Results 151 to 160 of about 108,077 (187)
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One Pot Synthesis of Acetylated Homoallyl Alcohols

Synthetic Communications, 1999
Abstract An efficient one pot procedure for the preparation of acetylated homoallyl alcohols mediated by TaCl5 is described.
S. Chandrasekhar   +2 more
openaire   +1 more source

Synthesis of homoallylic alcohols

The Journal of Organic Chemistry, 1968
Jack K. Crandall   +4 more
openaire   +1 more source

Methyltrioxorhenium-Catalyzed Epoxidation of Homoallylic Alcohols with Hydrogen Peroxide

The Journal of Organic Chemistry, 2012
Homoallylic alcohols were efficiently converted to the corresponding 3,4-epoxy alcohols in excellent yields by methyltrioxorhenium (MTO)-catalyzed epoxidation with aqueous hydrogen peroxide as the terminal oxidant and 3-methylpyrazole (10 mol %) as an additive.
openaire   +2 more sources

ChemInform Abstract: THE STEREOSELECTIVITY OF THE REDUCTION OF HOMOPROPARGYLIC ALCOHOLS TO HOMOALLYLIC ALCOHOLS

Chemischer Informationsdienst, 1981
AbstractDie Reduktion von 3‐Tetradecin‐1‐ol (I) wird unter verschiedenen Bedingungen in Hinblick auf eine möglichst selektive Bildung des E‐Olefins (II) untersucht.
openaire   +1 more source

Stereochemistry of epoxidation of allylic and homoallylic cyclohexene alcohols

J. Chem. Soc., Perkin Trans. 1, 1994
The reactivity of cyclohexene-type allylic alcohols towards epoxidation reagents (peroxy acids and ButO2H with transition metal catalysts) is largely dependent on the magnitude of steric hindrance in the substrate molecules. With unhindered [2(R = H)] or slightly hindered allylic alcohols (4, 8 and 12) the reaction is dominated by the syn ...
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Stereochemical Control via Chirality Pairing: Stereodivergent Syntheses of Enantioenriched Homoallylic Alcohols

Angewandte Chemie - International Edition, 2021
Shang Gao, Peiyuan Yu, Meng Duan
exaly  

Synthesis from Homoallylic Alcohols

2008
A. G. Griesbeck, T. Sokolova
openaire   +1 more source

Enantioselective Epoxidation of Homoallylic Alcohols

2011
K. Matsumoto   +2 more
openaire   +1 more source

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