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

切換: 標籤 | MARC模式 | ISBD

A Method for the Synthesis of Comple...

Sisto, Luke James.

FindBook

Google Book

Amazon

博客來

A Method for the Synthesis of Complex Polysulfide Linked Macrocycles via Sulfur Transalkylation and Applications thereof.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	A Method for the Synthesis of Complex Polysulfide Linked Macrocycles via Sulfur Transalkylation and Applications thereof./
作者:	Sisto, Luke James.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2021,
面頁冊數:	431 p.
附註:	Source: Dissertations Abstracts International, Volume: 82-09, Section: B.
Contained By:	Dissertations Abstracts International82-09B.
標題:	Organic chemistry. -
電子資源:	https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28320291
ISBN:	9798597066240

A Method for the Synthesis of Complex Polysulfide Linked Macrocycles via Sulfur Transalkylation and Applications thereof.
Sisto, Luke James.

A Method for the Synthesis of Complex Polysulfide Linked Macrocycles via Sulfur Transalkylation and Applications thereof. - Ann Arbor : ProQuest Dissertations & Theses, 2021 - 431 p.

Source: Dissertations Abstracts International, Volume: 82-09, Section: B.

Thesis (Ph.D.)--University of California, Los Angeles, 2021.

This item must not be sold to any third party vendors.

Peptidyl macrocycles are a compound class with a rich clinical history and great potential for drugging biological targets by mediating protein-protein interactions. Methods to forge S-S disulfide bonds largely rely on the oxidation of dithiol containing substrates. We have developed and implemented a sulfur transalkylative macrocyclization induced by an appended cinnamyl carbonate-based template. This is a mechanistically new method for the construction of peptide macrocycles. The resultant macrocyclic structures contain the functionality of the linear oligomer, while scaffolding this potential pharmacophore in a more conformationally rigid manner. We aim to improve these macrocyclic structure's biological stability and pharmacology relative to the linear oligomer.Chapter 2 details the synthesis of mono- and disulfides via sulfur transalkylation induced by a tethered cinnamyl cation. Scope, limitations, and competition with previously reported nucleophilic residues are discussed. Methods to synthetically elaborate these structures are demonstrated and attempted. Synthesis of a potential ghrelin O-acyl transferase inhibitor is disclosed.Chapter 3 covers the synthesis and development of two new templates designed to forge two macrocyclic bonds in one linear oligomer molecule. The use of these templates in the synthesis of bimacrocycles with sulfur and aryl linkages is divulged.Chapter 4 centers on the synthesis and chemistry macrocyclic trisulfides. Acidolysis of template capped peptides containing tert-butylate trisulfide residues furnishes a mixture of mono-, tri- and pentasulfide linked macrocyclic product. Confirmation of this S2 exchange event is demonstrated via independent synthesis of the relevant monosulfide congener obtained in these trisulfidation reactions. Additionally, our efforts toward the total synthesis of an antimicrobial trithiocane containing natural product via the trisulfidation reaction are detailed.

ISBN: 9798597066240Subjects--Topical Terms:

523952
Organic chemistry.
Subjects--Index Terms:

Disulfides

A Method for the Synthesis of Complex Polysulfide Linked Macrocycles via Sulfur Transalkylation and Applications thereof.
LDR:03182nmm a2200373 4500 001 2284285
005 20211115072425.5
008 220723s2021 ||||||||||||||||| ||eng d
020 $a 9798597066240
035 $a (MiAaPQ)AAI28320291
035 $a AAI28320291
040 $a MiAaPQ $c MiAaPQ
100 1 $a Sisto, Luke James. $3 3563445
245 1 0 $a A Method for the Synthesis of Complex Polysulfide Linked Macrocycles via Sulfur Transalkylation and Applications thereof.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2021
300 $a 431 p.
500 $a Source: Dissertations Abstracts International, Volume: 82-09, Section: B.
500 $a Advisor: Harran, Patrick G.
502 $a Thesis (Ph.D.)--University of California, Los Angeles, 2021.
506 $a This item must not be sold to any third party vendors.
520 $a Peptidyl macrocycles are a compound class with a rich clinical history and great potential for drugging biological targets by mediating protein-protein interactions. Methods to forge S-S disulfide bonds largely rely on the oxidation of dithiol containing substrates. We have developed and implemented a sulfur transalkylative macrocyclization induced by an appended cinnamyl carbonate-based template. This is a mechanistically new method for the construction of peptide macrocycles. The resultant macrocyclic structures contain the functionality of the linear oligomer, while scaffolding this potential pharmacophore in a more conformationally rigid manner. We aim to improve these macrocyclic structure's biological stability and pharmacology relative to the linear oligomer.Chapter 2 details the synthesis of mono- and disulfides via sulfur transalkylation induced by a tethered cinnamyl cation. Scope, limitations, and competition with previously reported nucleophilic residues are discussed. Methods to synthetically elaborate these structures are demonstrated and attempted. Synthesis of a potential ghrelin O-acyl transferase inhibitor is disclosed.Chapter 3 covers the synthesis and development of two new templates designed to forge two macrocyclic bonds in one linear oligomer molecule. The use of these templates in the synthesis of bimacrocycles with sulfur and aryl linkages is divulged.Chapter 4 centers on the synthesis and chemistry macrocyclic trisulfides. Acidolysis of template capped peptides containing tert-butylate trisulfide residues furnishes a mixture of mono-, tri- and pentasulfide linked macrocyclic product. Confirmation of this S2 exchange event is demonstrated via independent synthesis of the relevant monosulfide congener obtained in these trisulfidation reactions. Additionally, our efforts toward the total synthesis of an antimicrobial trithiocane containing natural product via the trisulfidation reaction are detailed.
590 $a School code: 0031.
650 4 $a Organic chemistry. $3 523952
650 4 $a Pharmaceutical sciences. $3 3173021
653 $a Disulfides
653 $a Macrocycles
653 $a Peptidomimetics
653 $a Total synthesis
653 $a Trisulfides
653 $a Sulfur transalkylation
690 $a 0490
690 $a 0572
710 2 $a University of California, Los Angeles. $b Chemistry 0153. $3 2096181
773 0 $t Dissertations Abstracts International $g 82-09B.
790 $a 0031
791 $a Ph.D.
792 $a 2021
793 $a English
856 4 0 $u https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28320291