LDR | | 00000nam u2200205 4500 |
001 | | 000000433459 |
005 | | 20200225142252 |
008 | | 200131s2019 ||||||||||||||||| ||eng d |
020 | |
▼a 9781085673259 |
035 | |
▼a (MiAaPQ)AAI22617915 |
040 | |
▼a MiAaPQ
▼c MiAaPQ
▼d 247004 |
082 | 0 |
▼a 540 |
100 | 1 |
▼a Dannatt, Jonathan E. |
245 | 10 |
▼a Advancing Frontiers in Reactive and Selective Iridium C-H Borylation Catalysis and Targeted Silsesquioxane Synthesis. |
260 | |
▼a [S.l.]:
▼b Michigan State University.,
▼c 2019. |
260 | 1 |
▼a Ann Arbor:
▼b ProQuest Dissertations & Theses,
▼c 2019. |
300 | |
▼a 521 p. |
500 | |
▼a Source: Dissertations Abstracts International, Volume: 81-03, Section: B. |
500 | |
▼a Advisor: Maleczka, Rob. |
502 | 1 |
▼a Thesis (Ph.D.)--Michigan State University, 2019. |
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▼a This item must not be sold to any third party vendors. |
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▼a The studies in this dissertation are aimed at uncovering reactive and selective Ir-catalyzed C-H borylation (CHB) catalysts. Due to the high versatility of organoboron species, green methodology to produce the C-B bond is poised to support a myriad of subsequent transformations. These transformations include Suzuki couplings, aminations, oxidations, halogenations, cyanations, and trifluoromethylations.Typical iridium catalyzed CHBs proceed through an iridium trisboryl with a bidentate ligand such as bipyridine or 1,10-phenanthroline. The selectivity of these standard catalysts is generally driven by sterics |
590 | |
▼a School code: 0128. |
650 | 4 |
▼a Organic chemistry. |
650 | 4 |
▼a Chemistry. |
690 | |
▼a 0490 |
690 | |
▼a 0485 |
710 | 20 |
▼a Michigan State University.
▼b Chemistry - Doctor of Philosophy. |
773 | 0 |
▼t Dissertations Abstracts International
▼g 81-03B. |
773 | |
▼t Dissertation Abstract International |
790 | |
▼a 0128 |
791 | |
▼a Ph.D. |
792 | |
▼a 2019 |
793 | |
▼a English |
856 | 40 |
▼u http://www.riss.kr/pdu/ddodLink.do?id=T15493503
▼n KERIS
▼z 이 자료의 원문은 한국교육학술정보원에서 제공합니다. |
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▼a 202002
▼f 2020 |
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▼a ***1008102 |
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▼a E-BOOK |