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    Chapter

    Synthesis of β-Halofurans

    Furans substituted with halogens at the beta carbon, which is less prone to electrophilic reactions compared to an alpha position, are important intermediates for accessing highly substituted furans. The regiosel...

    Roman Dembinski, Yan Li, Deepthi Gundapuneni, Alicia Decker in Halogenated Heterocycles (2012)

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    Chapter

    Chiral Ionic Liquids in Chromatographic Separation and Spectroscopic Discrimination

    Chiral ionic liquids (CILs) are a subclass of ionic liquids (ILs) in which the cation, anion, or both may be chiral. The chirality can be central, axial, or planar. CILs possess a number of unique advantageous...

    Min Li, David K. Bwambok, Sayo O. Fakayode in Chiral Recognition in Separation Methods (2010)

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    Chapter

    Cyclodextrin Inclusion Polymers Forming Hydrogels

    This chapter reviews the advances in the developments of supramolecular hydrogels based on the polypseudorotaxanes and polyrotaxanes formed by inclusion complexes of cyclodextrins threading onto polymer chains...

    Jun Li in Inclusion Polymers (2009)

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    Chapter

    Corey-Kim oxidation

    Oxidation of alcohol to the corresponding aldehyde or ketone using NCS/DMF, followed by treatment with a base.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Ring-closing metathesis (RCM) using Grubbs and Schrock catalysts

    A selenium dioxide oxidation of activated methylenes into ketones.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Herz reaction

    Treatment of anilines with sulfur monochloride to produce thiazothionium chlorides, which upon treatment with base give α-aminothiophenols.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Williamson ether synthesis

    Ether from the alkylation of alkoxides by alkyl halides.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Hodges-Vedejs metallation of oxazoles

    Metallation of an oxazole followed by treatment with benzaldehyde results in a 4-substituted oxazole as the major product [1]:

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Wohl-Ziegler reaction

    Radical-initiated allylic bromination using NBS, and catalytic AIBN as initiator or NBS under photolysis.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Stieglitz rearrangement

    Rearrangement of trityl N-haloamines.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Stobbe condensation

    Condensation of diethyl succinate and its derivatives with carbonyl compounds in the presence of a base.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Boord reaction

    Olefin from the treatment of β-halo-alkoxide with zinc.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Noyori asymmetric hydrogenation

    Asymmetric reduction of carbonyl via hydrogenation catalyzed by ruthenium(II) BINAP complex.

    Jie Jack Li Ph. D. in Name Reactions (2003)

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    Chapter

    Luche reduction

    1,2-Reduction of enones using NaBH4-CeCl3.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Madelung indole synthesis

    Indoles from the intramolecular cyclization of 2-(acylamino)-toluenes using strong bases.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Aldol condensation

    Condensation of a carbonyl with an enolate or an enol. A simple case is addition of an enolate to an aldehyde to afford an alcohol, thus the name aldol.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Fischer-Hepp rearrangement

    Transformation of N-nitroso-anilines to the corresponding para-nitroso anilines. Cf. Orton rearrangement.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Forster reaction

    α-Diazoketone formation from α-oximinoketones.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Reissert reaction (aldehyde synthesis)

    Aldehyde synthesis from the corresponding acid chloride, quinoline, and KCN.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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    Chapter

    Cornforth rearrangement

    Thermal rearrangement of keto-oxazoles.

    Jie Jack Li Ph.D. in Name Reactions (2003)

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