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Synthesis of Pharmaceutically Valued Molecules Enabled by Organophotoredox Catalysis.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Synthesis of Pharmaceutically Valued Molecules Enabled by Organophotoredox Catalysis./
作者:	Ji, Peng.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2022,
面頁冊數:	262 p.
附註:	Source: Dissertations Abstracts International, Volume: 83-08, Section: B.
Contained By:	Dissertations Abstracts International83-08B.
標題:	Pharmaceutical sciences. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28964456
ISBN:	9798780640424

Synthesis of Pharmaceutically Valued Molecules Enabled by Organophotoredox Catalysis.
Ji, Peng.

Synthesis of Pharmaceutically Valued Molecules Enabled by Organophotoredox Catalysis. - Ann Arbor : ProQuest Dissertations & Theses, 2022 - 262 p.

Source: Dissertations Abstracts International, Volume: 83-08, Section: B.

Thesis (Ph.D.)--The University of Arizona, 2022.

This item is not available from ProQuest Dissertations & Theses.

Photoredox catalysis has emerged as the currently most powerful strategy to manipulate the open-shell radicals for diverse chemical transformation that is impossible or difficult to accomplish using the conventional ionic pathways. This method is highlighted by the reaction mildness, biological compatibility, and broad substrates tolerance. Therefore, photoredox catalysis has been applied to total synthesis of nature products, modify the biomolecules (protein, DNA, saccharides, etc.), novel materials synthesis, etc. In the traditional polar strategy, a number of synthons such as organometal complexes are labile and/or less reactive, while the precursors of radicals (carboxylic acids, halogens, esters, amines, olefins, etc.) are usually bench stable, easily accessible, and the radicals are highly reactive, which demonstrate a quite distinct manner to construct the target molecules. Herein, we developed a series of novel approaches to constructing the pharmaceutically valued compounds using the photoredox catalysis. In the first effort, an approach for efficient synthesis of C-glycosyl amino acids is developed. Different from typical photoredox-catalyzed reactions of imines, the new process follows a pathway in which α-imino esters serve as electrophiles in chemoselective addition reactions with nucleophilic glycosyl radicals. The process is highlighted by the mild nature of the reaction conditions, the highly stereoselectivity attending C-C bond formation, and its applicability to C-glycosylation using both armed and disarmed pentose and hexose derivatives. In the second effort, a mild, versatile organophotoredox protocol has been developed for the preparation of diverse, enantioenriched α-deuterated α-amino acids. Distinct from the well established two-electron transformations, this radical-based strategy offers the unrivaled capacity of the convergent unification of readily accessible feedstock carboxylic acids and a chiral methyleneoxazolidinone fragment and the simultaneous highly diastereo-, chemo-, and regioselective incorporation of deuterium. Furthermore, the approach has addressed the longstanding challenge of the installation of sterically demanding side chains into α-amino acids. While strategies involving a 2e− transfer pathway have dictated glycosylation development, the direct glycosylation of readily accessible glycosyl donors as radical precursors is particularly appealing because of high radical anomeric selectivity and atom- and step-economy. However, the development of the radical process has been challenging owing to notorious competing reduction, elimination and/or SN side reactions of commonly used, labile glycosyl donors. Toward this end,15we introduce an organ ophotocatalytic strategy through which glycosyl bromides can be efficiently converted into corresponding anomeric radicals by photoredox mediated HAT catalysis without a transition metal or a directing group and achieve highly anomeric selectivity. The power of this platform has been demonstrated by the mild reaction conditions enabling the synthesis of challenging α-1,2-cis-thioglycosides, the tolerance of various functional groups and the broad substrate scope for both common pentoses and hexoses. Furthermore, this general approach is compatible with both sp2 and sp3 sulfur electrophiles and late-stage glyco diversification for a total of 50 substrates probed. Reactions that lead to destruction of aromatic ring systems often require harsh conditions and, thus, take place with poor selectivities. Selective partial dearomatization of fused arenes is even more challenging but it can be a strategic approach to creating versatile, complex polycyclic frameworks. We have developed a general organophotoredox approach for the chemo- and regioselective dearomatization of structurally diverse polycyclic aromatics, including quinolines, isoquinolines, quinoxalines, naphthalenes, anthracenes and phenanthrenes. The success of the new method for chemoselective oxidative rupture of aromatic moieties relies on precise manipulation of the electronic nature of the fused polycyclic arenes. Experimental and computational resultsshow that the key to overcoming the intrinsic thermodynamic and kinetic unfavorability of the dearomatization process is an ultimate hydrogen atom transfer (HAT) step, which enables dearomatization to predominate over the otherwise favorable aromatization pathway. We show that this strategy can be applied to rapid synthesis of biologically valued targets and late-stage skeletal remodeling en route to complex structures.

