Results 111 to 120 of about 1,571 (154)
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Diastereoselective Cycloadditions of Chiral Homoallylic Alcohols with Benzonitrile Oxide.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Martin G. Kociolek, Chayanant Hongfa
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Copper‐Catalyzed Trifluoromethylation of Trisubstituted Allylic and Homoallylic Alcohols
Chemistry – A European Journal, 2015AbstractAn efficient copper‐catalyzed trifluoromethylation of trisubstituted allylic and homoallylic alcohols with Togni’s reagent has been developed. This strategy, accompanied by a double‐bond migration, leads to various branched CF3‐substituted alcohols by using readily available trisubstituted cyclic/acyclic alcohols as substrates.
Jian, Lei +6 more
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General and Practical Approach to the Syntheses of Linear Homoallylic Alcohols
ChemInform, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
Hin-Soon Cheng, Teck-Peng Loh
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Chemistry Letters, 1993
Abstract Whereas platinum-catalyzed hydrogermylation of 3-hexenoxydipropylgermane provided five-membered ring product (5-propyl-1-germa-2-oxacyclopentane) as a main product, triethylborane induced radical cyclization gave six-membered ring product (6-ethyl-1-germa-2-oxacyclohexane) selectively.
Masahiko Taniguchi +2 more
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Abstract Whereas platinum-catalyzed hydrogermylation of 3-hexenoxydipropylgermane provided five-membered ring product (5-propyl-1-germa-2-oxacyclopentane) as a main product, triethylborane induced radical cyclization gave six-membered ring product (6-ethyl-1-germa-2-oxacyclohexane) selectively.
Masahiko Taniguchi +2 more
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One Pot Synthesis of Acetylated Homoallyl Alcohols
Synthetic Communications, 1999Abstract An efficient one pot procedure for the preparation of acetylated homoallyl alcohols mediated by TaCl5 is described.
S. Chandrasekhar +2 more
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Synthesis of homoallylic alcohols
The Journal of Organic Chemistry, 1968Jack K. Crandall +4 more
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Methyltrioxorhenium-Catalyzed Epoxidation of Homoallylic Alcohols with Hydrogen Peroxide
The Journal of Organic Chemistry, 2012Homoallylic 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.
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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.
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AbstractDie Reduktion von 3‐Tetradecin‐1‐ol (I) wird unter verschiedenen Bedingungen in Hinblick auf eine möglichst selektive Bildung des E‐Olefins (II) untersucht.
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Asymmetric Epoxidation of Homoallylic Alcohols
Synfacts, 2007H. Yamamoto, W. Zhang
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Stereochemistry of epoxidation of allylic and homoallylic cyclohexene alcohols
J. Chem. Soc., Perkin Trans. 1, 1994The 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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