東華大學圖書館 |

Language: English

Help

回圖書館首頁

手機版館藏查詢

Back

Switch To: Labeled | MARC Mode | ISBD

Linked to FindBook

Google Book

Amazon

博客來

Palladium-catalyzed mechanochemical cross-coupling reactions

Record Type:	Electronic resources : Monograph/item
Title/Author:	Palladium-catalyzed mechanochemical cross-coupling reactions/ by Tamae Seo.
Author:	Seo, Tamae.
Published:	Singapore :Springer Nature Singapore : : 2024.,
Description:	x, 278 p. :ill. (some col.), digital ;24 cm.
Notes:	"Doctoral Thesis accepted by Hokkaido University, Sapporo, Hokkaido, Japan."
[NT 15003449]:	1. General Introduction -- 2. Olefin Accelerated Solid State C N Cross Coupling Using Mechanochemistry -- 3. Solid State Suzuki-Miyaura Cross Coupling Reactions Using Mechanochemistry -- 4. Tackling Solubility Issues in Organic Synthesis: Solid State Cross Coupling of Insoluble Aryl Halides -- 5. Solid State Cross Coupling Reactions of Insoluble Aryl Halides Under Polymer Assisted Grinding Conditions -- 6. Mechanochemistry Directed Ligand Design: Development of a High Performance Phosphine Ligand for Palladium Catalyzed Suzuki Miyaura Cross Coupling Reactions -- 7. Mechanochemical Monoarylation of Dihaloarenes Enabled by In Situ Crystallization -- 8. Metallamechanoredox: Force induced Nickel Catalyzed Arylamination Using Ball Milling and Piezoelectric Materials.
Contained By:	Springer Nature eBook
Subject:	Mechanical chemistry. -
Online resource:	https://doi.org/10.1007/978-981-97-1991-4
ISBN:	9789819719914

Palladium-catalyzed mechanochemical cross-coupling reactions
Seo, Tamae.

Palladium-catalyzed mechanochemical cross-coupling reactions[electronic resource] /by Tamae Seo. - Singapore :Springer Nature Singapore :2024. - x, 278 p. :ill. (some col.), digital ;24 cm. - Springer theses,2190-5061. - Springer theses..

"Doctoral Thesis accepted by Hokkaido University, Sapporo, Hokkaido, Japan."

1. General Introduction -- 2. Olefin Accelerated Solid State C N Cross Coupling Using Mechanochemistry -- 3. Solid State Suzuki-Miyaura Cross Coupling Reactions Using Mechanochemistry -- 4. Tackling Solubility Issues in Organic Synthesis: Solid State Cross Coupling of Insoluble Aryl Halides -- 5. Solid State Cross Coupling Reactions of Insoluble Aryl Halides Under Polymer Assisted Grinding Conditions -- 6. Mechanochemistry Directed Ligand Design: Development of a High Performance Phosphine Ligand for Palladium Catalyzed Suzuki Miyaura Cross Coupling Reactions -- 7. Mechanochemical Monoarylation of Dihaloarenes Enabled by In Situ Crystallization -- 8. Metallamechanoredox: Force induced Nickel Catalyzed Arylamination Using Ball Milling and Piezoelectric Materials.

In this thesis, the author developed cross-coupling reactions that proceed in the solid state without using organic solvents, utilizing a mechanochemical synthesis method using a ball mill. Compared to conventional solution systems, the reactions realized a drastic reduction of chemical waste, a drastic acceleration of chemical reactions, and efficient transformations of insoluble compounds. The thesis demonstrates that mechanochemical synthesis method has the potential to revolutionize organic synthesis. Readers can learn not only about mechanochemical synthesis but also about new reactions and syntheses of new compounds that could not be obtained under solution conditions. Recently, mechanochemical synthesis has become increasingly popular among a wide range of researchers as an environmentally friendly and highly efficient method, so this thesis has a timely publication.

ISBN: 9789819719914

Standard No.: 10.1007/978-981-97-1991-4doiSubjects--Topical Terms:

790122
Mechanical chemistry.

LC Class. No.: QD850

Dewey Class. No.: 541.3413

Palladium-catalyzed mechanochemical cross-coupling reactions
LDR:02786nmm a2200349 a 4500 001 2372115
003 DE-He213
005 20240702131357.0
006 m d
007 cr nn 008maaau
008 241127s2024 si s 0 eng d
020 $a 9789819719914 $q (electronic bk.)
020 $a 9789819719907 $q (paper)
024 7 $a 10.1007/978-981-97-1991-4 $2 doi
035 $a 978-981-97-1991-4
040 $a GP $c GP
041 0 $a eng
050 4 $a QD850
072 7 $a PNN $2 bicssc
072 7 $a SCI013040 $2 bisacsh
072 7 $a PNN $2 thema
082 0 4 $a 541.3413 $2 23
090 $a QD850 $b .S478 2024
100 1 $a Seo, Tamae. $3 3718606
245 1 0 $a Palladium-catalyzed mechanochemical cross-coupling reactions $h [electronic resource] / $c by Tamae Seo.
260 $a Singapore : $b Springer Nature Singapore : $b Imprint: Springer, $c 2024.
300 $a x, 278 p. : $b ill. (some col.), digital ; $c 24 cm.
490 1 $a Springer theses, $x 2190-5061
500 $a "Doctoral Thesis accepted by Hokkaido University, Sapporo, Hokkaido, Japan."
505 0 $a 1. General Introduction -- 2. Olefin Accelerated Solid State C N Cross Coupling Using Mechanochemistry -- 3. Solid State Suzuki-Miyaura Cross Coupling Reactions Using Mechanochemistry -- 4. Tackling Solubility Issues in Organic Synthesis: Solid State Cross Coupling of Insoluble Aryl Halides -- 5. Solid State Cross Coupling Reactions of Insoluble Aryl Halides Under Polymer Assisted Grinding Conditions -- 6. Mechanochemistry Directed Ligand Design: Development of a High Performance Phosphine Ligand for Palladium Catalyzed Suzuki Miyaura Cross Coupling Reactions -- 7. Mechanochemical Monoarylation of Dihaloarenes Enabled by In Situ Crystallization -- 8. Metallamechanoredox: Force induced Nickel Catalyzed Arylamination Using Ball Milling and Piezoelectric Materials.
520 $a In this thesis, the author developed cross-coupling reactions that proceed in the solid state without using organic solvents, utilizing a mechanochemical synthesis method using a ball mill. Compared to conventional solution systems, the reactions realized a drastic reduction of chemical waste, a drastic acceleration of chemical reactions, and efficient transformations of insoluble compounds. The thesis demonstrates that mechanochemical synthesis method has the potential to revolutionize organic synthesis. Readers can learn not only about mechanochemical synthesis but also about new reactions and syntheses of new compounds that could not be obtained under solution conditions. Recently, mechanochemical synthesis has become increasingly popular among a wide range of researchers as an environmentally friendly and highly efficient method, so this thesis has a timely publication.
650 0 $a Mechanical chemistry. $3 790122
650 0 $a Palladium catalysts. $3 726223
650 1 4 $a Organic Chemistry. $3 890856
650 2 4 $a Chemical Synthesis. $3 3591854
650 2 4 $a Reaction Mechanisms. $3 3591956
650 2 4 $a Green Chemistry. $3 3241774
650 2 4 $a Catalysis. $3 560465
710 2 $a SpringerLink (Online service) $3 836513
773 0 $t Springer Nature eBook
830 0 $a Springer theses. $3 1314442
856 4 0 $u https://doi.org/10.1007/978-981-97-1991-4
950 $a Chemistry and Materials Science (SpringerNature-11644)