語系:
繁體中文
English
說明(常見問題)
圖資館首頁
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Asymmetric synthesis of bioactive la...
~
Doran, Robert.
Asymmetric synthesis of bioactive lactones and the development of a catalytic asymmetric synthesis of alpha-Aryl ketones
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Asymmetric synthesis of bioactive lactones and the development of a catalytic asymmetric synthesis of alpha-Aryl ketonesby Robert Doran.
作者:
Doran, Robert.
出版者:
Cham :Springer International Publishing :2015.
面頁冊數:
xxi, 202 p. :ill., digital ;24 cm.
Contained By:
Springer eBooks
標題:
Organic Chemistry.
電子資源:
http://dx.doi.org/10.1007/978-3-319-20544-1
ISBN:
9783319205441 (electronic bk.)
Asymmetric synthesis of bioactive lactones and the development of a catalytic asymmetric synthesis of alpha-Aryl ketones
Doran, Robert.
Asymmetric synthesis of bioactive lactones and the development of a catalytic asymmetric synthesis of alpha-Aryl ketones
[electronic resource] /by Robert Doran. - Cham :Springer International Publishing :2015. - xxi, 202 p. :ill., digital ;24 cm. - Springer theses,2190-5053. - Springer theses..
This thesis addresses two fundamental areas in contemporary organic chemistry: synthesis of natural products and catalytic asymmetric synthesis. Firstly, a new methodology, developed by our research group, which allows the asymmetric synthesis of lactones, a structural unit ubiquitous in natural products, was utilised in the synthesis of a number of natural product analogues that showed significant biological activity. Secondly, the development of a catalytic asymmetric synthesis of a key structural motif present in a number of natural products and pharmaceuticals was accomplished. During the course of this work we discovered dual stereocontrol, which is significant because it allows the configuration of a new stereocentre to be controlled by a simple change of proton source.
ISBN: 9783319205441 (electronic bk.)
Standard No.: 10.1007/978-3-319-20544-1doiSubjects--Topical Terms:
274120
Organic Chemistry.
LC Class. No.: QD262
Dewey Class. No.: 547.2
Asymmetric synthesis of bioactive lactones and the development of a catalytic asymmetric synthesis of alpha-Aryl ketones
LDR
:01810nmm a2200313 a 4500
001
471253
003
DE-He213
005
20160114152056.0
006
m d
007
cr nn 008maaau
008
160223s2015 gw s 0 eng d
020
$a
9783319205441 (electronic bk.)
020
$a
9783319205434 (paper)
024
7
$a
10.1007/978-3-319-20544-1
$2
doi
035
$a
978-3-319-20544-1
040
$a
GP
$c
GP
041
0
$a
eng
050
4
$a
QD262
072
7
$a
PNN
$2
bicssc
072
7
$a
SCI013040
$2
bisacsh
082
0 4
$a
547.2
$2
23
090
$a
QD262
$b
.D693 2015
100
1
$a
Doran, Robert.
$3
726379
245
1 0
$a
Asymmetric synthesis of bioactive lactones and the development of a catalytic asymmetric synthesis of alpha-Aryl ketones
$h
[electronic resource] /
$c
by Robert Doran.
260
$a
Cham :
$b
Springer International Publishing :
$b
Imprint: Springer,
$c
2015.
300
$a
xxi, 202 p. :
$b
ill., digital ;
$c
24 cm.
490
1
$a
Springer theses,
$x
2190-5053
520
$a
This thesis addresses two fundamental areas in contemporary organic chemistry: synthesis of natural products and catalytic asymmetric synthesis. Firstly, a new methodology, developed by our research group, which allows the asymmetric synthesis of lactones, a structural unit ubiquitous in natural products, was utilised in the synthesis of a number of natural product analogues that showed significant biological activity. Secondly, the development of a catalytic asymmetric synthesis of a key structural motif present in a number of natural products and pharmaceuticals was accomplished. During the course of this work we discovered dual stereocontrol, which is significant because it allows the configuration of a new stereocentre to be controlled by a simple change of proton source.
650
2 4
$a
Organic Chemistry.
$3
274120
650
2 4
$a
Catalysis.
$3
188259
650
2 4
$a
Medicinal Chemistry.
$3
275183
650
0
$a
Asymmetric synthesis.
$3
200035
650
0
$a
Biosynthesis.
$3
205687
650
0
$a
Ketones.
$3
563312
650
1 4
$a
Chemistry.
$3
188628
710
2
$a
SpringerLink (Online service)
$3
273601
773
0
$t
Springer eBooks
830
0
$a
Springer theses.
$3
557607
856
4 0
$u
http://dx.doi.org/10.1007/978-3-319-20544-1
950
$a
Chemistry and Materials Science (Springer-11644)
筆 0 讀者評論
全部
電子館藏
館藏
1 筆 • 頁數 1 •
1
條碼號
館藏地
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
000000117898
電子館藏
1圖書
電子書
EB QD262 D693 2015
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
多媒體檔案
http://dx.doi.org/10.1007/978-3-319-20544-1
評論
新增評論
分享你的心得
Export
取書館別
處理中
...
變更密碼
登入