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
Progress in enantioselective Cu(I)-c...
~
SpringerLink (Online service)
FindBook
Google Book
Amazon
博客來
Progress in enantioselective Cu(I)-catalyzed formation of stereogenic centers
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Progress in enantioselective Cu(I)-catalyzed formation of stereogenic centers/ edited by Syuzanna R. Harutyunyan.
其他作者:
Harutyunyan, Syuzanna R.
出版者:
Cham :Springer International Publishing : : 2016.,
面頁冊數:
vii, 224 p. :ill. (some col.), digital ;24 cm.
內容註:
Asymmetric allylic substitution using organolithium reagents -- 1,2- Versus 1,4- asymmetric addition of Grignard reagents to ketones and aldehydes -- Asymmetric addition of soft carbon nucleophiles -- Asymmetric addition of silicon and boron nucleophiles -- Asymmetric cycloaddition and cascade addition-cyclisation reactions -- 1,2- Versus 1,4-asymmetric reduction of ketones -- Generating quaternary stereogenic centers via asymmetric conjugate addition.
Contained By:
Springer eBooks
標題:
Copper catalysts. -
電子資源:
http://dx.doi.org/10.1007/978-3-319-33414-1
ISBN:
9783319334141
Progress in enantioselective Cu(I)-catalyzed formation of stereogenic centers
Progress in enantioselective Cu(I)-catalyzed formation of stereogenic centers
[electronic resource] /edited by Syuzanna R. Harutyunyan. - Cham :Springer International Publishing :2016. - vii, 224 p. :ill. (some col.), digital ;24 cm. - Topics in organometallic chemistry,581436-6002 ;. - Topics in organometallic chemistry ;38.
Asymmetric allylic substitution using organolithium reagents -- 1,2- Versus 1,4- asymmetric addition of Grignard reagents to ketones and aldehydes -- Asymmetric addition of soft carbon nucleophiles -- Asymmetric addition of silicon and boron nucleophiles -- Asymmetric cycloaddition and cascade addition-cyclisation reactions -- 1,2- Versus 1,4-asymmetric reduction of ketones -- Generating quaternary stereogenic centers via asymmetric conjugate addition.
The series Topics in organometallic chemistry presents critical overviews of research results in organometallic chemistry. As our understanding of organometallic structure, properties and mechanisms increases, new ways are opened for the design of organometallic compounds and reactions tailored to the needs of such diverse areas as organic synthesis, medical research, biology and materials science. Thus the scope of coverage includes a broad range of topics of pure and applied organometallic chemistry, where new breakthroughs are being achieved that are of significance to a larger scientific audience. The individual volumes of Topics in organometallic chemistry are thematic. Review articles are generally invited by the volume editors. All chapters from Topics in organometallic chemistry are published OnlineFirst with an individual DOI. In references, Topics in organometallic chemistry is abbreviated as Top Organomet Chem and cited as a journal.
ISBN: 9783319334141
Standard No.: 10.1007/978-3-319-33414-1doiSubjects--Topical Terms:
2040913
Copper catalysts.
LC Class. No.: QD505
Dewey Class. No.: 541.395
Progress in enantioselective Cu(I)-catalyzed formation of stereogenic centers
LDR
:02472nmm a2200325 a 4500
001
2035664
003
DE-He213
005
20160930165342.0
006
m d
007
cr nn 008maaau
008
161117s2016 gw s 0 eng d
020
$a
9783319334141
$q
(electronic bk.)
020
$a
9783319334127
$q
(paper)
024
7
$a
10.1007/978-3-319-33414-1
$2
doi
035
$a
978-3-319-33414-1
040
$a
GP
$c
GP
041
0
$a
eng
050
4
$a
QD505
072
7
$a
PNND
$2
bicssc
072
7
$a
SCI013040
$2
bisacsh
082
0 4
$a
541.395
$2
23
090
$a
QD505
$b
.P964 2016
245
0 0
$a
Progress in enantioselective Cu(I)-catalyzed formation of stereogenic centers
$h
[electronic resource] /
$c
edited by Syuzanna R. Harutyunyan.
260
$a
Cham :
$b
Springer International Publishing :
$b
Imprint: Springer,
$c
2016.
300
$a
vii, 224 p. :
$b
ill. (some col.), digital ;
$c
24 cm.
490
1
$a
Topics in organometallic chemistry,
$x
1436-6002 ;
$v
58
505
0
$a
Asymmetric allylic substitution using organolithium reagents -- 1,2- Versus 1,4- asymmetric addition of Grignard reagents to ketones and aldehydes -- Asymmetric addition of soft carbon nucleophiles -- Asymmetric addition of silicon and boron nucleophiles -- Asymmetric cycloaddition and cascade addition-cyclisation reactions -- 1,2- Versus 1,4-asymmetric reduction of ketones -- Generating quaternary stereogenic centers via asymmetric conjugate addition.
520
$a
The series Topics in organometallic chemistry presents critical overviews of research results in organometallic chemistry. As our understanding of organometallic structure, properties and mechanisms increases, new ways are opened for the design of organometallic compounds and reactions tailored to the needs of such diverse areas as organic synthesis, medical research, biology and materials science. Thus the scope of coverage includes a broad range of topics of pure and applied organometallic chemistry, where new breakthroughs are being achieved that are of significance to a larger scientific audience. The individual volumes of Topics in organometallic chemistry are thematic. Review articles are generally invited by the volume editors. All chapters from Topics in organometallic chemistry are published OnlineFirst with an individual DOI. In references, Topics in organometallic chemistry is abbreviated as Top Organomet Chem and cited as a journal.
650
0
$a
Copper catalysts.
$3
2040913
650
0
$a
Enantioselective catalysis.
$3
726242
650
1 4
$a
Chemistry.
$3
516420
650
2 4
$a
Organometallic Chemistry.
$3
892407
650
2 4
$a
Catalysis.
$3
560465
650
2 4
$a
Physical Chemistry.
$3
890828
700
1
$a
Harutyunyan, Syuzanna R.
$3
2191210
710
2
$a
SpringerLink (Online service)
$3
836513
773
0
$t
Springer eBooks
830
0
$a
Topics in organometallic chemistry ;
$v
38
$3
1565883
856
4 0
$u
http://dx.doi.org/10.1007/978-3-319-33414-1
950
$a
Chemistry and Materials Science (Springer-11644)
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
W9279508
電子資源
11.線上閱覽_V
電子書
EB QD505
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