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Building Up Three-Dimensional Molecules via Novel Lewis Acid and/or Photosensitization Promoted Cycloadditions.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Building Up Three-Dimensional Molecules via Novel Lewis Acid and/or Photosensitization Promoted Cycloadditions./
作者:
Guo, Renyu.
面頁冊數:
1 online resource (834 pages)
附註:
Source: Dissertations Abstracts International, Volume: 84-01, Section: B.
Contained By:
Dissertations Abstracts International84-01B.
標題:
Chemistry. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=29254506click for full text (PQDT)
ISBN:
9798834027089
Building Up Three-Dimensional Molecules via Novel Lewis Acid and/or Photosensitization Promoted Cycloadditions.
Guo, Renyu.
Building Up Three-Dimensional Molecules via Novel Lewis Acid and/or Photosensitization Promoted Cycloadditions.
- 1 online resource (834 pages)
Source: Dissertations Abstracts International, Volume: 84-01, Section: B.
Thesis (Ph.D.)--Indiana University, 2022.
Includes bibliographical references
Escaping from flatland to incorporate three-dimensional architectures often improves the drug-like properties of the resulting molecules, such as solubility, lipophilicity and metabolic stability. Cycloaddition reactions are among the most efficient and atom-economical approaches to quickly build up molecular complexity from readily available alkenes. This document discusses how we incorporate Lewis acid and/or photosensitization as novel tools in cycloadditions to access three-dimensional molecules, specifically for the following three prats: (1) Applying Lewis acid catalyzed chirality transfer [2+2]-cycloadditions into the enantioselectivetotal syntheses of (-)-cajanusine and (+)-hippilde J, and formal synthesis of endiandric acids; (2) Development and detailed mechanistic study of Lewis acid promoted dearomativecycloaddition of quinolines initiated by photosensitization; (3) Development of photosensitized strain release [2π+2σ] cycloaddition to synthesizeunderdeveloped bioisostere [2.1.1]-bicyclohexanes.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023
Mode of access: World Wide Web
ISBN: 9798834027089Subjects--Topical Terms:
516420
Chemistry.
Subjects--Index Terms:
BioisostereIndex Terms--Genre/Form:
542853
Electronic books.
Building Up Three-Dimensional Molecules via Novel Lewis Acid and/or Photosensitization Promoted Cycloadditions.
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Building Up Three-Dimensional Molecules via Novel Lewis Acid and/or Photosensitization Promoted Cycloadditions.
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Source: Dissertations Abstracts International, Volume: 84-01, Section: B.
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Thesis (Ph.D.)--Indiana University, 2022.
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Includes bibliographical references
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Escaping from flatland to incorporate three-dimensional architectures often improves the drug-like properties of the resulting molecules, such as solubility, lipophilicity and metabolic stability. Cycloaddition reactions are among the most efficient and atom-economical approaches to quickly build up molecular complexity from readily available alkenes. This document discusses how we incorporate Lewis acid and/or photosensitization as novel tools in cycloadditions to access three-dimensional molecules, specifically for the following three prats: (1) Applying Lewis acid catalyzed chirality transfer [2+2]-cycloadditions into the enantioselectivetotal syntheses of (-)-cajanusine and (+)-hippilde J, and formal synthesis of endiandric acids; (2) Development and detailed mechanistic study of Lewis acid promoted dearomativecycloaddition of quinolines initiated by photosensitization; (3) Development of photosensitized strain release [2π+2σ] cycloaddition to synthesizeunderdeveloped bioisostere [2.1.1]-bicyclohexanes.
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Mode of access: World Wide Web
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