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Enantioselective Hydrosilylation and Hydrogenation of Alkaloid Precursors

Brunner, H., Kürzinger, A., Mahboobi, Siavosh and Wiegrebe, Wolfgang (1988) Enantioselective Hydrosilylation and Hydrogenation of Alkaloid Precursors. Archiv der Pharmazie 321, pp. 73-76.

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Enantioselective hydrosilylations of the 3,4-dihydropyrrole derivatives 1a-c and 5 with in-situ catalysts consisting of [Rh(cod)Cl]2 and optically active phosphines yield the N-silyl compounds 2a-c and 6 in up to 66.1 % ee. The N-silyl derivatives were treated with acetic formic anhydride or trifluoroacetic anhydride to give the N-formyl and N-trifluoroacetyl compounds 3a-c, 4a-c, 7, and 8. The ...


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Item type:Article
Institutions:Chemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Wiegrebe
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Unknown
Item ID:15673
Owner only: item control page


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