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Co(II)-Based Metalloradical Catalysi...
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Cheng, Qigan.
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Co(II)-Based Metalloradical Catalysis for Asymmetric Radical Cyclopropanation.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Co(II)-Based Metalloradical Catalysis for Asymmetric Radical Cyclopropanation./
Author:
Cheng, Qigan.
Published:
Ann Arbor : ProQuest Dissertations & Theses, : 2016,
Description:
342 p.
Notes:
Source: Dissertation Abstracts International, Volume: 77-11(E), Section: B.
Contained By:
Dissertation Abstracts International77-11B(E).
Subject:
Organic chemistry. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10112567
ISBN:
9781339757216
Co(II)-Based Metalloradical Catalysis for Asymmetric Radical Cyclopropanation.
Cheng, Qigan.
Co(II)-Based Metalloradical Catalysis for Asymmetric Radical Cyclopropanation.
- Ann Arbor : ProQuest Dissertations & Theses, 2016 - 342 p.
Source: Dissertation Abstracts International, Volume: 77-11(E), Section: B.
Thesis (Ph.D.)--University of South Florida, 2016.
Metal-catalyzed cyclopropanation of olefins with diazo reagents is one of the most general and efficient method to prepare cyclopropanes. The resulting cyclopropyl units are found as a basic structural element in a wide range of naturally occurring compounds and biologically active compounds, and can serve as versatile synthetic intermediates in the synthesis of multifunctionalized cycloalkanes and acyclic compounds. Since Co(II) complexes of D 2-symmetric chiral amidoporphyrins [Co(D2-Por*)] were first introduced in 2004, Co(II)-metalloradical catalysis (MRC) have emerged as a new platform for asymmetric cyclopropanation. These metalloradical catalysts have been shown to be highly effective for asymmetric intermolecular cyclopropanation of a broad scope of substrates with different diazo reagents, with excellent diastereoselectivity and enantioselectivity.
ISBN: 9781339757216Subjects--Topical Terms:
523952
Organic chemistry.
Co(II)-Based Metalloradical Catalysis for Asymmetric Radical Cyclopropanation.
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Co(II)-Based Metalloradical Catalysis for Asymmetric Radical Cyclopropanation.
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342 p.
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Source: Dissertation Abstracts International, Volume: 77-11(E), Section: B.
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Advisers: Peter Zhang; Shengqian Ma.
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Thesis (Ph.D.)--University of South Florida, 2016.
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Metal-catalyzed cyclopropanation of olefins with diazo reagents is one of the most general and efficient method to prepare cyclopropanes. The resulting cyclopropyl units are found as a basic structural element in a wide range of naturally occurring compounds and biologically active compounds, and can serve as versatile synthetic intermediates in the synthesis of multifunctionalized cycloalkanes and acyclic compounds. Since Co(II) complexes of D 2-symmetric chiral amidoporphyrins [Co(D2-Por*)] were first introduced in 2004, Co(II)-metalloradical catalysis (MRC) have emerged as a new platform for asymmetric cyclopropanation. These metalloradical catalysts have been shown to be highly effective for asymmetric intermolecular cyclopropanation of a broad scope of substrates with different diazo reagents, with excellent diastereoselectivity and enantioselectivity.
520
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This dissertation aims to develop new Co(II)-MRC based enantioselective cyclopropanation systems. It will elaborate on three types of stereoselective cyclopropanation reactions from olefins: radical cyclopropanation with ?-halodiazoacetates, asymmetric bicyclization of diazoketones, and radical cyclopropanation with fluoroaryl diazomethanes. These three processes will be examined in the context of diastereo- and enantiocontrol. And also, the application of cyclopropanation products have been demonstrated, which could potentially lead to more exciting works.
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http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10112567
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