“I have provided chromatography services to many people at many companies Bill is one of the best. He fits the definition of a analytical chemist. He is creative and innovative. If I ever need advice on a separation Bill is one of the handful of chemist I would go to for that advice.”
About
With over 20 years of experience in analytical development and characterization of…
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1. We have more distractions than ever. 2. We default to meetings for too many workplace interactions.
1. We have more distractions than ever. 2. We default to meetings for too many workplace interactions.
Liked by William Barker
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We are pleased to announce the U.S. FDA has accepted our two New Drug Applications (NDAs) with a Priority Review designation for an investigational…
We are pleased to announce the U.S. FDA has accepted our two New Drug Applications (NDAs) with a Priority Review designation for an investigational…
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In our aging world, innovation and technology are lifelines for the elderly and disabled. I remember my grandfather, struggling in pain after hip…
In our aging world, innovation and technology are lifelines for the elderly and disabled. I remember my grandfather, struggling in pain after hip…
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Experience & Education
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Venatorx Pharmaceuticals, Inc.
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Publications
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High-performance liquid chromatographic enantioseparation of methanobenzazocines
J Chromatogr A, (2009), 1216 (45), 7708-7714.
Chiral recognition and resolution of methanobenzazocines was investigated by HPLC using polysaccharide, Pirkle-type, native and derivatized beta-cyclodextrin chiral stationary phases. Enantioseparation of phenyl substituted 2,6-methanobenzazocines was achieved with multiple chiral stationary phases throughout the classes described. Chiral resolution of the enantiomers of 1,5-methano-3-methyl-6-oxo-1,2,3,4,5,6-hexahydro-3-benzazocine was produced on both polysaccharide and Pirkle-type phases. In…
Chiral recognition and resolution of methanobenzazocines was investigated by HPLC using polysaccharide, Pirkle-type, native and derivatized beta-cyclodextrin chiral stationary phases. Enantioseparation of phenyl substituted 2,6-methanobenzazocines was achieved with multiple chiral stationary phases throughout the classes described. Chiral resolution of the enantiomers of 1,5-methano-3-methyl-6-oxo-1,2,3,4,5,6-hexahydro-3-benzazocine was produced on both polysaccharide and Pirkle-type phases. In the case of 1,5-methano-3-methyl-6-phenyl-1,2,3,4,5,6-hexahydro-3-benzazocine only a dinitrophenyl substituted beta-cyclodextrin produced a separation of enantiomers.
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Bravado Pharmaceuticals your CDMO experts for semi-solids development leading to GMP manufacturing. For more information contact Brian McMillan or…
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