Demand for bedside ultrasound in medicine has created a need for earlier exposure to ultrasound education during the clinical years of undergraduate medical education. Although bedside ultrasound is often used for invasive medical procedures, there is no standardized educational model for procedural skills that can provide the learner a real-life simulated experience. The objective of our study was to describe a unique fresh cadaver preparation model, and to determine the impact of a procedure-focused ultrasound training session. This study was a cross-sectional study at an urban academic medical center. A sixteen-item questionnaire was administered at the beginning and end of the session. Fifty-five third year medical students participated in this 1-day event during their surgical clerkship. Students were trained to perform the following ultrasound-guided procedures: internal jugular vein cannulation, femoral vein cannulation femoral artery cannulation and pericardiocentesis. Preparation of the fresh cadaver is easily replicated and requires minor manipulation of cadaver vessels and pericardial space. Fifty-five medical students in their third year participated in this study. All of the medical students agreed that US could help increase their confidence in performing procedures in the future. Eighty percent (95 % CI 70-91 %) of students felt that there was a benefit of learning ultrasound-based anatomy in addition to traditional methods. Student confidence was self-rated on a five-point Likert scale. Student confidence increased with statistical significance in all of the skills taught. The most dramatic increase was noted in central venous line placement, which improved from 1.95 (SD = 0.11) to 4.2 (SD = 0.09) (p < 0.001). The use of fresh cadavers for procedure-focused US education is a realistic method that improves the confidence of third year medical students in performing complex but critical procedures.

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A series of Michael‐initiated ring closing reactions of methyl dichloroacetate (II) with alkenes containing electron‐withdrawing groups, e.g. (I), (V), and (VIII), is reported.

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A New Synthesis of Alkyl (E)-(3-Dimethylamino)acrylates. -The stereoselective synthesis of title compounds (III) and (VI) is achieved by reaction of Vilsmeier reagent, in situ generated from DMF and SOCl2, with ketene acetals. Similar yield is achieved when the reagent is introduced directly. -(ROBERTSON, J. M.; JONES, I. W.; KAYNE, K. M.; CONTRERAS, C. G.; WITTER, D. J.; BATES*, R. B.; HALL, H. K. J.; Tetrahedron Lett. 52 (2011) 46, 6080-6081, http://dx.

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