| LDR | | 01931nmm uu200433 4500 |
| 001 | | 000000334038 |
| 005 | | 20240805175020 |
| 008 | | 181129s2018 |||||||||||||||||c||eng d |
| 020 | |
▼a 9780438404854 |
| 035 | |
▼a (MiAaPQ)AAI10827683 |
| 035 | |
▼a (MiAaPQ)colostate:14913 |
| 040 | |
▼a MiAaPQ
▼c MiAaPQ
▼d 248032 |
| 082 | 0 |
▼a 547 |
| 100 | 1 |
▼a Stache, Erin Elizabeth. |
| 245 | 10 |
▼a Dual Nickel- and Photoredox-catalyzed Enantioselective Desymmetrization of Meso Anhydrides and C-O Bond Activation via Phosphines and Photoredox Catalysis. |
| 260 | |
▼a [S.l.] :
▼b Colorado State University.,
▼c 2018 |
| 260 | 1 |
▼a Ann Arbor :
▼b ProQuest Dissertations & Theses,
▼c 2018 |
| 300 | |
▼a 375 p. |
| 500 | |
▼a Source: Dissertation Abstracts International, Volume: 80-02(E), Section: B. |
| 500 | |
▼a Advisers: Tomislav Rovis |
| 502 | 1 |
▼a Thesis (Ph.D.)--Colorado State University, 2018. |
| 520 | |
▼a Described herein is the application of photoredox catalysis in the development of new synthetic methods. A dual nickel- and photoredox catalyzed desymmetrization of meso succinic anhydrides was developed to generate stereodefined cis keto-acids |
| 520 | |
▼a A method for the C--O bond activation of aliphatic alcohols and carboxylic acids was developed using phosphines and photoredox catalysis. This novel reaction platform was used to generate aliphatic or acyl radicals directly from benzylic alcohol |
| 590 | |
▼a School code: 0053. |
| 650 | 4 |
▼a Organic chemistry. |
| 650 | 4 |
▼a Chemistry. |
| 650 | 4 |
▼a Physical chemistry. |
| 690 | |
▼a 0490 |
| 690 | |
▼a 0485 |
| 690 | |
▼a 0494 |
| 710 | 20 |
▼a Colorado State University.
▼b Chemistry. |
| 773 | 0 |
▼t Dissertation Abstracts International
▼g 80-02B(E). |
| 773 | |
▼t Dissertation Abstract International |
| 790 | |
▼a 0053 |
| 791 | |
▼a Ph.D. |
| 792 | |
▼a 2018 |
| 793 | |
▼a English |
| 856 | 40 |
▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999060
▼n KERIS |
| 980 | |
▼a 201812
▼f 2019 |
| 990 | |
▼a 관리자 |