| LDR | | 01978nmm uu200397 4500 |
| 001 | | 000000330431 |
| 005 | | 20240805161439 |
| 008 | | 181129s2018 |||||||||||||||||c||eng d |
| 020 | |
▼a 9780438369078 |
| 035 | |
▼a (MiAaPQ)AAI10844910 |
| 035 | |
▼a (MiAaPQ)purdue:23223 |
| 040 | |
▼a MiAaPQ
▼c MiAaPQ
▼d 248032 |
| 082 | 0 |
▼a 547 |
| 100 | 1 |
▼a Haskins, Chris William. |
| 245 | 10 |
▼a Gas-Phase and Condensed-Phase Studies of Small Reactive Intermediates. |
| 260 | |
▼a [S.l.] :
▼b Purdue University.,
▼c 2018 |
| 260 | 1 |
▼a Ann Arbor :
▼b ProQuest Dissertations & Theses,
▼c 2018 |
| 300 | |
▼a 147 p. |
| 500 | |
▼a Source: Dissertation Abstracts International, Volume: 80-01(E), Section: B. |
| 500 | |
▼a Adviser: Paul G. Wenthold. |
| 502 | 1 |
▼a Thesis (Ph.D.)--Purdue University, 2018. |
| 520 | |
▼a Nitriles are an integral functional group in many chemical industries. A new methodology for the dehydration of amides to nitriles has been developed using a palladium catalyst. The reaction conditions are robust and able to tolerate a wide var |
| 520 | |
▼a Cyclopropanols are important precursors for the generation of beta-carbonyl radicals. In the presence of a single-electron oxidant, the beta-carbonyl radical can be generated and trapped. In this methodology, N-aryl acrylamides were used as a tr |
| 520 | |
▼a Aryl Nitrenes are the other reactive intermediates of interest. Although extensively studied over the past 30 years, phenylnitrenes have a propensity for undergoing rearrangement reactions and forming polymeric tars. This is in direct contrast w |
| 590 | |
▼a School code: 0183. |
| 650 | 4 |
▼a Organic chemistry. |
| 690 | |
▼a 0490 |
| 710 | 20 |
▼a Purdue University.
▼b Chemistry. |
| 773 | 0 |
▼t Dissertation Abstracts International
▼g 80-01B(E). |
| 773 | |
▼t Dissertation Abstract International |
| 790 | |
▼a 0183 |
| 791 | |
▼a Ph.D. |
| 792 | |
▼a 2018 |
| 793 | |
▼a English |
| 856 | 40 |
▼u http://www.riss.kr/pdu/ddodLink.do?id=T15000023
▼n KERIS |
| 980 | |
▼a 201812
▼f 2019 |
| 990 | |
▼a 관리자 |