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Asymmetric [2,3]-sigmatropic rearrangement of allylic ammonium ylides
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Organic Chemistry.
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Organic Chemistry.
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Organic Chemistry.
2005 (English)In: Journal of the American Chemical Society, ISSN 0002-7863, E-ISSN 1520-5126, Vol. 127, no 26, 9352-9353 p.Article in journal (Refereed) Published
Abstract [en]

An asymmetric Lewis acid-mediated [2,3]-sigmatropic rearrangement of allylic amines has been developed, affording the corresponding homoallylic amines in good yield and excellent enantioselectivities. The rearrangement proceeds by complexation of the chiral Lewis acid to the amine followed by deprotonation and rearrangement.

Place, publisher, year, edition, pages
2005. Vol. 127, no 26, 9352-9353 p.
Keyword [en]
allyl compound, ammonium derivative, article, chirality, diastereoisomer, quantum yield, reaction analysis, stereochemistry
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:kth:diva-6874DOI: 10.1021/ja0510562ISI: 000230220900021Scopus ID: 2-s2.0-21644453480OAI: oai:DiVA.org:kth-6874DiVA: diva2:11706
Note
QC 20100831Available from: 2005-09-27 Created: 2005-09-27 Last updated: 2011-08-30Bibliographically approved
In thesis
1. Asymmetric [2,3]-Sigmatropic Rearrangement of Allylic Ammonium Ylides
Open this publication in new window or tab >>Asymmetric [2,3]-Sigmatropic Rearrangement of Allylic Ammonium Ylides
2005 (English)Doctoral thesis, comprehensive summary (Other scientific)
Abstract [en]

The thesis describes the realization of an asymmetric [2,3]-sigmatropic rearrangement of achiral allylic amines. It is divided into two parts; the first part deals with the development of a Lewis acid-mediated [2,3]-sigmatropic rearrangement and the second the asymmetric version thereof. Quaternization of an -amino amide with various Lewis acids established BBr3 and BF3 to be the most appropriate ones. Various allylic amines were subsequently rearranged into the corresponding homoallylic amines in good to excellent syn-diastereoselectivities, revealing the endo-transition state to be the preferred pathway. The structures of the intermediate Lewis acid-amine complexes were confirmed by NMR spectroscopy studies and DFT calculations.

Based on this investigation a chiral diazaborolidine was chosen as Lewis acid and was shown to efficiently promote the asymmetric [2,3]-sigmatropic rearrangement furnishing homoallylic amines in good yields and excellent enantiomeric excesses. In contrast to the achiral rearrangement mediated by BBr3 and BF3, the asymmetric version gave the opposite major diastereomer, revealing a preference for the exo-transition state in the asymmetric rearrangement. To account for the observed selectivities, a kinetic and thermodynamic pathway was presented. On the basis of a deuterium exchange experiment on a rearranged Lewis acid-amine complex and an NMR spectroscopic investigation, the kinetic pathway was shown to be favored.

Place, publisher, year, edition, pages
Stockholm: KTH, 2005. 68 p.
Series
Trita-IOK, ISSN 1100-7974 ; 2005:97
Keyword
asymmetric, [2, 3]-sigmatropic rearrangement, allylic amine, ammonium ylide, Lewis acid, enantioselective, boron, phosphazene base, NMR spectroscopy, DFT-calculations
National Category
Organic Chemistry
Identifiers
urn:nbn:se:kth:diva-430 (URN)91-7178-135-8 (ISBN)
Public defence
2005-10-07, Salongen, KTHB, KTH, Stockholm, 09:00
Opponent
Supervisors
Note
QC 20100927Available from: 2005-09-27 Created: 2005-09-27 Last updated: 2010-09-27Bibliographically approved

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