語系:
繁體中文
English
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
Reduction of Ketones to Alcohols and...
~
Varjosaari, Sami Ensio.
FindBook
Google Book
Amazon
博客來
Reduction of Ketones to Alcohols and Tertiary Amines Using 1-Hydrosilatrane.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Reduction of Ketones to Alcohols and Tertiary Amines Using 1-Hydrosilatrane./
作者:
Varjosaari, Sami Ensio.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2018,
面頁冊數:
437 p.
附註:
Source: Dissertation Abstracts International, Volume: 79-10(E), Section: B.
Contained By:
Dissertation Abstracts International79-10B(E).
標題:
Organic chemistry. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10785985
ISBN:
9780438032569
Reduction of Ketones to Alcohols and Tertiary Amines Using 1-Hydrosilatrane.
Varjosaari, Sami Ensio.
Reduction of Ketones to Alcohols and Tertiary Amines Using 1-Hydrosilatrane.
- Ann Arbor : ProQuest Dissertations & Theses, 2018 - 437 p.
Source: Dissertation Abstracts International, Volume: 79-10(E), Section: B.
Thesis (Ph.D.)--Northern Illinois University, 2018.
1-Hydrosilatrane is an easily synthesized, stable, solid silane which can be made into an efficient reducing agent in the presence of a Lewis base, by taking advantage of the properties of hypervalent silicon. Due to the simplicity of use and handling, 1-hydrosilatrane has the potential to be an appealing alternative to other more widely used reducing agents. Aromatic and aliphatic ketones were readily reduced with 1-hydrosilatrane in the presence of potassium tert-butoxide. The discovery of diastereoselectivity in the reduction of menthone, a chiral ketone, led to enantioselective reductions of prochiral ketones using chiral Lewis base activators. Enantiomeric excesses of up to 86% were observed. It was also shown that 1-hydrosilatrane could act as a chemoselective reducing agent in the formation of tertiary amines via direct reductive aminations, in the absence of activator or solvent. Attempts were also made to take advantage of the steric properties of silicon protecting groups in meta-directing electrophilic aromatic substitution of phenols, leading to a one-pot synthesis of O-aryl carbamates.
ISBN: 9780438032569Subjects--Topical Terms:
523952
Organic chemistry.
Reduction of Ketones to Alcohols and Tertiary Amines Using 1-Hydrosilatrane.
LDR
:02083nmm a2200301 4500
001
2202690
005
20190513114838.5
008
201008s2018 ||||||||||||||||| ||eng d
020
$a
9780438032569
035
$a
(MiAaPQ)AAI10785985
035
$a
(MiAaPQ)niu:13109
035
$a
AAI10785985
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Varjosaari, Sami Ensio.
$3
3429456
245
1 0
$a
Reduction of Ketones to Alcohols and Tertiary Amines Using 1-Hydrosilatrane.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2018
300
$a
437 p.
500
$a
Source: Dissertation Abstracts International, Volume: 79-10(E), Section: B.
500
$a
Advisers: Thomas M. Gilbert; Marc J. Adler.
502
$a
Thesis (Ph.D.)--Northern Illinois University, 2018.
520
$a
1-Hydrosilatrane is an easily synthesized, stable, solid silane which can be made into an efficient reducing agent in the presence of a Lewis base, by taking advantage of the properties of hypervalent silicon. Due to the simplicity of use and handling, 1-hydrosilatrane has the potential to be an appealing alternative to other more widely used reducing agents. Aromatic and aliphatic ketones were readily reduced with 1-hydrosilatrane in the presence of potassium tert-butoxide. The discovery of diastereoselectivity in the reduction of menthone, a chiral ketone, led to enantioselective reductions of prochiral ketones using chiral Lewis base activators. Enantiomeric excesses of up to 86% were observed. It was also shown that 1-hydrosilatrane could act as a chemoselective reducing agent in the formation of tertiary amines via direct reductive aminations, in the absence of activator or solvent. Attempts were also made to take advantage of the steric properties of silicon protecting groups in meta-directing electrophilic aromatic substitution of phenols, leading to a one-pot synthesis of O-aryl carbamates.
590
$a
School code: 0162.
650
4
$a
Organic chemistry.
$3
523952
650
4
$a
Chemistry.
$3
516420
690
$a
0490
690
$a
0485
710
2
$a
Northern Illinois University.
$b
Chemistry and Biochemistry.
$3
1672674
773
0
$t
Dissertation Abstracts International
$g
79-10B(E).
790
$a
0162
791
$a
Ph.D.
792
$a
2018
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10785985
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9379239
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入