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Catalytic Asymmetric Desymmetrisatio...

Yi, Yi.

Catalytic Asymmetric Desymmetrisation and Kinetic Resolution of Unsaturated Amides via Halofunctionalization.

Record Type:	Language materials, manuscript : Monograph/item
Title/Author:	Catalytic Asymmetric Desymmetrisation and Kinetic Resolution of Unsaturated Amides via Halofunctionalization./
Author:	Yi, Yi.
Description:	1 online resource (318 pages)
Notes:	Source: Dissertation Abstracts International, Volume: 79-09(E), Section: B.
Contained By:	Dissertation Abstracts International79-09B(E).
Subject:	Organic chemistry. -
Online resource:	click for full text (PQDT)
ISBN:	9780355890662

Catalytic Asymmetric Desymmetrisation and Kinetic Resolution of Unsaturated Amides via Halofunctionalization.
Yi, Yi.

Catalytic Asymmetric Desymmetrisation and Kinetic Resolution of Unsaturated Amides via Halofunctionalization. - 1 online resource (318 pages)

Source: Dissertation Abstracts International, Volume: 79-09(E), Section: B.

Thesis (Ph.D.)--Michigan State University, 2018.

Includes bibliographical references

My doctorate research work with professor Borhan is mainly focused on developing new asymmetric halofunctionalization reactions. Chapter 1 describes the catalytic asymmetric desymmetrisation of dienes via chlorocyclization. Chapter 2 describes the kinetic resolution of propargyl amides via chlorocyclization. Both desymmetrisation and kinetic resolution using cinchona alkaloid (DHQD) 2PHAL as catalyst afford good diastereoselectivity and enantioselectivity. Chapter 3 discloses efforts to develop asymmetric ipso-halocyclization via dearomatization of phenol derivatives. Chapter 4 describes a novel and practical method to access N,O-acetals using commercially available XtalFluor-ERTM as catalyst.

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

Mode of access: World Wide Web

ISBN: 9780355890662Subjects--Topical Terms:

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

554714
Electronic books.

Catalytic Asymmetric Desymmetrisation and Kinetic Resolution of Unsaturated Amides via Halofunctionalization.
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020 $a 9780355890662
035 $a (MiAaPQ)AAI10786363
035 $a (MiAaPQ)grad.msu:15903
035 $a AAI10786363
040 $a MiAaPQ $b eng $c MiAaPQ $d NTU
100 1 $a Yi, Yi. $3 1192679
245 1 0 $a Catalytic Asymmetric Desymmetrisation and Kinetic Resolution of Unsaturated Amides via Halofunctionalization.
264 0 $c 2018
300 $a 1 online resource (318 pages)
336 $a text $b txt $2 rdacontent
337 $a computer $b c $2 rdamedia
338 $a online resource $b cr $2 rdacarrier
500 $a Source: Dissertation Abstracts International, Volume: 79-09(E), Section: B.
500 $a Adviser: Babak Borhan.
502 $a Thesis (Ph.D.)--Michigan State University, 2018.
504 $a Includes bibliographical references
520 $a My doctorate research work with professor Borhan is mainly focused on developing new asymmetric halofunctionalization reactions. Chapter 1 describes the catalytic asymmetric desymmetrisation of dienes via chlorocyclization. Chapter 2 describes the kinetic resolution of propargyl amides via chlorocyclization. Both desymmetrisation and kinetic resolution using cinchona alkaloid (DHQD) 2PHAL as catalyst afford good diastereoselectivity and enantioselectivity. Chapter 3 discloses efforts to develop asymmetric ipso-halocyclization via dearomatization of phenol derivatives. Chapter 4 describes a novel and practical method to access N,O-acetals using commercially available XtalFluor-ERTM as catalyst.
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
655 7 $a Electronic books. $2 local $3 554714
690 $a 0490
710 2 $a ProQuest Information and Learning Co. $3 1178819
710 2 $a Michigan State University. $b Chemistry - Doctor of Philosophy. $3 1187121
773 0 $t Dissertation Abstracts International $g 79-09B(E).
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10786363 $z click for full text (PQDT)

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