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  2. Tsuji–Trost reaction - Wikipedia

    en.wikipedia.org/wiki/Tsuji–Trost_reaction

    The Tsuji–Trost reaction (also called the Trost allylic alkylation or allylic alkylation) is a palladium-catalysed substitution reaction involving a substrate that contains a leaving group in an allylic position. The palladium catalyst first coordinates with the allyl group and then undergoes oxidative addition, forming the π-allyl

  3. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    In organic chemistry, an allyl group is a substituent with the structural formula −CH 2 −HC=CH 2. It consists of a methylene bridge (−CH 2 −) attached to a vinyl group (−CH=CH 2). [1] [2] The name is derived from the scientific name for garlic, Allium sativum. In 1844, Theodor Wertheim isolated an allyl derivative from garlic oil and ...

  4. Krische allylation - Wikipedia

    en.wikipedia.org/wiki/Krische_allylation

    The excellent functional group compatibility of the Krische allylation combined with the tractability of the allyl acetate pronucleophiles enables the use of allyl donors bearing highly complex nitrogen-rich substituents. [20] insert a caption here. The figure below shows some of the different allyl donors that have been used in the Krische ...

  5. Transition-metal allyl complex - Wikipedia

    en.wikipedia.org/wiki/Transition-metal_allyl_complex

    The allyl ligand is commonly in organometallic chemistry.Usually, allyl ligands bind to metals via all three carbon atoms, the η 3-binding mode.The η 3-allyl group is classified as an LX-type ligand in the Green LXZ ligand classification scheme, serving as a 3e – donor using neutral electron counting and 4e – donor using ionic electron counting.

  6. Allylic rearrangement - Wikipedia

    en.wikipedia.org/wiki/Allylic_rearrangement

    Allylic shifts become the dominant reaction pathway when there is substantial resistance to a normal (non-allylic) substitution. For nucleophilic substitution, such resistance is known when there is substantial steric hindrance at or around the leaving group, or if there is a geminal substituent destabilizing an accumulation of positive charge.

  7. Category:Allyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Allyl_compounds

    Pages in category "Allyl compounds" The following 114 pages are in this category, out of 114 total. ... Allyl group; Allyl hexanoate; Allyl iodide; Allyl isothiocyanate;

  8. Department of Justice Announces Federal Review of 1921 Tulsa ...

    www.aol.com/department-justice-announces-federal...

    The violence took place in Tulsa, Okla., on May 31 and June 1, 1921 when a White mob descended on the city’s thriving Greenwood business district, known as “Black Wall Street,” burning and ...

  9. Allyl glycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Allyl_glycidyl_ether

    The synthesis of allyl glycidyl ether by condensation of allyl alcohol and epichlorohydrin. AGE can also be synthesized by monoepoxidation of diallyl ether. [6] [7] The synthesis of allyl glycidyl ether by epoxidation of diallyl ether. Diepoxidation of the second alkene would produce diglycidyl ether. Allyl glycidyl ether is chiral.