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 到查詢結果 [ subject:"Enantioselective catalysis." ]

切換: 標籤 | MARC模式 | ISBD

New organocatalytic strategies for t...

Iorio, Nicola Di.

FindBook

Google Book

Amazon

博客來

New organocatalytic strategies for the selective synthesis of centrally and axially chiral molecules

紀錄類型:	書目-電子資源 : 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:	Iorio, Nicola Di.
出版者:	Cham :Springer International Publishing : : 2018.,
面頁冊數:	xxi, 157 p. :ill., digital ;24 cm.
內容註:	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.
Contained By:	Springer eBooks
標題:	Enantioselective catalysis. -
電子資源:	http://dx.doi.org/10.1007/978-3-319-74914-3
ISBN:	9783319749143

New organocatalytic strategies for the selective synthesis of centrally and axially chiral molecules
Iorio, Nicola Di.

New organocatalytic strategies for the selective synthesis of centrally and axially chiral molecules[electronic resource] /by Nicola Di Iorio. - Cham :Springer International Publishing :2018. - xxi, 157 p. :ill., digital ;24 cm. - Springer theses,2190-5053. - Springer theses..

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:

726242
Enantioselective catalysis.

LC Class. No.: QD505 / .I575 2018

Dewey Class. No.: 547.215

New organocatalytic strategies for the selective synthesis of centrally and axially chiral molecules
LDR:02593nmm a2200325 a 4500 001 2136498
003 DE-He213
005 20180907143638.0
006 m d
007 cr nn 008maaau
008 181117s2018 gw s 0 eng d
020 $a 9783319749143 $q (electronic bk.)
020 $a 9783319749136 $q (paper)
024 7 $a 10.1007/978-3-319-74914-3 $2 doi
035 $a 978-3-319-74914-3
040 $a GP $c GP
041 0 $a eng
050 4 $a QD505 $b .I575 2018
072 7 $a PNRD $2 bicssc
072 7 $a SCI013060 $2 bisacsh
082 0 4 $a 547.215 $2 23
090 $a QD505 $b .I64 2018
100 1 $a Iorio, Nicola Di. $3 3307925
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.
260 $a Cham : $b Springer International Publishing : $b Imprint: Springer, $c 2018.
300 $a xxi, 157 p. : $b ill., digital ; $c 24 cm.
490 1 $a Springer theses, $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 Enantioselective catalysis. $3 726242
650 0 $a Asymmetric synthesis. $3 604596
650 1 4 $a Chemistry. $3 516420
650 2 4 $a Catalysis. $3 560465
650 2 4 $a Organic Chemistry. $3 890856
650 2 4 $a Medicinal Chemistry. $3 892420
710 2 $a SpringerLink (Online service) $3 836513
773 0 $t Springer eBooks
830 0 $a Springer theses. $3 1314442
856 4 0 $u http://dx.doi.org/10.1007/978-3-319-74914-3
950 $a Chemistry and Materials Science (Springer-11644)