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Enantioselective synthesis and react...

Panish, Robert A.

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Enantioselective synthesis and reactivity of bicyclobutanes: Strained molecular platforms for 4-, 5-, and 6-membered ring synthesis and rhodium(II)-catalyzed reactions of diazoesters with organozinc reagents.

Record Type:	Electronic resources : Monograph/item
Title/Author:	Enantioselective synthesis and reactivity of bicyclobutanes: Strained molecular platforms for 4-, 5-, and 6-membered ring synthesis and rhodium(II)-catalyzed reactions of diazoesters with organozinc reagents./
Author:	Panish, Robert A.
Published:	Ann Arbor : ProQuest Dissertations & Theses, : 2016,
Description:	429 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=10055790
ISBN:	9781339566993

Enantioselective synthesis and reactivity of bicyclobutanes: Strained molecular platforms for 4-, 5-, and 6-membered ring synthesis and rhodium(II)-catalyzed reactions of diazoesters with organozinc reagents.
Panish, Robert A.

Enantioselective synthesis and reactivity of bicyclobutanes: Strained molecular platforms for 4-, 5-, and 6-membered ring synthesis and rhodium(II)-catalyzed reactions of diazoesters with organozinc reagents. - Ann Arbor : ProQuest Dissertations & Theses, 2016 - 429 p.

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

Thesis (Ph.D.)--University of Delaware, 2016.

This dissertation is centered on reaction methodology and its application in the total synthesis of natural products. The results described herein include the development of a new method for enantioselective synthesis of cyclobutanes, the total synthesis of cyclobutane-containing natural products, the development of the first examples of transition-metal catalyzed vinylcyclobutane ring expansion reactions, and the rhodium-catalyzed organozincation of diazoesters.

ISBN: 9781339566993Subjects--Topical Terms:

523952
Organic chemistry.

Enantioselective synthesis and reactivity of bicyclobutanes: Strained molecular platforms for 4-, 5-, and 6-membered ring synthesis and rhodium(II)-catalyzed reactions of diazoesters with organozinc reagents.
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100 1 $a Panish, Robert A. $3 3280843
245 1 0 $a Enantioselective synthesis and reactivity of bicyclobutanes: Strained molecular platforms for 4-, 5-, and 6-membered ring synthesis and rhodium(II)-catalyzed reactions of diazoesters with organozinc reagents.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2016
300 $a 429 p.
500 $a Source: Dissertation Abstracts International, Volume: 77-08(E), Section: B.
500 $a Adviser: Joseph M. Fox.
502 $a Thesis (Ph.D.)--University of Delaware, 2016.
520 $a This dissertation is centered on reaction methodology and its application in the total synthesis of natural products. The results described herein include the development of a new method for enantioselective synthesis of cyclobutanes, the total synthesis of cyclobutane-containing natural products, the development of the first examples of transition-metal catalyzed vinylcyclobutane ring expansion reactions, and the rhodium-catalyzed organozincation of diazoesters.
520 $a The rich chemistry of diazocompounds rapidly builds complexity across many modes of reactivity. The propensity of Rh(II)-carbenes to undergo beta-hydride migration has been a long standing limitation to this chemistry. In Chapter 1, I will provide an overview of chemistries involving alpha-alkyl-beta-diazoesters that contain beta-hydrogens including the major contributions from our group. The ability to limit this undesired pathway by studying temperature and ligand effects has further extended the powerful chemistry of diazocompounds.
520 $a Rhodium(II)-catalyzed intermolecular cyclopropanation of diazoesters and alkenes has been widely studied and applied to complex synthesis; however, reports of intramolecular cyclopropanation had been quite limited. In Chapter 2, I will discuss the development of general conditions for the enantioselective intramolecular cyclopropanation or bicyclobutanation of alpha-diazoesters. Additionally, this chemistry has been coupled with a Cu(I)-catalyzed homoconjugate addition of Grignard reagents to bicyclobutanes in a one-pot procedure to provide rapid access to complex cyclobutanes in a highly stereocontrolled manner.
520 $a Cyclobutane-containing natural products exhibit diverse biological activity and have shown promise as therapeutic leads in areas including oncology, neurology, pain management, infectious diseases, and respiratory diseases. General and stereoselective methods to access unsymmetrical cyclobutane cores are still needed. In Chapter 3, I describe the application of the Rh(II)-catalyzed bicyclobutanation/Cu(I)-catalyzed homoconjugate addition of diazoesters for the synthesis of cyclobutane-containing natural products. I have completed the total synthesis of piperarborenine B in 0.4 g, 10 steps, and 8% overall yield in 1 week. I have also applied this methodology towards the synthesis of incarvillateine D and SB-FI-26 both of which have shown promise in pain management via adenosine receptor pathways.
520 $a In contrast to the well-known and widely-utilized vinylcyclopropane--cyclopentene rearrangement, the analogous vinylcyclobutane--cyclohexene rearrangement has found limited use due to the requirement of harsh conditions. In Chapter 4, I will discuss the development of the first examples of transition metal catalyzed ring expansions of vinylcyclobutanes. I have discovered the combination of Ni(0) and NHC ligands provides cyclohexenes while Rh(I)-catalysts provide exclusively cyclopentenes.
520 $a Organozinc reagents are widely used reagents in light of their excellent functional group tolerance; however, their use in Rh(II)-catalyzed reactions with diazoesters has not been reported. In Chapter 5, I describe the development of general conditions for the Rh(II)-catalyzed organozincation of diazoesters. The resulting hydrazone products have been elaborated to tertiary aminoesters and pyrazoles.
590 $a School code: 0060.
650 4 $a Organic chemistry. $3 523952
650 4 $a Chemistry. $3 516420
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690 $a 0485
710 2 $a University of Delaware. $b Chemistry and Biochemistry. $3 3174095
773 0 $t Dissertation Abstracts International $g 77-08B(E).
790 $a 0060
791 $a Ph.D.
792 $a 2016
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10055790