“I have known Amarjit for several years. He is a very competent and a very hard working professional. I am very impressed with his 'can-do' attitude, problem solving and critical thinking abilities. He is a very good team player with excellent leadership attributes. He never hesitates to take initiatives and has an impressive ability to prioritize goals with impressive ability to execute a plan. He believes in delivering promised results on time and exceeding client expectations. I am very confident that he will be an excellent and a very productive addition to any organization...”
About
Specialties:
ISO 10993-1, US FDA GLP testing, Biological Safety Evaluation…
Activity
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🔬 How Many Samples for Biocompatibility Tests? | Part 1: Chemical Characterization & Cytotoxicity When planning biocompatibility testing, one of…
🔬 How Many Samples for Biocompatibility Tests? | Part 1: Chemical Characterization & Cytotoxicity When planning biocompatibility testing, one of…
Liked by Amarjit Luniwal, PhD, DABT
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Hello! I'm looking for a new position and I hope you can help. I just left my last role as a biological safety specialist for a premier medical…
Hello! I'm looking for a new position and I hope you can help. I just left my last role as a biological safety specialist for a premier medical…
Liked by Amarjit Luniwal, PhD, DABT
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Medline Industries, LP closes on a $950 million acquisition in the #surgical space. " With this acquisition, we are eager to collaborate with…
Medline Industries, LP closes on a $950 million acquisition in the #surgical space. " With this acquisition, we are eager to collaborate with…
Liked by Amarjit Luniwal, PhD, DABT
Experience
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Education
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University of Toledo
Activities and Societies: American Chemical Society, Oganic Journal Club
Communication Director, Mid-Atlantic Graduate Student Symposium in Medicinal Chemistry (MAGSS)-2009 hosted by University of Toledo
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Activities and Societies: Molecular modeling, analog based drug designing, 3D-QSAR studies
Member, Indian Pharmaceutical Association
Licenses & Certifications
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Foreign Pharmacy Graduate Equivalency Committee (FPGEC) Certification
National Association of Boards of Pharmacy (NABP)
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Radiological Safety Certification
University of Toledo, Toledo, OH
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Research Commercialization Introductory Course Certification
National Council of Entrepreneurial Tech Transfer (NCET2)
Publications
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Molecular Docking and Enzymatic Evaluation to Identify Selective Inhibitors of Aspartate Semialdehyde Dehydrogenase
Bioorganic Medicinal Chemistry
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Multigram Synthesis of Glyceollin I
ACS/Organic Process Research and Development, 2011, 15, 1149–1162
Scaled-up procedures and prepn. of glyceollin I (I) in multigram quantities are described. The synthesis features construction of a cis-fused ring system in high enantiomeric excess after Sharpless asym. dihydroxylation of a key intermediate that is initially produced by an intramol. Wittig reaction to afford the requisite alkene while simultaneously forming the first ring. The overall yield is 12% after 11 steps.
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Total syntheses of (±)-vestitol and bolusanthin III using a wittig strategy
Synlett, 2011, 11, 1605-1607
An intramolecular Wittig olefination was utilized to produce the key isoflav-3-ene intermediate needed to prep. (±)-vestitol and bolusanthin III in ca. 30% and 20% resp. yields after eight steps.
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Total Syntheses of Racemic and Natural Glycinol
ACS/ Journal of Natural Products, 2009, 72, 11, 2072-2075.
Total syntheses of racemic and (-)-glycinol (I) are described. A Wittig reaction produced the isoflav-3-ene from which a Sharpless dihydroxylation introduced either the racemic or enantiomeric 6a-hydroxy group. A 5.5% overall yield of racemic material was obtained after 12 steps. A method was devised for a one-pot switch of protecting groups masking a sensitive resorcinolic para-functionality, and conditions were optimized to prompt spontaneous closure of the pterocarpanolic dihydrofuran…
Total syntheses of racemic and (-)-glycinol (I) are described. A Wittig reaction produced the isoflav-3-ene from which a Sharpless dihydroxylation introduced either the racemic or enantiomeric 6a-hydroxy group. A 5.5% overall yield of racemic material was obtained after 12 steps. A method was devised for a one-pot switch of protecting groups masking a sensitive resorcinolic para-functionality, and conditions were optimized to prompt spontaneous closure of the pterocarpanolic dihydrofuran upon subsequent exposure of its ortho-functionality. These improvements eliminated two steps and increased the overall yield to 9.8% during prodn. of the natural enantiomer.
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Patents
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Methods for synthesizing glycinols, glyceollins I and II and isoflavenes and chromanes using a Wittig reaction, and compositions made therewith
Issued USPTO 08507549
See patentMethods for synthesizing glycinols, glyceollins I and II, and isoflavene and chromane compounds using a Wittig reaction, compositions made therewith, and uses thereof are described.
Languages
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English
Full professional proficiency
Organizations
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American Chemical Society
Member
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Indian Pharmaceutical Association
Member
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Phi Kappa Phi
Member
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Society of Toxicology
Full Member
Recommendations received
2 people have recommended Amarjit
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