93455-29-9Relevant academic research and scientific papers
Synthesis of Ethyl (2RS,3SR)-1-Tosyl-3-vinylazetidine-2-carboxylate and Ethyl (2RS,E)-3-Ethylidene-1-tosylazetidine-2-carboxylate (=rac-Ethyl N-Tosylpolyoximate)
Baumann, Hans,Duthaler, Rudolf O.
, p. 1025 - 1034 (1988)
The synthesis of 3-ethylideneazetidine-2-carboxylic acid (=polyoximic acid; 3) is approached in two different ways leading to potential precursors of 3.The first way involved a ring closure to a vinyl-substituted azetidine.Thus, Ireland-Claiser rearrangem
Stereochemical Studies of Thermal Intermolecular and Intramolecular N-Sulfonylimine Ene Reactions
Tschaen, David M.,Turos, Edward,Weinreb, Steven M.
, p. 5058 - 5064 (2007/10/02)
N-Sulfonylimine 2 has been found to undergo highly stereoselective thermal ene reactions with cyclohexene and trans-2-butene.In the cyclohexene example, the exclusive product was unsaturated amino acid derivative 6, the product of an endo transition state.With trans-2-butene, a 9:1 mixture of 18:22 was obtained, with the endo product again predominating.Intramolecular ene processes have been effected with the N-sulfonylimines derived from glyoxylates 25c and 26c.In the former case, the sole ene product was γ-lactone 30 derived from exo addition.In the latter process, a 9:1 mixture of cis-(E)-lactone 32 and cis-(Z)-lactone 33 was produced.Lactone 32 results from endo ene transition state 35 and 33 results from endo transition state 36.All attempts to effect intermolecular ene reactions of N-benzoylimine 39 failed.In trying to perform an intramolecular N-acylimine ene reaction, only Diels-Alder adduct 45 was produced from precursor 42.
