to calix[4]arene Mo(VI) dioxo complexes.

Synthesis and structure of cyclopropano-annelated homosesquinorbornene derivatives containing pyramidalized double bonds: evidence for the sterical effect of a cyclopropyl group on the degree of C=C double-bond pyramidalization.

[reaction: see text] endo- and exo-2,3,4,7-tetrahydro-1H-1,4-methanobenzocycloheptene-7-carboxylic acid ethyl esters have been synthesized, and their Diels-Alder cycloaddition reactions with maleic anhydride, dimethyl acetylenedicarboxylate and singlet oxygen have been investigated. The X-ray analysis of four adducts indicated the pyramidalization of the central double bond. Density functional theory calculations on the isolated products and model compounds showed excellent agreement between the experimental and theoretical determined butterfly angles.

Facile formation of molybdenum(VI) monooxo aryloxides MoO(OAr)4-nCln from molybdenum dioxo dichloride.

Molybdenum monooxo compoundsMoO(OAr)4-nCln (n=0-2, Ar=2,6-Me2C6H3 or 2,6-i-Pr2C6H3) have been synthesized starting from the dioxo precursor MoO2Cl2. The complexes are characterized spectroscopically and by X-ray diffraction. The formation mechanism likely involves phenol precoordination followed by addition across the Mo=O bond.

Steric control of coordination number: A series of Mo(VI) dioxo diaryloxide complexes bearing 4-, 5-, and 6-coordinate environments.

The design, synthesis, and structure determination of a series of Mo(VI) dioxo diaryloxide complexes have been reported. By varying the steric bulk of the aryloxide ligand, control of the coordination number around the Mo(VI) center was achieved. All the complexes are characterized by analytical and spectroscopic techniques.

Synthesis, structures, and conformational characteristics of calixarene monoanions and dianions.

The synthesis, complete characterization, and solid state structural and solution conformation determination of calix[n]arenes (n = 4, 6, 8) is reported. A complete series of X-ray structures of the alkali metal salts of calix[4]arene (HC4) illustrate the great influence of the alkali metal ion on the solid state structure of calixanions (e.g.

Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry.

The Chuvash form of polycythemia is an autosomal recessive disorder common to a large number of families in central Russia. Affected individuals have been reported to be homozygous for an Arg200Trp mutation in the von Hippel-Lindau (VHL) gene. We have screened 78 patients with erythrocytosis and found 8 of Bangladeshi and Pakistani origin to be homozygous for the Arg200Trp mutation and another of English descent to be heterozygous.

Synthesis, structure, and reactivity of some sterically hindered (Silylamino)phosphines.

A series of new (silylamino)phosphines that contain sterically bulky silyl groups on nitrogen were prepared by deprotonation/substitution reactions of the hindered disilylamines t-BuR(2)Si(Me(3)Si)NH (1, R = Me; 2, R = Ph) and (Et(3)Si)(2)NH (3). Sequential treatment of the N-lithio derivatives of 1-3 with PCl(3) or PhPCl(2) and MeLi gave the corresponding (silylamino)phosphines t-BuR(2)Si(Me(3)Si)NP(R')Me (5, R = Me, R' = Ph; 6, R = Ph, R' = Me) and (Et(3)Si)(2)NP(R)Me (11, R = Me; 12, R = Ph) in high yields. Two of the P-chloro intermediates t-BuR(2)Si(Me(3)Si)NP(Ph)Cl (7, R = Ph; 9, R = Me) were also isolated and fully characterized.

Synthesis, structure, and reactivity of some N-phosphorylphosphoranimines.

A large series of new N-phosphorylphosphoranimines that bear potentially reactive functional groups on both phosphorus centers were prepared by silicon-nitrogen bond cleavage reactions of N-silylphosphoranimines. Thus, treatment of the N-silylphosphoranimines, Me(3)SiN=P(Me)(R)X (R = Me, Ph; X = OCH(2)CF(3) and R = Me, X = OPh), with phosphoryl chlorides, RP(=O)Cl(2) (R' = Cl, Me, Ph), readily afforded the corresponding N-phosphoryl derivatives, R'P(=O)(Cl)-N=P(Me)(R)X, in high yields. Subsequent reaction with 1 or 2 equiv of the silylamine, Me(3)SiNMe(2), resulted in ligand exchange at the phosphoryl (P=O) group to give the P-dimethylamino analogues, R'P(=O)(NMe(2))N=P(Me)(R)X (R' = Cl, NMe(2), Me, Ph; R = Me, Ph; X = OCH(2)CF(3), OPh).

Reactions of N-silylphosphoranimines with alcohols: synthesis and structure of cyclotriphosphazenes with nongeminal methyl and phenyl substituents.

The reactions of Me(3)SiN=P(OR")RR'(R" = Ph, CH(2)CF(3); R, R' = Me, Ph) with alcohols were investigated. With nonequivalent amounts of CF(3)CH(2)OH, the reactions produced high yields of the cyclic phosphazene (Me(2)PN)(3) and both the cis and trans isomers of nongeminally substituted [(Ph)(Me)PN](3). The isomers of this new cyclic phosphazene were separated by column chromatography and characterized by NMR and IR spectroscopy, elemental analysis, and X-ray crystallography.

Enantiospecific Formation of Trans 1,3-Disubstituted Tetrahydro-beta-carbolines by the Pictet-Spengler Reaction and Conversion of Cis Diastereomers into Their Trans Counterparts by Scission of the C-1/N-2 Bond.

The factors which effect the stereoselective formation of trans-1-alkyl-2-benzyl-3-(alkoxycarbonyl)-1,2,3,4-tetrahydro-beta-carbolines and trans-3-(alkoxycarbonyl)-1-alkyl-2-(diphenylmethyl)-1,2,3,4-tetrahydro-beta-carbolines by the Pictet-Spengler cyclization were examined by heating tryptophan derivatives with aldehydes of varied steric bulk under aprotic and acidic conditions, followed by determination of the ratio of cis to trans diastereomers so formed. The presence of a benzyl group at the N(b)-nitrogen atom alters the diastereochemical outcome of this condensation to provide 100% trans stereoselectivity when the cyclization is carried out with cyclohexanecarboxaldehyde. Furthermore, when N(b)-(diphenylmethyl)tryptophan isopropyl ester was condensed with aldehydes of any size, trans diastereomers are formed with 100% stereoselectively.