ROBERT B. KARGBO, PH.D.
Robert B. Kargbo, Ph.D., Senior Research Scientist I at Albany Molecular Research Inc. (AMRI), was born in Freetown, Sierra Leone. He completed his BSc (Hons) in Chemistry Fourah Bay College, University of Sierra Leone. He lectured at the College of Medicine and Allied Health Sciences in Freetown, Sierra Leone. He obtained a Ph.D. in Organic Chemistry from North Dakota State University (with Professor Gregory R. Cook). He received a number of awards including the Pfizer Global Reseach & Development Research Fellowship, McNair Scholar Award and Graduate Research Fellowship, ND-EPSCoR. Dr. Kargbo joined AMRI as a Senior Research Scientist, working his way to his current position of Senior Research Scientist I in the Medicinal Chemistry Department.
Dr. Kargbo spent most of his time at AMRI in projects involved in drug discovery for small biotech and large pharmaceutical clients. The most recent collaborative work involves the NIH National Institute of Neurological Disorders and Stroke as part of the Medicinal Chemistry for Neurotherapeutics Program (NINDS MCNP). Dr. Kargbo occasional review articles and maintains active Independent Research Projects.
links
links
http://www.amrismartsourcing.com/meet-the-bloggers/robert-b-kargbo-ph-d/
https://www.linkedin.com/pub/robert-kargbo/27/a30/a5b
https://www.researchgate.net/profile/Robert_Kargbo/publications
– Present (1 year 3 months)Albany, New York Area
– Present (5 years 6 months)Albany, New York
– (2 years 11 months)
– (1 year 9 months)FREETOWN SIERRA LEONE
Christopher Conway, Senior Vice President,
Albany Molecular Research Inc. (AMRI)
26 Corporate Circle
Albany, NY 12203
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https://www.linkedin.com/pub/robert-kargbo/27/a30/a5b
https://www.researchgate.net/profile/Robert_Kargbo/publications
Experience
Blogger (AMRI)
AMRI (Albany Molecular Research Inc.)
Highlight interesting event or discovery:
Blog posting: http://www.amrismartsourcing.com/amri-events/a-recap-of-the-florida-heterocyclic-and-synthetic-conference/
Blog posting: http://www.amrismartsourcing.com/amri-events/a-recap-of-the-florida-heterocyclic-and-synthetic-conference/
Senior Research Scientist I
AMRI (Albany Molecular Research Inc.)
TRACKER
CARDINAL IG
• Expert in statistical and analytical experience in the manufacturing of high quality glass product for various customers.
• Organizes and directs resources effectively, efficiently and execute complex experimental plans.
• Collaborates to enhance team efforts through personal contributions.
• First recipient of the “Employer of the year award” in 2001.
• Organizes and directs resources effectively, efficiently and execute complex experimental plans.
• Collaborates to enhance team efforts through personal contributions.
• First recipient of the “Employer of the year award” in 2001.
RESEARCH TEACHING ASSISTANT
COLLEGE OF MEDICINE AND ALLIED HEALTH SCIENCES
Education
North Dakota State University
PHD, SYNTHETIC ORGANIC CHEMISTRY
Faculty Search Committee, Student Representative, North Dakota State University. Fargo, ND.
Laboratory Safety Program, Student Representative, North Dakota State University, Fargo, ND.
Organizer, New Graduate Welcome Ceremony. North Dakota State University, Fargo, ND.
Laboratory Safety Program, Student Representative, North Dakota State University, Fargo, ND.
Organizer, New Graduate Welcome Ceremony. North Dakota State University, Fargo, ND.
Fourah Bay College
BS Chemistry (Hons)
Publications
Tricyclic Compounds and PBK Inhibitors Containing the Same
US 8,962,648
February 24, 2015
Synthesis of tricyclic compounds and their use as PBK inhibitors. These compounds are useful for the treatment of PBK related diseases, including cancer.
