dc.contributor.advisor | Omer, Humair Bin Md | |
dc.contributor.author | Mim, Md. Rasel Mahmud | |
dc.date.accessioned | 2024-06-04T06:51:04Z | |
dc.date.available | 2024-06-04T06:51:04Z | |
dc.date.copyright | 2023 | |
dc.date.issued | 2023-02 | |
dc.identifier.other | ID 19146081 | |
dc.identifier.uri | http://hdl.handle.net/10361/23114 | |
dc.description | This thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2023. | en_US |
dc.description | Cataloged from the PDF version of thesis. | |
dc.description | Includes bibliographical references (pages 59-66). | |
dc.description.abstract | Nebivolol is a potent beta-blocker used to treat heart failure and hypertension. With the increasing prevalence of cardiovascular diseases and the demand for effective and well-tolerated treatments, the global market for beta-blockers, including nebivolol, was worth approximately US$8.5 billion in 2020 and is projected to grow by 5.5% in the coming years. There are several techniques for synthesizing nebivolol, including Sharpless asymmetric epoxidation, Pd-, Zr-, and Mo-catalyzed processes, photochemical reconfiguration, and homochiral sulfoxide-directed reaction (Jiang et al., 2021). Among these techniques, Zr- and Mo-catalyzed processes produce the highest efficiency of 99%. However, using natural chiral starting materials and Sharpless asymmetric epoxidation is more efficient in terms of time and cost. This review article provides an in-depth analysis of the effectiveness of the various nebivolol synthesis techniques. The commercial expansion of beta-blockers and the rising need for efficient and well-tolerated medicines emphasize how critical it is to conduct further research in this area. | en_US |
dc.description.statementofresponsibility | Md. Rasel Mahmud Mim | |
dc.format.extent | 66 pages | |
dc.language.iso | en | en_US |
dc.publisher | Brac University | en_US |
dc.rights | Brac University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. | |
dc.subject | Sharpless asymmetric epoxidation | en_US |
dc.subject | Asymmetric dihydroxylation | en_US |
dc.subject | Chiral photochemical synthesis | en_US |
dc.subject.lcsh | Hypertension. | |
dc.title | Synthesis and characterization of nebivolol: a review of different synthetic approaches and their efficiencies | en_US |
dc.type | Thesis | en_US |
dc.contributor.department | School of Pharmacy, Brac University | |
dc.description.degree | B. Pharmacy | |