ISBN: 9798780640424Subjects--Topical Terms:

3173021
Pharmaceutical sciences.
Subjects--Index Terms:

Dearomative functionalization

Synthesis of Pharmaceutically Valued Molecules Enabled by Organophotoredox Catalysis.
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245 1 0 $a Synthesis of Pharmaceutically Valued Molecules Enabled by Organophotoredox Catalysis.
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300 $a 262 p.
500 $a Source: Dissertations Abstracts International, Volume: 83-08, Section: B.
500 $a Advisor: Wang, Wei.
502 $a Thesis (Ph.D.)--The University of Arizona, 2022.
506 $a This item is not available from ProQuest Dissertations & Theses.
506 $a This item must not be sold to any third party vendors.
520 $a Photoredox catalysis has emerged as the currently most powerful strategy to manipulate the open-shell radicals for diverse chemical transformation that is impossible or difficult to accomplish using the conventional ionic pathways. This method is highlighted by the reaction mildness, biological compatibility, and broad substrates tolerance. Therefore, photoredox catalysis has been applied to total synthesis of nature products, modify the biomolecules (protein, DNA, saccharides, etc.), novel materials synthesis, etc. In the traditional polar strategy, a number of synthons such as organometal complexes are labile and/or less reactive, while the precursors of radicals (carboxylic acids, halogens, esters, amines, olefins, etc.) are usually bench stable, easily accessible, and the radicals are highly reactive, which demonstrate a quite distinct manner to construct the target molecules. Herein, we developed a series of novel approaches to constructing the pharmaceutically valued compounds using the photoredox catalysis. In the first effort, an approach for efficient synthesis of C-glycosyl amino acids is developed. Different from typical photoredox-catalyzed reactions of imines, the new process follows a pathway in which α-imino esters serve as electrophiles in chemoselective addition reactions with nucleophilic glycosyl radicals. The process is highlighted by the mild nature of the reaction conditions, the highly stereoselectivity attending C-C bond formation, and its applicability to C-glycosylation using both armed and disarmed pentose and hexose derivatives. In the second effort, a mild, versatile organophotoredox protocol has been developed for the preparation of diverse, enantioenriched α-deuterated α-amino acids. Distinct from the well established two-electron transformations, this radical-based strategy offers the unrivaled capacity of the convergent unification of readily accessible feedstock carboxylic acids and a chiral methyleneoxazolidinone fragment and the simultaneous highly diastereo-, chemo-, and regioselective incorporation of deuterium. Furthermore, the approach has addressed the longstanding challenge of the installation of sterically demanding side chains into α-amino acids. While strategies involving a 2e− transfer pathway have dictated glycosylation development, the direct glycosylation of readily accessible glycosyl donors as radical precursors is particularly appealing because of high radical anomeric selectivity and atom- and step-economy. However, the development of the radical process has been challenging owing to notorious competing reduction, elimination and/or SN side reactions of commonly used, labile glycosyl donors. Toward this end,15we introduce an organ ophotocatalytic strategy through which glycosyl bromides can be efficiently converted into corresponding anomeric radicals by photoredox mediated HAT catalysis without a transition metal or a directing group and achieve highly anomeric selectivity. The power of this platform has been demonstrated by the mild reaction conditions enabling the synthesis of challenging α-1,2-cis-thioglycosides, the tolerance of various functional groups and the broad substrate scope for both common pentoses and hexoses. Furthermore, this general approach is compatible with both sp2 and sp3 sulfur electrophiles and late-stage glyco diversification for a total of 50 substrates probed. Reactions that lead to destruction of aromatic ring systems often require harsh conditions and, thus, take place with poor selectivities. Selective partial dearomatization of fused arenes is even more challenging but it can be a strategic approach to creating versatile, complex polycyclic frameworks. We have developed a general organophotoredox approach for the chemo- and regioselective dearomatization of structurally diverse polycyclic aromatics, including quinolines, isoquinolines, quinoxalines, naphthalenes, anthracenes and phenanthrenes. The success of the new method for chemoselective oxidative rupture of aromatic moieties relies on precise manipulation of the electronic nature of the fused polycyclic arenes. Experimental and computational resultsshow that the key to overcoming the intrinsic thermodynamic and kinetic unfavorability of the dearomatization process is an ultimate hydrogen atom transfer (HAT) step, which enables dearomatization to predominate over the otherwise favorable aromatization pathway. We show that this strategy can be applied to rapid synthesis of biologically valued targets and late-stage skeletal remodeling en route to complex structures.
590 $a School code: 0009.
650 4 $a Pharmaceutical sciences. $3 3173021
650 4 $a Chemistry. $3 516420
653 $a Dearomative functionalization
653 $a Glycoamino acids
653 $a Photoredox catalysis
653 $a Thioglycosides
653 $a Unnatural amino acids
690 $a 0572
690 $a 0485
710 2 $a The University of Arizona. $b Pharmacology & Toxicology. $3 3189648
773 0 $t Dissertations Abstracts International $g 83-08B.
790 $a 0009
791 $a Ph.D.
792 $a 2022
793 $a English
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