Scott Hasty
Appearances
- : [CHED] Division of Chemical Education
Speakers
University of Nevada, RenoUniversity of Notre DameAssociate Professor, Mississippi CollegeIndiana State UniversityNortheastern UnivMuhlenberg CollegeAssociate Professor of Chemistry, Rhodes CollegeHigh Point University, High Point University, High Point, NC, US, academicUniversity of TampaPostdoctoral Research and Teaching Fellow, UNC AshevilleAssistant Professor, Lafayette CollegeMelvin Druelinger, Ph.D.Professor of Chemistry, Colorado State Univ PuebloSalt Lake Community CollegeDenison UniversitySoutheast Missouri State UniversityAllison Hurley Predecki, Ph.D.Associate Professor of Chemistry and Biochemistry, Shippensburg University of PennsylvaniaAssociate Professor, Shippensburg UniversityNorthern Kentucky UniversityTrinity UniversityCollege of the Holy CrossProvidence CollegeDavidson CollegeUSC UpstateProfessor, Eastern Oregon UniversityMichael S. Leonard, Ph.D.Professor of Chemistry, Washington & Jefferson CollegeNaresh Gunaganti, Ph.D.Associate Research Scientist, Northeastern UniversityBaljinder Singh, PhDSenior Research Scientist, AstraZeneca Pharmaceuticals LPResearch Assistant Professor, Northeastern UniversityWhitworth UniversityProfessor, Penn State Berks - : [CHED] Division of Chemical Education
Speakers
University of Nevada, RenoUniversity of Notre DameAssociate Professor, Mississippi CollegeIndiana State UniversityNortheastern UnivMuhlenberg CollegeAssociate Professor of Chemistry, Rhodes CollegeHigh Point University, High Point University, High Point, NC, US, academicUniversity of TampaPostdoctoral Research and Teaching Fellow, UNC AshevilleAssistant Professor, Lafayette CollegeMelvin Druelinger, Ph.D.Professor of Chemistry, Colorado State Univ PuebloSalt Lake Community CollegeDenison UniversitySoutheast Missouri State UniversityAllison Hurley Predecki, Ph.D.Associate Professor of Chemistry and Biochemistry, Shippensburg University of PennsylvaniaAssociate Professor, Shippensburg UniversityNorthern Kentucky UniversityTrinity UniversityCollege of the Holy CrossProvidence CollegeDavidson CollegeUSC UpstateProfessor, Eastern Oregon UniversityMichael S. Leonard, Ph.D.Professor of Chemistry, Washington & Jefferson CollegeNaresh Gunaganti, Ph.D.Associate Research Scientist, Northeastern UniversityBaljinder Singh, PhDSenior Research Scientist, AstraZeneca Pharmaceuticals LPResearch Assistant Professor, Northeastern UniversityWhitworth UniversityProfessor, Penn State Berks - : [CHED] Division of Chemical Education
Speakers
University of Nevada, RenoUniversity of Notre DameAssociate Professor, Mississippi CollegeIndiana State UniversityNortheastern UnivMuhlenberg CollegeAssociate Professor of Chemistry, Rhodes CollegeHigh Point University, High Point University, High Point, NC, US, academicUniversity of TampaPostdoctoral Research and Teaching Fellow, UNC AshevilleAssistant Professor, Lafayette CollegeMelvin Druelinger, Ph.D.Professor of Chemistry, Colorado State Univ PuebloSalt Lake Community CollegeDenison UniversitySoutheast Missouri State UniversityAllison Hurley Predecki, Ph.D.Associate Professor of Chemistry and Biochemistry, Shippensburg University of PennsylvaniaAssociate Professor, Shippensburg UniversityNorthern Kentucky UniversityTrinity UniversityCollege of the Holy CrossProvidence CollegeDavidson CollegeUSC UpstateProfessor, Eastern Oregon UniversityMichael S. Leonard, Ph.D.Professor of Chemistry, Washington & Jefferson CollegeNaresh Gunaganti, Ph.D.Associate Research Scientist, Northeastern UniversityBaljinder Singh, PhDSenior Research Scientist, AstraZeneca Pharmaceuticals LPResearch Assistant Professor, Northeastern UniversityWhitworth UniversityProfessor, Penn State Berks - DateMarch 27, 2023Ongoing development of novel thio-based carbohydrate leaving groups creates methods for additional oligosaccharide assembly methods. The use of heterocyclic anomeric leaving groups containing nitrogens have been proven quite useful in the glycosylation reaction…
Presenter
Speaker
- DateMarch 27, 2023It is widely known that protecting groups and solvents can have an impact on the stereo-outcome of carbohydrates during the glycosylation reaction. It has also been established that hydrogen bonding influences the coupled carbohydrate product…
Presenters
Speaker
- DateMarch 27, 2023The on-going exploration of thiol-based carbohydrate leaving groups have led us to the heterocyclic compound 2-mercapto-6-methylpyridine. The leaving group was affixed to the pyranose series containing glucose, galactose, and mannose…
Presenter
Speaker
- DateMarch 18, 2024It is widely known that protecting groups can have an impact on the stereo-outcome of carbohydrates during the glycosylation reaction. It has also been well established that hydrogen bonding influences the coupled carbohydrate product…
Presenters
- DateMarch 18, 2024Novel thio-based carbohydrate leaving groups help create methods for oligosaccharide assembly. Additionally, implementation of heterocyclic anomeric leaving groups containing nitrogens have proven quite useful in the glycosylation reaction…
Presenters
Speaker
- DateMarch 23, 2025Efforts toward the development of thioimidate-based carbohydrate leaving groups are a continual endeavor with glycochemists. Over the past few years our group has explored the use of 4,2’pyridine-2-mercaptopyrimidine as a glycosyl donor leaving group…
Presenter
Co-Author
- DateMarch 24, 2025Many institutions search for chemical experiments that are cost effective and pedagogically practical. Additionally, chemist are embracing the need for more green chemistry reacting in recent years. Microwavable reactions fit nicely at this interface of financial constraints and green chemistry…
Presenter
Co-Author
- DateMarch 24, 2025Carbohydrate glycosyl donors bearing nitrogens have displayed some stereoselective outcomes during the coupling reaction. With two nitrogens and a thiol, thiouracil is an attractive moiety to employ as an anomeric carbohydrate leaving group…
Presenter
Co-Author
- DateMarch 24, 2025The quest for stereoselective coupling of carbohydrates is always evolving. The use of thiopyrimidine has been used by glycoscientists for many years as a carbohydrate leaving group. While its selectivity has been less than reasonable, here we investigate its role hydrogen bonding during departure…
Presenter
Co-Author
