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New Lewis Bases for Enantioselective Catalysis.

Record Type:	Language materials, manuscript : Monograph/item
Title/Author:	New Lewis Bases for Enantioselective Catalysis./
Author:	Schwamb, Charles Benjamin.
Description:	1 online resource (277 pages)
Notes:	Source: Dissertation Abstracts International, Volume: 79-08(E), Section: B.
Contained By:	Dissertation Abstracts International79-08B(E).
Subject:	Organic chemistry. -
Online resource:	click for full text (PQDT)
ISBN:	9780355824544

New Lewis Bases for Enantioselective Catalysis.
Schwamb, Charles Benjamin.

New Lewis Bases for Enantioselective Catalysis. - 1 online resource (277 pages)

Source: Dissertation Abstracts International, Volume: 79-08(E), Section: B.

Thesis (Ph.D.)--Northwestern University, 2018.

Includes bibliographical references

The discovery and tailoring of new useful organic molecules for applications such as medicine and materials science is highly driven by meaningful developments in chemical methodology, and some of the most impactful advances have invoked catalysis to increase efficiency and specificity. N-heterocyclic carbenes (NHCs) have continuously occupied a prominent space in catalytic methodology due to their unique steric features, electronic properties, and versatility as both metal ligands and organocatalysts. This thesis describes our efforts to invoke unusual molecular topology in extending the value of this ligand class in enantioselective catalysis. The first chapter details our initial attempts to incorporate metallocenes as effective control units in NHC-mediated asymmetric catalysis. The unique product of these efforts is employed in chapter two for the asymmetric synthesis of the privileged, but challenging alpha-aminoboronate motif. Lastly, chapter three briefly describes our initial foray into the development of exotic NHC precursors which incorporate a metal atom at the "wingtip N" position.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2018

Mode of access: World Wide Web

ISBN: 9780355824544Subjects--Topical Terms:

1148722
Organic chemistry.
Index Terms--Genre/Form:

554714
Electronic books.

New Lewis Bases for Enantioselective Catalysis.
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500 $a Source: Dissertation Abstracts International, Volume: 79-08(E), Section: B.
500 $a Adviser: Karl A. Scheidt.
502 $a Thesis (Ph.D.)--Northwestern University, 2018.
504 $a Includes bibliographical references
520 $a The discovery and tailoring of new useful organic molecules for applications such as medicine and materials science is highly driven by meaningful developments in chemical methodology, and some of the most impactful advances have invoked catalysis to increase efficiency and specificity. N-heterocyclic carbenes (NHCs) have continuously occupied a prominent space in catalytic methodology due to their unique steric features, electronic properties, and versatility as both metal ligands and organocatalysts. This thesis describes our efforts to invoke unusual molecular topology in extending the value of this ligand class in enantioselective catalysis. The first chapter details our initial attempts to incorporate metallocenes as effective control units in NHC-mediated asymmetric catalysis. The unique product of these efforts is employed in chapter two for the asymmetric synthesis of the privileged, but challenging alpha-aminoboronate motif. Lastly, chapter three briefly describes our initial foray into the development of exotic NHC precursors which incorporate a metal atom at the "wingtip N" position.
533 $a Electronic reproduction. $b Ann Arbor, Mich. : $c ProQuest, $d 2018
538 $a Mode of access: World Wide Web
650 4 $a Organic chemistry. $3 1148722
650 4 $a Chemistry. $3 593913
655 7 $a Electronic books. $2 local $3 554714
690 $a 0490
690 $a 0485
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