Myra Beaudoin Bertrand, MBA, PhD
Denver, Colorado, United States
2K followers
500+ connections
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- Business Development professional with experience as Search & Evaluation Lead in areas…
Activity
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Such an important thing to know. One wonders what the benefit is of Harvard University hiding it 🧐
Such an important thing to know. One wonders what the benefit is of Harvard University hiding it 🧐
Liked by Myra Beaudoin Bertrand, MBA, PhD
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I'm excited to attend BIO-Europe 2023, November 6–8, 2023 in Munich. Join me to meet one-to-one! https://lnkd.in/gs8j-wbE Informa Connect
I'm excited to attend BIO-Europe 2023, November 6–8, 2023 in Munich. Join me to meet one-to-one! https://lnkd.in/gs8j-wbE Informa Connect
Shared by Myra Beaudoin Bertrand, MBA, PhD
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University of Michigan College of Literature, Science, and the Arts
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Graduate advisor: John P. Wolfe
Thesis title: Methodology development for the stereoselective synthesis of protected pyrrolidines and alpha-alkyl-alpha-beta-dihydroxy esters -
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Activities and Societies: https://www.rider.edu/outcomes/stories/myra-beaudoin-bertrand
Executive MBA program
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Medicinal Chemistry, COOP program
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Volunteer Experience
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Closing ceremony host
Expo-Sciences
- Present 25 years
Science and Technology
1999-2003
Publications
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From Benchside to Business: My Career Path as a Chemist in the Pharmaceutical Industry
University of Michigan, Chemistry Department, CALCIUM Seminar Series
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Rationally Designed, Conformationally Constrained Inverse Agonists of RORγt-Identification of a Potent, Selective Series with Biologic-Like in Vivo Efficacy
J. Med. Chem. 2019, 62, 9931–9946
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Discovery of Branebrutinib (BMS-986195): A Strategy for Identifying a Highly Potent and Selective Covalent Inhibitor Providing Rapid in Vivo Inactivation of Bruton's Tyrosine Kinase (BTK)
J. Med. Chem. 2019, 62, 3228–3250
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Identification of a Potent, Selective, and Efficacious Phosphatidylinositol 3-Kinase δ (PI3Kd) Inhibitor for the Treatment of Immunological Disorders
J. Med. Chem. 2017, 60, 5193–5208
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Discovery of 6-Fluoro-5-(R)-(3-(S)-(8-fluoro-1-methyl-2,4-dioxo-1,2-dihydroquinazolin-3(4H)-yl)-2-methylphenyl)-2-(S)-(2-hydroxypropan-2-yl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide (BMS-986142)
J. Med. Chem. 2016, 59, 9173–9200
Other authors -
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Small Molecule Reversible Inhibitors of Bruton's Tyrosine Kinase (BTK): Structure-Activity Relationships Leading to the Identificationof7-(2-Hydroxypropan-2-yl)-4-[2-methyl-3-(4-oxo-3,4-dihydroquinazolin-3-yl)phenyl]-9H-carbazole-1-(BMS-935177)
J. Med. Chem. 2016, 59, 7915–7935
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SAR Studies on Peptide Agonists of Proteinase Activated Receptor-2 (PAR-2)
American Chemical Society National Meeting, Denver (CO), August 28, 2011. (poster presentation)
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[1,1'-Biphenyl]2-yldicyclohexylphosphine
The Electronic Encyclopedia of Reagents for Organic Synthesis
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Mild Conditions for Pd-Catalyzed Carboamination of N-Protected Hex-4-enylamines and 1-, 3-, and 4-Substituted Pent-4-enylamines. Scope, Limitations, and Mechanism of Pyrrolidine Formation
J. Org. Chem. 2008, 73, 8851–8860
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Mild Conditions for the Synthesis of Functionalized Pyrrolidines via Pd-Catalyzed Carboamination Reactions
Org. Lett. 2007, 9, 457–460
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Palladium-Catalyzed Synthesis of Cyclopentane-Fused Benzocyclobutenes via Tandem Directed Carbopalladation/C-H Bond Functionalization
Org. Lett. 2007, 9, 3073–3075
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A Concise Stereoselective Synthesis of Preussin, 3-epi-Preussin, and Analogs
Org. Lett. 2006, 8, 2353–2356
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Stereoselective Synthesis of N-Protected Pyrrolidines via Pd-Catalyzed Reactions of y-(N-Acylamino)alkenes and y-(N-Boc-amino)alkenes with Aryl Bromides
Tetrahedron, 2005, 61, 6447–6459
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Tandem Wittig Rearrangement/Aldol Reactions for the Synthesis of Glycolate Aldols
Org. Lett. 2006, 8, 4661–4663
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Polyester Based Antireflectant Coatings Having Shorter Etch Times
Advances in Imaging Materials and Processes 2004, 357–367
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Patents
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Tricyclic sulfones as ROR modulators and their preparations
Issued US WO 2016/179460 A1
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Indolecarboxamides compounds useful as kinase inhibitors and their preparation
Issued US WO 2016/065226 A1
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Preparation of 4-phenylcarbazole-1-carboxamide compounds useful as Bruton's tyrosine kinase (Btk) inhibitors
Issued US WO 2014210087
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Substituted carbazolecarboxamide derivatives as Btk inhibitors and their preparation and use for the treatment of diseases
Issued US US 20140378475
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Courses
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BIO Advanced Business Development Executive Training Program, Boston, MA
June 1-3, 2018
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Digital Health Courses (Artificial Intelligence and Machine Learning in Drug Discovery and Development, Digital Medicine), Molecular Med Tri-Con, San Francisco, March 1-3, 2020
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Project Management Fundamentals, Bristol-Myers Squibb, June 23-24, 2014
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Honors & Awards
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Bristol-Myers Squibb Graduate Fellowship in Organic Chemistry
Bristol-Myers Squibb
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Pfizer Graduate Student Award in Chemistry and Chemical Biology
Pfizer
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University of Ottawa Scholarship
University of Ottawa
1999-2003
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Collège de l’Outaouais Scholarship
Collège de l’Outaouais
1997-1999
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Chemical Institute of Canada Prize
Chemical Institute of Canada
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Esso Scholarship
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High School
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Ordre des Chimistes du Québec Prize
Ordre des Chimistes du Québec
High School
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Agence Canadienne-Française pour l’Avancement des Sciences Prize
Agence Canadienne-Française pour l’Avancement des Sciences
High School
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Governor General's Bronze Medal
Governor General of Canada
High Scool (École secondaire Hormisdas-Gamelin, Buckingham, Québec, Canada)
Languages
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Englisch
Native or bilingual proficiency
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French
Native or bilingual proficiency
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Chinese (Mandarin)
Limited working proficiency
Organizations
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American Chemical Society
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- Present
More activity by Myra
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I'm excited about BIO-Europe: Spring 2023, to join me click here https://lnkd.in/guYT3azq Informa Connect
I'm excited about BIO-Europe: Spring 2023, to join me click here https://lnkd.in/guYT3azq Informa Connect
Shared by Myra Beaudoin Bertrand, MBA, PhD
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