Allylic alkylation reactions involve the addition of a nucleophile to the allylic position of a substrate, often an allylic carbonate or similar compound. Asymmetric allylic alkylation is a powerful method for the synthesis of chiral molecules, as it allows for the creation of new stereocenters with high enantioselectivity.
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3-[2-{[(1S)-1-(hydroxymethyl)-2,2-dimethylpropyl]amino}-2-oxoethyl]-1-cyclohexyl-1H-benzimidazolium chloride
(R)-(2-(tert-butylsulfinyl) phenyl) (methyl) sulfane
(-)-t-butyl trans-2,3-bis(diphenylphosphinyl)-1-methyl-1-cyclopropanecarboxylate
tert-butyl bis(2-methoxyphenyl)phosphine oxide
Propanedioic acid, [(1R)-1,3-diphenyl-2-propenyl]-, diethyl ester
(R)-2-phenyl-2-cyclohexen-1-ylmalonic acid di-tert-butyl ester
