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P R Verhoest

Showing results (1-10 of 5) with videos related to

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Journal of the American Chemical Society|November 1, 2001
Total synthesis of (+)-phorboxazole A exploiting the Petasis-Ferrier rearrangementA B Smith, K P Minbiole, P R Verhoest, et al.
Organic Letters|May 24, 2000
Phorboxazole synthetic studies. 1. Construction of a C(3-19) subtarget exploiting an extension of the Petasis-Ferrier rearrangementA B Smith, P R Verhoest, K P Minbiole, et al.
Organic Letters|May 24, 2000
Phorboxazole synthetic studies. 2. Construction of a C(20-28) subtarget, a further extension of the Petasis-Ferrier rearrangementA B Smith, K P Minbiole, P R Verhoest, et al.
The Journal of Pharmacology and Experimental Therapeutics|August 9, 2011
Pharmacological characterization of 2-methyl-N-((2'-(pyrrolidin-1-ylsulfonyl)biphenyl-4-yl)methyl)propan-1-amine (PF-04455242), a high-affinity antagonist selective for κ-opioid receptorsS Grimwood, Y Lu, A W Schmidt, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 22, 2008
Preclinical characterization of selective phosphodiesterase 10A inhibitors: a new therapeutic approach to the treatment of schizophreniaC J Schmidt, D S Chapin, J Cianfrogna, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Journal of the American Chemical Society|November 1, 2001
Total synthesis of (+)-phorboxazole A exploiting the Petasis-Ferrier rearrangementA B Smith, K P Minbiole, P R Verhoest, et al.
Organic Letters|May 24, 2000
Phorboxazole synthetic studies. 1. Construction of a C(3-19) subtarget exploiting an extension of the Petasis-Ferrier rearrangementA B Smith, P R Verhoest, K P Minbiole, et al.
Organic Letters|May 24, 2000
Phorboxazole synthetic studies. 2. Construction of a C(20-28) subtarget, a further extension of the Petasis-Ferrier rearrangementA B Smith, K P Minbiole, P R Verhoest, et al.
The Journal of Pharmacology and Experimental Therapeutics|August 9, 2011
Pharmacological characterization of 2-methyl-N-((2'-(pyrrolidin-1-ylsulfonyl)biphenyl-4-yl)methyl)propan-1-amine (PF-04455242), a high-affinity antagonist selective for κ-opioid receptorsS Grimwood, Y Lu, A W Schmidt, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 22, 2008
Preclinical characterization of selective phosphodiesterase 10A inhibitors: a new therapeutic approach to the treatment of schizophreniaC J Schmidt, D S Chapin, J Cianfrogna, et al.
Pageof 1