Thomas D. Greenwood
Virginia Tech
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Featured researches published by Thomas D. Greenwood.
Tetrahedron Letters | 1989
Mukta S. Hendi; Kenneth J. Natalie; Shivakumar B. Hendi; James A. Campbell; Thomas D. Greenwood; James F. Wolfe
Abstract N-acyl-2-bromobenzamides participate in metal-halogen exchange with n -BuLi to form N-acyl-2-lithiobenzamides, which undergo cyclization to afford 3-alkylidenephthalimidines.
Expert Opinion on Therapeutic Patents | 1998
James F. Wolfe; Thomas D. Greenwood; Joyal M Mulheron
This article summarises reports of new compounds with anticonvulsant activity that have appeared in the patent literature over the past five years. The subject compounds are arranged and discussed according to the following two major categories: new candidate drugs with structural features in common with established anti-epileptic drugs (AEDs), and new candidate drugs with novel structures. The first category includes derivatives and analogues of carbamazepine and oxcarbazepine, felbamate, lamotrigine, phenytoin, tiagabine, topiramate and valproate. The second category describes compounds structurally unrelated to these AEDs, and includes acids and their derivatives, amides and vinylogous amides, aliphatic amines, benzimidazoles and imidazoles, benzodiazepines and benzothiazepines, benzopyrans, benzothiazoles, isoindolinones, lactams, lactones and thiolactones, 2(1H)-quinolones, quinoxalines and quinazolines, steroids and tricyclic steroid analogues, ureas and carbamates, and miscellaneous structural type...
Polymer | 1982
Thomas D. Greenwood; David M Armistead; James F. Wolfe; Anne K. St. Clair; Terry L. St. Clair; J. Barrick
Abstract A series of high molecular weight aromatic polyamide copolymers derived from 4,4′-bis(methylamino)-diphenylmethane, 4,4′-bis(propargylamino)diphenylmethane and isophthaloyl dichloride was prepared as potential candidates for use as matrix resins in Kevlar(R) fibre composites. These polyamides, which contain pendant propargyl groups, underwent facile crosslinking at 280°C as evidenced by dramatic increases in their glass transition temperatures (Tg) and accompanying loss of solubility. Other attempts to effect crosslinking by exposure to ultraviolet light, electron beam or gamma radiation were unsuccessful.
Journal of Medicinal Chemistry | 1990
James F. Wolfe; Terry L. Rathman; Mark C. Sleevi; James A. Campbell; Thomas D. Greenwood
Journal of Medicinal Chemistry | 1996
Patrick T. Flaherty; Thomas D. Greenwood; and Amy L. Manheim; James F. Wolfe
Journal of Organic Chemistry | 2005
William J. Layman; Thomas D. Greenwood; and Aaron L. Downey; James F. Wolfe
Journal of Organic Chemistry | 1983
Thomas D. Greenwood; James S. Hubbard; Andrew P. Komin; Yesh P. Sachdeva; James F. Wolfe
Journal of Medicinal Chemistry | 1990
R. Richard Goehring; Thomas D. Greenwood; Godson C. Nwokogu; Jyothi S. Pisipati; Tommie Gene. Rogers; James F. Wolfe
Bioorganic & Medicinal Chemistry | 2004
David White; Thomas D. Greenwood; Aaron L. Downey; Jeffrey R. Bloomquist; James F. Wolfe
Journal of Polymer Science Part A | 1980
Thomas D. Greenwood; Richard A. Kahley; James F. Wolfe; Anne K. St. Clair; Norman J. Johnston