Synthesis of 3-benzazepines and azepino[4,5-b]heterocyclic ring systems via intramolecular Friedel–Crafts cyclization
Tetrahedron Letters
2013
The intramolecular Friedel–Crafts cyclization was found to be effective for the synthesis of 3-benzazepines and azepino[4,5-b]heterocyclic ring systems using simple allylic bromides tethered to activated aromatic nuclei. Amongst the various Lewis acids screened, Bi(OTf)3 was found to be the most effective ‘ecofriendly’ catalyst for the cyclization.
Synlett
2012
An efficient one-pot synthesis of 2-substituted benzimidazoles via triacyloxyborane intermediates is reported. The mild protocol is efficient and tolerant of acid-labile functional groups.
Preparation of thieno[2,3-c]quinoline derivatives as PKB inhibitors for treating cancer
PCT Int. Appl
2012
Title compds. I [R1, R2, R3, and R4 independently = H, OH, halogen, CN, NO2, NH2, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, alkoxy, aryl, indanyl, heteroaryl, etc.; R5 = H or alkyl; X, Y and Z together form S-CR7=CR6, CH2-CH2-CH2, NR108-CH=CR109; wherein R6 = H, OH, alkyl or (un)substituted aryl; R7 = H, halo, or (un)substituted alkyl; R108 = H, or (un)substituted alkyl; R109 = H, CH3, or...more
Asymmetric Synthesis of Aminochromanes via Intramolecular Indium-Mediated Allylation of Chiral Hydrazones
J. Org. Chem.
August 24, 2009
Debasis Samanta, Robert B. Kargbo and Gregory R. Cook
J. Org. Chem., 2009, 74 (18), pp 7183–7186
Publication Date (Web): August 24, 2009 (Note)
DOI: 10.1021/jo901195g
The asymmetric intramolecular indium-mediated cyclization reaction delivers chromanes with excellent diastereoselectivity (68−91% yield, dr >99:1). The reaction was efficient for aryl substrates with both electron-withdrawing...more
J. Org. Chem., 2009, 74 (18), pp 7183–7186
Publication Date (Web): August 24, 2009 (Note)
DOI: 10.1021/jo901195g
The asymmetric intramolecular indium-mediated cyclization reaction delivers chromanes with excellent diastereoselectivity (68−91% yield, dr >99:1). The reaction was efficient for aryl substrates with both electron-withdrawing...more
Stereoselective Indium-Mediated Allylation Reactions
Current Organic Chemistry
2009
Since the discovery that indium could affect a Barbier-type allylation of carbonyls in water over a decade ago, interest in the utility of indium metal and its salts to influence organic transformations has increased exponentially. Control of chemo-, regio-, and especially stereoselectivity in indium-mediated reactions has proven to be a challenge, however, examples of such discerning processes...more
March 13, 2007
Robert Kargbo, Yoko Takahashi, Santosh Bhor, Gregory R. Cook, Guy C. Lloyd-Jones, and Ian R. Shepperson
J. Am. Chem. Soc., 2007, 129 (13), pp 3846–3847
Publication Date (Web): March 13, 2007 (Communication)
DOI: 10.1021/ja070742t
Thia−Fries rearrangement of BINOL perfluoroalkylsulfonates affords readily derivatized novel mono- and disulfone ligands in just two steps from enantiomerically pure...more
J. Am. Chem. Soc., 2007, 129 (13), pp 3846–3847
Publication Date (Web): March 13, 2007 (Communication)
DOI: 10.1021/ja070742t
Thia−Fries rearrangement of BINOL perfluoroalkylsulfonates affords readily derivatized novel mono- and disulfone ligands in just two steps from enantiomerically pure...more
Catalytic Enantioselective Indium-Mediated Allylation of Hydrazones
Gregory R. Cook, Robert Kargbo, and Bikash Maity
Org. Lett., 2005, 7 (13), pp 2767–2770
Publication Date (Web): May 28, 2005 (Letter)
DOI: 10.1021/ol051160o
A facile and highly selective indium-mediated allylation of hydrazones utilizing BINOL ligands is described. Chiral (R)-3,3‘-bistrifluoromethylBINOL afforded homoallylic amines in up to 97% ee with stoichiometric ligand. Employing only 10...more
Org. Lett., 2005, 7 (13), pp 2767–2770
Publication Date (Web): May 28, 2005 (Letter)
DOI: 10.1021/ol051160o
A facile and highly selective indium-mediated allylation of hydrazones utilizing BINOL ligands is described. Chiral (R)-3,3‘-bistrifluoromethylBINOL afforded homoallylic amines in up to 97% ee with stoichiometric ligand. Employing only 10...more
Highly Diastereoselective Indium-Mediated Allylation of Chiral Hydrazones
Gregory R. Cook, Bikash C. Maity, and Robert Kargbo
Org. Lett., 2004, 6 (11), pp 1741–1743
Publication Date (Web): May 04, 2004 (Letter)
DOI: 10.1021/ol0496172
The indium-mediated allylation of chiral hydrazones was investigated. Essentially complete diastereoselectivity and quantitative yields were obtained for substrates derived from both aromatic and aliphatic aldehydes.
