語系:
繁體中文
English
說明(常見問題)
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
New Organocatalytic Strategies for t...
~
Di Iorio, Nicola.
New Organocatalytic Strategies for the Selective Synthesis of Centrally and Axially Chiral Molecules
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
New Organocatalytic Strategies for the Selective Synthesis of Centrally and Axially Chiral Molecules/ by Nicola Di Iorio.
作者:
Di Iorio, Nicola.
面頁冊數:
XXI, 157 p. 33 illus., 28 illus. in color.online resource. :
Contained By:
Springer Nature eBook
標題:
Catalysis. -
電子資源:
https://doi.org/10.1007/978-3-319-74914-3
ISBN:
9783319749143
New Organocatalytic Strategies for the Selective Synthesis of Centrally and Axially Chiral Molecules
Di Iorio, Nicola.
New Organocatalytic Strategies for the Selective Synthesis of Centrally and Axially Chiral Molecules
[electronic resource] /by Nicola Di Iorio. - 1st ed. 2018. - XXI, 157 p. 33 illus., 28 illus. in color.online resource. - Springer Theses, Recognizing Outstanding Ph.D. Research,2190-5053. - Springer Theses, Recognizing Outstanding Ph.D. Research,.
Introduction -- The Vinylogous Reactivity of Oxindoles Bearing Non-symmetric 3-Alkylidene Groups -- Targeting the Remote Control of Axial Chirality in N-(2-tert-Butylphenyl)Succinimides via a Desymmetrization Strategy -- Direct Catalytic Synthesis of C(sp2)-C(sp3) Atropisomers with Simultaneous Control of Central and Axial Chirality.
This thesis discusses the use of asymmetric organic catalysis for the direct enantioselective synthesis of complex chiral molecules, and by addressing the many aspects of both vinylogy and atropisomerism, it appeals to researchers and scholars interested in both areas. Organocatalysis is a relatively modern and “hot” topic in the chemical community; it is constantly expanding and its use has been extended to interesting areas like vinylogous reactivity and atropisomerism. Vinylogous systems are very important for their synthetic applications but also pose a number of challenges, the most notable of which are their reduced reactivity and the reduced stereocontrol at these positions. On the other hand, atropisomeric systems are even more important because of the huge potential they have as drugs, ligands and catalysts. Chemists have only recently “recognized” the importance of these two areas and are focusing their efforts on studying them and the challenges they pose. This thesis offers an extensive introduction on the general aspects of chirality and organocatalysis and an equally extensive experimental section that allow nonexperts to understand the discussion section and reproduce the experiments.
ISBN: 9783319749143
Standard No.: 10.1007/978-3-319-74914-3doiSubjects--Topical Terms:
673438
Catalysis.
LC Class. No.: QD505
Dewey Class. No.: 541.395
New Organocatalytic Strategies for the Selective Synthesis of Centrally and Axially Chiral Molecules
LDR
:03062nam a22004095i 4500
001
991649
003
DE-He213
005
20200701232834.0
007
cr nn 008mamaa
008
201225s2018 gw | s |||| 0|eng d
020
$a
9783319749143
$9
978-3-319-74914-3
024
7
$a
10.1007/978-3-319-74914-3
$2
doi
035
$a
978-3-319-74914-3
050
4
$a
QD505
072
7
$a
PNRD
$2
bicssc
072
7
$a
SCI013060
$2
bisacsh
072
7
$a
PNRD
$2
thema
082
0 4
$a
541.395
$2
23
100
1
$a
Di Iorio, Nicola.
$e
author.
$4
aut
$4
http://id.loc.gov/vocabulary/relators/aut
$3
1283326
245
1 0
$a
New Organocatalytic Strategies for the Selective Synthesis of Centrally and Axially Chiral Molecules
$h
[electronic resource] /
$c
by Nicola Di Iorio.
250
$a
1st ed. 2018.
264
1
$a
Cham :
$b
Springer International Publishing :
$b
Imprint: Springer,
$c
2018.
300
$a
XXI, 157 p. 33 illus., 28 illus. in color.
$b
online resource.
336
$a
text
$b
txt
$2
rdacontent
337
$a
computer
$b
c
$2
rdamedia
338
$a
online resource
$b
cr
$2
rdacarrier
347
$a
text file
$b
PDF
$2
rda
490
1
$a
Springer Theses, Recognizing Outstanding Ph.D. Research,
$x
2190-5053
505
0
$a
Introduction -- The Vinylogous Reactivity of Oxindoles Bearing Non-symmetric 3-Alkylidene Groups -- Targeting the Remote Control of Axial Chirality in N-(2-tert-Butylphenyl)Succinimides via a Desymmetrization Strategy -- Direct Catalytic Synthesis of C(sp2)-C(sp3) Atropisomers with Simultaneous Control of Central and Axial Chirality.
520
$a
This thesis discusses the use of asymmetric organic catalysis for the direct enantioselective synthesis of complex chiral molecules, and by addressing the many aspects of both vinylogy and atropisomerism, it appeals to researchers and scholars interested in both areas. Organocatalysis is a relatively modern and “hot” topic in the chemical community; it is constantly expanding and its use has been extended to interesting areas like vinylogous reactivity and atropisomerism. Vinylogous systems are very important for their synthetic applications but also pose a number of challenges, the most notable of which are their reduced reactivity and the reduced stereocontrol at these positions. On the other hand, atropisomeric systems are even more important because of the huge potential they have as drugs, ligands and catalysts. Chemists have only recently “recognized” the importance of these two areas and are focusing their efforts on studying them and the challenges they pose. This thesis offers an extensive introduction on the general aspects of chirality and organocatalysis and an equally extensive experimental section that allow nonexperts to understand the discussion section and reproduce the experiments.
650
0
$a
Catalysis.
$3
673438
650
0
$a
Organic chemistry.
$3
1148722
650
0
$a
Medicinal chemistry.
$3
1253747
650
2 4
$a
Organic Chemistry.
$3
673440
650
2 4
$a
Medicinal Chemistry.
$3
668872
710
2
$a
SpringerLink (Online service)
$3
593884
773
0
$t
Springer Nature eBook
776
0 8
$i
Printed edition:
$z
9783319749136
776
0 8
$i
Printed edition:
$z
9783319749150
776
0 8
$i
Printed edition:
$z
9783030091033
830
0
$a
Springer Theses, Recognizing Outstanding Ph.D. Research,
$x
2190-5053
$3
1253569
856
4 0
$u
https://doi.org/10.1007/978-3-319-74914-3
912
$a
ZDB-2-CMS
912
$a
ZDB-2-SXC
950
$a
Chemistry and Materials Science (SpringerNature-11644)
950
$a
Chemistry and Material Science (R0) (SpringerNature-43709)
筆 0 讀者評論
多媒體
評論
新增評論
分享你的心得
Export
取書館別
處理中
...
變更密碼[密碼必須為2種組合(英文和數字)及長度為10碼以上]
登入