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Advancing Frontiers in Reactive and Selective Iridium C-H Borylation Catalysis and Targeted Silsesquioxane Synthesis
Advancing Frontiers in Reactive and Selective Iridium C-H Borylation Catalysis and Targeted Silsesquioxane Synthesis
- 자료유형
- 학위논문
- Control Number
- 0015493503
- International Standard Book Number
- 9781085673259
- Dewey Decimal Classification Number
- 540
- Main Entry-Personal Name
- Dannatt, Jonathan E.
- Publication, Distribution, etc. (Imprint
- [Sl] : Michigan State University, 2019
- Publication, Distribution, etc. (Imprint
- Ann Arbor : ProQuest Dissertations & Theses, 2019
- Physical Description
- 521 p
- General Note
- Source: Dissertations Abstracts International, Volume: 81-03, Section: B.
- General Note
- Advisor: Maleczka, Rob.
- Dissertation Note
- Thesis (Ph.D.)--Michigan State University, 2019.
- Restrictions on Access Note
- This item must not be sold to any third party vendors.
- Summary, Etc.
- 요약The 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
- Subject Added Entry-Topical Term
- Organic chemistry
- Subject Added Entry-Topical Term
- Chemistry
- Added Entry-Corporate Name
- Michigan State University Chemistry - Doctor of Philosophy
- Host Item Entry
- Dissertations Abstracts International. 81-03B.
- Host Item Entry
- Dissertation Abstract International
- Electronic Location and Access
- 로그인을 한후 보실 수 있는 자료입니다.
- Control Number
- joongbu:569234
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