Wake Forest College: The Undergraduate College of Arts & Scienceshttp://hdl.handle.net/10339/259602014-04-19T09:25:41Z2014-04-19T09:25:41ZSchwarzschildBates, Jason D.http://hdl.handle.net/10339/391492014-01-21T20:44:27Z2012-01-01T00:00:00ZSchwarzschild
Bates, Jason D.
Mathematica programs which allow for the computation of an approximation to the noise kernel in Schwarzschild spacetime
2012-01-01T00:00:00ZTab DS for MathematicaAnderson, Paul R.Hiscock, William A.Samuel, David A.http://hdl.handle.net/10339/391482014-01-16T18:51:21Z1995-01-01T00:00:00ZTab DS for Mathematica
Anderson, Paul R.; Hiscock, William A.; Samuel, David A.
The DeWitt-Schwinger approximation for massive scalar fields in static spherically symmetric spacetimes.
This is in the form of an input file for Mathematica. We ask only that, if you use this file, you reference the appropriate paper. The appropriate reference is given as a comment in the file.
1995-01-01T00:00:00ZTab analytic for MathematicaAnderson, Paul R.Hiscock, William A.Samuel, David A.http://hdl.handle.net/10339/391472014-01-16T18:53:18Z1995-01-01T00:00:00ZTab analytic for Mathematica
Anderson, Paul R.; Hiscock, William A.; Samuel, David A.
The analytic approximation which can be used for massless and small mass scalar fields in static spherically symmetric spacetimes.
This is in the form of an input file for Mathematica. We ask only that, if you use these files, you reference the appropriate paper. The appropriate reference is given as a comment in the file.
1995-01-01T00:00:00ZSyntheses of 2-Silicon-Substituted 1,3-DienesChoudhury, Partha P.Junker, Christopher S.Pidaparthi, Ramakrishna R.Welker, Mark E.http://hdl.handle.net/10339/391452014-01-17T18:07:01Z2014-01-01T00:00:00ZSyntheses of 2-Silicon-Substituted 1,3-Dienes
Choudhury, Partha P.; Junker, Christopher S.; Pidaparthi, Ramakrishna R.; Welker, Mark E.
A number of 2-silicon substituted 1,3â€“dienes have been prepared by one of three routes: 1) Reactions of 1,3-dienyl Grignard reagents with silyl electrophiles or silyl Grignard reagents with 1,3-dienyl electrophiles; 2) Hydrosilylation of enynes; 3) Enyne cross metathesis. The strengths and limitations of each preparative method are discussed.
This manuscript has been accepted for publication in the Journal of Organometallic Chemistry. It was accepted for publication on 24 December 2013, and first published online on 3 January 2014. It is available at http://dx.doi.org/10.1016/j.jorganchem.2013.12.046.
2014-01-01T00:00:00Z