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Introducing Dynamic Combinatorial Chemistry: Probing the Substrate Selectivity of Acetylcholinesterase
KTH, Skolan för kemivetenskap (CHE), Kemi, Organisk kemi.
KTH, Skolan för kemivetenskap (CHE), Kemi, Organisk kemi.
KTH, Skolan för kemivetenskap (CHE), Kemi, Organisk kemi.
KTH, Skolan för kemivetenskap (CHE), Kemi, Organisk kemi.ORCID-id: 0000-0002-1533-6514
2010 (Engelska)Ingår i: Journal of Chemical Education, ISSN 0021-9584, E-ISSN 1938-1328, Vol. 87, nr 11, s. 1248-1251Artikel i tidskrift (Refereegranskat) Published
Ort, förlag, år, upplaga, sidor
2010. Vol. 87, nr 11, s. 1248-1251
Nationell ämneskategori
Organisk kemi
Identifikatorer
URN: urn:nbn:se:kth:diva-13743DOI: 10.1021/ed100400vISI: 000282868100032Scopus ID: 2-s2.0-78449272682OAI: oai:DiVA.org:kth-13743DiVA, id: diva2:327074
Anmärkning
QC20100628, QC 20111109. Ändrad från accepted till published 20111109Tillgänglig från: 2010-06-28 Skapad: 2010-06-28 Senast uppdaterad: 2019-12-20Bibliografiskt granskad
Ingår i avhandling
1. Discovery-Oriented Screening of Dynamic Systems: Combinatorial and Synthetic Applications
Öppna denna publikation i ny flik eller fönster >>Discovery-Oriented Screening of Dynamic Systems: Combinatorial and Synthetic Applications
2010 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

This thesis is divided into six parts, all centered around the development of dynamic (i.e., reversibly interacting) systems of molecules and their applications in dynamic combinatorial chemistry (DCC) and organic synthesis.

Part one offers a general introduction, as well as a more detailed description of DCC, being the central concept of this thesis. Part two explores the potential of the nitroaldol reaction as a tool for constructing dynamic systems, employing benzaldehyde derivatives and nitroalkanes. This reaction is then applied in part three where a dynamic nitroaldol system is resolved by lipase-catalyzed transacylation, selecting two out of 16 components.

In part four, reaction and crystallization driven DCC protocols are developed and demonstrated. The discovery of unexpected crystalline properties of certain pyridine β-nitroalcohols is used to resolve a dynamic system and further expanded into asynthetic procedure. Furthermore, a previously unexplored tandem nitroaldol-iminolactone rearrangement reaction between 2-cyanobenzaldehyde and primarynitroalkanes is used for the resolution of dynamic systems. It is also coupled with diastereoselective crystallization to demonstrate the possibility to combine several selection processes. The mechanism of this reaction is investigated and a synthetic protocol is developed for asymmetric synthesis of 3-substituted isoindolinones.

Part five continues the exploration of tandem reactions by combining dynamic hemithioacetal or cyanohydrin formation with intramolecular cyclization to synthesize a wide range of 3-functionalized phthalides.

Finally, part six deals with the construction of a laboratory experiment to facilitate the introduction of DCC in undergraduate chemistry education. The experiment is based on previous work in our group and features an acetylcholinesterase-catalyzed resolution of a dynamic transthioacylation system.

Ort, förlag, år, upplaga, sidor
Stockholm: KTH, 2010. s. 82
Serie
Trita-CHE-Report, ISSN 1654-1081 ; 2010:13
Nyckelord
chemical education, crystallization, dynamic combinatorial chemistry, dynamic combinatorial resolution, dynamic system, enzyme catalysis, isoindolinone, lipase, nitroalcohol, nitroaldol reaction, phthalide, reversible, secondary alcohol, systems chemistry, tandem reaction
Nationell ämneskategori
Organisk kemi Organisk kemi
Identifikatorer
urn:nbn:se:kth:diva-12524 (URN)978-91-7415-617-1 (ISBN)
Disputation
2010-05-28, F3, Lindstedtsvägen 26, KTH, Stockholm, 10:00 (Engelska)
Opponent
Handledare
Anmärkning
QC 20100628Tillgänglig från: 2010-05-12 Skapad: 2010-05-03 Senast uppdaterad: 2011-02-11Bibliografiskt granskad

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Angelin, MarcusLarsson, RikardVongvilai, PornrapeeRamström, Olof
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