東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Methodologies of Bicyclo[2.2.2]octan...

Roberts, Courtney Arielle.

FindBook

Google Book

Amazon

博客來

Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide./
作者:	Roberts, Courtney Arielle.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2016,
面頁冊數:	141 p.
附註:	Source: Dissertation Abstracts International, Volume: 78-03(E), Section: B.
Contained By:	Dissertation Abstracts International78-03B(E).
標題:	Organic chemistry. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10196321
ISBN:	9781369337921

Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide.
Roberts, Courtney Arielle.

Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide. - Ann Arbor : ProQuest Dissertations & Theses, 2016 - 141 p.

Source: Dissertation Abstracts International, Volume: 78-03(E), Section: B.

Thesis (Ph.D.)--University of California, Los Angeles, 2016.

In Chapter 1, rearrangements of 4-substituted bicyclo[2.2.2]oct-2-enyl-5-selenophenyl esters are explored. Reduction of the esters under radical-generating conditions initially generates a bicyclo[2.2.2]oct-5-en-2-yl radical which can rearrange to a bicyclo[3.2.1]oct-6-en-2-yl radical via a cyclopropylcarbinyl radical. Although the bicyclo[3.2.1]octene system exhibits greater strain than does the bicyclo[2.2.2]octene system, radical-stabilizing substituents can reverse this preference. The product ratios are influenced by the interplay of ring strain and radical stability. In addition, the rearranged products favored the equatorial over the axial isomers, which can be explained by torsional steering.

ISBN: 9781369337921Subjects--Topical Terms:

523952
Organic chemistry.

Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide.
LDR:02562nmm a2200301 4500 001 2118913
005 20170614101411.5
008 180830s2016 ||||||||||||||||| ||eng d
020 $a 9781369337921
035 $a (MiAaPQ)AAI10196321
035 $a AAI10196321
040 $a MiAaPQ $c MiAaPQ
100 1 $a Roberts, Courtney Arielle. $3 3280757
245 1 0 $a Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2016
300 $a 141 p.
500 $a Source: Dissertation Abstracts International, Volume: 78-03(E), Section: B.
500 $a Adviser: Michael E. Jung.
502 $a Thesis (Ph.D.)--University of California, Los Angeles, 2016.
520 $a In Chapter 1, rearrangements of 4-substituted bicyclo[2.2.2]oct-2-enyl-5-selenophenyl esters are explored. Reduction of the esters under radical-generating conditions initially generates a bicyclo[2.2.2]oct-5-en-2-yl radical which can rearrange to a bicyclo[3.2.1]oct-6-en-2-yl radical via a cyclopropylcarbinyl radical. Although the bicyclo[3.2.1]octene system exhibits greater strain than does the bicyclo[2.2.2]octene system, radical-stabilizing substituents can reverse this preference. The product ratios are influenced by the interplay of ring strain and radical stability. In addition, the rearranged products favored the equatorial over the axial isomers, which can be explained by torsional steering.
520 $a In Chapter 2, different approaches to the synthesis of the optically active bicyclo[2.2.2]octane-2,5-diones are presented. A stereoselective Diels-Alder cycloaddition was explored to construct the bicyclo[2.2.2]octane skeleton in an efficient manner. This approach was hindered by unexpected polymerization and lack of stereoselectivity. A different method of synthesizing the optically active bicyclo[2.2.2]octane-2,5-dione featuring a diastereoselective 1,4-addition is also presented.
520 $a In Chapter 3, progress toward the total synthesis of parthenolide is described. The synthetic route relies on ring-closing metathesis to close the 10-membered carbocycle of the natural product. The efforts leading up to and including the key ring-closing step are described. Specific attention is given to different methods for overcoming the difficulties associated with medium-sized ring formation.
590 $a School code: 0031.
650 4 $a Organic chemistry. $3 523952
690 $a 0490
710 2 $a University of California, Los Angeles. $b Chemistry. $3 2104984
773 0 $t Dissertation Abstracts International $g 78-03B(E).
790 $a 0031
791 $a Ph.D.
792 $a 2016
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10196321