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020 ▼a 9780438348462
035 ▼a (MiAaPQ)AAI10830696
035 ▼a (MiAaPQ)unc:17959
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0491 ▼f DP
0820 ▼a 540
1001 ▼a Roselli, Christina A.
24510 ▼a Strategies for Achieving Selectivity in Homogeneous Catalysis.
260 ▼a [S.l.] : ▼b The University of North Carolina at Chapel Hill., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 383 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 80-01(E), Section: B.
500 ▼a Adviser: Michel R. Gagne.
5021 ▼a Thesis (Ph.D.)--The University of North Carolina at Chapel Hill, 2018.
520 ▼a A hallmark of gold(I)-catalyzed enyne cycloisomerization reactions is their unique ability to generate complex scaffolds from simple unsaturated starting materials. Initial work focused on the development of a gold-catalyzed cascading cycloisome
520 ▼a A second area of research focused on a computational study on the transfer of silylium from triphenylphosphine to other heteroatom containing Lewis bases. In various examples of tris(pentafluorophenyl)borane (BCF) catalyzed hydrosilylative reduc
520 ▼a The final chapter focuses on the development of a living, chain-growth polymerization of a donor-acceptor (D-A)monomer. While donor-acceptor conjugated polymers have many applications in organic electric materials, they are typically synthesized
590 ▼a School code: 0153.
650 4 ▼a Chemistry.
650 4 ▼a Organic chemistry.
690 ▼a 0485
690 ▼a 0490
71020 ▼a The University of North Carolina at Chapel Hill. ▼b Chemistry.
7730 ▼t Dissertation Abstracts International ▼g 80-01B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0153
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999471 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자 ▼b 관리자