D. Armistead

发表

Cellular and biochemical characterization of VX-710 as a chemosensitizer: reversal of P-glycoprotein-mediated multidrug resistance in vitro.

J. Saunders, V. Galullo, U. Germann, 1997, Anti-cancer drugs.

Synthetic studies on the immunosuppressive agent FK-506: Enantioselective synthesis of a C22C34 fragment

J. Boger, K. Hoogsteen, P. J. Hodges, 1998 .

Free-radicals in synthesis. I. A two-step carbolactonization procedure

D. Armistead, W. Fobare, S. D. Burke, 1982 .

The total synthesis of avermectin A1a

R. Hungate, S. Danishefsky, H. Selnick, 1989 .

Total synthesis of ionophore antibiotic X-14547 A (indanomycin)

M. Kort, D. Armistead, M. H. Parker, 1994 .

The total synthesis of the aglycon of avermectin A1a

R. Hungate, S. Danishefsky, H. Selnick, 1987 .

An enolate claisen route to c-pyranosides : Development and application to an ionophore synthon

F. Schoenen, D. Armistead, S. D. Burke, 1986 .

Polysubstituted dihydropyrans via the enolate Claisen rearrangement. A stereocontrolled route to C-pyranosides

F. Schoenen, D. Armistead, S. D. Burke, 1984 .

A Novel Immunophilin Ligand: Distinct Branching Effects on Dopaminergic Neurons in Culture and Neurotrophic Actions after Oral Administration in an Animal Model of Parkinson's Disease

P. Chaturvedi, P. Mccaffrey, O. Isacson, 1998, Neurobiology of Disease.

Total Synthesis of Ionophore Antibiotic X-14547A (Indanomycin).

M. Kort, D. Armistead, M. H. Parker, 1994 .

The Total Synthesis of the Aglycon of Avermectin A1a.

R. Hungate, S. Danishefsky, H. Selnick, 1988 .

Ionophore synthesis. An enantioselective route to the left-wing of indanomycin (X- 14547A).

D. Armistead, S. D. Burke, J. Fevig, 1985 .

Not the enolate Claisen rearrangement: a surprising route to the right-wing of indanomycin (X-14547A)

D. Armistead, S. D. Burke, K. Shankaran, 1986 .

The total synthesis of avermectin A1a. New protocols for the synthesis of novel 2-deoxypyranose systems and their axial glycosides

S. Danishefsky, H. Selnick, D. Armistead, 1987 .

Stereocontrolled one-pot conversions of α-alkoxy esters to syn- and anti-1,2-diol derivatives

B. Blough, R. Olsen, D. N. Deaton, 1987 .

Model studies directed toward the avermectins: A route to the oxahydrindene subunit

S. Danishefsky, D. Armistead, 1987 .

Non‐FK506‐binding protein‐12 neuroimmunophilin ligands increase neurite elongation and accelerate nerve regeneration

B. Gold, D. Armistead, Min‐Sheng Wang, 2005, Journal of neuroscience research.

A Nonimmunosuppressant FKBP-12 Ligand Increases Nerve Regeneration

P. Chaturvedi, B. Gold, D. Armistead, 1997, Experimental Neurology.

Chapter 22. Immunophilins and Immunosuppressive Drug Action

M. Harding, D. Armistead, 1993 .

Mechanistic aspects of acid-catalyzed reactions of 2,2,2-trifluorodiazoethane with alcohols

H. Dorn, D. Armistead, D. T. Loehr, 1988 .

Carbon-13 and fluorine-19 nuclear magnetic resonance chemical shift studies of carbon-13 enriched p-fluorobenzoyl derivatives

M. P. Spratt, E. Motell, H. Dorn, 1985 .

(2‐Dimethylaminoethyl)triphenylphosphonium Bromide

D. Armistead, 2001 .

N-Propargyl-substituted aromatic polyamides: preparation and thermal crosslinking

J. F. Wolfe, T. L. Clair, A. K. Clair, 1982 .

Novel 2-aminopyrimidine carbamates as potent and orally active inhibitors of Lck: synthesis, SAR, and in vivo antiinflammatory activity.

P. Gallant, M. Morrison, D. Elbaum, 2006, Journal of medicinal chemistry.

Design, synthesis and structure of non-macrocyclic inhibitors of FKBP12, the major binding protein for the immunosuppressant FK506.

M. Murcko, M. Navia, J. Saunders, 1995, Acta crystallographica. Section D, Biological crystallography.