ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
Collection
Keywords
Publisher
Years
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 69 (1986), S. 1137-1146 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The structure of the α-chloronitroso ether 1, obtained from the hydroximolactone 2 and tert-butyl hypochlorite (89%), was established by X-ray crystallographic analysis. The [4 + 2] cycloadditions of 1 with the dienes 3 and 8-11 led to the N-unsubstituted 3,6-dihydro-2H-1,2-oxazines 6 and 12-16 in high enantiomeric excess (Table 1). Due to the additional α-alkoxy group, the reactivity of 2 is much superior to the one of known α-chloronitrosoalkanes. The reactive conformation of 1 was deduced from the X-ray analysis as well as the high diastereoselectivity of the cycloadditions. The importance of the α-alkoxy group was evidenced from the similar reactivity of the racemic α-chloronitroso ethers 25-27 which were prepared from the hydroximo ethers 28-30 and tert-butyl hypochlorite.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Chemistry of Sulfur Diimides, III. Reactions of Aromatic Bis-amino Compounds with N-Sufinyl Sulfonamides and N,N'-Bis-arylsulfonyl-sulfur DiimidesBifunctional amino compounds 1 react with N-sulfinyl-p-toluene sulfonamide (2) and N,N'-bis-[p-toluenesulfonyl]-sulfur diimide (3) to give the derivatives 4-8, depending on the nature of X. By reaction with 2,3-dimethyl-1,3-butadiene the cyclic sulfur diimide 8b gives the adduct 11, the alkaline cleavage of which yields the pyrrole 12.
    Notes: Bifunktionelle Aminoverbindungen 1 reagieren mit N-Sulfinyl-p-toluolsulfonamid (2) und N.N'-Bis-[p-toluolsulfonyl]-schwefeldiimid (3) in Abhängigkeit von der Art der Gruppe X zu den Derivaten 4-8. Das cyclische Schwefeldiimid 8b liefert mit 2.3-Dimethyl-1.3-butadien das Addukt 11, dessen alkalische Spaltung zum Pyrrol 12 führt.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1975 (1975), S. 1721-1724 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemistry of Sulfur Diimides V - Reaction of N,N′-Ditosylsulfur Diimide with Nucleophilic and Electrophilic ReagentsN,N′-Ditosylsulfur diimide (1) reacts smoothly with organic sulfides as nucleophilic reagents. The structure of the products and the mechanism of their formation are discussed. If the SN bond in 1 possessed ylid character, a reactivity towards electrophilic reagents could be foreseen. This is not observed.
    Notes: N,N′-Ditosylschwefeldiimid (1) reagiert infolge der starken Positivierung des S-Atoms glatt mit Sulfiden als nucleophilen Reaktionspartnern. Die Struktur der Produkte und der Verlauf der Umsetzung werden diskutiert. Eine bei Ylidcharakter der SN-Bindung in 1 zu erwartende Reaktivität gegenüber elektrophilen Reagentien konnte nicht nachgewiesen werden.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...