Alan W. Schwabacher, James W. Lane, Matthew W. Schiesher, Krista M. Leigh, Christopher W. Johnson The Journal of Organic Chemistry | 1998 | 10.1021/jo971802o
Laura L. Kiessling, Laura E. Strong Journal of the American Chemical Society | 1999 | 10.1021/ja990223t
A new, general strategy for the synthesis of biologically active multivalent arrays displaying diverse functionality has been developed. This method exploits the ability of ring-opening metathesis polymerizations to produce polymers of defined lengths. By...
Juan Z. Dávalos, Rafael Notario, Carlos A. Cuevas, Josep M. Oliva, Alfonso Saiz-Lopez Computational and Theoretical Chemistry | 2017 | 10.1016/j.comptc.2016.11.009
Thomas E. Nielsen, Sebastian Le Quement, David Tanner* Synthesis | 2004 | 10.1055/s-2004-822380
Tanner et al. reported the silastannation reaction of several secondary terminal propargylic alcohols (protected and unprotected) with Pd2(dba)3ââ¬Â¢CHCl3/ Ph3P (1-2 equivalents of per Pd). Excellent regio and stereoselectivity (cis addition with tin always...
Concentrated colloidal solutions of well-dispersed YVO %sub%4 %/sub%:Eu nanoparticles are synthesized by precipitation reactions at room temperature and stabilized by sodium hexametaphosphate. X-ray diffraction and electron microscopy characterizations show...
Mitchell A. McCarthy, Bo Liu, Andrew G. Rinzler Nano Letters | 2010 | 10.1021/nl101589x
State-of-the-art performance is demonstrated from a carbon nanotube enabled vertical field effect transistor using an organic channel material. The device exhibits an on/off current ratio >10 %sup%5 %/sup% for a gate voltage range of 4 V with a current...
A study of some parameters which influence the oxidation of 2-
and 4-methylquinolines with selenium dioxide (or selenious acid) in dioxane has allowed to correct some erroneous opinions of this method and to elaborate a general, simple, fast, and cheap...
Michal Szostak, Malcolm Spain, Andrew J. Eberhart, David J. Procter Journal of the American Chemical Society | 2014 | 10.1021/ja412578t
Highly chemoselective direct reduction of primary, secondary, and tertiary amides to alcohols using SmI %sub%2 %/sub%/amine/H %sub%2 %/sub%O is reported. The reaction proceeds with CâN bond cleavage in the carbinolamine intermediate, shows excellent...
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