Org. Lett., 2004, 6 (11), pp 1741–1743
Publication Date (Web): May 04, 2004 (Letter)
DOI: 10.1021/ol0496172
The indium-mediated allylation of chiral hydrazones was investigated. Essentially complete diastereoselectivity and quantitative yields were obtained for substrates derived from both aromatic and aliphatic aldehydes.
Synthetic applications of tris(pentafluorophenyl)borane
Synlett
2004
Hydrosilation of arom. compds. catalyzed by 1-4 mol% of tris(pentafluorophenyl)borane is a mild and selective addn. of Ph3SiH at room temp. Yields and conversion rates for this transformation are high and the reactivity order is esters >> ketone > aldehyde which is paradoxical to the normal reactivity pattern. Secondary benzylic alc. derivs. undergo allylation with allylsilanes in the...more
Asymmetric addition of organoindium reagent to hydrazones
Diss. Abstr. Int., B 2008, 69(4), 2332.
2008
Dissertation (2008), 209 pp
Christopher Conway has been appointed to lead AMRI ’s discovery business strategy as SrVP of Discovery and Development and Global Commercial Sales.
Christopher Conway, Senior Vice President,
Global Sales and Marketing
Christopher Conway has been appointed to lead the company’s discovery business strategy as Senior Vice President of Discovery and Development and Global Commercial Sales.
September 3, 2015
SEE AN UPDATEFRO AMRI
QUOTE
Dear industry colleague,
As we continue to support the research and development that leads to the commercialization of pharmaceutical products, it is critical that we align our focus on R&D with the commercial demands of the market. Today, AMRI has announced an organizational change in our Discovery and Development Services (DDS) business. These changes are expected to drive top and bottom line growth for the Discovery and Development Solutions (DDS) business through strong commercial leadership; strengthen the DDS strategy and aggressively pursue the most valuable growth opportunities, externally and internally; and ensure that our service offerings are well aligned with your needs and the needs of the market.
Effective immediately, Christopher Conway has been appointed to lead the company’s discovery business strategy as Senior Vice President of Discovery and Development and Global Commercial Sales. In this role, Chris will head up the global Discovery and Development Solutions (DDS) business leading these businesses in the United States, Europe and Asia. Sales and marketing will also continue to report to him. He succeeds Michael A. Luther, Ph.D., MBA, who will be leaving AMRI to pursue other opportunities. We thank Dr. Luther for his efforts in moving the DDS business along over the last year and wish him the best in his future endeavors.
Related to this announcement, we would like to take the opportunity to announce the hiring of Rory Curtis, Ph.D., who has joined AMRI as Vice President of Discovery Biology and Pharmacology. Rory will also serve as site head with responsibility for scientific operations at AMRI’s Buffalo, N.Y. location. Rory was most recently Senior Director of Human Diseases in Discovery at Cubist Pharmaceuticals, where he developed Cubist’s antibacterial drug discovery into new disease areas such as pain, inflammation and gastro-intestinal disease. Before this, he held positions of increasing responsibility at Elixir Pharmaceuticals, Millennium Pharmaceuticals and Regeneron Pharmaceuticals.
