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Alfred Häßner

Researcher Next ID · RN-042265

Researcher · Biochemistry, Genetics and Molecular Biology

Bar-Ilan University

Ramat Gan, Israel

Accepting doctoral researchersFunding unknown
Works count
424
Citation count
10,090
H-index
48
i10-index
228

Research interests

Biochemistry, Genetics and Molecular Biology
Chemistry
Synthesis and Catalytic Reactions
Asymmetric Synthesis and Catalysis
Organic Chemistry Cycloaddition Reactions
Chemical Synthesis and Analysis
Chemical Synthesis and Reactions

Publications

  • Di- tert -butyl Dicarbonate and 4-(Dimethylamino)pyridine Revisited. Their Reactions with Amines and Alcohols 1

    The Journal of Organic Chemistry · 2000 · https://doi.org/10.1021/jo000257f

  • An Improved Method for Preparation of Nitrile Oxides from Nitroalkanes for In Situ Dipolar Cycloadditions

    Synthesis · 1997 · 10.1055/s-1997-1181

  • Synthetic methods. 33. Utility of a polymeric azide reagent in the formation of di- and triazidomethane. Their NMR spectra and the x-ray structure of derived triazoles

    The Journal of Organic Chemistry · 1990 · https://doi.org/10.1021/jo00295a014

  • A New Method for the Generation of Nitrile Oxides and Its Application to the Synthesis of 2-Isoxazolines

    Synthesis · 1989 · https://doi.org/10.1055/s-1989-27152

  • Kinetics of thermolysis of vinyl azides. Empirical rules for formation of azirines and rearranged nitriles

    The Journal of Organic Chemistry · 1986 · 10.1021/jo00366a019

  • Synthesis of Alkyl Azides with a Polymeric Reagent

    Angewandte Chemie International Edition in English · 1986 · 10.1002/anie.198604781

  • Synthetic methods. 19. Lewis acid catalyzed conversion of alkenes and alcohols to azides

    The Journal of Organic Chemistry · 1984 · 10.1021/jo00196a025

  • Synthetic methods. 15. Unsaturated acyl derivatives of silicon, germanium, and tin from metalated enol ethers

    Journal of the American Chemical Society · 1980 · 10.1021/ja00525a019

  • Aminopyridines as acylation catalysts for tertiary alcohols

    Tetrahedron · 1978 · 10.1016/0040-4020(78)89005-x

  • Cycloadditions. 24. An improved procedure for the addition of dichloroketene to unreactive olefins

    The Journal of Organic Chemistry · 1978 · https://doi.org/10.1021/jo00408a028

  • Direct room temperature esterification of carboxylic acids

    Tetrahedron Letters · 1978 · https://doi.org/10.1016/s0040-4039(01)95256-6

  • Recent developments in the synthetic uses of chlorosulfonyl isocyanate

    Chemical Reviews · 1976 · https://doi.org/10.1021/cr60301a004

  • Levulinic esters. Alcohol protecting group applicable to some nucleosides

    Journal of the American Chemical Society · 1975 · 10.1021/ja00839a077

  • Synthetic methods. VIII. Hydroxylation of carbonyl compounds via silyl enol ethers

    The Journal of Organic Chemistry · 1975 · https://doi.org/10.1021/jo00911a027

  • Synthetic methods. IV. Halogenation of carbonyl compounds via silyl enol ethers

    The Journal of Organic Chemistry · 1974 · 10.1021/jo00925a051

  • New Methods for the Synthesis of Vinyl Azides

    Angewandte Chemie International Edition in English · 1971 · 10.1002/anie.197100981

  • Regiospecific and stereospecific introduction of azide functions into organic molecules

    Accounts of Chemical Research · 1971 · https://doi.org/10.1021/ar50037a002

  • Stereochemistry. XLI. Reduction of .beta.-iodo azides. Stereospecific synthesis of aziridines

    Journal of the American Chemical Society · 1969 · 10.1021/ja01046a019

  • Stereochemistry. XXXIX. Ionic and free-radical addition of bromine azide to olefins

    Journal of the American Chemical Society · 1968 · 10.1021/ja01003a042

  • Stereochemistry. XXXII. Synthesis and reactions of 1-azirines

    Journal of the American Chemical Society · 1968 · https://doi.org/10.1021/ja01013a025

  • General synthesis of vinyl azides from olefins. Stereochemistry of elimination from .beta.-iodo azides

    The Journal of Organic Chemistry · 1968 · https://doi.org/10.1021/jo01271a016

  • Addition of iodine isocyanate to olefins. Scope and synthetic utility

    The Journal of Organic Chemistry · 1967 · https://doi.org/10.1021/jo01278a006

  • Stereospecific Introduction of Azide Functions into Organic Molecules

    Journal of the American Chemical Society · 1967 · 10.1021/ja00985a019

  • Additions of Iodine Azide to Olefins. Stereospecific Introduction of Azide Functions1

    Journal of the American Chemical Society · 1965 · https://doi.org/10.1021/ja01096a045

  • Reaction of Nitrosyl Chloride with Steroid 5-Enes.1 Nuclear Magnetic Resonance as a Stereochemical Tool in Steroids

    The Journal of Organic Chemistry · 1964 · 10.1021/jo01029a019

Current projects

    No projects listed.