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  1. Ring contraction via a Favorskii-type rearrangement: cycloundecanoneRearrangement Org. Synth. Coll. Vol. 6, p. 368; Vol. 56, p. 107 · Wohllebe and Jr
  2. Silver-catalyzed rearrangement of propargylic sulfinates: synthesis of allenic sulfonesRearrangement Org. Synth. Vol. 88, p. 309 · Harmata et al.
  3. Stereocontrolled preparation of 3-acyltetrahydrofurans from acid-promoted rearrangements of allylic ketals: (2S,3S)-3-acetyl-8-carboethoxy-2,3-dimethyl-1-oxa-8-azaspiro[4.5]decaneRearrangement Org. Synth. Coll. Vol. 9, p. 4; Vol. 71, p. 63 · Overman and Rishton
  4. Synthesis of an N-substituted lactam using an intramolecular Schmidt reaction: formation of 2,3,11,11a-tetrahydro-1H-benzo[d]pyrrolo[1,2-a]azepin-5(6H)-oneRearrangement Org. Synth. Vol. 84, p. 347 · Grecian and Aubé
  5. Synthesis of Arylboronic Pinacol Esters from Corresponding ArylaminesRearrangement Org. Synth. Vol. 91, p. 106 · Qiu et al.
  6. The Carroll rearrangement: 5-dodecen-2-oneRearrangement Org. Synth. Coll. Vol. 8, p. 235; Vol. 68, p. 210 · Wilson and Augelli
  7. α-Unsubstituted γ,δ-unsaturated aldehydes by Claisen rearrangement: 3-phenyl-4-pentenalRearrangement Org. Synth. Coll. Vol. 8, p. 536; Vol. 66, p. 29 · Vogel and Büchi