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C.Y. Prescott W.B. Atwood R.L.A. Cottrell H. DeStaebler Edward L. Garwin A. Gonidec R.H. Miller L.S. Rochester T. Sato D.J. Sherden C.K. Sinclair S. Stein R.E. Taylor C. Young J.E. Clendenin V.W. Hugnes N. Sasao K.P. Schüler W. Jentschke 《Physics letters. [Part B]》1979,84(4):524-528
We have extended our earlier measurements of parity violating asymmetries in the inelastic scattering of longitudinally polarized electrons from deuterium to cover the range 0.15≤y≤0.36. The observed asymmetry shows only slight y dependence over this range. Our results are consistent with the expectations of the Weinberg-Salam model for a value of sin2θw= 0.224±0.020. 相似文献
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Behenna DC Mohr JT Sherden NH Marinescu SC Harned AM Tani K Seto M Ma S Novák Z Krout MR McFadden RM Roizen JL Enquist JA White DE Levine SR Petrova KV Iwashita A Virgil SC Stoltz BM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(50):14199-14223
α-Quaternary ketones are accessed through novel enantioselective alkylations of allyl and propargyl electrophiles by unstabilized prochiral enolate nucleophiles in the presence of palladium complexes with various phosphinooxazoline (PHOX) ligands. Excellent yields and high enantiomeric excesses are obtained from three classes of enolate precursor: enol carbonates, enol silanes, and racemic β-ketoesters. Each of these substrate classes functions with nearly identical efficiency in terms of yield and enantioselectivity. Catalyst discovery and development, the optimization of reaction conditions, the exploration of reaction scope, and applications in target-directed synthesis are reported. Experimental observations suggest that these alkylation reactions occur through an unusual inner-sphere mechanism involving binding of the prochiral enolate nucleophile directly to the palladium center. 相似文献
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