Zobrazeno 1 - 10
of 35
pro vyhledávání: '"E. Starbuck"'
Publikováno v:
Physiotherapy. 107:e188
Publikováno v:
Value in Health. 22:S103-S104
Akademický článek
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Akademický článek
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Publikováno v:
Tetrahedron Letters. 37:4113-4116
By using a benzyl copper reagent (e.g. 10→11) in combination with titanium enolate chemistry (e.g. 12→13) a concise sequence has been developed for the rapid introduction of functionality found in the cytochalasin HIV protease inhibitor (1).
Autor:
A, Kc, K, Thapa, Y V, Pradhan, N P, Kc, S R, Upreti, R K, Adhikari, N, Khadka, B, Acharya, J R, Dhakwa, D R, Aryal, S, Aryal, E, Starbuck, D, Paudel, S, Khanal, M D, Devkota
Publikováno v:
Journal of Nepal Health Research Council. 9(2)
In Nepal, the proportion of under 5 deaths that are neonatal (0-28 days) has been increasing in the last decade, due to faster declines in infant and child mortality than in neonatal mortality. This trend is likely due to a focus on maternal and chil
Autor:
P.M.D. Fitzgerald, Joel R. Huff, Ken E. Starbuck, L.J. Chen, Hungate Randall W, Paul L. Darke, P. S. Anderson, M. K. Holloway, J. P. Vacca
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:499-504
The synsthesis and structure activity relationships of conformationally constrained analogs of the HIV-1 protease inhibitor L-685,434 are described. In addition, the X-ray crystal structure of a complex between L-700,497 and the HIV-1 protease is sho
Publikováno v:
ChemInform. 23
Versatile and concise routes to both racemic and chiral cyclopentane analogs of valinol are described. These compounds are constrained analogs of a key amino acid found in the aspartyl protease inhibitors of HIV-1.
Publikováno v:
ChemInform. 27
By using a benzyl copper reagent (e.g. 10→11) in combination with titanium enolate chemistry (e.g. 12→13) a concise sequence has been developed for the rapid introduction of functionality found in the cytochalasin HIV protease inhibitor (1).
Publikováno v:
Tetrahedron Letters. 32:6851-6854
Versatile and concise routes to both racemic and chiral cyclopentane analogs of valinol are described. These compounds are constrained analogs of a key amino acid found in the aspartyl protease inhibitors of HIV-1.