Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Robert D. Baird"'
Autor:
Robert N. Minor, Robert D. Baird
Publikováno v:
Bulletin for the Study of Religion. 49:38-42
In 1983 Robert N. Minor and Robert D. Baird wrote a piece for The Bulletin that discussed what it means to teach religion academically in a public university in the United States. By dismantling other popular notions of what it meant to teach religio
Autor:
Robert D. Baird
Since its founding by Jacques Waardenburg in 1971, Religion and Reason has been a leading forum for contributions on theories, theoretical issues and agendas related to the phenomenon and the study of religion. Topics include (among others) category
Autor:
Robert D. Baird
Sinceits founding by Jacques Waardenburg in 1971, Religion and Reason has been a leading forum for contributions on theories, theoretical issues and agendas related to the phenomenon and the study of religion. Topics include (among others) category f
Autor:
Steven M. Allin, Robert D. Baird
Publikováno v:
Current Organic Chemistry. 5:395-415
Publikováno v:
Tetrahedron Letters. 43:4195-4197
We report a novel and enantioselective approach to 2,4-disubstituted tetrahydropyrans that utilises the asymmetric amino-Cope rearrangement as a key synthetic step.
Publikováno v:
ChemInform. 30
Autor:
Robert D. Baird, Steven M. Allin
Publikováno v:
ChemInform. 32
Autor:
William F. Newberry, Robert D. Baird
Publikováno v:
ASME 2009 12th International Conference on Environmental Remediation and Radioactive Waste Management, Volume 2.
This paper reports evaluations of the adequacy of the Barnwell Extended Care Fund in light of identified risks, with the conclusion that the fund is sufficient to cover the costs and uncertainties associated with planned post-closure care of the Barn
Publikováno v:
Synlett. 1998:1117-1119
Autor:
Mark R. J. Elsegood, Pritom Shah, Vickie McKee, Catarina Horro Pita, Munira Essat, Steven M. Allin, Robert D. Baird, David M. Andrews, Mark Edgar, Ian Aspinall
Publikováno v:
Organicbiomolecular chemistry. 3(5)
We report a novel approach to some chiral tetrahydropyran and delta-lactone targets that utilizes the asymmetric amino-Cope rearrangement as a key synthetic step. Products of amino-Cope rearrangement chemistry have also been applied to access piperid