| LDR | | 01817nmm uu200385 4500 |
| 001 | | 000000334628 |
| 005 | | 20240805180706 |
| 008 | | 181129s2017 |||||||||||||||||c||eng d |
| 020 | |
▼a 9780438373891 |
| 035 | |
▼a (MiAaPQ)AAI10603568 |
| 035 | |
▼a (MiAaPQ)wisc:14655 |
| 040 | |
▼a MiAaPQ
▼c MiAaPQ
▼d 248032 |
| 082 | 0 |
▼a 547 |
| 100 | 1 |
▼a Alderson, Juliet Marie. |
| 245 | 10 |
▼a Development and Extensions of Tunable, Selective Aminations via Silver-Catalyzed Nitrene Transfer Reactions. |
| 260 | |
▼a [S.l.] :
▼b The University of Wisconsin - Madison.,
▼c 2017 |
| 260 | 1 |
▼a Ann Arbor :
▼b ProQuest Dissertations & Theses,
▼c 2017 |
| 300 | |
▼a 514 p. |
| 500 | |
▼a Source: Dissertation Abstracts International, Volume: 80-01(E), Section: B. |
| 500 | |
▼a Adviser: Jennifer M. Schomaker. |
| 502 | 1 |
▼a Thesis (Ph.D.)--The University of Wisconsin - Madison, 2017. |
| 520 | |
▼a The advancement of selective carbon-nitrogen (C--N) bond forming reactions represents an important research area because amines are a common functional group in biologically active natural products, pharmaceuticals, agrochemicals, and ligands. T |
| 520 | |
▼a Chapter 1 serves as an introduction by providing a selected review of literature on transition metal-catalyzed nitrene transfer reactions emphasizing the common problems associated with selectivity and tunability. Chapter 2 describes a method fo |
| 590 | |
▼a School code: 0262. |
| 650 | 4 |
▼a Organic chemistry. |
| 690 | |
▼a 0490 |
| 710 | 20 |
▼a The University of Wisconsin - Madison.
▼b Chemistry. |
| 773 | 0 |
▼t Dissertation Abstracts International
▼g 80-01B(E). |
| 773 | |
▼t Dissertation Abstract International |
| 790 | |
▼a 0262 |
| 791 | |
▼a Ph.D. |
| 792 | |
▼a 2017 |
| 793 | |
▼a English |
| 856 | 40 |
▼u http://www.riss.kr/pdu/ddodLink.do?id=T14996621
▼n KERIS |
| 980 | |
▼a 201812
▼f 2019 |
| 990 | |
▼a 관리자 |