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Journal of Medicinal Chemistry | 2009

Hit to lead account of the discovery of a new class of inhibitors of Pim kinases and crystallographic studies revealing an unusual kinase binding mode.

Kevin Chungeng Qian; Lian Wang; Charles L. Cywin; Bennett T. Farmer; Eugene R. Hickey; Carol Ann Homon; Scott Jakes; Mohammed A. Kashem; George E. Lee; Scott Leonard; Jun Li; Ronald Magboo; Wang Mao; Edward J. Pack; Charlene Peng; Anthony S. Prokopowicz; Morgan Welzel; John P. Wolak; Tina Morwick

A series of inhibitors of Pim-2 kinase identified by high-throughput screening is described. Details of the hit validation and lead generation process and structure-activity relationship (SAR) studies are presented. Disclosure of an unconventional binding mode for 1, as revealed by X-ray crystallography using the highly homologous Pim-1 protein, is also presented, and observed binding features are shown to correlate with the Pim-2 SAR. While highly selective within the kinase family, the series shows similar potency for both Pim-1 and Pim-2, which was expected on the basis of homology, but unusual in light of reports in the literature documenting a bias for Pim-1. A rationale for these observations based on Pim-1 and Pim-2 K(M(ATP)) values is suggested. Some interesting cross reactivity with casein kinase-2 was also identified, and structural features which may contribute to the association are discussed.


Tetrahedron Letters | 1979

Thienamycin. A solution of the stereochemical problem

Joseph J. Tufariello; George E. Lee; Pushpananda A. Senaratne; Mohammed Al-Nuri

Abstract A new nitrone-based synthesis of β-lactams is described which makes provision for the 1-hydroxyethyl moiety in the potent antibiotic thienamycin. Moreover, the relative stereochemical features of the natural product are defined in a step involving the cycloaddition of a nitrone with methyl crotonate.


Synthetic Communications | 1980

A Synthesis of γ-Ketocarboxylic Acids and its Application in the Preparation of Benzo [B]Furans

Wayne K. Anderson; George E. Lee

Abstract The aldol addition-pinacol rearrangement sequence starting with 1,2-bis(trimethylsilyloxy)cyclobutene and a ketal or acetal provides facile entry into a series of substituted 1,3-cyclopentadiones.2 This, combined with the known propensity for 1,3-diketones to undergo cleavage reactions, affords a useful sequence for the synthesis of γ-ketocarboxylic acids: Application of this sequence is demonstrated in a new synthesis of 2,3-dihydrobenzo [b] furan (ergo, benzo[b] furan).


Journal of the American Chemical Society | 1980

Functionalized nitrones. A highly stereoselective and regioselective synthesis of dl-retronecine

Joseph J. Tufariello; George E. Lee


Journal of the American Chemical Society | 1999

CARBENES AS SUBSTRATES : BIMOLECULAR FRAGMENTATION OF ALKOXYCHLOROCARBENES

Robert A. Moss; Lauren A. Johnson; Dina C. Merrer; George E. Lee


Journal of Organic Chemistry | 1980

Synthesis of C-ring-functionalized A-ring-aromatic trichothecane analogs

Wayne K. Anderson; George E. Lee


Organic Process Research & Development | 2001

Facile Preparation of 3-(1-Piperazinyl)-1H-indazoles

Vincent Leroy; George E. Lee; Jiang Lin; and Sandra H. Herman; Thomas B. K. Lee


Journal of Organic Chemistry | 1977

Synthesis of 6.9-bisnormethyl-8-methoxy-12,13-epoxy-6,8,10-trichothecatriene.

Wayne K. Anderson; Edmond J. LaVoie; George E. Lee


Journal of Medicinal Chemistry | 1980

Synthesis of 8-methoxy-15,16-dinor-6,8,10-trichothecatriene 12,13 alpha-epoxide and 12,13 beta-epoxide as potential antineoplastic agents.

Wayne K. Anderson; George E. Lee


Organic Process Research & Development | 2011

N-Amination of Indoles on Pilot-Plant Scale via Simultaneous and Proportional Metering of Reagents

Franz J. Weiberth; Reda G. Hanna; George E. Lee; Yvonne Polverine; Joseph T. Klein

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