Zobrazeno 1 - 10
of 35
pro vyhledávání: '"J. E. Cochran"'
Publikováno v:
Applied Mathematics and Computation. 117:301-312
Orbital motion of a tethered satellite system, composed of two satellites and an inextensible tether, is considered by using a perturbed two-body model. This approach is adopted so that the determination of the orbit of one of the satellites can be a
Publikováno v:
The Journal of the Astronautical Sciences. 48:477-493
This paper addresses the problem of characterizing the information available in observations of one of the satellites of a two-satellite tethered system. Generally, both satellites in a two-satellite tethered system are observed if it is known a prio
Publikováno v:
Journal of Applied Mechanics. 64:935-939
The fundamental theory of wire ropes developed by Costello and Phillips is utilized to obtain closed-form expressions for maximum contact stresses in single strand cables with fibrous cores. These should be useful for gaining an insight into the infl
Publikováno v:
The Journal of Organic Chemistry. 62:2786-2797
The alpha-thiocarbocation generated from the Pummerer reaction of an o-amido-substituted sulfoxide is intercepted by the adjacent amido carbonyl group to produce a 2-amino-substituted isobenzofuran as a transient intermediate. In the presence of an e
Publikováno v:
Tetrahedron Letters. 37:2903-2906
Methyl 5-aminofuroate undergoes a facile [4+2]-cycloaddition with a variety of dienophiles to afford ring opened cycloadducts which are readily dehydrated using BF3·OEt2 to give polysubstituted anilines.
Publikováno v:
Tetrahedron Letters. 36:9285-9288
The α-thiocarbocation generated from the Pummerer reaction of an o-amido substituted sulfoxide is intercepted by the adjacent carbonyl group to produce an α-amino isobenzofuran as a transient intermediate which undergoes a subsequent Diels-Alder cy
Autor:
J. E. Cochran, Albert Padwa
Publikováno v:
ChemInform. 26
Autor:
J. E. Cochran, Albert Padwa
Publikováno v:
ChemInform. 26
The α-thiocarbocation generated from the Pummerer reaction of an o -benzoyl substituted sulfoxide is intercepted by the adjacent keto group to produce an α-thio-isobenzofuran as a transient intermediate which undergoes a subsequent Diels-Alder cycl
Publikováno v:
ChemInform. 27
Publikováno v:
ChemInform. 27