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

Cycloaddition Reactions of Silyloxy ...

Haynes, Jamie-Ann Elaine.

FindBook

Google Book

Amazon

博客來

Cycloaddition Reactions of Silyloxy Vinylketene Iron Carbonyl Complexes with Alkynes.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Cycloaddition Reactions of Silyloxy Vinylketene Iron Carbonyl Complexes with Alkynes./
作者:	Haynes, Jamie-Ann Elaine.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2018,
面頁冊數:	97 p.
附註:	Source: Masters Abstracts International, Volume: 57-06.
Contained By:	Masters Abstracts International57-06(E).
標題:	Chemistry. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10868692
ISBN:	9780438079038

Cycloaddition Reactions of Silyloxy Vinylketene Iron Carbonyl Complexes with Alkynes.
Haynes, Jamie-Ann Elaine.

Cycloaddition Reactions of Silyloxy Vinylketene Iron Carbonyl Complexes with Alkynes. - Ann Arbor : ProQuest Dissertations & Theses, 2018 - 97 p.

Source: Masters Abstracts International, Volume: 57-06.

Thesis (M.S.)--Long Island University, The Brooklyn Center, 2018.

The focus of the series of experiments centers around [4+2] cycloaddition reactions between tricarbonyl iron(0) vinylketene complexes and alkynes. The procedure includes confirmation of a viable technique which allows for affordability without diminished productivity or effectiveness, with the substitution of iron, as it meets these requirements. The compounds selected included tricarbonyl [2-triisoproylsilyloxy (TIP SO) vinylketene] iron, tricarbonyl [2-TIPSO-3-methyl vinylketene] iron, tricarbonyl [2-TIPS0-4-methyl vinylketene] iron, tricarbonyl [2-TIPSO-3-phenyl vinylketene] iron, and tricarbonyl [2ethoxy-3phenyl vinylketene] iron; the alkynes vary between chlorohexyne and methyl propiolate (which was also analyzed as it reacted with tricarbonyl [2-TIPSO-3-methyl vinylketene] iron). These compounds were authenticated and used in the purest forms that could be provided, within the cyclization process, and cycloadducts then purified and identified through spectroscopic analysis. The success of high yields from the cycloadditions could provide cost effective means for synthesizing medications.

ISBN: 9780438079038Subjects--Topical Terms:

516420
Chemistry.

Cycloaddition Reactions of Silyloxy Vinylketene Iron Carbonyl Complexes with Alkynes.
LDR:02019nmm a2200289 4500 001 2202763
005 20190513114840.5
008 201008s2018 ||||||||||||||||| ||eng d
020 $a 9780438079038
035 $a (MiAaPQ)AAI10868692
035 $a AAI10868692
040 $a MiAaPQ $c MiAaPQ
100 1 $a Haynes, Jamie-Ann Elaine. $3 3429534
245 1 0 $a Cycloaddition Reactions of Silyloxy Vinylketene Iron Carbonyl Complexes with Alkynes.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2018
300 $a 97 p.
500 $a Source: Masters Abstracts International, Volume: 57-06.
500 $a Adviser: Samuel Watson.
502 $a Thesis (M.S.)--Long Island University, The Brooklyn Center, 2018.
520 $a The focus of the series of experiments centers around [4+2] cycloaddition reactions between tricarbonyl iron(0) vinylketene complexes and alkynes. The procedure includes confirmation of a viable technique which allows for affordability without diminished productivity or effectiveness, with the substitution of iron, as it meets these requirements. The compounds selected included tricarbonyl [2-triisoproylsilyloxy (TIP SO) vinylketene] iron, tricarbonyl [2-TIPSO-3-methyl vinylketene] iron, tricarbonyl [2-TIPS0-4-methyl vinylketene] iron, tricarbonyl [2-TIPSO-3-phenyl vinylketene] iron, and tricarbonyl [2ethoxy-3phenyl vinylketene] iron; the alkynes vary between chlorohexyne and methyl propiolate (which was also analyzed as it reacted with tricarbonyl [2-TIPSO-3-methyl vinylketene] iron). These compounds were authenticated and used in the purest forms that could be provided, within the cyclization process, and cycloadducts then purified and identified through spectroscopic analysis. The success of high yields from the cycloadditions could provide cost effective means for synthesizing medications.
590 $a School code: 0198.
650 4 $a Chemistry. $3 516420
650 4 $a Organic chemistry. $3 523952
690 $a 0485
690 $a 0490
710 2 $a Long Island University, The Brooklyn Center. $3 1017735
773 0 $t Masters Abstracts International $g 57-06(E).
790 $a 0198
791 $a M.S.
792 $a 2018
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10868692