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  • 1
    ISSN: 0009-2940
    Keywords: Cyclopentadienes, synthesis of ; [3 + 2] Cycloadditions of 1-metalla-1,3-dienes and alkynes ; 1-Metalla-1,3,5-trienes of tungsten, cyclization to cyclopentadiene complexes ; η1-Cyclopentadiene tungsten complexes ; Aminocarbene complexes of chromium and tungsten ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Syntheses via Transition Metal Complexes, 54.  -  Cyclopentadienes from 1-Metalla-1,3-dienes and Alkynes by Cyclization of Intermediate 1-Metalla-1,3,5-trienes (Metal = Tungsten)We report on first examples of the formation of cyclopentadienes from a 1-metalla-1,3-diene LnM=C-C=C [LnM = W(CO)5] and an alkyne in [3 + 2] cycloaddition multistep reactions. In a first step the alkyne Et2N-C=C-Me (2) adds to the 1-metalla-1,3-diene (CO)5W = C(OEt)-CH=CHPh (1b) to give 1-metalla-1,3,5-trienes (CO)5W=C(NEt2)-CMe=C(OEt)-CH=CHPh (3b) and (CO)5W=C(OEt)-CH=C(NEt2)-CMe=CHPh (4b). In a second step 3b cyclizes to thecyclopentadiene complex 5, which has an η1 ylide-type structure as established by an X-ray analysis. Hydrolysis of 5 leads to the formation of a 3-aminocyclopentenone 7. The 1-metalla-1,3,5-triene 4b yields a cyclopentadiene complex 8. In contrast to 5 the carbon skeleton of 8 has a connectivity different from that of the C3 unit of the 1-metalla-1,3-diene 1.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1988 (1988), S. 695-704 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Diastereoselective Syntheses of rac-Slaframine and rac-6-epi-SlaframineIndolizidinones 8 have been obtained from thalidomide (5) and cyclopropylphosphonium salts 6 in good yields. Acid-catalyzed rearrangement of 8a gave the isomer 11. A regio- and stereoselective acetoxylation of 8a and 11 was achieved with lead tetraacetate: using standard conditions, acetates 15 and 16 were obtained; in the presence of triethylamine, however, 8a has been transformed into the acetoxy derivative 17. rac-6-epi-Slaframine (4) and rac-slaframine (1) were obtained from acetates 16 and 17 on conventional routes.
    Notes: Indolizidinone 8 wurden aus Thalidomid (5) und Cyclopropylphosphoniumsalzen 6 in guten Ausbeuten erhalten. 8a ließ sich mit Säuren zu 11 isomerisieren. Eine regio- und stereoselektive Acetoxylierung von 8a und 11 gelang mit Blei(IV)-acetat: unter den üblichen Bedingungen entstanden die Acetate 15 und 16; in Gegenwart von Triethylamin reagierte 8a jedoch zum Acetoxyderivat 17. rac-6-epi-Slaframin (4) und rac-Slaframin (1) wurden aus 16 und 17 auf konventionellen Wegen erhalten.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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