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I. Syntheses and reactions of ynamid...

Zhang, Xuejun.

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I. Syntheses and reactions of ynamides. II. 1,3-dipolar cycloadditions of ynamides.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	I. Syntheses and reactions of ynamides. II. 1,3-dipolar cycloadditions of ynamides./
作者:	Zhang, Xuejun.
面頁冊數:	263 p.
附註:	Source: Dissertation Abstracts International, Volume: 68-04, Section: B, page: 2370.
Contained By:	Dissertation Abstracts International68-04B.
標題:	Chemistry, Organic. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3261442

I. Syntheses and reactions of ynamides. II. 1,3-dipolar cycloadditions of ynamides.
Zhang, Xuejun.

I. Syntheses and reactions of ynamides. II. 1,3-dipolar cycloadditions of ynamides. - 263 p.

Source: Dissertation Abstracts International, Volume: 68-04, Section: B, page: 2370.

Thesis (Ph.D.)--The University of Wisconsin - Madison, 2007.

A general and efficient method for the coupling of a wide range of amides with alkynyl bromides is described here. This novel amidation reaction involves a catalytic protocol using copper(II) sulfate-pentahydrate and 1,10-phenanthroline to direct the sp-C-N bond formation, leading to a structurally diverse array of ynamides including macrocyclic amides via an intramolecular amidation.Subjects--Topical Terms:

516206
Chemistry, Organic.

I. Syntheses and reactions of ynamides. II. 1,3-dipolar cycloadditions of ynamides.
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245 1 0 $a I. Syntheses and reactions of ynamides. II. 1,3-dipolar cycloadditions of ynamides.
300 $a 263 p.
500 $a Source: Dissertation Abstracts International, Volume: 68-04, Section: B, page: 2370.
500 $a Adviser: Richard P. Hsung.
502 $a Thesis (Ph.D.)--The University of Wisconsin - Madison, 2007.
520 $a A general and efficient method for the coupling of a wide range of amides with alkynyl bromides is described here. This novel amidation reaction involves a catalytic protocol using copper(II) sulfate-pentahydrate and 1,10-phenanthroline to direct the sp-C-N bond formation, leading to a structurally diverse array of ynamides including macrocyclic amides via an intramolecular amidation.
520 $a Both intermolecular and intramolecular Rh(I)-catalyzed [4+2] cycloadditions of ynamides were developed, leading to interesting anilides and indolizidines compounds.
520 $a A Bronsted acid-catalyzed highly stereoselective cyclization of arene-ynamides through a novel keteniminium intermediate was developed. And this methodology has been applied to the total syntheses of (+/-)-10-Desbromoarborescidine A.
520 $a A one-pot synthesis of amide-substituted triazoles from alkyl bromides and amides is described here along with syntheses of novel bis-ynamides and their applications in [3+2] cycloadditions with azides to construct unique bis-triazoles.
520 $a Tandem azidination- and hydroazidination Huisgen [3+2] cycloadditions of ynamides are described here. These processes are regioselective and chemoselective, leading to the syntheses of chiral amide-substituted triazoles.
520 $a A tandem azide-[3+2]-vinyl copper trapping employing ynamides and applications of these triazoles as templates for ring-closing metathesis are described here, combining the two powerful reactions to construct novel fused-triazoles and bridged-triazoles.
520 $a A copper(I)-catalyzed highly regioselective dipolar [3+2] cycloadditions of ynamides and nitrile oxides was described here, leading to novel 5-amino isoxazoles.
520 $a A copper(I)-catalyzed highly diastereoselective Kinugasa reaction of ynamides and nitrones was described here, leading to various cis-alpha-amino-beta-lactams, which are very important compounds in medicine and chemistry.
590 $a School code: 0262.
650 4 $a Chemistry, Organic. $3 516206
650 4 $a Health Sciences, Pharmacy. $3 1017737
690 $a 0490
690 $a 0572
710 2 0 $a The University of Wisconsin - Madison. $3 626640
773 0 $t Dissertation Abstracts International $g 68-04B.
790 1 0 $a Hsung, Richard P., $e advisor
790 $a 0262
791 $a Ph.D.
792 $a 2007
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