Rory Curtis
Vice President of Discovery Biology and Pharmacology, Site Head AMRI Buffalo
In addition to Chris’ current direct reports and Rory, he will have a scientific leadership team reporting into him, which includes Michael P. Trova, Ph.D., Senior Vice President of Chemistry; Raj Shenoy, Senior Director of Global Chemical Development; and Pete Michels, Ph.D., Senior Director of Metabolism and Biotransformations.
Michael P. Trova, Ph.D.
Pete C. Michels, Ph.D., Senior Director, Chemical Development, Fermentation and Biocatalysis, AMRI
We are very excited about the future of AMRI Drug Discovery and Development and are pleased to welcome Rory to the AMRI discovery team. Market demand for our DDS services continues to grow and these changes will help us increase our market share and strengthen AMRI’s global position in Discovery and Development.
As we approach the second half of 2015, we are looking forward to working with you on a great number of new opportunities in 2016 and beyond. We appreciate your loyalty and support, and continue to remain dedicated to enhancing your pharmaceutical services experience from early discovery through to the commercialization and delivery of drug product. If you have any questions, please feel free to read today’s related press release atwww.amriglobal.com, or contact us here.
Sincerely,
William S. Marth. President and Chief Executive Officer Albany Molecular Research, Inc.
Albany Molecular Research Inc. (AMRI)
26 Corporate Circle
Albany, NY 12203
Albany Molecular Research Inc. provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. Our services include Drug Discovery, such as medicinal chemistry, discovery biology and in vitro ADME; Development, such as pre-formulation, formulation and validation; and Manufacturing, such as cGMP API manufacturing.
SINGAPORE RESEARCH CENTRE
AMRI’s Singapore Research Centre, Pte. Ltd. provides chemistry and biology services to support drug discovery and development programs. AMRI is one of the first drug discovery R&D companies to establish operations in Singapore. Fully integrated with AMRI’s locations in the United States, Asia, and Europe, the Singapore centre offers medicinal chemistry services such as hit-to-lead andlead optimization as well as focused library synthesis / custom synthesis. In the area of biology / in vitro pharmacology, the Singapore Research Centre provides target validation; assay development; HTS; rapid production of SAR quality data; and in vitro ADMET support, including CYP inhibition, metabolic stability (liver microsome assays), and aqueous solubility. As a signatory to the World Patent Treaty, Singapore provides an environment that protects intellectual property, enabling our scientists to conduct proprietary and cutting-edge research on behalf of our customers.
Areas of Expertise: Discovery Services
Contact Information:
61 Science Park Road
#05-01 The Galen
Singapore Science Park II
Singapore 117525
Phone: +65-6398-5500
Fax: +65-6398-5511
61 Science Park Road
#05-01 The Galen
Singapore Science Park II
Singapore 117525
Phone: +65-6398-5500
Fax: +65-6398-5511
HYDERABAD RESEARCH CENTRE
The Hyderabad Research Centre, Pvt. Ltd. (AMRHRC) is located in Hyderabad, India, an emerging technology metropolis located in South Central India.
All fully integrated with AMRI’s U.S.-based resources, this Centre’s core area of expertise is in the areas ofmedicinal chemistrysupport, chemical development, custom synthesis of scaffolds and building blocks, process development, GMP analytical services,scale-up and preparation of reference standards.
Areas of Expertise: Chemical Development and Small Scale Manufacturing
Contact Information:
Hyderabad Research Centre Pvt. Ltd.
Plot # 9, Alexandria Knowledge Park, Turkapally, Shameerpet
Genome Valley, RR District, Hyderabad – 500 078, India
Tel : +91 – 40 – 6687 6666 (Board)
Fax : +91 – 40 – 6687 6600
Hyderabad Research Centre Pvt. Ltd.
Plot # 9, Alexandria Knowledge Park, Turkapally, Shameerpet
Genome Valley, RR District, Hyderabad – 500 078, India
Tel : +91 – 40 – 6687 6666 (Board)
Fax : +91 – 40 – 6687 6600
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