| dc.contributor |
Timothy F. Jamison |
|
| dc.contributor |
Massachusetts Institute of Technology. Department of Chemistry |
|
| dc.creator |
McGeough, Catherine P. |
|
| dc.date |
2023-01-26T14:46:26Z |
|
| dc.date |
2023-01-26T14:46:26Z |
|
| dc.date |
2021-06 |
|
| dc.date |
2021-06-16T17:29:07.599Z |
|
| dc.date.accessioned |
2023-03-01T07:23:12Z |
|
| dc.date.available |
2023-03-01T07:23:12Z |
|
| dc.identifier |
https://hdl.handle.net/1721.1/147730 |
|
| dc.identifier.uri |
http://localhost:8080/xmlui/handle/CUHPOERS/275844 |
|
| dc.description |
Chapter 1: Skipped polyenes featuring high (E)-selectivity and varying methyl substitution patterns are synthesized using a nickel-catalyzed cross-coupling reaction between allyl trifluoroacetates and vinyl bromides. The utility of this cross-electrophile coupling is showcased in part by the synthesis of the RST fragment of the marine ladder polyether, maitotoxin. Construction of this fragment is particularly challenging due to the alternating methyl substitution pattern.
Chapter 2.1: A two-step route to MK-4482 (EIDD-2801, 1) was developed consisting of an esterification and hydroxamination of cytidine. The selective acylation and direct amination eliminate the need for protecting and activating groups and proceed in overall yield of 75%, a significant advancement over the reported yield of 17%. The step count is reduced from five transformations to two, and expensive uridine is replaced with the more available cytidine.
Chapter 2.2: Molnupiravir (MK-4482, EIDD-2801) is a promising orally bioavailable drug candidate for treatment of COVID-19. Herein we describe a supply-centered and chromatography- free synthesis of molnupiravir from cytidine, consisting of two steps: a selective enzymatic acylation followed by transamination to yield the final drug product. Both steps have been successfully performed on decagram scale: the first step at 200 g, and the second step at 80 g. Overall, molnupiravir has been obtained in a 41% overall isolated yield compared to a maximum 17% isolated yield in the patented route. This route provides many advantages to the initial route described in the patent literature and would decrease the cost of this pharmaceutical should it prove safe and efficacious in ongoing clinical trials.
Chapter 3: Tea is the second most consumed beverage world-wide (after water), however, approximately 90% of the tea leaf is not soluble in water and is therefore disposed of. Extracted cellulose from tea leaf waste fiber (TLWF) could be utilized around the globe as a locally sourced absorbent in the manufacturing of menstrual pads. In this chapter, an FDA friendly procedure is developed for cellulose extraction from TLWF as well as attempts to modify the texture of this material.
Chapter 4: The approach to reproductive health and safety in academic laboratories requires increased focus and a shift in paradigm. Our analysis of the current guidance from more than 100 academic institutions’ Chemical Hygiene Plans (CHPs) indicates that the burden to implement laboratory reproductive health and safety practices is often placed on those already pregnant or planning conception. We also found inconsistencies in the classification of potential reproductive toxins by resources generally considered to be authoritative, adding further confusion. In the interest of human health and safe laboratory practice, we suggest straightforward changes that institutions and individual laboratories can make to address these present deficiencies: Provide consistent and clear information to laboratory researchers about reproductive health and normalize the discussion of reproductive health among all researchers. Doing so will promote safer and more inclusive laboratory environments. |
|
| dc.description |
Ph.D. |
|
| dc.format |
application/pdf |
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| dc.publisher |
Massachusetts Institute of Technology |
|
| dc.rights |
In Copyright - Educational Use Permitted |
|
| dc.rights |
Copyright MIT |
|
| dc.rights |
http://rightsstatements.org/page/InC-EDU/1.0/ |
|
| dc.title |
Catalysis, Synthesis, and Materials in Support of Chemical Understanding and Global Health |
|
| dc.type |
Thesis |
|