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I. Catalytic Enantioselective Synthe...

Zeng, Bi-Shun.

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I. Catalytic Enantioselective Synthesis of 2-Aryl Chromenes II. Total Syntheses of Alstonine and Serpentine via Cooperative Catalysis III. Progress Towards Enantioselective Oxa-Pictet-Spengler Cyclization via Phosphoric Acids.

Record Type:	Electronic resources : Monograph/item
Title/Author:	I. Catalytic Enantioselective Synthesis of 2-Aryl Chromenes II. Total Syntheses of Alstonine and Serpentine via Cooperative Catalysis III. Progress Towards Enantioselective Oxa-Pictet-Spengler Cyclization via Phosphoric Acids./
Author:	Zeng, Bi-Shun.
Description:	242 p.
Notes:	Source: Dissertation Abstracts International, Volume: 77-08(E), Section: B.
Contained By:	Dissertation Abstracts International77-08B(E).
Subject:	Organic chemistry. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10043997
ISBN:	9781339554501

I. Catalytic Enantioselective Synthesis of 2-Aryl Chromenes II. Total Syntheses of Alstonine and Serpentine via Cooperative Catalysis III. Progress Towards Enantioselective Oxa-Pictet-Spengler Cyclization via Phosphoric Acids.
Zeng, Bi-Shun.

I. Catalytic Enantioselective Synthesis of 2-Aryl Chromenes II. Total Syntheses of Alstonine and Serpentine via Cooperative Catalysis III. Progress Towards Enantioselective Oxa-Pictet-Spengler Cyclization via Phosphoric Acids. - 242 p.

Source: Dissertation Abstracts International, Volume: 77-08(E), Section: B.

Thesis (Ph.D.)--Northwestern University, 2016.

An enantioselective Pd-catalyzed 6-endo-trig reaction to generate 2-aryl chromenes is presented in the first chapter. A novel monodentate phosphoramidite ligand -- identified through a systematic optimization of a TADDOL-derived ligand set -- enanbled the synthesis of a wide range of 2-aryl-2H-chromenes with high yield and enantioselectivity under mild conditions. To illustrate the utility of this new methodology, the products obtained from this reaction were transformed into two bioactive flavonoids (namely, catechin and hydroxyflavanone) through functionalization of the benzopyran olefin. The syntheses of alstonine and serpentine, two potential neurotherapeutics, are disclosed in chapter two. The key step involves a cooperative hydrogen bonding/enamine-catalyzed Michael addition. In the last chapter, efforts toward the enantioselective oxa-Pictet-Spengler cyclization to oxazinoindole using BINOL- and SPINOL-derived chiral phosphoric acids are described.

ISBN: 9781339554501Subjects--Topical Terms:

523952
Organic chemistry.

I. Catalytic Enantioselective Synthesis of 2-Aryl Chromenes II. Total Syntheses of Alstonine and Serpentine via Cooperative Catalysis III. Progress Towards Enantioselective Oxa-Pictet-Spengler Cyclization via Phosphoric Acids.
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100 1 $a Zeng, Bi-Shun. $3 3192656
245 1 0 $a I. Catalytic Enantioselective Synthesis of 2-Aryl Chromenes II. Total Syntheses of Alstonine and Serpentine via Cooperative Catalysis III. Progress Towards Enantioselective Oxa-Pictet-Spengler Cyclization via Phosphoric Acids.
300 $a 242 p.
500 $a Source: Dissertation Abstracts International, Volume: 77-08(E), Section: B.
500 $a Adviser: Karl A. Scheidt.
502 $a Thesis (Ph.D.)--Northwestern University, 2016.
520 $a An enantioselective Pd-catalyzed 6-endo-trig reaction to generate 2-aryl chromenes is presented in the first chapter. A novel monodentate phosphoramidite ligand -- identified through a systematic optimization of a TADDOL-derived ligand set -- enanbled the synthesis of a wide range of 2-aryl-2H-chromenes with high yield and enantioselectivity under mild conditions. To illustrate the utility of this new methodology, the products obtained from this reaction were transformed into two bioactive flavonoids (namely, catechin and hydroxyflavanone) through functionalization of the benzopyran olefin. The syntheses of alstonine and serpentine, two potential neurotherapeutics, are disclosed in chapter two. The key step involves a cooperative hydrogen bonding/enamine-catalyzed Michael addition. In the last chapter, efforts toward the enantioselective oxa-Pictet-Spengler cyclization to oxazinoindole using BINOL- and SPINOL-derived chiral phosphoric acids are described.
590 $a School code: 0163.
650 4 $a Organic chemistry. $3 523952
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710 2 $a Northwestern University. $b Chemistry. $3 1030729
773 0 $t Dissertation Abstracts International $g 77-08B(E).
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791 $a Ph.D.
792 $a 2016
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10043997