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The small peptide-catalyzed direct asymmetric aldol reaction in water
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
2006 (Engelska)Ingår i: Organic and biomolecular chemistry, ISSN 1477-0520, E-ISSN 1477-0539, Vol. 4, s. 38-40Artikel i tidskrift (Refereegranskat) Published
Ort, förlag, år, upplaga, sidor
2006. Vol. 4, s. 38-40
Nationell ämneskategori
Annan medicinsk grundvetenskap
Forskningsämne
organisk kemi
Identifikatorer
URN: urn:nbn:se:su:diva-39047DOI: 10.1039/b515880jOAI: oai:DiVA.org:su-39047DiVA, id: diva2:318116
Tillgänglig från: 2010-05-06 Skapad: 2010-05-06 Senast uppdaterad: 2018-01-12Bibliografiskt granskad
Ingår i avhandling
1. Amino acid-catalyzed synthesis of amino acid derivatives: Application and semi-synthesis of Paclitaxel, Docetaxel and their derivatives
Öppna denna publikation i ny flik eller fönster >>Amino acid-catalyzed synthesis of amino acid derivatives: Application and semi-synthesis of Paclitaxel, Docetaxel and their derivatives
2010 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

This thesis deals with different applications of organocatalysis, where amino acid derivatives and small peptides are applied as catalysts. First, the development of environmentally friendly aldol reactions, carried out in aqueous media is illustrated. The corresponding β-hydroxy ketones are formed with ee´s up to 99%. Chapter 3 describes the ability of β3-amino acids to selectively catalyze Mannich-type reactions and govern the formation of products with high anti-selectivity (up to >19:1) and ee´s up to 99%. In the following chapter, an amino acid-catalyzed one-pot three component Mannich reaction between dihydroxyacetone and PMP-protected imines, is presented. The corresponding a,a’-dihydroxy-b-aminoketones are obtained in high yields and with 82-95% ee. Next, an aza-Morita-Baylis-Hillman reaction was investigated where L-proline is the catalyst. The reaction proceeds with excellent chemo- and enantioselectivity to give the corresponding compounds in good yields and with 97-99% ee. Finally, the last part describes development of a proline-catalyzed Mannich reation between N-acyl imines and protected α-hydroxyaldehyes, providing access to different α-hydroxy-β-amino acids in good yields and high enantioselctivity (92-99% ee). The obtained amino acids were further applied in the semisynthesis of paclitaxel and docetaxel derivatives.

Ort, förlag, år, upplaga, sidor
Stockholm: Department of Organic Chemistry, Stockholm University, 2010. s. 73
Nyckelord
Organocatlysis, amino acids, syntesis, Taxol and Taxotere derivatives
Nationell ämneskategori
Annan medicinsk grundvetenskap
Forskningsämne
organisk kemi
Identifikatorer
urn:nbn:se:su:diva-39138 (URN)978-91-7447-091-8 (ISBN)
Disputation
2010-06-11, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16b, Stockholm, 10:00 (Engelska)
Opponent
Handledare
Anmärkning
At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 7: Manuscript.Tillgänglig från: 2010-05-20 Skapad: 2010-05-10 Senast uppdaterad: 2018-01-12Bibliografiskt granskad

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Dziedzic, PawelCórdova, Armando
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Institutionen för organisk kemi
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Organic and biomolecular chemistry
Annan medicinsk grundvetenskap

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