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
  • Synthetic methods  (2)
  • Cross-coupling reaction  (1)
  • Cyanide addition to unsaturated ketones  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2759-2763 
    ISSN: 0009-2940
    Keywords: Dichloroketene ; Stereoselective ketone reduction ; Mitsunobu reaction ; Cyclobutyl bromides ; Cross-coupling reaction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stereoselective Synthesis of 3-Substituted Cyclobutanols and Products Derived Therefrom3-Substituted cyclobutanones 2 are prepared by alkene/dichloroketene cycloadditions and subsequent dehalogenation. Reduction with LiAlH(OtBu)3 furnishes cis-cyclobutanols 3 in 95-100% selectivity. Mitsunobu inversion turned out to be the only practical method to get trans isomers 4 in high selectivity. A stereoselective cyclobutanol→bromocyclobutane conversion could be achieved only by a modified Mitsunobu reaction. Cross coupling between zinc derivatives of bromocyclobutanes 9 and aromatic bromides is not stereoselective.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1989 (1989), S. 181-185 
    ISSN: 0170-2041
    Keywords: Phase-Transfer catalysis, enantioselective ; Crown ethers, chiral ; Cyanide addition to unsaturated ketones ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Enantioselective Phase-Transfer Catalysis by Optically Active Crown Ethers1)1,2-Bis(hydroxymethyl)-15-crown-5 (1a), its dibenzyl ether (1b), and a series of esters with substituted benzoic acids (3) were probed as enantioselective phase-transfer catalysts. Optical yields were observed in epoxidations of unsaturated ketones by hypochlorite and in cyanide additions to such compounds. The maximum ee value was 45%. Polar side groups of the optically active crown ethers proved to be vital for enantiomeric excesses.
    Notes: 1,2-Bis(hydroxymethyl)-15-krone-5 (1a), ihr Dibenzylether (1b) und eine Anzahl von Estern mit substituierten Benzoesäuren (3) wurden als enantioselektive Phasentransfer-Katalysatoren erprobt. Optische Ausbeuten wurden bei der Epoxidierung von ungesättigten Ketonen mit Hypochlorit und bei der Cyanid-Addition an solche Verbindungen beobachtet, wobei das erreichte Maximum bei 45% ee lag. Polare Seitengruppen der optisch aktiven Kronenether erwiesen sich als notwendig für Enantiomerenüberschüsse.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 16 (1977), S. 493-505 
    ISSN: 0570-0833
    Keywords: Phase-transfer catalysis ; Catalysis ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phase-transfer catalysis (PTC) has grown into a versatile preparative method in the last few years. The most notable new developments include the use of crown ethers as phase-transfer catalysts and the introduction of solid-liquid PTC. Some representative examples have been selected from the large number of new PTC reactions and some of them are summarized in tables.
    Additional Material: 11 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 13 (1974), S. 170-179 
    ISSN: 0570-0833
    Keywords: Phase-transfer catalysis ; Catalysis ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Quaternary ammonium and phosphonium salts catalyze reactions between substances located partly in an aqueous and partly in an organic phase. Use of such phase-transfer catalysts simplifies and accelerates numerous reactions traditionally conducted in nonaqueous media. These reactions include carbene reactions, nucleophilic substitutions, alkylations of ketones and nitriles, Wittig and Darzens reactions, formation of ethers and esters. Other reactions such as hydrolysis and oxidation can be accelerated.
    Additional Material: 5 Tab.
    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...