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020 ▼a 9780438170346
035 ▼a (MiAaPQ)AAI10287524
035 ▼a (MiAaPQ)umn:18231
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 540
1001 ▼a Eiden, Carter G.
24510 ▼a Room Temperature Chemoselective Phosphine Oxide Reduction and Mechanism-Based Inhibitors of BioA.
260 ▼a [S.l.] : ▼b University of Minnesota., ▼c 2017
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2017
300 ▼a 344 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
500 ▼a Adviser: Courtney Aldrich.
5021 ▼a Thesis (Ph.D.)--University of Minnesota, 2017.
520 ▼a The reduction of phosphine oxides with silanes occurs with high specificity and fidelity and represents one of the most useful methods for synthesis of phosphines. The chemoselectivity of this process also allows for in situ recycling of phosph
520 ▼a Abnormal patterns in the reduction rates of phosphetane oxides by phenylsilane were noted, causing initiation of a comprehensive investigation of silane-mediated phosphine oxide reduction which revealed widespread misunderstandings of the reduct
520 ▼a Mechanism-based inhibitors (MBIs) are widely employed in chemistry, biology, and medicine due to their exquisite specificity and sustained duration of inhibition. The global kinetic parameters kinact and KI have been used to characterize MBIs, b
520 ▼a 1 inactivates tubercular BioA through a four-step mechanism, and kinetic analysis revealed the rate-limiting step is the removal of the alpha-proton of 1. This knowledge was subsequently applied to rationally design dihydro-4-pyranone 42, dihydr
590 ▼a School code: 0130.
650 4 ▼a Chemistry.
650 4 ▼a Biochemistry.
650 4 ▼a Organic chemistry.
690 ▼a 0485
690 ▼a 0487
690 ▼a 0490
71020 ▼a University of Minnesota. ▼b Medicinal Chemistry.
7730 ▼t Dissertation Abstracts International ▼g 79-12B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0130
791 ▼a Ph.D.
792 ▼a 2017
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14996596 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자