LDR | | 02105nam u200421 4500 |
001 | | 000000419864 |
005 | | 20190215164021 |
008 | | 181129s2018 |||||||||||||||||c||eng d |
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▼a 9780438384545 |
035 | |
▼a (MiAaPQ)AAI10931905 |
035 | |
▼a (MiAaPQ)columbia:14873 |
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▼a MiAaPQ
▼c MiAaPQ
▼d 247004 |
082 | 0 |
▼a 547 |
100 | 1 |
▼a Radtke, Mark Alexander. |
245 | 10 |
▼a Synthesis and Reactivity of Highly Stabilized Cyclopentadienes. |
260 | |
▼a [S.l.]:
▼b Columbia University.,
▼c 2018. |
260 | 1 |
▼a Ann Arbor:
▼b ProQuest Dissertations & Theses,
▼c 2018. |
300 | |
▼a 164 p. |
500 | |
▼a Source: Dissertation Abstracts International, Volume: 80-02(E), Section: B. |
500 | |
▼a Adviser: Tristan H. Lambert. |
502 | 1 |
▼a Thesis (Ph.D.)--Columbia University, 2018. |
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▼a This dissertation focuses on the development of cyclopentadienes as an emerging class of compounds for use in catalysis. Previous work in the Lambert group had established pentacarboxycyclopentadienes (PCCPs) as a promising class of Bronsted aci |
520 | |
▼a Initial efforts were focused on the synthesis of leading to the development of two complementary methods for their synthesis. Chapter 2 details the improvements made to the transesterification of penta(methoxycarbonyl)cyclopentadiene, which allo |
520 | |
▼a The second half of the dissertation examines the use of electrophilic silicon reagents and their use as Lewis acids. Given our ability to access highly electron-deficient cyclopentadienes, the silyl cyclopentadienes were targeted as potential Le |
590 | |
▼a School code: 0054. |
650 | 4 |
▼a Organic chemistry. |
650 | 4 |
▼a Chemistry. |
690 | |
▼a 0490 |
690 | |
▼a 0485 |
710 | 20 |
▼a Columbia University.
▼b Chemistry. |
773 | 0 |
▼t Dissertation Abstracts International
▼g 80-02B(E). |
773 | |
▼t Dissertation Abstract International |
790 | |
▼a 0054 |
791 | |
▼a Ph.D. |
792 | |
▼a 2018 |
793 | |
▼a English |
856 | 40 |
▼u http://www.riss.kr/pdu/ddodLink.do?id=T15001065
▼n KERIS
▼z 이 자료의 원문은 한국교육학술정보원에서 제공합니다. |
980 | |
▼a 201812
▼f 2019 |
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▼a ***1012033 |